Loading...

Table of Content

    28 November 2026, Volume 30 Issue 33 Previous Issue    Next Issue
    For Selected: Toggle Thumbnails
    Relationship of hip bone mineral density and geometry with age and body mass index in women
    Gao Haiyan, Zheng Hongyin, Xiao Yi, Huang Jiyuan
    2026, 30 (33):  8577-8582.  doi: 10.12307/2026.315
    Abstract ( 36 )   PDF (1462KB) ( 3 )   Save
    BACKGROUND: Bone mineral density measured by dual-energy X-ray absorptiometry is the gold standard for diagnosing osteoporosis. The hip is an important site for osteoporosis and fractures. Bone mineral density can only reflect 70% of bone strength. Hip geometric mechanical parameters also have an important impact on hip fractures.
    OBJECTIVE: To observe the changes in bone mineral density and geometry of the proximal femur of female subjects and their value in predicting fracture risk through a large sample of female data in Chengdu, and to provide a reference for the prevention and treatment of osteoporosis and hip fractures. 
    METHODS: Bone mineral densities of 37 682 women aged 20 to 104.3 years were measured using Prodigy Advance dual-energy X-ray absorptiometry (GE LUNAR, USA). Measurement sites included the left femoral neck, greater trochanter, Wards area, femoral shaft, and total hip. The hip structure analysis software of the dual-energy X-ray absorptiometry was used to measure the geometric structure parameters of the proximal femur, including hip axis length, cross-sectional moment of inertia, femur strength index, neck-shaft angle, and cross-sectional area, to explore the relationship between age, body mass index and proximal femoral bone mineral density and geometry.  
    RESULTS AND CONCLUSION: (1) The bone mineral density of the femoral neck, greater trochanter, and total hip in women peaked at ages 30 to 39 and gradually decreased with increasing age. Hip axis length, cross-sectional moment of inertia, cross-sectional area, and femur strength index peaked at ages 30 to 39 and gradually decreased with age. (2) With increasing body mass index, bone mineral density at hip skeletal sites gradually increased, and the detection rate of osteoporosis gradually decreased. (3) With increasing body mass index, hip axis length, cross-sectional moment of inertia, and cross-sectional area of the femoral neck gradually increased (P < 0.001), and the femur strength index gradually decreased (P < 0.001). (4) Hip bone mineral density showed a positive correlation with height, body mass, and body mass index (r=0.095-0.425) and a negative correlation with age (r=-0.445 to -0.623). The hip axis length, cross-sectional moment of inertia, and cross-sectional area were positively correlated with height, body mass, body mass index, and hip bone mineral density (r=0.059-0.444), and negatively correlated with age (r=-0.055 to -0.555). (5) This data provided reference values for hip bone mineral density and geometric parameters in the Chengdu region. There was a loss of bone mineral density and changes geometry in women with increasing age, which become more pronounced after age 50. Women with low body mass index should be particularly cautious regarding the prevention of osteoporosis and fracture risk.
    Figures and Tables | References | Related Articles | Metrics
    Jiawei Yanghe Decoction-containing serum attenuates hydrogen peroxide-induced oxidative damage in osteoblasts
    Wu Fan, Yang Wenlong, Liu Jiangyuan, Xia Hanting, Zeng Zhikui, Yang Fengyun
    2026, 30 (33):  8583-8590.  doi: 10.12307/2026.476
    Abstract ( 29 )   PDF (2342KB) ( 6 )   Save
    BACKGROUND: Activation of nuclear factor erythroid 2-related factor 2 may be an effective strategy for antioxidant stress in osteoblasts and prevention of osteoporosis.
    OBJECTIVE: To investigate the protective effect and mechanism of Jiawei Yanghe Decoction-containing serum on hydrogen peroxide-induced osteoblast injury. 
    METHODS: The mouse osteoblast cell line MC3T3-E1 was divided into five groups: control group, model group, and low-, medium-, and high-dose Jiawei Yanghe Decoction-containing serum groups. Cells in the control group were routinely cultured. Cells in the model group were treated with hydrogen peroxide to establish an oxidative stress injury model of osteoblasts. Cells in the low-, medium-, and high-dose Jiawei Yanghe Decoction-containing serum groups were treated with final volume fractions of 5%, 10%, and 15% Jiawei Yanghe Decoction-containing serum for 24 hours based on the model group. Cell status, osteogenic function, oxidative stress level, inflammatory response, and protein expression related to the nuclear factor erythroid 2-related factor 2/heme oxygenase 1 signaling pathway were detected.
    RESULTS AND CONCLUSION: Compared with the control group, the model group showed significantly decreased cell viability, alkaline phosphatase activity, osteogenic mineralization capacity, antioxidant enzyme activities, and protein expression levels of nuclear factor erythroid 2-related factor 2 and heme oxygenase 1, and significantly increased apoptosis rate, reactive oxygen species levels, and levels of the inflammatory factors interleukin-6 and interleukin-1β (P < 0.05). Compared with the model group, the Jiawei Yanghe Decoction-containing serum groups showed varying degrees of improvement in the above indicators (P < 0.05). These findings indicate that Jiawei Yanghe Decoction-containing serum can restore the viability and bone formation function of MC3T3-E1 cells and alleviate oxidative stress injury by activating the nuclear factor erythroid 2-related factor 2/heme oxygenase 1 antioxidant signaling pathway.
    Figures and Tables | References | Related Articles | Metrics
    Mechanism by which curcumin promotes osteogenic differentiation in the treatment of osteoporosis
    Yan Xiaolong, Zhao Canbin, Shao Jiang, Sun Hongzhang, Guan Donghui, Qin Ying, Li Xiaoyang, Chen Dongfeng
    2026, 30 (33):  8591-8606.  doi: 10.12307/2026.477
    Abstract ( 27 )   PDF (43519KB) ( 5 )   Save
    BACKGROUND: The diseased osteogenic differentiation function of bone marrow mesenchymal stem cells is a key pathological link in the occurrence and development of osteoporosis. Curcumin can promote osteogenic differentiation and treat osteoporosis by regulating the phosphatidylinositol 3-kinase/protein kinase B signaling pathway, but the specific mechanism of action remains unclear.
    OBJECTIVE: To investigate the mechanism by which curcumin regulates the phosphatidylinositol 3-kinase/protein kinase B signaling pathway to promote osteogenic differentiation for the treatment of osteoporosis. 
    METHODS: Network pharmacology was used to screen the drug action targets of curcumin and target genes related to osteogenic differentiation and osteoporosis. The intersection targets of the three were used to construct a protein-protein interaction network diagram and perform Gene Ontology and Kyoto Encyclopedia of Genes and Genomes enrichment analyses and molecular docking. Bioinformatics was used to screen potential signature genes in the protein-protein interaction network and construct a clinical prediction model. Single-cell transcriptomics technology was used to analyze the expression patterns of signature genes in osteoblast lineage subpopulations. Finally, cell and animal experiments were conducted for verification.
    RESULTS AND CONCLUSION: (1) A total of 366 drug targets of curcumin were screened, and 134 intersection targets were identified among curcumin, osteogenic differentiation, and osteoporosis. (2) Kyoto Encyclopedia of Genes and Genomes enrichment analysis showed that the intersection targets were involved in the phosphatidylinositol 3-kinase/protein kinase B signaling pathway. (3) Molecular docking showed that the main active components of curcumin could be well docked with the targets related to the phosphatidylinositol 3-kinase/protein kinase B signaling pathway. (4) Osteoporosis-related gene sets were downloaded from the Gene Expression Omnibus database. The 134 target genes in the protein-protein interaction network were screened by 113 combinations of machine learning algorithms to obtain 14 potential signature genes, including target genes in the phosphatidylinositol 3-kinase/protein kinase B signaling pathway: PIK3R1, PIK3CG, GSK3β, and AKT1. These 14 genes may play important roles in curcumin promoting osteogenic differentiation for the treatment of osteoporosis. (5) Single-cell transcriptomics analysis showed that there was a cell subpopulation with high GSK3β expression in the osteoblast lineage of osteoporosis patients, and this cell subpopulation might be closely related to the occurrence and development of osteoporosis. (6) Pseudotime analysis found that during the development of osteoporosis, the expression level of GSK3β gradually increased, while the expression levels of PIK3R1, PIK3CG, and AKT1 gradually decreased. (7) Cell experiments showed that after GSK3β knockout, the osteogenic differentiation of mouse MC3T3-E1 subclone 14 was promoted, as evidenced by deeper staining in alkaline phosphatase staining and Alizarin Red S staining, and significantly increased alkaline phosphatase activity and calcium deposition (P < 0.05). The mRNA and protein expression levels of β-catenin were significantly increased (P < 0.05). Cell counting kit-8 and EdU results showed that 5 and 10 μmol/L curcumin had no obvious toxicity and could significantly promote the proliferation of MC3T3-E1 subclone 14 cells. In addition, intervention with 5 and 10 μmol/L curcumin significantly promoted the osteogenic differentiation of MC3T3-E1 subclone 14. (8) Animal experiments showed that curcumin improved osteoporosis in the femoral tissue of ovariectomized rats by increasing the number of trabecular bones and ameliorating the disorder of trabecular bone arrangement. After curcumin intervention, the expression and phosphorylation levels of phosphatidylinositol 3-kinase and protein kinase B1 in the distal femoral bone tissue of osteoporotic rats were significantly increased (P < 0.05), and the phosphorylation level of GSK3β was significantly decreased (P < 0.05). In addition, the expression levels of c-MYC, Cyclin D1, bone morphogenetic protein 2, osteocalcin, osteopontin, and Osterix were significantly increased (P < 0.05). In conclusion, the increased expression of GSK3β in the phosphatidylinositol 3-kinase/protein kinase B signaling pathway may be a key factor leading to the decline of osteogenic differentiation function and the occurrence and development of osteoporosis. Curcumin treats osteoporosis by activating the phosphatidylinositol 3-kinase/protein kinase B signaling pathway to promote osteogenic differentiation.
    Figures and Tables | References | Related Articles | Metrics
    Regulatory role of mediating plasma protein alpha-2-HS glycoprotein in celiac disease and its predictive efficacy analysis for osteoporosis
    Duan Yudong, Zhao Piqian, Guo Qianping, Xie Jile
    2026, 30 (33):  8607-8617.  doi: 10.12307/2026.394
    Abstract ( 24 )   PDF (20283KB) ( 4 )   Save
    BACKGROUND: Recent studies have suggested an association between celiac disease and osteoporosis. However, the causal nature of this association has not been fully established. More evidence is required to enhance the prevention and treatment of osteoporosis.
    OBJECTIVE: To investigate the causal relationship between celiac disease and osteoporosis and to screen plasma proteins that may mediate this relationship to reveal the underlying mechanisms through a combination of cross-sectional analysis and Mendelian randomization.
    METHODS: A multi-stage analytical approach was used to analyze the association between celiac disease and osteoporosis and its underlying mechanisms. Initially, logistic regression analysis was used to assess the risk of osteoporosis in patients with celiac disease. Subsequently, a two-sample Mendelian randomization analysis was applied to delve into the causal relationship between celiac disease and osteoporosis, leveraging data from two major databases: IEU OpenGWAS and Finngen R10. In terms of data sources, the study primarily relied on two authoritative databases. The first, the IEU OpenGWAS database, established by the University of Exeter, UK, aggregates a variety of genome-wide association study data, providing open resource support for genetic research. The celiac disease dataset used (GCST90014442) comprised 2 364 cases and 324 074 controls. The second, the Finngen R10 database, constructed by the Finnish Biobank Network, specializes in providing health data support for the Finnish population. For this study, the osteoporosis dataset included 8 017 patients and 391,037 controls. As this study uses publicly available aggregated statistical databases, it is exempt from ethical approval. To further elucidate the potential mechanisms, the study conducted colocalization analysis using the deCODE and UKBPPP databases to screen for possible mediating plasma proteins. Gene expression analysis was performed to explore the expression trends of these proteins in patients with celiac disease, and the diagnostic value was assessed using receiver operating characteristic curves.
    RESULTS AND CONCLUSION: (1) Logistic regression analysis showed that the risk of osteoporosis was significantly increased in patients with celiac disease compared with those without celiac disease (OR=56.000, P=0.008). (2) Mendelian randomization analysis further indicated that there was a causal effect between celiac disease and osteoporosis (OR=2.363, P < 0.01). (3) Colocalization analysis showed that alpha-2-HS glycoprotein (AHSG) is a mediating factor (PPH3+PPH4=0.862, PPH4=0.793). The results of gene expression detection showed that the expression level of AHSG was significantly increased in patients with celiac disease, and was significantly negatively correlated with bone mineral density (r=-0.805, P < 0.05). (4) Receiver operating characteristic curve analysis showed that AHSG had a certain diagnostic efficiency, and the area under the curve (AUC) was 0.667, especially when combined with other biomarkers, the diagnostic efficiency was further improved (AUC=0.706). This study reveals a possible mechanism for the increased risk of osteoporosis in patients with celiac disease and suggests AHSG as a potential key mediator that may play an important role in the early diagnosis and risk assessment of celiac disease-associated osteoporosis. These findings provide new biomarkers and potential intervention targets for the prevention and treatment of osteoporosis in patients with celiac disease, and provide an important reference for clinical practice.

    Figures and Tables | References | Related Articles | Metrics
    Epimedium in the treatment of alcohol-induced osteonecrosis of the femoral head: action mechanism through network pharmacology and molecular dynamics simulation
    Lai Yu, Chen Yueping, Zhang Xiaoyun, Zhuo Yinghong
    2026, 30 (33):  8618-8630.  doi: 10.12307/2026.285
    Abstract ( 29 )   PDF (5722KB) ( 6 )   Save
    BACKGROUND: Currently, the treatment, early intervention, and delaying the progression of alcoholic osteonecrosis of the femoral head are not satisfactory. Preliminary studies have found that the active components of Epimedium have the effects on maintaining bone homeostasis and promoting fracture healing.
    OBJECTIVE: To investigate the potential mechanism of Epimedium in the treatment of alcohol-induced osteonecrosis of the femoral head by integrated approaches, including network pharmacology, molecular docking technology, molecular dynamics simulations, and in vitro cell experiments.
    METHODS: After identifying the main constituents of Epimedium via ultra-high performance liquid chromatography coupled with quadrupole-exactive Orbitrap high-resolution mass spectrometry, potential active compounds were screened firstly based on the TCMSP database, and their corresponding targets were retrieved using the TCMSP and Uniprot databases. Subsequently, disease-related targets associated with alcohol-induced osteonecrosis of the femoral head were extracted from multiple disease databases. An intersection analysis was conducted between drug targets with disease targets, and the results were imported into the STRING platform to construct a protein-protein interaction network. The network topology was analyzed using Cytoscape software to identify key targets. An “active ingredient–target” interaction network was then constructed to determine core active compounds. On this basis, Gene Ontology annotation and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analyses were performed on the key targets. Molecular docking was conducted between core compounds and key targets. The most stable compound-target complex, based on binding affinity, was further subjected to molecular dynamics simulations to validate its structural stability and interaction mechanisms. Finally, cell counting kit-8 and western blot assays were performed on MC3T3-E1 cells in the blank group, model group and drug group.
    RESULTS AND CONCLUSION: (1) A total of 88 active compounds were identified from Epimedium extract. Fifty overlapping targets were obtained by intersecting the compound-related and disease-related targets, from which five core compounds and six key targets were identified. Gene Ontology enrichment involved 1 321 terms, and Kyoto Encyclopedia of Genes and Genomes analysis revealed 79 signaling pathways. (2) Molecular docking showed strong binding affinities between the core compounds and key targets, with icariin exhibiting the lowest binding energy to serine/threonine protein kinase 1. Subsequent molecular dynamics simulations demonstrated good structural stability between icariin and serine/threonine protein kinase 1. (3) In vitro experiments confirmed that alcohol exerted significant cytotoxic effects on MC3T3-E1 osteoblasts, impairing their osteogenic differentiation, while icariin effectively alleviated these detrimental effects, potentially through activation of the serine/threonine protein kinase signaling pathway. A systematic analysis of the chemical constituents of Epimedium suggests that it may exert therapeutic effects against alcohol-induced osteonecrosis of the femoral head via multi-component synergy, multi-target regulation, and multi-pathway modulation. These mechanisms may involve immune regulation, anti-inflammatory activity, mitigation of oxidative stress, promotion of angiogenesis, and maintenance of bone metabolic homeostasis, ultimately contributing to the improvement of alcohol-induced osteonecrosis of the femoral head pathological progression.
    Figures and Tables | References | Related Articles | Metrics
    Promoting fracture healing in rats: mechanism of the compound Miao medicine Jiuxian Luohan Jiegu Decoction
    Deng Lincheng, Yu Liang, Wan Haoran, Ning Zhong, Xie Zhengxing, Zheng Jiabao, Tang Lianghua
    2026, 30 (33):  8631-8638.  doi: 10.12307/2026.492
    Abstract ( 23 )   PDF (11690KB) ( 4 )   Save
    BACKGROUND: Previous in vitro experiments have shown that the compound Miao medicine Jiuxian Luohan Jiegu Decoction may activate autophagy by regulating the phosphatidylinositol 3-kinase/protein kinase B/mammalian target of rapamycin signaling pathway, thereby promoting the proliferation and differentiation of osteoblasts.
    OBJECTIVE: To investigate the effect of Jiuxian Luohan Jiegu Decoction on the phosphatidylinositol 3-kinase/protein kinase B/mammalian target of rapamycin signaling pathway in rats during fracture healing.
    METHODS: Thirty Sprague-Dawley rats were used to establish a femoral fracture model in the right hind limb. After modeling, the rats were randomly divided into five intervention groups, with six rats in each group: the model group received intragastric administration of normal saline; the low-, medium-, and high-dose Jiuxian Luohan Jiegu Decoction groups received intragastric administration of 2.95, 5.9, and 11.8 g/(kg·d) of the decoction, respectively; and the Shangke Jiegu Tablet group received intragastric administration of 0.24 g/(kg·d) of Shangke Jiegu Tablets. All administrations were given twice daily for 28 consecutive days. After 2 and 4 weeks of administration, fracture healing was assessed by X-ray. After 4 weeks of administration, fracture healing was evaluated by Micro-CT; mRNA expression of phosphatidylinositol 3-kinase, protein kinase B, mammalian target of rapamycin, microtubule-associated protein 1 light chain 3II, and P62 in the fracture callus was detected by q-PCR; protein expression of phosphorylated phosphatidylinositol 3-kinase, phosphatidylinositol 3-kinase, phosphorylated protein kinase B, protein kinase B, phosphorylated mammalian target of rapamycin, mammalian target of rapamycin, microtubule-associated protein 1 light chain 3II, and P62 in the fracture callus was detected by western blot; and fracture healing and callus formation were observed by hematoxylin-eosin staining.
    RESULTS AND CONCLUSION: After 2 and 4 weeks of administration, X-ray examination showed that fracture healing and callus formation in the high-dose Jiuxian Luohan Jiegu Decoction group were superior to those in the other four groups. Micro-CT analysis showed that fracture healing in the high-dose Jiuxian Luohan Jiegu Decoction group was better than that in the other four groups, characterized by callus circumferentially surrounding the fracture ends, denser and more regularly arranged trabecular bone structure, and blurred fracture lines. Compared with the model group, the mRNA expression of phosphatidylinositol 3-kinase, protein kinase B, mammalian target of rapamycin, and P62 was decreased in the other four groups, while microtubule-associated protein 1 light chain 3II mRNA expression was increased; protein expression of phosphorylated phosphatidylinositol 3-kinase, phosphorylated protein kinase B, phosphorylated mammalian target of rapamycin, and P62 was decreased, while microtubule-associated protein 1 light chain 3II protein expression was increased. The most significant changes were observed in the high-dose Jiuxian Luohan Jiegu Decoction group. Hematoxylin-eosin staining showed that the number of osteoblasts, the amount of new bone tissue, and the quality of bone formation at the fracture site in the high-dose Jiuxian Luohan Jiegu Decoction group were superior to those in the other four groups. To conclude, these findings indicate that Jiuxian Luohan Jiegu Decoction may enhance the level of autophagy in osteoblasts by regulating the phosphatidylinositol 3-kinase/protein kinase B/mammalian target of rapamycin signaling pathway, thereby accelerating the process of fracture healing in rats.
    Figures and Tables | References | Related Articles | Metrics
    Acupoint-pressing and knee-regulating therapy improves the morphological structure and inflammatory level of articular cartilage in rats with knee osteoarthritis
    Xu Hui, Wang Zhen, Yang Fangli, Li Mengmeng, Shi Mingwei, Wang Xiaoyan, Shi Hongxia, Yang Tao, Diao Jieyao, Zhou Yunfeng
    2026, 30 (33):  8639-8644.  doi: 10.12307/2026.429
    Abstract ( 30 )   PDF (1749KB) ( 1 )   Save
    BACKGROUND: Preliminary studies have found that massage therapy can alleviate damage to cartilage tissue, reduce inflammation, and inhibit chondrocyte apoptosis in knee osteoarthritis.
    OBJECTIVE: To observe the effects of acupoint-pressing and knee-regulating therapy on the morphological structure of articular cartilage and inflammatory levels in rats with knee osteoarthritis. 
    METHODS: Thirty-two Sprague-Dawley rats were randomly divided into a blank group, a model group, a medication group, and a massage group, with eight rats in each group. Rats in the model, medication, and massage groups were subjected to intra-articular injection of a mixture of papain and L-cysteine into the right knee joint (on days 1, 4, and 7) to establish a rat model of knee osteoarthritis. After modeling, the massage group received acupoint-pressing and knee-regulating therapy, while the medication group was treated with celecoxib via gavage. The remaining two groups received intraperitoneal injection of saline solution, once daily, for continuous 2 weeks. The diameter of the right knee joint, range of motion, and the paw withdrawal threshold were recorded. ELISA was used to detect serum levels of interleukin-6, interleukin-18, tumor necrosis factor-α, and matrix metallopeptidase 1. Hematoxylin-eosin staining was used to observe the degree of cartilage degeneration.
    RESULTS AND CONCLUSION: (1) The knee joint diameter in the model group was greater than that in the blank group (P < 0.05), while knee joint range of motion and paw withdrawal threshold were lower than those in the blank group (P < 0.05). In the massage and medication groups, the knee joint diameter was smaller than that in the model group (P < 0.05), while knee joint range of motion and paw withdrawal threshold were higher than those in the model group (P < 0.05). (2) Compared with the blank group, there were elevated levels of interleukin-6, interleukin-18, tumor necrosis factor-α, and matrix metalloproteinase-1 in the model group (P < 0.05). Compared with the model group, the levels of interleukin-6, interleukin-18, tumor necrosis factor-α, and matrix metalloproteinase-1 were reduced in both the massage and medication groups (P < 0.05). (3) Hematoxylin-eosin staining revealed that the articular cartilage surface in the blank group was smooth, with normal chondrocyte morphology and regular arrangement. However, the articular cartilage surface in the model group appeared irregular, showing chondrocyte necrosis and dissolution in local areas, unclear tidal line structure, and no significant inflammatory cell infiltration. The massage group exhibited relatively smooth articular cartilage surface, increased chondrocyte counts, visible cell clusters, unclear tide line structure, and no significant inflammatory cell infiltration. The medication group also showed relatively smooth articular cartilage surface, increased chondrocyte counts, visible cell clusters, unclear tide line structure, and no significant inflammatory cell infiltration. The Markin score in the model group was higher than that in the other three groups (P < 0.05). To conclude, acupoint-pressing and knee-regulating therapy can effectively improve the articular cartilage ultrastructure and reduce inflammatory reactions in rats with knee osteoarthritis.
    Figures and Tables | References | Related Articles | Metrics
    Application of isobaric tags for relative and absolute quantification for identifying serum biomarkers in patients with cervical spinal cord syndrome
    Xu Wei, Cui Zizheng, Hu Minggao, Liu Chunzhi, Li Zhifei, Zhong Yuanming, Yang Hanli
    2026, 30 (33):  8645-8652.  doi: 10.12307/2026.490
    Abstract ( 23 )   PDF (2627KB) ( 1 )   Save
    BACKGROUND: Cervical spondylotic myelopathy is the most severe type of cervical spondylosis, yet its specific serum biomarkers that can distinguish it from healthy individuals remain unclear.  
    OBJECTIVE: To analyze the differential expression of serum proteins between patients with cervical spondylotic myelopathy of Qi deficiency and blood stasis type and healthy individuals using isobaric tags for relative and absolute quantification (iTRAQ), and to screen and identify potential serum biomarkers for this condition.  
    METHODS: Serum samples were collected from 13 patients with cervical spondylotic myelopathy of Qi deficiency and blood stasis type and 8 healthy individuals. Proteomic analysis was performed using iTRAQ with liquid chromatography-tandem mass spectrometry. Functional annotation and pathway enrichment analysis of differentially expressed proteins were conducted using bioinformatics methods to reveal their potential biological significance and involved signaling pathways.  
    RESULTS AND CONCLUSION: (1) Mass spectrometry analysis identified a total of 78 differentially expressed proteins (P < 0.05). Compared with healthy individuals, 12 differential proteins, including vasodilator-stimulated phosphoprotein, multiple epidermal growth factor-like domains protein 9, complement factor H-related protein 3, and mitogenin A, were significantly upregulated, while 66 differential proteins, including transferrin, cartilage intermediate layer protein 2, fibronectin, and fibrinogen beta chain, were significantly downregulated. (2) These differentially expressed proteins were primarily involved in various biological processes such as nucleic acid transport and protein activation cascade, and exhibited molecular functions including protein kinase B binding, immunoglobulin receptor binding, and translation elongation factor activity. They were associated with seven signaling pathways, including mineral absorption, oxidative phosphorylation, and platelet activation. (3) Among the differentially expressed proteins in the serum of patients with cervical spondylotic myelopathy of Qi deficiency and blood stasis type compared with healthy individuals, IGLC2, IGLC7, IGLL5, IGLV2-8, IGLV3-25, and IGKV3D-11 showed extensive interactions with other proteins in the functional network. (4) Validation of the differentially expressed protein IGLC2 using western blot yielded results consistent with the proteomics analysis. To conclude, these findings indicate that iTRAQ combined with liquid chromatography-tandem mass spectrometry successfully screened differentially expressed proteins between patients with cervical spondylotic myelopathy of Qi deficiency and blood stasis type and healthy individuals, and preliminarily suggest that seven proteins, including IGLC2, IGLL5, and IGLV3-25, may serve as specific serum biomarkers for this population.  

    Figures and Tables | References | Related Articles | Metrics
    Gait kinematics and electromyography features in patients with Lenke type 5 adolescent idiopathic scoliosis
    Liu Jiaqi, Zhou Ding, Jiang Yawen, Ni Simin, Li Ning, Zhu Zhitao, Liu Yue, Chen Qinghua, Mei Zhao, Yao Yifei, Wang Jinwu
    2026, 30 (33):  8653-8661.  doi: 10.12307/2026.494
    Abstract ( 53 )   PDF (1535KB) ( 3 )   Save
    BACKGROUND: Static imaging parameters in adolescents with Lenke type 5 adolescent idiopathic scoliosis suggest that lumbar deformity may alter relative pelvic alignment. However, quantitative evidence on segmental kinematics of the trunk–pelvis–lower limb complex during walking and on compensatory control by core musculature remains limited.
    OBJECTIVE: To evaluate the kinematic characteristics during walking in patients with Lenke type 5 adolescent idiopathic scoliosis.
    METHODS: Twenty patients with Lenke type 5 adolescent idiopathic scoliosis (Cobb angle 20°-36°, age 10-15 years) and 20 age-matched healthy adolescents were enrolled. Spatiotemporal gait parameters, kinematic parameters, and electromyographic differences during walking at a constant speed were simultaneously collected and analyzed between the two groups. 
    RESULTS AND CONCLUSION: (1) Gait parameters: Step width, the percentage of convex-side double-support phase, and percentage of concave-side swing phase over the gait cycle were significantly greater in the Lenke type 5 adolescent idiopathic scoliosis group compared with the healthy control group (P < 0.05). The percentages of convex-side stance phase and double-support phase were significantly greater than those on the concave side (P < 0.05), while convex-side step length and swing phase percentage were significantly smaller than those on the concave side (P < 0.05). (2) Kinematic parameters: The range of motion in the coronal plane for the lumbar spine and spine-pelvis relative movement was significantly greater in the Lenke type 5 adolescent idiopathic scoliosis group than the healthy control group (P < 0.05). Convex-side peak hip flexion angle and peak ankle plantarflexion angle were significantly smaller than those in the healthy control group, and these angles were greater on the concave side than on the convex side (P < 0.05). (3) Surface electromyography results: Electromyographic signals of the bilateral erector spinae, bilateral gluteus medius, convex-side external oblique, and convex-side gluteus maximus were significantly greater in the Lenke type 5 adolescent idiopathic scoliosis group compared with the healthy control group (P < 0.05). Signals from the convex-side erector spinae and external oblique were significantly greater than those on the concave side, while convex-side gluteus medius signals were significantly smaller than those on the concave side (P < 0.05). (4) Overall, these findings suggest that during walking, in patients with Lenke type 5 adolescent idiopathic scoliosis, the convex-side lower limb serves as the primary support. The concave-side lower limb compensates during the swing phase by increasing range of motion at the hip and ankle joints. Increased coronal-plane trunk mobility helps maintain gait stability. Convex-side erector spinae–external oblique co-activation and concave-side gluteus medius recruitment indicate side-specific neuromuscular compensation to maintain balance. This indicates that adolescents with Lenke Type 5 idiopathic scoliosis maintain body balance and stability through bilateral imbalanced muscle control strategies based on joint mobility.
    Figures and Tables | References | Related Articles | Metrics
    Long non-coding RNA-TNFRSF13C improves periodontal pathomorphology in rat models of periodontitis via target regulation
    Zhou Dayu, Dong Na, Geng Ganshu, Zhang Xue
    2026, 30 (33):  8662-8668.  doi: 10.12307/2026.491
    Abstract ( 25 )   PDF (1760KB) ( 1 )   Save
    BACKGROUND: Studies have found that long non-coding RNAs (lncRNAs) play a key regulatory role in the pathogenesis of periodontitis. The signaling axis composed of hypoxia-inducible factor 1α (HIF1α) and peroxisome proliferator-activated receptor γ (PPARγ) is of great significance in the regulation of inflammation, and its association with lncRNA-TNFRSF13C has become a key entry point for research in this field.  
    OBJECTIVE: To investigate the mechanism of lncRNA-TNFRSF13C targeting the HIF1α-PPARγ signaling axis in periodontitis. 
    METHODS: (1) Periodontal ligament cells were divided into periodontal ligament cell group, lipopolysaccharide+periodontal ligament cell group, lipopolysaccharide+periodontal ligament cell+lncRNA-TNFRSF13C-NC group, lipopolysaccharide+periodontal ligament cell+lncRNA-TNFRSF13C sno group, and lipopolysaccharide+periodontal ligament cell+lncRNA-TNFRSF13C siRNA group. RT-PCR was used to detect the expression of lncRNA-TNFRSF13C, HIF1α, and PPARγ. MTT assay was used to detect cell proliferation, DAPI staining was used to detect cell apoptosis, and western blot was used to detect HIF1α and PPARγ protein expression. Dual-luciferase reporter assay was performed by designing and cloning the full-length sequence of lncRNA-TNFRSF13C and its mutant to confirm the interaction between lncRNA-TNFRSF13C and the HIF1α-PPARγ signaling axis. (2) Thirty SPF-grade male Sprague-Dawley rats were randomly divided into normal group, model group, and lncRNA-TNFRSF13C siRNA group, with 10 rats in each group. Periodontitis models were established in the latter two groups by periodontal injection of Porphyromonas gingivalis. After successful modeling, the lncRNA-TNFRSF13C siRNA group was injected with 40 mg/kg lncRNA-TNFRSF13C siRNA via the tail vein. Hematoxylin-eosin staining was used to detect the pathological morphology of periodontal tissue in each group.   
    RESULTS AND CONCLUSION: (1) Compared with the periodontal ligament cell group, the expression of lncRNA-TNFRSF13C and HIF1α mRNA was increased in the lipopolysaccharide+periodontal ligament cell group (P < 0.05), while PPARγ mRNA expression was decreased (P < 0.05). Compared with the lipopolysaccharide+periodontal ligament cell group, there was no significant difference in the expression of lncRNA-TNFRSF13C, HIF1α, and PPARγ mRNA in the lncRNA-TNFRSF13C-NC group (P > 0.05); and the expression of lncRNA-TNFRSF13C and HIF1α mRNA was increased in the lncRNA-TNFRSF13C sno group (P < 0.05), while PPARγ mRNA expression was decreased (P < 0.05). Compared with the lncRNA-TNFRSF13C sno group, the expression of lncRNA-TNFRSF13C and HIF1α mRNA was decreased in the lncRNA-TNFRSF13C siRNA group (P < 0.05), while PPARγ mRNA expression was increased (P < 0.05). (2) Compared with the periodontal ligament cell group, cell proliferation was decreased and apoptosis was increased in the lipopolysaccharide+periodontal ligament cell group (P < 0.05). Compared with the lipopolysaccharide+periodontal ligament cell group, there was no significant difference in cell proliferation in the lncRNA-TNFRSF13C-NC group (P > 0.05); and cell proliferation was decreased and apoptosis was increased in the lncRNA-TNFRSF13C sno group (P < 0.05). Compared with the lncRNA-TNFRSF13C sno group, cell proliferation was increased and apoptosis was decreased in the lncRNA-TNFRSF13C siRNA group (P < 0.05). (3) Compared with the periodontal ligament cell group, HIF1α protein expression was increased and PPARγ protein expression was decreased in the lipopolysaccharide+periodontal ligament cell group (P < 0.05). Compared with the lipopolysaccharide+periodontal ligament cell group, there was no significant difference in HIF1α and PPARγ protein expression in the lncRNA-TNFRSF13C-NC group (P > 0.05); and HIF1α protein expression was increased and PPARγ protein expression was decreased in the lncRNA-TNFRSF13C sno group (P < 0.05). Compared with the lncRNA-TNFRSF13C sno group, HIF1α protein expression was decreased and PPARγ protein expression was increased in the lncRNA-TNFRSF13C siRNA group (P < 0.05). (4) Dual-luciferase reporter assay results showed that transfection with lncRNA-TNFRSF13C significantly increased the luciferase activity of HIF1α-3′-UTR-WT (P < 0.05) and decreased the luciferase activity of PPARγ-3′-UTR-WT (P < 0.05), but had no significant effect on the mutant genes (P > 0.05). (5) In the model group, the periodontal tissue of rats showed congestion, edema, and infiltration by a large number of inflammatory cells, with disorganized and ruptured periodontal ligament fibers, and epithelial hyperplasia or ulcers were observed. Compared with the model group, the pathological structure of rats was significantly improved in the lncRNA-TNFRSF13C siRNA group. To conclude, inhibition of lncRNA-TNFRSF13C can effectively regulate the activity of lipopolysaccharide-induced periodontal ligament cells and improve the pathological morphology of periodontal tissue in rats with periodontitis. Its mechanism of action may be related to the targeted regulation of the HIF1α-PPARγ signaling axis.  
    Figures and Tables | References | Related Articles | Metrics
    Effects of risedronate sodium on periodontal inflammation and osteoclasts in rats with orthodontic tooth movement
    Wang Anran, Zhang Xihong, Zhao Yijun
    2026, 30 (33):  8669-8675.  doi: 10.12307/2026.493
    Abstract ( 24 )   PDF (1633KB) ( 2 )   Save
    BACKGROUND: Studies have found that risedronate sodium can influence bone remodeling by regulating osteoclast and osteoblast activity, thereby accelerating orthodontic tooth movement. However, its mechanism of action has not been fully elucidated.
    OBJECTIVE: To investigate the effects of risedronate sodium on periodontal inflammation, osteoclasts, and the bone morphogenetic protein 2/Smad1 signaling pathway in rats with orthodontic tooth movement.
    METHODS: Thirty Sprague-Dawley rats were used to establish orthodontic tooth movement models. At 24 hours after modeling, the rats were randomly divided into model group, high-dose risedronate sodium group, and low-dose risedronate sodium group, with 10 rats in each group. Another 10 Sprague-Dawely rats were set as the control group. The high- and low-dose risedronate sodium groups received intragastric administration of 1 and 0.5 mg/kg risedronate sodium, respectively, while the model group and control group received intragastric administration of normal saline, once daily for 21 consecutive days. At 24 hours after the final administration, the orthodontic tooth movement distance was measured. Serum levels of tumor necrosis factor α, interleukin 1β, and interleukin 6 were detected by ELISA. The number of osteoclasts in periodontal tissue was detected by tartrate-resistant acid phosphatase staining. Maxillary tissue morphology was observed by hematoxylin-eosin staining. Protein expression of bone morphogenetic protein 2 and Smad1 in alveolar bone tissue was detected by western blot.
    RESULTS AND CONCLUSION: (1) Compared with the control group, the model group showed significantly increased levels of interleukin 1β, tumor necrosis factor α, and interleukin 6, and a significantly increased number of osteoclasts (P < 0.05), while protein expression of bone morphogenetic protein 2 and Smad1 was significantly decreased (P < 0.05). Compared with the model group, the low-dose risedronate sodium group showed significantly decreased levels of interleukin 1β, tumor necrosis factor α, and interleukin 6, and a significantly decreased number of osteoclasts (P < 0.05), while orthodontic tooth movement distance and protein expression of bone morphogenetic protein 2 and Smad1 were significantly increased (P < 0.05). Compared with the low-dose risedronate sodium group, the high-dose risedronate sodium group showed significantly decreased levels of interleukin 1β, tumor necrosis factor α, and interleukin 6, and a significantly decreased number of osteoclasts (P < 0.05), while orthodontic tooth movement distance and protein expression of bone morphogenetic protein 2 and Smad1 were significantly increased (P < 0.05). (2) Hematoxylin-eosin staining showed normal maxillary bone structure in the control group. In the model group, the periodontal space on the pressure side was narrowed, the periodontal ligament on the tension side was widened, cementum resorption lacunae were increased, and bone remodeling was active. In the low- and high-dose risedronate sodium groups, the pressure side space was reduced, new bone deposition on the tension side was enhanced, and bone resorption was decreased. To conclude, these findings indicate that risedronate sodium inhibits inflammatory response and osteoclast activity in the periodontal tissue induced by orthodontic force, promotes bone formation by upregulating the bone morphogenetic protein 2/Smad1 signaling pathway, and accelerates the process of orthodontic tooth movement.

    Figures and Tables | References | Related Articles | Metrics
    Bioinformatics analysis of cuproptosis in periodontitis and verification in a periodontitis rat model 
    Qin Yufeng, Feng Xiaoyun, Gao Hongli, Xiong Lin, Zhang Yuehan, Chen Helin
    2026, 30 (33):  8676-8686.  doi: 10.12307/2026.482
    Abstract ( 25 )   PDF (8232KB) ( 2 )   Save
    BACKGROUND: Through analyzing the expression of cuproptosis-related genes in periodontitis tissues, this study attempted to explore the significance of cuproptosis-related biomarkers in the diagnosis and treatment of periodontitis during the development of periodontitis. 
    OBJECTIVE: To explore the expression of cuproptosis-related genes in periodontitis and their potential mechanisms through bioinformatics analysis. 
    METHODS: Periodontitis transcriptome datasets GSE10334 and GSE156993 were obtained from the Gene Expression Omnibus (GEO) database. After eliminating batch effects, they were integrated into a meta-cohort. Hub genes were screened and identified using the Least Absolute Shrinkage and Selection Operator, Support Vector Machine-Recursive Feature Elimination, and Venn analysis. Subsequently, a comprehensive analysis of the distribution and role of these hub genes in periodontitis was performed using receiver operating characteristic curves, functional enrichment analysis, immune cell infiltration analysis, single-cell analysis (dataset GSE171213), gene-drug network analysis, nomogram model construction, and consensus clustering. Further validation was conducted in a Sprague-Dawley rat periodontitis model.

    RESULTS AND CONCLUSION: (1) Three hub cuproptosis signature genes (NOD-like receptor pyrin domain-containing protein 3, dihydrolipoamide succinyltransferase and glutamine synthetase) in periodontitis were identified using machine learning algorithms. These genes were significantly upregulated in periodontal tissues, with NOD-like receptor pyrin domain-containing protein 3 (the area under the curve=0.828) and glutamine synthetase (the area under the curve=0.830) showing good diagnostic value, suggesting their potential as diagnostic biomarkers for periodontitis. (2) Dihydrolipoamide succinyltransferase induced mitochondrial dysfunction by regulating the tricarboxylic acid cycle and lipoic acid metabolism; NOD-like receptor pyrin domain-containing protein 3 amplified inflammatory responses through inflammasome activation; and glutamine synthetase supported immune cell function by enhancing glutamine metabolism. These three genes synergistically regulated cuproptosis to drive the progression of periodontitis. (3) The expression levels of NOD-like receptor pyrin domain-containing protein 3, dihydrolipoamide succinyltransferase and glutamine synthetase were upregulated in the Sprague-Dawley rat model of periodontitis and positively correlated with the amount of alveolar bone resorption, providing in vivo evidence for the proposed mechanistic hypothesis. These findings indicate that NOD-like receptor pyrin domain-containing protein 3, dihydrolipoamide succinyltransferase and glutamine synthetase, as hub genes of cuproptosis, play important roles in the occurrence and development of periodontitis and possess potential diagnostic value.

    Figures and Tables | References | Related Articles | Metrics
    Regulatory effect of low-frequency pulsed magnetic field on body fat composition in female athletes during high-intensity upper limb resistance training
    Sun Shiqiang, Li Wenhao, Du Xinran, Bai Shi, Li Zhongshan
    2026, 30 (33):  8687-8694.  doi: 10.12307/2026.914
    Abstract ( 11 )   PDF (2051KB) ( 1 )   Save
    BACKGROUND: In recent years, low-frequency pulsed magnetic field regulation technology has garnered widespread attention for its ability to regulate cellular metabolism and mitochondrial function. Its efficacy has been demonstrated in improving skeletal muscle strength, structural morphology, and overall body fat composition. However, there is a lack of research on its regulatory effect on body fat composition during high-intensity upper limb resistance training in female athlete, and its potential mechanisms and practical outcomes are still unclear.
    OBJECTIVE: To observe the effect of low-frequency pulsed magnetic field on improving body fat composition during a high-intensity upper limb resistance training cycle in women, and to infer its potential molecular mechanisms.
    METHODS: Thirteen female athletes (aged 18–23 years) undergoing long-term systematical training were recruited and randomly divided into an experimental group (n=6) and a control group (n=7). Both groups underwent 4 weeks of high-intensity upper limb resistance training (3 times per week, 75%–90% one-repetition maximum). The experimental group received 10 minutes of low-frequency pulsed magnetic field intervention (intensity 1.5 mT, frequency 3300 Hz) after each training session, while the control group received sham intervention (device with no output). Pre- and post-intervention measurements included maximum voluntary contraction of the biceps brachii, body composition (fat-free mass, subcutaneous fat mass, and total fat mass), and exercise performance (bench press and pull-ups) to observe and analyze the regulatory effect of low-frequency pulsed magnetic field on body fat composition.
    RESULTS AND CONCLUSION: Intra-group comparisons revealed: (1) In the control group, only the left-arm biceps brachii maximum voluntary contraction showed a significant decrease, whereas in the experimental group, significant decreases were observed in the maximum voluntary contraction of the biceps brachii in both arms. (2) No significant changes were observed in fat-free mass, total fat mass, or subcutaneous fat mass in either the control group or the experimental group. (3) Bench press performance was significantly improved in both the experimental group (P=0.017) and the control group (P=0.041), while no significant changes were observed in pull-up performance in both groups. Inter-group comparisons revealed: (1) No significant differences were found between the two groups in maximum voluntary contraction of the biceps brachii, fat-free mass, or exercise performance. (2) After intervention, total fat mass (P=0.041) and subcutaneous fat mass (P=0.038) were significantly lower in the experimental group compared with the control group. These data confirmed that after 4 weeks (12 sessions) of high-intensity upper limb resistance training combined with low-frequency pulsed electromagnetic field intervention, both groups showed consistent trends in maximal strength and exercise performance, while the experimental group receiving the low-frequency pulsed electromagnetic field intervention exhibited significantly superior body fat composition (total fat mass and subcutaneous fat mass) compared with the control group. Therefore, as a non-metabolic physical adjunct modality, low-frequency pulsed magnetic field may promote body fat optimization during high-intensity resistance training in female athletes without affecting strength adaptation, and possesses potential advantages in mitigating concurrent training interference effects. Overall, this study preliminarily validates the feasibility of low-frequency pulsed magnetic field in improving body fat composition during high-intensity upper limb resistance training in women, providing a scientific basis for promoting safe, low-burden body composition regulation methods among female training populations in the future.
    Figures and Tables | References | Related Articles | Metrics
    Mechanisms by which polygonatum sibiricum polysaccharides ameliorate skeletal muscle senescence in a mouse model of sarcopenia
    Zhao Liang, Zhao Rongcan, Shi Long, Chen Gang, Yuan Chaonong, Deng Zhiyuan, Peng Yi, Lei Jie, Wen Feng, Li Yang
    2026, 30 (33):  8695-8702.  doi: 10.12307/2026.487
    Abstract ( 25 )   PDF (1788KB) ( 1 )   Save
    BACKGROUND: The phosphatidylinositol 3-kinase/serine protein kinase B signaling pathway is closely related to the regulation of cell proliferation, growth, and metabolism. As a traditional Chinese medicine for invigorating the spleen and tonifying the kidney, the active ingredient of Polygonatum sibiricum, Polygonatum sibiricum polysaccharide, has the potential to improve skeletal muscle aging and treat sarcopenia, but the specific molecular mechanism remains unclear.
    OBJECTIVE: To investigate the protective effect and mechanism of Polygonatum sibiricum polysaccharide on skeletal muscle aging in sarcopenia mice by regulating the phosphatidylinositol 3-kinase/serine protein kinase B signaling pathway.
    METHODS: Forty C57BL/6 male mice were randomly divided into control group, model group, and low-, medium-, and high-dose Polygonatum sibiricum polysaccharide groups. The latter four groups received intraperitoneal injections of 400 mg/kg D-galactose every other day for 12 weeks to establish a sarcopenia model. Modeling and drug administration were performed simultaneously. The low-, medium-, and high-dose Polygonatum sibiricum polysaccharide groups were administered 30, 60, and 120 mg/kg by gavage, respectively, while the control and model groups received an equal volume of normal saline by gavage every other day for 12 consecutive weeks. Physiological functions were assessed by body mass, grip strength, and endurance. Western blot and real-time quantitative PCR were used to detect the expression of phosphatidylinositol 3-kinase/protein kinase B pathway proteins (phosphorylated phosphatidylinositol 3-kinase, phosphatidylinositol 3-kinase, phosphorylated serine protein kinase B, and protein kinase B) and aging-related p21 and p53 proteins and mRNAs in skeletal muscle. Immunofluorescence staining was used to detect the expression of aging-related protein p21. Hematoxylin-eosin staining and Sirius red staining were used to observe myofiber pathology and fibrosis degree.
    RESULTS AND CONCLUSION: (1) After 12 weeks of intervention, compared with the control group, body mass, grip strength, and endurance were significantly reduced in the model group (P < 0.01). Compared with the model group, only grip strength showed an upward trend in the low-dose Polygonatum sibiricum polysaccharide group (P < 0.05), while body mass, grip strength, and endurance were all increased in the medium- and high-dose Polygonatum sibiricum polysaccharide groups (P < 0.05 or P < 0.01). (2) Western blot results showed that compared with the control group, the expression levels of phosphorylated phosphatidylinositol 3-kinase/phosphatidylinositol 3-kinase and phosphorylated protein kinase B/protein kinase B proteins were decreased in the model group (P < 0.01). Compared with the model group, there were no significant changes in the low-dose Polygonatum sibiricum polysaccharide group, but these indexes were significantly increased in the medium- and high-dose Polygonatum sibiricum polysaccharide groups (P < 0.01). Compared with the control group, p21 and p53 protein expression was increased in the model group (P < 0.01). Compared with the model group, there was no significant change in p21 and p53 protein expression in the low-dose Polygonatum sibiricum polysaccharide group, but p21 and p53 protein expression was significantly decreased in the medium- and high-dose Polygonatum sibiricum polysaccharide groups (P < 0.01). (3) Real-time quantitative PCR results showed that compared with the control group, p21 and p53 mRNA expression was increased in the model group (P < 0.01). Compared with the model group, there was no significant change in p21 and p53 mRNA expression in the low-dose Polygonatum sibiricum polysaccharide group, but p21 and p53 mRNA expression was significantly decreased in the medium- and high-dose Polygonatum sibiricum polysaccharide groups (P < 0.05 or P < 0.01). (4) Immunofluorescence staining showed that compared with the control group, the mean fluorescence intensity was significantly increased in the model group (P < 0.01). Compared with the model group, the mean fluorescence intensity of p21 was significantly decreased in all Polygonatum sibiricum polysaccharide groups (P < 0.01). (5) Hematoxylin-eosin staining showed that compared with the model group, all doses of Polygonatum sibiricum polysaccharide improved the degree of skeletal muscle cell atrophy and degeneration. (6) Sirius red staining showed that compared with the model group, low-, medium-, and high-dose Polygonatum sibiricum polysaccharide interventions improved skeletal muscle fibrosis. To conclude, these findings indicate that Polygonatum sibiricum polysaccharides can improve the physiological function, pathological changes, and fibrosis degree of skeletal muscle aging in sarcopenia model mice, and its mechanism is related to the regulation of the phosphatidylinositol 3-kinase/protein kinase B signaling pathway.
    Figures and Tables | References | Related Articles | Metrics
    Relationship between diaphragmatic ultrasound parameters and core stability tests in young adults
    Ma Tian, Luo Yu
    2026, 30 (33):  8703-8711.  doi: 10.12307/2026.480
    Abstract ( 27 )   PDF (5821KB) ( 1 )   Save
    BACKGROUND: Core stability tests are regarded as an important indicator for evaluating the function of core muscles. They not only reflect the functional state of the human trunk but also have a close connection with the structure and function of the diaphragm. 
    OBJECTIVE: To investigate the relationship between diaphragmatic ultrasound parameters and core stability in young adults. 
    METHODS: From January to April 2024, diaphragmatic ultrasound parameters and core stability indicators were assessed in 163 young participants. Subjects were categorized into a sedentary group (n=83) and an exercise group (n=80). Intergroup differences were evaluated using independent samples t-tests or Mann–Whitney U tests. Simple correlation and canonical correlation analyses were conducted to examine the relationships between diaphragmatic ultrasound measures and core stability parameters. 
    RESULTS AND CONCLUSION: (1) The sedentary group showed lower values than the exercise group in diaphragmatic thickness at the end of quiet inspiration, diaphragmatic thickness at the end of quiet expiration, diaphragmatic thickness at the end of deep inspiration, and diaphragmatic thickening fraction during deep breathing (P < 0.001); the sedentary group showed lower values than the exercise group in prone pressure, supine pressure, dominant side single-leg hop, sit-ups, and trunk extensor endurance (P < 0.01); the sedentary group showed higher values than the exercise group in prone trunk proprioception and supine trunk proprioception (P < 0.01). (2) Most diaphragmatic ultrasound parameters and core stability parameters showed statistically significant correlations among subjects. However, dominant side single-leg standing was not statistically correlated with most diaphragmatic ultrasound indicators. The correlation between deep inspiratory diaphragmatic slope and various core stability indicators was not statistically significant. The first two canonical correlation coefficients of diaphragmatic ultrasound parameters and core stability parameters were 0.900 and 0.572, accounting for 81.60% and 9.29% of the variance, respectively. (3) The proportion of variance in diaphragmatic ultrasound parameters explained by their own first canonical variable and the opposing first canonical variable was 33.30% and 27.00%, respectively. The proportion of variance in core stability variables explained by their own first canonical variable and the opposing first canonical variable was 64.40% and 52.20%, respectively. These findings indicate that significant differences exist in diaphragmatic ultrasound parameters and core stability between sedentary and exercising young adults, and there is a strong canonical correlation between diaphragmatic ultrasound parameters and core stability. 
    Figures and Tables | References | Related Articles | Metrics
    Mechanisms of secondary demyelinating injury and inflammatory response in mice with acute ischemic stroke
    Zhang Ziwei, Pu Meng, Tang Yibin, Zheng Lulu, Liang Yajie, Liu Jian, Chen Ying, Wang Qing, Li Yanqing, Li Yanhua
    2026, 30 (33):  8712-8720.  doi: 10.12307/2026.465
    Abstract ( 25 )   PDF (4289KB) ( 1 )   Save
    BACKGROUND: Distal middle cerebral artery occlusion in mice leads to secondary demyelinating lesions. In the acute phase, the progression of demyelinating injury is closely related to the inflammatory response of microglia. Microglia possess phagocytic functions and clear degraded myelin debris through relevant mechanisms post-injury, thereby repairing the microenvironment of the damaged area.
    OBJECTIVE: To establish a mouse model of ischemic stroke using electrocoagulation and investigate demyelination, inflammatory responses, and related mechanisms.
    METHODS: Kunming mice were randomly divided into a sham operation group and an electrocoagulation group. The electrocoagulation group was further subdivided into 12-hour, 1-day, 3-day, 5-day, and 7-day subgroups, with nine mice in each group. Using the sham group as the control, motor and memory abilities were compared via Bederson scoring and Y-maze tests. 2,3,5-Triphenyl tetrazolium chloride staining was used to observe the infarct area, while Luxol fast blue staining was employed to detect the degree of myelin loss in the cerebral cortex. Immunofluorescence staining was performed to detect the expression of myelin basic protein, degraded myelin basic protein, ionized calcium-binding adapter molecule 1, Janus kinase 2 (JAK2), and signal transducer and activator of transcription 3 (STAT3). Western blot was used to measure JAK2 and STAT3 protein expression, and ELISA was conducted to quantify levels of interleukin-6, tumor necrosis factor-α, interleukin-1β, interferon-γ, and interleukin-10. These experiments were employed to analyze the mechanisms of myelin injury and inflammatory responses in the model mice.
    RESULTS AND CONCLUSION: The ischemic stroke model was successfully established in mice using electrocoagulation. Compared with the sham group, the following results were observed: (1) Mice in the electrocoagulation subgroups exhibited varying degrees of motor dysfunction, with significant differences in total distance traveled within the same time frame. (2) At 1 day of electrocoagulation, the ischemic area identified by 2,3,5-triphenyl tetrazolium chloride staining (P < 0.001) and the demyelinated area in the cerebral cortex detected by Luxol fast blue staining (P < 0.001) reached their maximum extent. (3) Immunofluorescence staining showed that myelin basic protein significantly decreased at 1 day of electrocoagulation (P < 0.05), degraded myelin basic protein significantly increased at 1 day of electrocoagulation (P < 0.001), ionized calcium-binding adapter molecule 1 significantly increased at 3-5 days of electrocoagulation (P < 0.001), JAK2 significantly increased at 1 day of electrocoagulation (P < 0.01), and STAT3 significantly increased at 1-3 days of electrocoagulation (P < 0.01). (4) ELISA results indicated that inflammatory factor levels significantly increased after electrocoagulation. (5) Western blot results revealed significantly elevated protein expression of JAK2 and STAT3 in the electrocoagulation group. These findings indicate that electrocoagulation induces central nervous system demyelination, impairs motor and memory functions, triggers cerebral inflammatory responses, and activates the JAK2-STAT3 pathway, which may be involved in microglial phagocytosis of myelin debris.

    Figures and Tables | References | Related Articles | Metrics
    Effects of different flavors on neurobehaviors and cellular molecular networks of mice: high-throughput transcriptome sequencing analysis
    Gao Yang, Zhang Lina, Zhao Zhihuang, Wang Hui, Liu Chongsheng, Xie Yongheng, Xu Liping, Chen Peixian, Yang Wei, Hua Ning, Zhao Xuming
    2026, 30 (33):  8721-8734.  doi: 10.12307/2026.280
    Abstract ( 19 )   PDF (19874KB) ( 1 )   Save
    BACKGROUND: Fragrances and flavorts are closely associated with the brain’s nervous system; however, their long-term effects on brain tissue under the context of cigarette smoke delivery systems remain poorly understood.
    OBJECTIVE: To focus on the molecular mechanisms by which fragrances and flavors influence the neural system of brain tissue and reveal their potential neuroregulatory value in cigarette products by systematically evaluating the effects of different flavoring interventions on mouse neurobehaviors and cellular molecular networks.
    METHODS: Adult male C57BL/6J mice were randomly assigned to two experimental systems. In Experiment I, mice were divided into a solvent aerosol group, a control flavoring aerosol group, and a modified flavoring aerosol group. In Experiment II, mice were divided into a control group, a blank flavored cigarette group, a control flavored cigarette group, and a modified flavored cigarette group. Mice were concentrated exposed to flavors and fragrances either via aerosol inhalation or through combustion in cigarette smoke for 45 consecutive days, twice daily, with each exposure lasting 45 minutes. Open field tests were conducted at weeks 2 and 4 to evaluate spontaneous locomotor activity within a 10-minute observation period. RNA sequencing was performed to identify differentially expressed genes and enriched Kyoto Encyclopedia of Genes and Genomes pathways in brain tissue, while single-nucleus RNA sequencing was employed to characterize major cellular subpopulations and associated biological processes of Gene Ontology. 
    RESULTS AND CONCLUSION: (1) In Experiment I, open field test results demonstrated that mice exposed to both control and modified flavoring aerosols exhibited significantly enhanced locomotor activity and increased central zone exploration compared with the solvent group (P < 0.05). (2) RNA sequencing results revealed a markedly higher number of differentially expressed genes in the modified flavoring aerosol group compared with the solvent group. Kyoto Encyclopedia of Genes and Genomes pathway enrichment indicated significant involvement of glutamatergic synapse, amphetamine addiction, and neuroactive ligand-receptor interaction pathways, with notable upregulation of the G protein-coupled receptor ligand binding pathway in the modified group. (3) snRNA sequencing results identified neurons and microglia as the primary responsive cell populations following flavoring aerosol exposure. Differentially expressed genes in neuronal subpopulations were predominantly enriched in processes such as trans-synaptic signaling, mitochondrial electron transport chain, and oxidative phosphorylation, while oligodendrocyte lineage cells were predominantly enriched in electron transport, myelination formation, and their regulatory pathways. (4) In Experiment II, mice exposed to modified flavored cigarettes also demonstrated significantly increased locomotor activity and exploratory behavior in the central zone compared with the blank flavored cigarette group (P < 0.05). (5) RNA sequencing analysis showed comparable numbers of differentially expressed genes between the groups. Among them, the control flavored cigarette group exhibited enrichment in neuroactive ligand-receptor interaction, cholinergic and glutamatergic synapses, whereas the modified group was predominantly associated with neurotransmitter homeostasis, excitability regulation, and metabolic pathways. (6) Single-nucleus RNA sequencing analysis revealed significant alterations in neuronal and microglial subpopulations. In the modified flavored cigarette group, neuronal differentially expressed genes were enriched in GABAergic synapse, membrane potential regulation, transmembrane transport, and chemical synaptic transmission; oligodendrocyte-related differentially expressed genes were enriched in dendrite development, postsynaptic neurotransmitter receptor regulation, and synaptic organization. These findings suggest that modified flavors and fragrances, through targeted effects on neurons and oligodendrocytes, modulate synaptic plasticity, neurotransmitter metabolism, myelination, and mitochondrial energy pathways, thereby altering neuronal excitability and functional states in the brain. This study offers a theoretical foundation and research paradigm for investigating the regulatory functions of flavors, fragrances, and their applied products in the nervous system of brain tissue. 

    Figures and Tables | References | Related Articles | Metrics
    Mechanism of exercise in regulating the function of vascular endothelial progenitor cells in hypertensive rats
    Zhu Jing, Wang Hexia, Pi Yihua, Wang Qingbo
    2026, 30 (33):  8735-8743.  doi: 10.12307/2026.474
    Abstract ( 22 )   PDF (1771KB) ( 1 )   Save
    BACKGROUND: Irisin is a myokine induced by exercise. In addition to its metabolic regulatory effects, it can also improve endothelial function. However, its relationship with endothelial progenitor cells has not yet been fully clarified. 
    OBJECTIVE: To investigate the effects of irisin induced by regular exercise on the function of bone marrow endothelial progenitor cells in spontaneously hypertensive rats and to reveal the role of the phosphatidylinositol-3-kinase/protein kinase B/endothelial nitric oxide synthase signaling pathway in this process. 
    METHODS: Thirty 10-week-old male spontaneously hypertensive rats were randomly divided into a hypertensive control group and a hypertensive exercise group using a random number table. Fifteen age- and sex-matched Wistar-Kyoto rats served as the normotensive group. The normotensive group and hypertensive control group were kept quietly in cages, while the hypertensive exercise group underwent voluntary wheel running exercise for 5 days per week over 8 weeks. Seventy-two hours after the last intervention, tail artery blood pressure was measured using plethysmography. Blood samples were collected from the abdominal aorta, and plasma irisin concentration was measured by enzyme-linked immunosorbent assay. The thoracic aorta was collected to assess endothelium-dependent vasodilation (representing endothelial function) via vascular ring experiments. The gastrocnemius muscle was collected to detect capillary density using CD31 immunohistochemical staining, to measure irisin levels by enzyme-linked immunosorbent assay, and to determine fibronectin type III domain-containing protein 5 mRNA and protein expression by real-time quantitative polymerase chain reaction and western blot, respectively. The left tibia was isolated to measure irisin content and fibronectin type III domain-containing protein 5 expression. Bone marrow was collected from the femur and right tibia to isolate and culture endothelial progenitor cells. Matrigel tube formation assay was used to assess in vitro angiogenesis capacity. A nude rat model of carotid artery endothelial denudation was established to evaluate the in vivo vascular endothelial repair capacity of endothelial progenitor cells (a carotid endothelium injury model was established by tail vein injection of endothelial progenitor cell suspension. Vascular staining using Evans blue and the area of vascular re-endothelialization was observed). Protein expression of the phosphatidylinositol-3-kinase/protein kinase B/endothelial nitric oxide synthase signaling pathway was measured by western blot. Recombinant human irisin was co-incubated with bone marrow endothelial progenitor cells. Endothelial progenitor cell function was assessed after treatment with the endothelial nitric oxide synthase inhibitor L-nitroarginine methyl ester. Protein expression levels of protein kinase B and endothelial nitric oxide synthase were measured after treatment with the phosphatidylinositol-3-kinase inhibitor LY-294002 or the protein kinase B inhibitor GSK-690693. 
    RESULTS AND CONCLUSION: (1) Exercise reduced blood pressure, improved vascular endothelial function, and promoted angiogenesis (increased capillary density) in spontaneously hypertensive rats (P < 0.05). (2) Exercise increased irisin levels in the circulation, skeletal muscle, and bone (P < 0.05); however, fibronectin type III domain-containing protein 5 mRNA expression was only upregulated in skeletal muscle (P < 0.05). (3) Exercise enhanced the angiogenic and vascular endothelial repair capacity of bone marrow endothelial progenitor cells and activated the phosphatidylinositol-3-kinase/protein kinase B/endothelial nitric oxide synthase signaling pathway (P < 0.05). (4) Exogenous irisin also improved the function of bone marrow endothelial progenitor cells in spontaneously hypertensive rats (P < 0.05). Endothelial progenitor cell function decreased after treatment with the endothelial nitric oxide synthase inhibitor L-nitroarginine methyl ester (P < 0.05). After treatment with phosphatidylinositol-3-kinase or protein kinase B inhibitors, the protein expression levels of protein kinase B and endothelial nitric oxide synthase were downregulated (P < 0.05). To conclude, irisin induced by regular exercise improves the function of bone marrow endothelial progenitor cells in spontaneously hypertensive rats via the phosphatidylinositol-3-kinase/protein kinase B/endothelial nitric oxide synthase signaling pathway, thereby correcting vascular endothelial dysfunction and promoting angiogenesis. These findings suggest that irisin, as a potential "exercise mimetic," may provide health benefits to hypertensive patients who are unable to engage in physical activity by mimicking the protective effects of exercise on the cardiovascular system.
    Figures and Tables | References | Related Articles | Metrics
    Herbal cake-separated moxibustion improves cognitive function in immunosuppressed rats
    Shi Linjuan, Xu Xiaoshan, Zhai Chuntao, Li Wei, Tian Yuefeng
    2026, 30 (33):  8744-8750.  doi: 10.12307/2026.388
    Abstract ( 19 )   PDF (2867KB) ( 2 )   Save
    BACKGROUND: Immunosuppressants such as cyclophosphamide impair immune function, leading to cognitive impairment. Herbal cake-separated moxibustion and moxa-stick moxibustion effectively modulate immune function and improve cognitive dysfunction; however, their mechanisms of action remain incompletely understood.
    OBJECTIVE: To investigate potential mechanisms by which different moxibustion methods influence cognitive impairment in immunosuppressed rats.
    METHODS: Forty SD rats were randomly divided into a blank control group, a model group, a cake-separated moxibustion group, and a moxa-stick moxibustion group, with 10 rats in each group. Cyclophosphamide (30 mg/kg) was intraperitoneally injected for 3 consecutive days to induce immunosuppression rat models, in the latter three groups. Following modeling, rats in the cake-separated moxibustion group and moxa-stick moxibustion groups received corresponding interventions for 10 consecutive days. After intervention, cognitive function was assessed using the open field test. Serum levels of interleukin-1β, interleukin-6, and tumor necrosis factor-α, as well as brain tissue levels of interleukin-18, were measured by enzyme-linked immunosorbent assay. Hematoxylin-eosin staining and immunohistochemistry were used to observe morphological changes and detect nuclear factor κB expression in brain tissue, respectively.
    RESULTS AND CONCLUSION: (1) Compared with the blank control group, the number of rearings, total travel distance, distance traveled in the central zone, and time spent in the central zone in the open field test were decreased (P < 0.01); serum levels of interleukin-1β, interleukin-6, and tumor necrosis factor-α were significantly decreased (P < 0.01, P < 0.001, P < 0.001, respectively); nuclear factor κB expression and IL-18 levels in brain tissue were significantly increased (P < 0.001); and hippocampal neurons exhibited disorganized alignment, with some nuclei showing deep staining due to nuclear condensation and lymphocytic infiltration in the model group. (2) Compared with the model group, the number of rearings, total travel distance, distance traveled in the central zone, and time spent in the central zone in the open field test were significantly increased (P < 0.05); serum levels of interleukin-1β, interleukin-6, and tumor necrosis factor-α were significantly elevated (P < 0.05, P < 0.01, P < 0.01), while nuclear factor κB expression was significantly reduced (P < 0.05); brain tissue IL-18 levels in brain tissue were significantly decreased (P < 0.01); and hippocampal neuronal alignment was more orderly, lymphocytic infiltration was reduced, and nuclear condensation and vacuolation were markedly less pronounced in the cake-separated moxibustion group. (3) Compared with the model group, total travel distance and time spent in the central zone in the open field test were significantly increased (P < 0.05), with no significant difference in the number of rearings and distance traveled in the central zone; and serum levels of interleukin-1β, interleukin-6, and tumor necrosis factor-α significantly increased (P < 0.05), while no significant difference in nuclear factor κB and interleukin-18 levels were found in brain tissues in the moxa-stick moxibustion group. (4) Compared with the moxa-stick moxibustion group, interleukin-18 levels in brain tissue significantly reduced (P < 0.05), with no significant differences in other indicators in the cake-separated moxibustion group. These results suggest that herb cake-separated moxibustion may alleviate neuroinflammation by inhibiting nuclear factor-κB signaling pathway activation, thereby improving cognitive function in immunosuppressed rats. The cake-separated moxibustion shows superior therapeutic efficacy for immunosuppression to moxa-stick moxibustion.

    Figures and Tables | References | Related Articles | Metrics
    Targeted inhibition of poly(ADP-ribose) polymerase 1 attenuates neutrophil-mediated acute lung injury in mice
    Su Tong, Wang Meng, Lyu Yanfang, Xu Xiaodi, Zhong Weixiang, Gao Wanjun, Gao Ge, Han Lulu
    2026, 30 (33):  8751-8760.  doi: 10.12307/2026.481
    Abstract ( 20 )   PDF (6058KB) ( 1 )   Save
    BACKGROUND: In acute lung injury, the activation and tissue infiltration of neutrophils are key contributing factors. Inhibiting poly(ADP-ribose) polymerase 1 activity can reduce the number of infiltrating neutrophils in lung tissue following lipopolysaccharide treatment and alleviate lung injury. However, the specific mechanism by which poly(ADP-ribose) polymerase 1 regulates neutrophil activation and function has not been fully elucidated.
    OBJECTIVE: To investigate the effect and mechanism of poly(ADP-ribose) polymerase 1 in regulating neutrophil activation on acute lung injury in mice.
    METHODS: (1) Using the human promyelocytic leukemia cell line HL-60 as a basis, cells were induced to differentiate into neutrophil-like cells (dHL-60) with dimethyl sulfoxide. Lipopolysaccharide was used to stimulate dHL-60 to obtain activated neutrophils, and Western blot was used to detect poly(ADP-ribose) polymerase 1 expression in activated neutrophils. (2) A neutrophil cell line with low poly(ADP-ribose) polymerase 1 expression was prepared using shRNA targeting human poly(ADP-ribose) polymerase 1, and the knockdown efficiency of poly(ADP-ribose) polymerase 1 was verified by western blot. (3) Western blot and immunofluorescence assays were used to detect the effect of low poly(ADP-ribose) polymerase 1 expression on neutrophil polarization; cell migration assays were used to detect the effect on neutrophil migration; real-time quantitative PCR and flow cytometry were used to detect the effect on chemokine receptor expression; and reactive oxygen species, interleukin 1β, and neutrophil extracellular traps were used to assess the effect on neutrophil activity. (4) Primary mouse neutrophils with low poly(ADP-ribose) polymerase 1 expression were prepared using shRNA targeting mouse poly(ADP-ribose) polymerase 1. In a mouse neutrophil adoptive transfer model, the effect of low poly(ADP-ribose) polymerase 1 expression on lipopolysaccharide-induced acute lung injury was verified by assessing pulmonary edema, myeloperoxidase activity, and hematoxylin-eosin staining. (5) A mouse sepsis survival experiment was performed to evaluate the effect of the poly(ADP-ribose) polymerase 1 inhibitor AG14361 on acute lung injury and survival time in mice.
    RESULTS AND CONCLUSION: (1) Poly(ADP-ribose) polymerase 1 expression was significantly upregulated in activated neutrophils. (2) A neutrophil cell line with low poly(ADP-ribose) polymerase 1 expression was successfully constructed. (3) Compared with the control group, low poly(ADP-ribose) polymerase 1 expression did not affect neutrophil polarization but significantly inhibited neutrophil migration, activation, and inflammatory factor expression. The expression of C-X-C chemokine receptor 2 and C-X-C chemokine receptor 4 on the neutrophil surface was significantly downregulated. (4) Neutrophil adoptive transfer experiments confirmed that specifically knocking down poly(ADP-ribose) polymerase 1 expression in neutrophils reduced neutrophil infiltration in lung tissue and alleviated lipopolysaccharide-induced acute lung injury. (5) The poly(ADP-ribose) polymerase 1 inhibitor AG14361 alleviated lipopolysaccharide-induced acute lung injury and prolonged the survival time of septic mice. Overall, these findings indicate that poly(ADP-ribose) polymerase 1 affects neutrophil migration and inflammatory effector functions by regulating the expression of C-X-C chemokine receptor 2 and C-X-C chemokine receptor 4. Targeted inhibition of poly(ADP-ribose) polymerase 1 can reduce neutrophil infiltration in lung tissue, thereby alleviating lung injury and prolonging survival in mice.
    Figures and Tables | References | Related Articles | Metrics
    Causal relationships between immune cells and childhood asthma and the mediating role of inflammatory proteins
    Gong Jiaxuan, Lin Lin, Wang Chun, Zhang Xingxing, Xiong Ying
    2026, 30 (33):  8761-8777.  doi: 10.12307/2026.484
    Abstract ( 18 )   PDF (54609KB) ( 1 )   Save
    BACKGROUND: Asthma is one of the most prevalent chronic respiratory diseases in children. Existing studies have indicated significant associations among immune cells, inflammatory proteins, and childhood asthma, but the specific causal relationships remain unclear.
    OBJECTIVE: To investigate the causal relationship between immune cells and childhood asthma mediated by inflammatory proteins.
    METHODS: Utilizing data from the largest genome-wide association studies on immune cells, inflammatory proteins, and childhood asthma, we performed bidirectional two-sample Mendelian randomization analyses to explore the causal links between these variables. The inverse variance weighted method served as the primary analytical approach. Cochran’s Q test, MR-Egger intercept test, and MR-PRESSO were employed to assess heterogeneity, outliers, and horizontal pleiotropy, respectively. Mediation analysis was conducted to determine whether inflammatory proteins mediate the effect of immune cells on childhood asthma. Key inflammatory mediators were detected in an established asthmatic rat model using quantitative real-time PCR and western blot assay.
    RESULTS AND CONCLUSION: (1) Inverse variance weighted analyses identified significant causal associations of 40 immune-cell phenotypes and 7 inflammatory proteins with childhood asthma (P < 0.05), but there was no evidence of reverse causality. (2) Mediation analysis revealed that interleukin-33 could play a mediating role between two types of immune cells (T cell %leukocyte and CD86 on myeloid dendritic cells) and childhood asthma, with mediating ratios of 12.7% and 9.3%, respectively. (3) Animal experiments verified that compared with the normal control group, the mRNA and protein levels of interleukin-33 in the lung tissue of rats in the asthma model group were significantly increased (P < 0.01). (4) Protein-protein interaction networks revealed that interleukin-33 and molecules such as interleukin-1 receptor-like 1 formed a pivotal hub in inflammation regulation, and drug screening revealed the potential of targeted therapies like Astegolimab. (5) By integrating genetics with experimental validation, this study establishes interleukin-33 as the pivotal inflammatory mediator linking immune-cell dysregulation to childhood asthma onset. Leveraging bioinformatic pipelines and algorithmic frameworks developed by international multi-omics platforms, we provide a new avenue for refining variant-interpretation workflows tailored to the Chinese population, improving the efficiency of asthma-susceptibility-gene identification, and elucidating the biological basis of childhood asthma for the development of early-intervention therapies.
    Figures and Tables | References | Related Articles | Metrics
    Effects of 12-week blood flow restriction training combined with aerobic exercise on cardiorespiratory endurance and cardiovascular function in overweight and obese individuals
    Hao Yilin, Bao Chunyu
    2026, 30 (33):  8778-8784.  doi: 10.12307/2026.489
    Abstract ( 25 )   PDF (1454KB) ( 7 )   Save
    BACKGROUND: Overweight and obese college students experience a decline in cardiorespiratory endurance, and the long-term tendency may lead to an increased risk of cardiovascular disease. Studies have confirmed that blood flow restriction training can significantly improve muscle morphology and function under the same load, enhance cardiorespiratory endurance, and optimize cardiovascular function.
    OBJECTIVE: To investigate the effects of 12-week blood flow restriction training combined with aerobic exercise on cardiorespiratory endurance and cardiovascular function in overweight and obese college students.
    METHODS: A total of 64 overweight and obese college students were randomly divided into an experimental group and a control group (32 participants in each group). The experimental group participated in blood flow restriction training combined with aerobic exercise, with a 12-week low-intensity blood flow-restricted aerobic exercise program, 3 times per week, 60 minutes each session. The control group underwent regular aerobic exercise during the same period. Before and after the exercise intervention, body composition (body mass index, body fat percentage, and lean body mass), cardiovascular function (systolic blood pressure, diastolic blood pressure, ankle-brachial index, pulse wave velocity, stroke volume, and left ventricular ejection fraction), and cardiorespiratory endurance (vital capacity, oxygen pulse, maximal oxygen uptake, metabolic equivalents, rating of perceived exertion, and respiratory quotient) were measured.
    RESULTS AND CONCLUSION: After 12 weeks of exercise intervention, compared with the control group, the experimental group showed significant changes in body composition, with a 1.51% decrease in body fat percentage (P < 0.05) and a 0.93 kg increase in lean body mass (P < 0.05); resting heart rate decreased by 3.05 beats/min (P < 0.05), systolic blood pressure decreased by 6.51 mmHg (P < 0.05), diastolic blood pressure decreased by 2.16 mmHg (P < 0.05), ankle-brachial index decreased by 0.12 units (P < 0.05), and brachial-ankle pulse wave velocity decreased by 64.93 m/s (P < 0.05); stroke volume increased by 6.86 mL 
    (P < 0.05), and left ventricular ejection fraction increased by 5.17% (P < 0.05); cardiorespiratory endurance improved, with vital capacity increasing by 
    335.94 mL (P < 0.05), VO2max increasing by 4.67 mL/kg/min (P < 0.05), oxygen pulse increasing by 1.73 mL/b (P < 0.05), and metabolic equivalents increasing by 1.34 units (P < 0.05). These findings indicate that blood flow-restricted aerobic exercise can effectively improve cardiorespiratory endurance and cardiovascular function in overweight and obese college students without imposing additional cardiac burden, providing a low-risk and high-efficiency exercise modality for improving cardiorespiratory endurance and cardiovascular function in this population.
    Figures and Tables | References | Related Articles | Metrics
    Probiotic supplementation regulates the gut microbiota to improve intestinal inflammation in gestational diabetes mellitus
    He Biyun, Wu Anqin, Yang Tao, Cao Ting, Xiao Yan, Guo Yi, Zeng Ling, Hua Zhaozhao
    2026, 30 (33):  8785-8793.  doi: 10.12307/2026.496
    Abstract ( 29 )   PDF (2236KB) ( 1 )   Save
    BACKGROUND: Probiotics can help alleviate abnormal glucose and lipid metabolism and insulin resistance in patients with type 2 diabetes by remodeling the structure of the gut microbiota, affecting gut microbiota metabolites, and improving intestinal barrier function. Therefore, therapeutic approaches such as adjusting dietary structure, taking probiotic supplements, and fecal microbiota transplantation are expected to become new targets for the prevention and treatment of gestational diabetes mellitus.
    OBJECTIVE: To investigate the effects of probiotic supplements on the structure of the gut microbiota, inflammatory response, and glucose and lipid metabolism in rats with gestational diabetes mellitus, providing experimental evidence for clinical application.
    METHODS: A total of 62 SPF-grade female Sprague-Dawley rats and 42 male Sprague-Dawley rats were housed together at a ratio of 1.5:1 for mating. After successful mating, eight female rats were randomly selected using a random number table as the blank group. The remaining female rats were fed a high-fat and high-sugar diet combined with an intraperitoneal injection of streptozotocin (35 mg/kg) to establish a rat model of gestational diabetes mellitus. They were then randomly divided into a model control group, a probiotic group, a prebiotic group, a synbiotic group, and a metformin group, with eight rats in each group. The probiotic group was administered 418 mg/(kg·d) of Bifidobacterium quadruple viable tablets by gavage, the prebiotic group was administered 315 mg/(kg·d) of fructooligosaccharides by gavage, the synbiotic group was administered a combination of both drugs by gavage, the metformin group was administered 
    52.5 mg/(kg·d) of metformin by gavage, and the blank group and model control group were administered an equal volume of normal saline by gavage, once daily for 14 consecutive days. After 14 days of administration, the serum levels of fasting blood glucose, fasting insulin, total cholesterol, triglycerides, high-density lipoprotein cholesterol, tumor necrosis factor alpha, interleukin-1β, interleukin-6, lipopolysaccharide, C-reactive protein, and glucagon-like peptide-1 were measured in the rats. Changes in the structure of the gut microbiota were analyzed based on 16S rRNA sequencing, and the levels of short-chain fatty acids in the colonic contents were detected by gas chromatography.
    RESULTS AND CONCLUSION: (1) The serum levels of fasting blood glucose, fasting insulin, total cholesterol, lipopolysaccharide, C-reactive protein, interleukin-1β, and interleukin-6, as well as the relative abundance of Spirochaetota, Desulfobacteroae, Actinobactera, Proteobacteria, Cyanobacteria, and Campilobacteria in the gut microbiota of rats in the model control group were significantly higher than those in the blank group (all P < 0.05). (2) The serum levels of glucagon-like peptide 1, the relative abundance of beneficial bacterial phyla, and the levels of short-chain fatty acids (acetic acid, propionic acid, butyric acid, isobutyric acid, isovaleric acid, and isocaproic acid) in the colonic contents of rats in the model control group were significantly lower than those in the blank group (all P < 0.05). (3) The serum levels of fasting blood glucose, fasting insulin, total cholesterol, lipopolysaccharide, C-reactive protein, interleukin-1β, and interleukin-6 in the probiotic group, synbiotic group, and metformin group were significantly lower than those in the model control group (all P < 0.05). (4) The serum levels of glucagon-like peptide 1, the relative abundance of Verrucomicrobiota, Firmicutes, and Bacteroidota in the gut microbiota, and the levels of short-chain fatty acids (acetic acid, valeric acid, isobutyric acid, isovaleric acid, and isocaproic acid) in the colonic contents of rats in the probiotic group, synbiotic group, and metformin group were significantly higher than those in the model control group (all P < 0.05). To conclude, these findings suggest that probiotic supplements may significantly improve insulin resistance and glucose and lipid metabolism disorders in rats with gestational diabetes mellitus by activating the gut microbiota-short-chain fatty acid-glucagon-like peptide 1 regulatory axis, upregulating the abundance of beneficial bacteria, promoting short-chain fatty acid synthesis, enhancing intestinal mucosal barrier function, and alleviating systemic inflammatory responses.

    Figures and Tables | References | Related Articles | Metrics
    Construction and validation of a nomogram prediction model for cognitive impairment at admission in elderly patients with acute cerebral infarction
    Gao Lin, Hu Yirong, Deng Xinbo, Zeng Ying, Xiong Juan, Shi Xin
    2026, 30 (33):  8794-8801.  doi: 10.12307/2026.483
    Abstract ( 23 )   PDF (16940KB) ( 1 )   Save
    BACKGROUND: Previous studies have predominantly focused on long-term cognitive outcomes, and an instrument that can be applied immediately upon admission to quantify, based on serum biochemical markers, the risk of cognitive impairment at discharge in elderly patients with acute cerebral infarction is still lacking.
    OBJECTIVE: To construct and validate a prediction model based on serum biochemical indicators at admission to evaluate the risk of cognitive impairment at discharge in elderly patients with acute cerebral infarction.
    METHODS: A total of 280 elderly patients with acute cerebral infarction treated at the Department of Neurology, Yichun People’s Hospital from July 2023 to June 2024 were selected and divided into a cognitive impairment group (n=157) and a non-cognitive impairment group (n=123) based on the presence or absence of cognitive impairment at discharge. Another 120 patients treated from July 2024 to January 2025 were selected as the validation set in a 7:3 training-to-validation ratio. Clinical and serum biochemical indicators were collected. Independent risk factors were identified using univariate analysis, least absolute shrinkage and selection operator regression, and multivariate logistic regression. Spearman correlation analysis was used to assess the relationship between serum biochemical indicators at admission and clinical indicators. A restricted cubic spline model was employed to analyze the nonlinear relationship between serum biochemical indicators and cognitive impairment occurrence. Logistic models incorporating independent risk factors were constructed, and nomograms were developed. Model performance was comprehensively evaluated using the area under the area under the receiver operating characteristic curve (AUC), confusion matrix metrics (accuracy, precision, recall, and F1 score), calibration curves, and decision curves, with validation performed in the validation set.
    RESULTS AND CONCLUSION: Among 400 patients, the incidence of cognitive impairment was 55.00%. (1) Eleven independent risk factors for cognitive impairment were identified: age (odds ratio [OR]=1.095, P < 0.001), National Institutes of Health Stroke Scale score (OR=1.121, P=0.013), cerebral infarction location (OR=1.785, P=0.006), cerebral infarction type (OR=1.587, P=0.017), hypertension (OR=2.200, P=0.014), diabetes (OR=2.249, P=0.011), leukoaraiosis (OR=2.031, P=0.022), homocysteine (OR=1.088, P=0.020), C-reactive protein (OR=1.142, P=0.025), high-density lipoprotein (OR=0.208, P=0.021), and 25-hydroxyvitamin D (OR=0.973, P=0.013). (2) The results of the Spearman correlation analysis showed that in elderly patients with acute cerebral infarction, the level of homocysteine was positively correlated with the location of cerebral infarction (r=0.127, P < 0.05); the level of C-reactive protein was positively correlated with hypertension and the type of cerebral infarction (r=0.259, P < 0.001; r=0.178, P < 0.001); the level of high-density lipoprotein was negatively correlated with age (r=-0.131, P < 0.05); and the level of 25-hydroxyvitamin D was negatively correlated with diabetes (r=-0.145, P < 0.05). (3) After adjusting for other independent risk factors, elevated homocysteine and C-reactive protein levels increased the risk of cognitive impairment, whereas increased levels of high-density lipoprotein and 25-hydroxyvitamin D decreased the risk of cognitive impairment. (4) Critical thresholds for homocysteine, C-reactive protein, high-density lipoprotein, and 25-hydroxyvitamin D were 21.44 μmol/L, 11.73 mg/L, 0.56 mmol/L, and 48.22 nmol/L, respectively. (5) The AUC values for the biochemical indicator model were 0.852 (0.809-0.895) in the training set and 0.836 (0.790-0.882) in the validation set, while those for the total prediction model were 0.918 (0.886-0.950) and 0.895 (0.857-0.933), respectively. Both models demonstrated good predictive performance, calibration, and clinical utility. These findings indicate that the nomogram model based on serum biochemical markers at hospital admission exhibits robust predictive power for the risk of cognitive impairment following ischemic stroke in elderly patients with acute cerebral infarction. It serves as a visual aid for the early clinical identification of patients at high risk for cognitive impairment.

    Figures and Tables | References | Related Articles | Metrics
    Effects of different non-invasive brain stimulation modalities on unilateral spatial neglect after stroke: a network meta-analysis
    Wang Dehua, Liang Chunting, Cheng Xiaofei, Li Sihui, Yao Xiaoduo, Tang Jiqin
    2026, 30 (33):  8802-8810.  doi: 10.12307/2026.386
    Abstract ( 27 )   PDF (2353KB) ( 1 )   Save
    OBJECTIVE: Using network Meta-analysis to systematically evaluate the effects of various non-invasive brain stimulation modalities for unilateral spatial neglect after stroke and provide a scientific basis for selecting clinical treatment options.
    METHODS: The researchers independently searched Scopus, PubMed, CNKI, WanFang Database, and other commonly used Chinese and English literature databases to collect relevant randomized controlled trials of non-invasive brain stimulation for the treatment of unilateral spatial neglect after stroke from the establishment of the database to June 24, 2025. The quality of the included studies was assessed by Version 2 of the Cochrane Tool for Assessing Risk of Bias in Randomized Trials (Rob 2). RevMan 5.3 and Stata 17 were used to conduct traditional and network meta-analysis, draw the network evidence map, and offset funnel plot. Finally, GRADE was used to evaluate the level of evidence for each outcome.
    RESULTS: (1) A total of 20 articles with a total sample size of 900 were included, 3 of which were rated as low-risk, 17 were classified as having some risk, and none were classified as high-risk. (2) The results of network meta-analysis showed that single channel transcranial direct current stimulation was conducted to the right parietal lobe with the best efficacy in improving the line bisection test and mini-mental state examination in patients with unilateral spatial neglect. The continuous theta burst transcranial magnetic stimulation targeted the left parietal lobe with the best effect in improving the modified Barthel index and the Fugl-Meyer assessment scale. (3) The GRADE evidence level evaluation results showed that the three levels of evidence were low for line bisection test, Modified Barthel index, and the Fugl-Meyer assessment scale, and were moderate for the Mini-Mental State Examination.
    CONCLUSION: The available clinical evidence of low to moderate intensity suggests that non-invasive brain stimulation is effective in improving cognitive, motor, and daily living abilities in patients with unilateral spatial neglect after stroke. However, due to the number and quality of the included studies, this conclusion still needs to be further verified by more high-quality studies.

    Figures and Tables | References | Related Articles | Metrics
    Effects of exercise intensity on cognitive function in different age groups: a meta-analysis
    Li Bing, Su Yu, Quan Jialin, Yuan Yufeng, Wang Quanjun, Xie Ke, Wang Ping'an, Yu Songyuan
    2026, 30 (33):  8811-8821.  doi: 10.12307/2026.392
    Abstract ( 23 )   PDF (10929KB) ( 1 )   Save
    OBJECTIVE: To investigate the effects of exercise intervention on cognitive function in different age groups and to explore the optimal intensity of exercise intervention for improving cognitive function in different age groups.
    METHODS: Based on the PRISMA guidelines, we searched five databases (PubMed, Web of Science, Cochrane Library, Embase, and CNKI) for randomized controlled trials on the effects of different exercise intensities on cognitive functions from their inception to December 2024. The Risk of Bias 2 (ROB2) tool was used to assess the risk of bias in the included studies. Bayesian network Meta-analysis was performed using R 4.2.0 software and JAGS 4.3.0. A random-effects model was applied, and standardized mean differences (SMDs) were used as pooled effect sizes. The optimal exercise intensities for improving outcome indicators (global cognition, memory performance, inhibitory control, and cognitive flexibility) were explored.
    RESULTS: A total of 63 articles with 4 167 participants were included. (1) Overall cognitive function: in the age of > 45 years, moderate intensity exercise [SMD=1.34, 95% confidence interval (CI)=0.83-1.85, P < 0.05] and high-intensity exercise (SMD=1.30, 95% CI=0.29-2.33, P < 0.05) significantly improved the overall cognitive level, and moderate-intensity exercise was better than high-intensity exercise. (2) Memory performance: In the age of < 18 years, moderate-intensity exercise (SMD=0.68, 95% CI=0.29-1.09, P < 0.05) significantly improved the level of memory performance. In people aged ≤ 45 years, moderate-intensity exercise (SMD=0.60, 95% CI=0.33-0.89, P < 0.05) significantly improved memory performance. In the age of > 45 years, high-intensity exercise (SMD=0.40, 95% CI=0.06-0.75, P < 0.05) significantly improved memory performance. (3) Inhibitory control: In people aged < 18 years, moderate-intensity exercise (SMD=0.56, 95% CI=0.31-0.81, P < 0.05) and high-intensity exercise (SMD=0.43, 95% CI=0.05-0.83, P < 0.05) could significantly improve the level of inhibitory control, and moderate-intensity exercise was better than high-intensity exercise. In the age of ≤ 45 years, moderate-intensity exercise (SMD=0.55, 95%CI=0.35-0.77, P < 0.05) and high-intensity exercise (SMD=0.51, 95% CI=0.19-0.85, P < 0.05) significantly improved the level of inhibitory control, and moderate-intensity exercise had a better effect than high-intensity exercise. However, there was no significant effect on the three exercise intensities in the age of > 45 years (P > 0.05). (4) Cognitive flexibility: In people aged ≤ 18 years, moderate-intensity exercise (SMD=0.62, 95% CI=0.25-1.01, P < 0.05) significantly improved cognitive flexibility. In the age of > 18 years, moderate-intensity exercise (SMD=0.47, 95% CI=0.01-1.03, P < 0.05) significantly improved cognitive flexibility.
    CONCLUSION: Compared with the other exercise intensities, moderate-intensity exercise shows better effects in improving memory performance, inhibitory control, and cognitive flexibility in children, adolescents, and young adults. High-intensity exercise can effectively improve inhibitory control in children, adolescents, and young adults, as well as overall cognition and memory performance in middle-aged and older adults, with particularly optimal improvements in memory performance. In practical applications, factors such as exercise type, duration, and age should be comprehensively considered to select the optimal exercise intensity. 

    Figures and Tables | References | Related Articles | Metrics
    Association between peri-implantitis and tuberculosis: sample analysis based on GEO and GWAS databases
    Mu Wenbo, Wang Yan, Cheng Yao
    2026, 30 (33):  8822-8828.  doi: 10.12307/2026.378
    Abstract ( 24 )   PDF (3923KB) ( 2 )   Save
    BACKGROUND: There is a correlation between peri-implantitis and tuberculosis, but the specific causal relationship and immunological mechanisms remain unclear.
    OBJECTIVE: To explore the association between peri-implantitis and tuberculosis using Mendelian randomization and bioinformatics methods.
    METHODS: (1) Four groups of expression profile data of peri-implantitis (the study has been approved by the relevant institutional review board) were obtained from the Gene Expression Omnibus (GEO) database (an open database developed by the National Center for Biotechnology Information (NCBI) in the United States, which collects high-throughput gene expression data, chip data, sequencing data, and other information from around the world, providing a wealth of resources for biomedical research). After batch correction, differential analysis, Gene Ontology (GO) enrichment analysis, and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis were performed. (2) The most significant pathway from the results of the KEGG enrichment analysis was extracted as the exposure factor for the study. Data on tuberculosis and peri-implantitis (the study has been approved by the relevant institutional review board) were obtained from the Genome-Wide Association Study (GWAS) database (an open-access database developed by the MRC Integrative Epidemiology Unit at the University of Bristol, which integrates GWAS summary data from large cohorts such as UK Biobank and FinnGen, covering a wide range of human phenotypes and disease-related outcomes) as outcome factors for Mendelian randomization analysis. The inverse variance weighting method, MR-Egger regression method, weighted median method, simple mode, and weighted mode were used to evaluate the causal relationship between peri-implantitis and tuberculosis. Heterogeneity analysis, horizontal pleiotropy test, and leave-one-out sensitivity analysis were conducted to assess the reliability of the results of the Mendelian randomization analysis. (3) Immunocyte infiltration analysis was carried out to explore the correlation between tuberculosis pathway genes and immune cells. The differential expression of pathway genes was verified through differential analysis in the validation group.
    RESULTS AND CONCLUSION: (1) GO enrichment analysis revealed that peri-implantitis was significantly associated with biological functions such as leukocyte-mediated immunity, lymphocyte-mediated immunity, regulation of monocyte proliferation, and phagocytosis. KEGG enrichment analysis revealed that peri-implantitis was primarily associated with tuberculosis, phagosomes, cytokine-cytokine receptor interactions, Staphylococcus aureus infection, alcoholic liver disease, and COVID-19. The most significant pathway obtained from the KEGG enrichment analysis was tuberculosis. (2) The results of the Mendelian randomization analysis showed that when tuberculosis was regarded as the exposure factor, there was a significant positive correlation between tuberculosis and peri-implantitis (inverse variance weighting: odds ratio=1.490, 95% confidence interval=1.218-1.823, P < 0.001). The results of the weighted median method were consistent with those of the inverse variance weighting method. The results of the heterogeneity analysis indicated no heterogeneity. The results of the horizontal pleiotropy test showed that there was no horizontal pleiotropy in this study. The results of the leave-one-out sensitivity analysis showed that removing any single nucleotide polymorphism individually would not affect the results of the Mendelian randomization. (3) Correlation analysis between immune cells showed that tuberculosis may increase the risk of peri-implantitis through immunosuppressive effects and promoting alveolar bone resorption. To conclusion, there is a causal association between tuberculosis and peri-implantitis, and tuberculosis may increase the risk of peri-implantitis. This study provides a new theoretical perspective for the prevention and treatment of diseases in the field of dental implantation, and is expected to promote the improvement of the risk assessment system for implant treatment in tuberculosis patients in clinical practice, and provide an important reference for reducing the incidence of peri-implantitis and optimizing treatment strategies.

    Figures and Tables | References | Related Articles | Metrics
    Role of m6A methylation modification in the treatment of steroid-induced osteonecrosis of the femoral head and its regulation by traditional Chinese medicine
    Zhang Mianyu, Han Jie, Chai Yuan
    2026, 30 (33):  8829-8837.  doi: 10.12307/2026.397
    Abstract ( 21 )   PDF (2716KB) ( 1 )   Save
    BACKGROUND: Research has shown that both m6A methylation modification and steroid-induced osteonecrosis of the femoral head are closely related to bone and lipid metabolism.
    OBJECTIVE: To explore the relationship between m6A methylation modification and steroid-induced osteonecrosis of the femoral head, as well as the potential mechanism by which Chinese herbal medicine regulates m6A methylation modification to treat steroid-induced osteonecrosis of the femoral head.
    METHODS: Using "m6A methylation, steroid-induced avascular necrosis of femoral head/SANFH, bone metabolism, lipid metabolism, Chinese herbal medicine, glucocorticoid" as Chinese and English search terms, a literature search was conducted in Web of Science, PubMed, CNKI, Wanfang, and VIP databases. According to the inclusion and exclusion criteria, 75 articles were included in the final review.
    RESULTS AND CONCLUSION: Steroid-induced osteonecrosis of the femoral head has a multifactorial pathogenesis involving imbalances in bone and lipid metabolism. It results from the combined effects of multiple pathological mechanisms. m6A methylation plays a crucial role in bone and lipid metabolism. It influences the proliferation, apoptosis, and differentiation of osteoblasts, osteoclasts, and bone marrow mesenchymal stem cells. It also affects lipid metabolism and angiogenesis. Therefore, m6A methylation may significantly impact the onset and progression of steroid-induced avascular necrosis of the femoral head. Certain traditional Chinese medicines, including monomers, compound formulations, and patented drugs, can modulate osteogenesis by regulating m6A methylation. This process could contribute to preventing and treating steroid-induced avascular necrosis of the femoral head. However, the bidirectional regulatory mechanisms of certain m6A methyltransferases and demethylases, such as methyltransferase-like 3 and demethylase, remain to be fully elucidated. Further research into the interaction between m6A methylation and the development of steroid-induced avascular necrosis of the femoral head is warranted, with the potential to provide novel therapeutic strategies for clinical management.
    Figures and Tables | References | Related Articles | Metrics
    Positive effects of transcranial direct current stimulation in improving muscle and cardiopulmonary endurance
    Zhang Yi, Wu Huaduo, Song Yu, Dong Yumo, Zhang Yiguang, Wang Qian, Gao Xin, Jiang Ning
    2026, 30 (33):  8838-8844.  doi: 10.12307/2026.405
    Abstract ( 18 )   PDF (1959KB) ( 2 )   Save

    BACKGROUND: In recent years, transcranial direct current stimulation technology has gained widespread attention as a non-invasive means of neuromodulation to improve endurance.
    OBJECTIVE: To analyze and summarize the application of transcranial direct current stimulation in improving endurance performance, and to explore the application effect of transcranial direct current stimulation in muscle endurance and cardiopulmonary endurance.
    METHODS: The effects of transcranial direct current stimulation on endurance performance were searched through data knowledge service platforms such as CNKI, WanFang, VIP, PubMed and Dimension Academic (SPIS). The Chinese search terms were “transcranial direct current stimulation,” “endurance performance,” “endurance exercise,” and “exercise performance.” The English search terms were “tDCS,” “transcranial direct current stimulation,” “endurance performance,” “endurance exercise,” and “sports performance.” The literature was screened to find out the Chinese and English journal papers that fit the theme. Finally, 73 articles were included for review.
    RESULTS AND CONCLUSION: Transcranial direct current stimulation has yielded promising research results in enhancing endurance performance. By modulating the resting membrane potential of cortical neurons to induce depolarization, it increases cortical excitability and strengthens connectivity between the cerebral cortex and neuromuscular systems, thereby improving muscle recruitment efficiency and endurance performance. Transcranial direct current stimulation may also prolong endurance performance by modulating an individual’s perception of effort, allowing the individual to better tolerate fatigue during endurance training. Transcranial direct current stimulation may have a positive effect on cardiopulmonary endurance by influencing brain function. It should be noted that there are still some controversies and uncertainties regarding the improvement of endurance in transcranial direct current stimulation, and future studies need to further explore the mechanism of action, applicable populations and sustained effects of this technology in order to provide a more reliable basis for clinical practice.






    Figures and Tables | References | Related Articles | Metrics