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    11 March 2016, Volume 20 Issue 11 Previous Issue    Next Issue
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    Effect of hyperbaric oxygen pretreatment on the expressions of vascular endothelial growth factor and transforming growth factor beta in over-length dorsal random skin flaps
    Zhu Jiang-ying, Yin Guo-qian, Pang Jin-jun, Chen Zi-xiang, Pan Xin-yuan, Lu Si-ding, Wei Qin-xi, Xie Zhao-di
    2016, 20 (11):  1525-1531.  doi: 10.3969/j.issn.2095-4344.2016.11.001
    Abstract ( 265 )   PDF (729KB) ( 412 )   Save

    BACKGROUND: Hyperbaric oxygen (HBO) therapy can alleviate the skin flap congestion by improving the angiogenesis and increasing the oxygen content of blood in skin flaps. Although the HBO therapy ability to increase flap survival has been well described, the research on the application of HBO pretreatment in skin flap transplantation does not arouse adequate concern.
    OBJECTIVE: To investigate the effect of HBO pretreatment on early-stage flap congestion in the rat model of over-length dorsal random skin flaps.
    METHODS: Thirty-six SD rats were randomly divided into control group (n=12), HBO pretreatment group (n=12) and HBO treatment group (n=12). Rats in the HBO pretreatment group received 4 days of HBO therapy prior to transplantation, once a day. Rats in the HBO treatment group received 4 days of HBO therapy after transplantation. Rats in the control group were raised in the normal conditions after flap transplantation. At postoperative days 3 and 5, rats were sacrificed and the samples were collected. The inflammation of flap tissues was detected using hematoxylin-eosin staining. The expression of vascular endothelial growth factor and transforming growth factor-β was analyzed by immunohistochemistry staining. The flap survival rate was calculated at postoperative day 5.
    RESULTS AND CONCLUSION: The flap survival area of the HBO pretreatment group and HBO treatment group was larger than that of the control group (P < 0.05). At postoperative days 3 and 5, the expression levels of vascular endothelial growth factor and transforming growth factor-β in the flap tissue were higher in the HBO pretreatment group and HBO treatment group than the control group (P < 0.05). However, there was no significant difference in the flap survival area and the expression of vascular endothelial growth factor and transforming growth factor-β between HBO pretreatment and HBO treatment groups  (P > 0.05). HBO pretreatment can increase the expression of vascular endothelial growth factor and transforming growth factor-β and promotes angiogenesis in random pattern flaps, thereby improving skin flap survival. 

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    Amniotic membrane implantation into the corneal stroma for the treatment of bullous keratopathy
    Zhang Feng, Meng Wei-zhe
    2016, 20 (11):  1532-1537.  doi: 10.3969/j.issn.2095-4344.2016.11.002
    Abstract ( 274 )   PDF (448KB) ( 316 )   Save

    BACKGROUND: Bullous keratopathy has an increasing annual incidence, but its treatment is restricted by few sources of materials for corneal transplantation and high cost of operation. Additionally, some patients who present with serious symptoms have little chance of recovery and low success in corneal transplantation. Amniotic membrane from the corneal stroma has a rich source with low cost, which can effectively relieve the symptoms and improve the quality of life in patients.
    OBJECTIVE: To observe the therapeutic efficacy of amniotic membrane implantation into the corneal stroma in the treatment of bullous keratopathy.
    METHODS: Forty healthy adult New Zealand rabbits (half male and female) were randomly divided into four groups (A, B, C, D groups), with 10 rats in each group. Rabbit models of bullous keratopathy were made in the groups A, B, C. At 2 weeks after modeling, amniotic membrane implantation into the corneal stroma and corneal surface was performed in groups A and B, respectively, and in group C, corneal lamellar dissection was done but with no amniotic membrane transplantation. In group D, there was no surgical treatment (blank control). A slit lamp microscope with constant crack width and angle of light projection was used to observe the central corneal thickness, and corneal opacification degree, corneal epithelial bulla of rabbits were observed at different time in each group. Under microscope, the rabbit corneal endothelial cells and healing were observed at different time.
    RESULTS AND CONCLUSION: At 1 day and 2 weeks after transplantation, the central corneal thickness of rabbits had significant differences in the four groups (P < 0.05). At 4, 8, 12 weeks after transplantation, the central corneal thickness of rabbits showed no difference between groups A and B as well as between groups C and D (both P > 0.05), but there was a significant difference between groups A, B and group C  (P < 0.05). At 4 and 8 weeks after transplantation, the degree of corneal opacity was significantly better in group A than the other three groups (P < 0.05). There were obvious scars forming at the incision of rabbits in the group C. Compared with the other three groups, the bulla was improved better in the group A (P < 0.05). At 2 weeks after transplantation, bullous keratopathy relapsed in the group B, and symptoms of edema with bulla were still seen in groups C and D at 12 weeks after transplantation. These findings indicate that amniotic membrane implantation into the corneal stroma can effectively repair rabbit corneal endothelial cells and alleviate the symptoms of edema, but its specific mechanism need to be further studies.

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    Substance P effects on aggregation and differentiation control of epidermal stem cells and skin wound repair
    Peng Xi-liang, Zhang Yu-hong, Ni Wen-qiong
    2016, 20 (11):  1538-1543.  doi: 10.3969/j.issn.2095-4344.2016.11.003
    Abstract ( 348 )   PDF (577KB) ( 787 )   Save

    BACKGROUND: Epidermal stem cells are the source of cells for repairing the skin and its appendages. To study differentiation and migration of epidermal stem cells is crucial for perfect healing.
    Objective: To investigate the effects of substance P in skin wound repair.
    METHODS: Thirty Wistar rats were randomized into groups of substance P, capsaicin and control (n=10 per group). After the establishment of skin defect models, exogenous neuropeptide substance P, capsaicin, and normal saline were daily injected at the wound for continuous 5 days. Skin thickness, skin wound area, BrdU-positive cells were detected in the three groups at different time after injection.
    Results and conclusions: No difference n the skin thickness was found in the three groups at 14 days after injection (P > 0.05), but with time, the epidermal thickness was reduced. At 42 days, the epidermal thickness was reduced remarkably in the substance P group and decreased certainly in the capsaicin group, but unchanged in the control group. The wound area of the substance P group was significantly lower than that in the control and capsaicin groups at 3, 5, 7 days after injection (P < 0.05), but there was no difference between the control and capsaicin group (P > 0.05). The BrdU positive rates in the three groups were significantly different at 3, 5, 7, 12 days after injection: the substance P group > the control group > the capsaicin group (P < 0.05). These results show that substance P can promote epidermal cell proliferation and accelerate wound healing. 

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    Chondrocyte-like differentiation of synovial mesenchymal stem cells co-cultured with chondrocytes on a three-dimensional scaffold
    Yang Meng, Shao Bo, Gong Zhong-cheng, Ning Xiao-ting, Liu Hui, Rekemu Abasi, Ling Bin, Yin Xiao-peng, Wang Bing, Hu Lu-lu, Wang Yue, Hu Xin, Lin Zhao-quan
    2016, 20 (11):  1544-1560.  doi: 10.3969/j.issn.2095-4344.2016.11.004
    Abstract ( 237 )   PDF (672KB) ( 387 )   Save

    BACKGROUND: The co-culture of chondrocytes and synovial mesenchymal stem cells can induce the cartilage differentiation of synovial mesenchymal stem cells in vitro, but the cell differentiation induced by co-culture in vivo is rarely reported. OBJECTIVE: To investigate the chondrogenic differentiation of synovial mesenchymal stem cells co-cultured with chondrocytes on the chitosan/type I collagen composite scaffolds after being transplanted into the subcutaneous layer of Sprague-Dawley rats.
    METHODS: The synovial mesenchymal stem cells and chondrocytes harvested from the synovial membrane and articular cartilage of Sprague-Dawley rats were obtained by enzyme digestion method and cultured respectively. Passage 3 synovial mesenchymal stem cells and passage 2 chondrocytes, which were divided into four groups: group A (chondrocytes alone), group B (synovial mesenchymal stem cells alone), group C (ratio of synovial mesenchymal stem cells:chondrocytes=1:2) and group D (scaffold material without cells), were cultured on chitosan/type I collagen composite scaffolds and transplanted into the subcutaneous layer of rats followed by morphological observation and immunohistochemical staining at 4 and 8 weeks.   .
    RESULTS AND CONCLUSION: After 4 and 8 weeks, the discoid-like scaffold was visible. The immunohistochemical staining of type II collagen and the toluidine blue staining of aggrecan were significantly positive in groups A and C. These results show that the co-culture of synovial mesenchymal stem cells and chondrocytes on the scaffold in vivo can form cartilage-like tissues. 

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    Feasibility of different xenogeneic (porcine) acellular dermal matrices in the repair of deep burn wounds: a 12-month follow-up
    Zeng Ming, Wei Di-nan, Zhi Yan, Wang Hong, Chen Zong-hua
    2016, 20 (11):  1551-1557.  doi: 10.3969/j.issn.2095-4344.2016.11.005
    Abstract ( 283 )   PDF (553KB) ( 530 )   Save

    BACKGROUND: Skin grafting is crucial for patients with deep burns, but limited source of autologous skin grafts is an existing difficulty.
    OBJECTIVE: To investigate the effect of xenogeneic (porcine) acellular dermal matrix in the treatment of deep burn wounds and the feasibility of its application.
    METHODS: Forty-one patients with deep burn were divided into two groups according to the intention of the patients, 21 cases in control group and 20 cases in observational group, followed by autologous split-thickness skin grafting alone or combined with different (porcine) acellular dermal matrix, respectively. After 12 months of follow-up, the graft success rate at postoperative 1, 2, 3, 4 weeks and skin graft contraction rate and wound repair at postoperative 3, 6, 9, 12 months were observed and compared between two groups. Moreover, levels of inflammatory factors were detected and compared between two groups at postoperative 1, 2, 3 months.
    RESULTS AND CONCLUSION: The skin graft success rates showed no difference between two groups at postoperative 1, 2, 3, 4 weeks (P > 0.05). The skin graft contraction rates also showed no difference between two groups at postoperative 3, 6, 9, 12 months (P > 0.05). After 12 months of follow-up, no serious scar hyperplasia, but soft texture appeared in the control group. In the observational group, three cases presented with local pigmentation at the early stage, but it gradually subsided with time; no obvious scar, but only small, point-like scar, was visible, and the repaired wound exhibited soft touch. No adverse events and death occurred in both two groups. Experimental results show that the treatment of deep burns with autologous split-thickness skin grafting combined with xenogeneic (porcine) acellular dermal matrix is safe and effective, which can improve the quality of wound healing. 

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    Expression of Livin, Smac and Caspase-3 in keloids and their correlation
    Zhang Yuan-gui, Duan Dong, Li Pan-deng, Chen Run-fang, Li Zhi-hua, Gao Xin-yu, Wu Wei
    2016, 20 (11):  1558-1583.  doi: 10.3969/j.issn.2095-4344.2016.11.006
    Abstract ( 228 )   PDF (533KB) ( 412 )   Save

    BACKGROUND: Currently, there is no effective treatment for keloids that often recur. Its pathogenesis is still entirely unclear, and fibroblast proliferation and apoptosis have become a research hotspot.
    OBJECTIVE: To investigate the expression of Livin, Smac and Caspase-3 in keloids and to analyze their relationship so as to preliminarily explore the significance of Livin, Smac and Caspase-3 in the pathogenesis of keloids.
    METHODS: RT-PCR and immunohistochemical methods were used to detect the mRNA and protein expressions of Livin, Smac and Caspase-3 in keloids (n=20) and normal skin tissues (n=20).
    RESULTS AND CONCLUSION: Compared with the normal skin tissue, the mRNA and protein positive expressions of Livin were significantly higher in keloids (P < 0.05), while the mRNA and protein positive expressions of Smac and Caspase-3 were lower in keloids (P < 0.05). There was a negative association between Livin and Smac, Caspase-3 protein expression in keloids. These findings indicate that the high mRNA expression of Livin may cause the imbalance between proliferation and apoptosis of fibroblasts by inhibiting the mRNA expression of Smac and Caspase-3, and eventually lead to the formation of keloid. 

     

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    Changes of mouse hippocampal neurogenesis during aging
    Liu Pin-yue, Jin Zhen-chao, Deng Xiao-lan, Yuan Li, Zheng Min, Wang Ya-ping, Wang Jian, Jiang Rong
    2016, 20 (11):  1564-1569.  doi: 10.3969/j.issn.2095-4344.2016.11.007
    Abstract ( 446 )   PDF (572KB) ( 515 )   Save

    BACKGROUND: Abnormal hippocampal neurogenesis during aging has been reported to result in learning and memory dysfunction. But its mechanism is unclear.
    OBJECTIVE: To understand the changes of mouse neurogenesis in the hippocampal subgranular zone during aging.
    METHODS: C57BL/6 mice 2, 6 and 20 months of age were used. Immunochemistry was used to count the number of neural stem cells (nestin+), neuroblasts (Doublecortin+, DCX+), and proliferative cells (proliferating cell nuclear antigen+, PCNA+) in the hippocampal subgranular zone. mRNA expressions of aging-related genes, p19Arf and p21Cip1/Waf1, in the hippocampus were detected by reverse transcription-PCR.
    RESULTS AND CONCLUSION: Compared with the young and middle age groups, the number of PCNA+ cells, nestin+ and DCX+ cells in the hippocampal subgranular zone of the aged group decreased dramatically; the expression of p19Arf and p21Cip1/Waf1 mRNA increased in the aged group. Proliferation activity, the number of neural stem cells and neuronal differentiation all decreased. These findings indicate that the decline of hippocampal neurogenesis may be associated with increased expression of aging-related genes p19Arf and p21Cip1/Waf1 in the p19Arf-Mdm2-p53-p21Cip1/Waf1pathway. 

     

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    Five kinds of vitrified cryoprotectants: toxicity of their alone or combination to nucleus pulposus cells
    Li Jian-guo, Li Pan, Yin He-yong, Liu Xi, Zhou Yu-jun, Li Hai-tao,Li Yan-fei, Wang Fei, Hu Cheng-dong
    2016, 20 (11):  1570-1576.  doi: 10.3969/j.issn.2095-4344.2016.11.008
    Abstract ( 265 )   PDF (692KB) ( 446 )   Save

    BACKGROUND: Transplantation of allogeneic intervertebral disc can be facilitated by the cryopreservation of the intervertebral disc. But the traditional cryopreservation methods always lead to the appearing of ice crystals inside and outside the cells which can cause cellular injury. The vitrification method that can avoid the formation of ice crystals have been widely applied in the cryopreservation field. However, only a few reports have assessed the vitrified cryopreservation of the intervertebral disc, and the toxicity of cryoprotectants to the nucleus pulposus cells have not been fully explored.
    OBJECTIVE: To determine the order of toxicity of five commonly used cryoprotectants that are used alone or in combination to rabbit nucleus pulposus cells, and to select the optimal cryoprotectant for the vitrification of the intervertebral disc.
    METHODS: We chose five most commonly used cryoprotectants including dimethyl sulphoxide, formamide, ethylene glycol, propylene glycol and glycerol. Then, 5 single commonly used cryoprotectants, 10 mixed agents containing any 2 commonly used cryoprotectants, and 10 mixed agents containing any 3 commonly used cryoprotectants were formulated. Cell viability of nucleus pulposus cells was determined using cell counting kit-8 and fluorescein diacetate/propidium iodide method. All data obtained were analyzed statistically to choose the appropriate combining scheme with less toxicity.
    RESULTS AND CONCLUSION: The order of the toxicity of these five commonly used cryoprotectants from low to high was ethylene glycol, glycerol, formamide, dimethyl sulphoxide, and propylene glycol. The toxicity of the combined agents containing two or three commonly used cryoprotectants was lower than that of any commonly used cryoprotectants that were used to formulate them. The toxicity of the mixed agents that contained ethylene glycol or glycerol was lower than that of any other mixed agents. So we can choose the mixed cryoprotectants that contain ethylene glycol and (or) glycerol for the vitrification of the intervertebral disc.
     

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    Effect of sodium arsenite on malignant transformation of human immortalized keratinocyte cell lines
    Li Yan-ling, Hu Yu-xian, Zhang Xiao-guang, Wang Ling
    2016, 20 (11):  1577-1583.  doi: 10.3969/j.issn.2095-4344.2016.11.009
    Abstract ( 389 )   PDF (441KB) ( 364 )   Save

    BACKGROUND: Studies have found that sodium arsenite can cause the malignant transformation and tumorigenicity of HaCaT cells, but whether low concentrations of sodium arsenite can cause the malignant transformation is rarely reported.
    OBJECTIVE: To study the effect of sodium arsenite on the malignant transformation of human immortalized keratinocyte cell lines.
    METHODS: HaCaT cells were treated with different concentrations of sodium arsenite. MTT assay was used to determine the effect of sodium arsenite on HaCaT cell morphology and proliferation, flow cytometry used to detect the effect of sodium arsenite on HaCaT cell cycle, and soft agar colony formation experiments assay used to determine the effect of sodium arsenite on HaCaT cell colony formation capacity.
    RESULTS AND CONCLUSION: HaCaT cells grew well when the concentration of sodium arsenite was 5 mol/L, but the cell growth was inhibited under intervention with 10 and 50 mol/L sodium arsenite. HaCaT cells treated with 0.1 mol/L sodium arsenite were passaged to the 20th generation, and cell morphology had no notable changes; cells at passage 25 exhibited enlarged size and multiple nucleoli, which had a continued proliferation trend. Compared with the primarily cultured cells, 0.1 mol/L sodium arsenite-treated HaCaT cells at passages 15 and 25 had an increased proportion at S phase and G2/M phase, with strengthened proliferation ability and increased colony-forming efficiency, and moreover, the proliferation ability and colony-forming efficiency of passage 25 cells were higher than those of passage 15 cells. These experimental data show that high concentrations of sodium arsenite reduce HaCaT cell viability, and low concentrations of sodium sulfite have a certain influence on the morphology, cell cycle, proliferation ability and colony-forming efficiency of HaCaT cells, and moreover, the proliferation ability and colony-forming efficiency of human immortalized keratinocytes will be strengthened with the increase of passage. 

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    Effect of miR-25 on the differentiation of P19 cells into cardiomyocytes and its mechanism
    Li Lian-chong
    2016, 20 (11):  1584-1590.  doi: 10.3969/j.issn.2095-4344.2016.11.010
    Abstract ( 312 )   PDF (546KB) ( 442 )   Save

    BACKGROUND: Previous studies have found that the expression level of miR-25 in differentiated P19 cells is significantly lower than that in undifferentiated P19 cells. However, the effect of miR-25 on cardiomyogenesis and the relevant mechanism remain unclear.
    OBJECTIVE: To explore the effect and mechanism of miR-25 on the differentiation of P19 cells into cardiomyocytes.
    METHODS: P19 cells were cultured and differentiated into cardiomyocytes in vitro. The expression of miR-25 in differentiated and undifferentiated P19 cells was detected by real-time PCR. miR-25-overexpressing P19 cells were constructed by lipofection transfection, and were used to investigate the effect of miR-25 on the differentiation of P19 cells into cardiomyocytes. MicroRNA target analysis tools were used to explore potential targets of miR-25, and dual luciferase reporter assay was used to identify whether the 3’UTR of Pax3 mRNA was a binding target of miR-25. In addition, we transfected P19 cells with Pax3 shRNAs to silence the expression of Pax3, and investigated the effect of Pax3 on the differentiation of P19 cells into cardiomyocytes.
    RESULTS AND CONCLUSION: Expression level of miR-25 in differentiated P19 cells was obviously down-regulated compared with that in undifferentiated P19 cells. miR-25 overexpression promoted the differentiation of P19 cells into cardiomyocytes. By target prediction analysis, we confirmed that Pax3 was a potential target gene of miR-25. Luciferase assay further confirmed that miR-25 targeted Pax3 directly. Moreover, knockdown of Pax3 promoted the differentiation of P19 cells into cardiomyocytes. Taken together, miR-25 promotes the differentiation of P19 cells into cardiomyocytes by targeting Pax3. These findings offer new clues and theoretical basis for cardiomyogenesis and prevention and cure of congenital heart disease.
     

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    Dexamethasone inhibits the expression of microRNA-155 in macrophages induced by lipopolysaccharide
    Wang Zhong-hua, Wang Shou-hong, Wu Yan, Li Zhou, Liao Xiao-long, Qin Tie-he
    2016, 20 (11):  1591-1596.  doi: 10.3969/j.issn.2095-4344.2016.11.011
    Abstract ( 274 )   PDF (493KB) ( 415 )   Save

    BACKGROUND: It is unclear about dexamethasone effect on the regulation of microRNA-155 expression in macrophages.
    OBJCTIVE: To explore whether dexamethasone can regulate the expression of microRNA-155 in macrophages.
    METHODS: (1) Lipopolysaccharide stimulation of mouse macrophages: mouse macrophage cell lines, Raw264.7 cells, were cultured in vitro and stimulated by lipopolysaccharide. Cultured cells were collected at 0, 0.5, 2, 6 hours after culture to detect the dynamical expression of microRNA-155. (2) Dexamethasone intervention for macrophages: Macrophages were divided into four groups: control group treated with phosphate buffer; lipopolysaccharide group stimulated by lipopolysaccharide; combined group given intervention with dexamethasone and lipopolysaccharide; dexamethasone group cultured with dexamethasone. At 6 hours after culture, cell supernatant was collected to detect the expression of tumor necrosis factor α and interleukin-6 using ELISA method. Real-time fluorescence quantitative PCR was used to detect the expression of microRNA-155 in the Raw264.7 macrophages.
    RESULTS AND CONCLUSION: Lipopolysaccharide significantly increased the expression of tumor necrosis factor α, interleukin-6 and microRNA-155 after 6 hours of culture (P < 0.05). Combined use of dexamethasone and lipopolysaccharide slightly increased the expression of tumor necrosis factor α, interleukin-6 and microRNA-155 (P < 0.05). Dexamethasone alone had no influence on the expression of tumor necrosis factor α and interleukin-6, but significantly decreased the expression of microRNA-155 (P < 0.05). These findings indicate that dexamethasone can inhibit the expression of microRNA-155 in the macrophages induced by lipopolysaccharide. 

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    Effect of gastric cancer stem cells CSC-G on invasion and metastasis of gastric cancer cells
    Li Xiang-hui, Wang Gui-ji
    2016, 20 (11):  1597-1602.  doi: 10.3969/j.issn.2095-4344.2016.11.012
    Abstract ( 270 )   PDF (455KB) ( 372 )   Save

    BACKGROUND: Studies have shown that cancer stem cells play an important role in tumor invasion and metastasis, but studies on the role of gastric cancer stem cells in invasion and metastasis of gastric cancer cells were rarely reported.
    OBJECTIVE: To study the effect of gastric cancer stem cells CSC-G on invasion and metastasis of gastric cancer cells.
    METHODS: Gastric cancer stem cells CSC-G and gastric cancer cells SGC7901 were cultured in vitro for 10 days followed by spherical colony formation assay, western blot assay for detecting OCT4, SOX2, E-cadherin and CD44 protein expression levels in gastric cancer stem cells CSC-G and gastric cancer cells SGC7901, and Transwell assay for detecting the invasion and migration of gastric cancer stem cells and gastric cancer cells SGC7901.
    RESULTS AND CONCLUSION: Gastric cancer cells SGC7901 in RPMI1640 medium presented with adherent growth and were quadrilateral or polygonal after passage; gastric cancer stem cells CSC-G in serum-free medium presented with suspension growth, and adherent gastric cancer stem cells were spindle-shaped or round. Compared with gastric cancer cells SGC7901, the protein expressions of OCT4, SOX2 and CD44, the number of cancer cell spheres and the number of trans-membrane cells were significantly increased in the gastric cancer stem cells CSC-G (P < 0.05), and the expression of E-cadherin protein was significantly decreased (P < 0.05). These findings indicate that the gastric cancer stem cells CSC-G can be successfully cultured in vitro, and have enhanced invasion and migration compared with the gastric cancer cells SGC7901, which play an important role in gastric cancer invasion and metastasis. 

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    Daily water loss in Chinese young men
    Hao Wen-rui, Quan Hai-ying, Li Lu, Zhang Cheng, Wu Da-wei, Zhang Kuan
    2016, 20 (11):  1603-1609.  doi: 10.3969/j.issn.2095-4344.2016.11.013
    Abstract ( 389 )   PDF (525KB) ( 437 )   Save

    BACKGROUND: No studies currently focus on the measurement of daily water loss under certain physical activity level continuously and precisely.
    OBJECTIVE: To provide evidence for daily water requirement in Chinese young men based on the measurement of the daily water loss in Chinese young men under moderate physical activity.
    METHODS: Twenty male subjects were enrolled, and 23-hour whole-body sweat loss and urine output were measured using high-precision body weighting scale in whole-room indirect calorimeter. The results were converted to daily (24-hour) water requirement to determine the daily water requirement. Daily whole-body sweat loss per unit body weight, daily whole-body sweat loss per unit fat free mass and daily whole-body sweat loss per unit surface area were calculated.
    RESULTS AND CONCLUSION: In Chinese young men, daily water loss was (3 339.7±509.9) g, daily urine output was (1 982.9±449.5) g and daily whole-body sweat loss was (1 356.7±215.6) g. There was a linear correlation between water intake and water loss (r=0.616, P < 0.05). Daily whole-body sweat loss per unit body weight was (21.0±3.6) g/kg, daily whole-body sweat loss per unit fat free mass was  (25.8±3.9) g/kg and daily whole-body sweat loss per unit surface area was (799.4±129.4) g/m2. Daily water requirement of Chinese young men under moderate physical activity is approximately 3 340g, and moreover, water loss increases with the increase of water intake. 

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    Internal fixation with intermaxillary traction nail combined with small/mini-titanium plate in the treatment of mandibular fractures
    Hu Chao, Xiao Jin-gang, Hu Wen-jian, Wang Wen, Pan Qing, Zeng Xin
    2016, 20 (11):  1610-1615.  doi: 10.3969/j.issn.2095-4344.2016.11.014
    Abstract ( 201 )   PDF (447KB) ( 477 )   Save

    BACKGROUND: Mandibular fractures often harm patient’s work and life. Intermaxillary traction nail with small/mini-titanium plate, relative to traditional dental arch splint combined with small/mini titanium plate treatment alone, is characterized by short treatment time and good fixation effect, which can improve the maxillofacial dysfunction and promote the early completion of the treatment.
    OBJECTIVE: To explore the curative effect of intermaxillary traction nail with mini-titanium plate versus dental arch splint combined with small/mini-titanium plate on mandibular fractures
    METHODS: Ninety cases of mandibular fractures hospitalized at the Department of Oral and Maxillofacial Surgery, Stomatological Hospital of Southwest Medical University in China from July 2011 to May 2015 were enrolled in this study. These patients were equivalently randomized into control group subjected to dental arch splint combined with small/mini-titanium plate and observation group subjected to intermaxillary traction nail with mini-titanium plate. All the patients were followed up for 4-6 months. Curative effects, including excellent and good rate and total efficiency, were compared between the two groups. Maxillofacial function and incidence of adverse reactions were observed and recorded, respectively, to analyze the experimental data and assess their clinical values.
    RESULTS AND CONCLUSION: The total efficiency and the maxillofacial function were significantly better in the observation group than the control group (P < 0.05). Plaque and debris index was increased significantly in the control group compared with the experimental group before and after treatment (P < 0.05). The gingival index had no significant changes in the observation, but it was increased significantly in the control group before and after treatment (P < 0.05). The number of cases of adverse reactions was significantly less in the experimental group than the control group (P < 0.05). These results show that the effect of internal fixation with intermaxillary traction nail combined with small/mini-titanium plate mini titanium plate and mini titanium plate was good, safe and reliable. 

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    Tightrope versus Endobutton in the reconstruction of the cruciate ligament
    Yuan Ling-li, Xu Bin, Jiang Shao-wei, Tu Jun
    2016, 20 (11):  1616-1622.  doi: 10.3969/j.issn.2095-4344.2016.11.015
    Abstract ( 606 )   PDF (566KB) ( 777 )   Save

    BACKGROUND: Because of its advantages, Endobutton has been widely used in clinic. Currently, its shortcomings are increasingly recognized. Tightrope that overcomes the shortcomings of Endobutton has been gradually accepted by a doctor skilled in sports injuries.
    OBJECTIVE: To analyze and compare the differences in the effects of Tightrope and Endobutton in the reconstruction of the cruciate ligament.
    METHODS: Totally 60 cases of anterior cruciate ligament rupture were selected and subjected to anterior cruciate ligament reconstruction under arthroscopy, of which 30 cases were randomly assigned to reconstruction by Endobutton device and 30 cases underwent reconstruction by Tightrope device. All operations were performed by the same surgeon. All patients were subjected to regular functional exercise and were followed up regularly after operation. Effects of Tightrope and Endobutton in the cruciate ligament reconstruction were evaluated by comparing various indexes in the two groups.
    RESULTS AND CONCLUSION: Compared to the Endobutton fixation system, the Tightrope fixation system could shorten the operation time, reduce the length of tendon incision, and decrease the loss of bone mass in the femoral bone tunnel. There were no significant differences in the maximum knee flexion, knee joint score and Tegner movement level score between the two groups at 3 and 6 months after operation. These findings indicate that the Tightrope fixation system is superior to the Endobutton fixation system, because it is more simple and convenient to operate and has less bone loss. However, their clinical efficacy has no difference after 6 months. 

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    Cholecystokinin promotes regeneration of the injured common peroneal nerve: study protocol for a prospective, randomized, controlled clinical trial
    Chen Xuan-huang, Zheng Feng, Zhang Guo-dong, Li Rong-yi, Lin Hai-bin, Zheng Zu-gao, Cai Han-hua
    2016, 20 (11):  1623-1629.  doi: 10.3969/j.issn.2095-4344.2016.11.016
    Abstract ( 219 )   PDF (538KB) ( 324 )   Save

    BACKGROUND: Cholecystokinin as an endogenous neuroprotective factor in the nervous system has garnered increasing attention. Findings from previous animal studies show that cholecystokinin can effectively promote the regeneration of the injured peripheral nerve. On this basis, further clinical trials will be performed to observe whether local application of cholecystokinin at nerve anastomosis can promote peripheral nerve regeneration.
    METHODS/DESIGN: As a prospective randomized controlled trial, this study will enroll 100 patients with complete rupture of the peroneal nerve, who will be randomly divided into two groups: after nerve suture and partial gelatin sponge infiltration at nerve anastomosis, the patients will be treated with 8 nmol/kg cholecystokinin (treatment group) or saline (control group). At 6, 12, 24 weeks after treatment, common peroneal nerve conduction velocity and electromyography and nerve fiber morphology will be detected; the clinical efficacy at the last follow-up will be assessed; and all adverse events during the follow-up will be recorded to assess the therapeutic efficacy and safety.
    DISCUSSION: In this study, cholecystokinin as an inducing agent for nerve growth factor synthesis will be observed and studied, with a view to providing a new idea for seeking peripheral nerve therapy.
    ETHICAL APPROVAL: The study protocol was approved by the Medical Ethics Committee of the Affiliated Hospital of Putian University (approval No. 2014116). Written informed consent will be obtained from patients before treatment. 

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    Application of cell sheet technology in tissue engineering
    Zhou Shu-kui, Zhang Kai-le, Wang Ying, Fu Qiang
    2016, 20 (11):  1630-1636.  doi: 10.3969/j.issn.2095-4344.2016.11.017
    Abstract ( 566 )   PDF (613KB) ( 973 )   Save

    BACKGROUND: The cell sheet technology that is applied with the absence of scaffolds and enzymatic digestion can effectively repair tissue defects and improve organ function, by stimulating the secretion of extracellular matrix to form a dense membrane tissue.
    OBJECTIVE: To review the recent progress in cell sheet technology used in tissue engineering, thereby providing a new idea for relevant basic and clinical research.
    METHODS: The first author retrieved CNKI database, Wanfang database and PubMed with the keywords of “cell sheet, tissue engineering” in Chinese and English, respectively. Literature retrieval period was from January 2010 to July 2015.
    RESULTS AND CONCLUSION: Cell sheet technology combined with scaffold materials can be used for reconstruction and repair of tissues and organs. With the emerging of new technologies, multi-layer cell sheets are stratified to form a three-dimensional tissue for repair of soft tissues and organs. Compared with the monolayer cell sheet, the three-dimensional cell sheet that is laminated by same or different cell sheets has stronger regenerative ability and can be used to construct the ideal target tissue model in vitro. Cell sheet technology combined with scaffolds can improve the mechanical strength of the composite and reduce cell loss, which has made great progress in the repair of tooth, bone and cartilage tissue. Currently, the cell sheet technology is at the laboratory stage, and little is reported on its clinical applications. We look forward to more innovative technologies that can be integrated into the cell sheet technology. 

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    Microenvironment of cell growth factors and early embryonic development
    Wang Fang, Chen Shao-wei
    2016, 20 (11):  1637-1643.  doi: 10.3969/j.issn.2095-4344.2016.11.018
    Abstract ( 330 )   PDF (552KB) ( 678 )   Save

    BACKGROUND: Early mammalian embryonic development and implantation is a very complex process, which is regulated by a variety of cytokines. Moreover, epidermal growth factor, transforming growth factor, leukemia inhibitory factor, insulin-like growth factor and vascular endothelial growth factor play an important role in this regulation process.
    OBJECTIVE: To introduce cytokines related to early embryonic development, including types, structural features and molecular mechanisms, and meanwhile to review the effects of epidermal growth factor, transforming growth factor, leukemia inhibitory factor, insulin-like growth factor and vascular endothelial growth factor in the early embryonic development.
    METHODS: A literature retrieval was performed to search relevant articles published from 1989 to 2015 using the keywords of “embryos development, epidermal growth factor, transforming growth factor, leukemia inhibitory factor, insulin-like growth factor, vascular endothelial growth factor”. Active effects of these five kinds of cytokines in overcoming the mammalian embryonic development block were reviewed and summarized to provide theoretical and experimental basis for further optimization of the embryonic culture system in vitro.
    RESULTS AND CONCLUSION: Cell growth factors involved in embryonic development is the focus of the study. Insulin-like growth factor is capable of promoting the embryonic growth; epidermal growth factor exhibits multiform functions in the embryonic development; leukemia inhibitory factor directly affects oocyte cell development, and progesterone increases the expression of leukemia inhibitory factor to provide a good cytokine microenvironment for embryonic development; vascular endothelial growth factor promotes in vitro oocyte maturation, and plays a very important role in various stages of embryonic development. To clarify these regulatory patterns of cytokines cannot only contribute to in vitro embryonic culture, but also reduce embryonic apoptosis, which is of great significance for promoting embryonic development.
     

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    Role of vascular endothelial growth factor and its receptors in the corneal tissue and corneal lesions
    Feng Lu, Di Guo-hu, Zhou Qing-jun
    2016, 20 (11):  1644-1650. 
    Abstract ( 216 )   PDF (516KB) ( 346 )   Save

    BACKGROUND: Vascular endothelial growth factors are a family of multifunctional cytokines that can enhance vascular permeability, induce angiogenesis, promote endothelial cell growth and migration, and inhibit cell apoptosis.
    OBJECTIVE: To elaborate the latest progress in the role of vascular endothelial growth factor and its receptors in the corneal tissue.
    METHODS: A computer-based search of PubMed databases was performed for relevant articles published from 2005 to 2015. The key words were “vascular endothelial growth factor, cornea”. According to the inclusion and exclusion criteria, 43 articles were included in result analysis.
    RESULTS AND CONCLUSION: Vascular endothelial growth factor and its receptors are involved in the regulation of corneal neovascularization by causing Tip cell activation that affects the Notch signaling pathways. Corneal lymphatic regeneration mainly relies on macrophages to secrete vascular endothelial growth factor-C or vascular endothelial growth factor-D that further activate vascular endothelial growth factor receptor-3 in the lymphatic endothelial cells to cause cell proliferation and migration, and eventually lead to the formation of new lymphatic vessels. But herpes simplex keratitis HSK induces the corneal lymphatic regeneration by vascular endothelial growth factor-A/vascular endothelial growth factor receptor-2 pathway. Vascular endothelial growth factor family can significantly improve the damaged corneal nerve endings, epithelium and corneal sensitivity, has the function of nerve nutrition and promote restoration of the corneal epithelium.
     

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    Tissue engineering technology for repair of meniscus injury: from basic to clinic
    Hou Li-gang, Yang Jian-yi
    2016, 20 (11):  1651-1657.  doi: 10.3969/j.issn.2095-4344.2016.11.020
    Abstract ( 263 )   PDF (675KB) ( 606 )   Save

    BACKGROUND: The use of tissue engineering technology to build a functional meniscus is a new idea for repair of meniscus injury.
    OBJECTIVE: To analyze the research progress of seed cells and scaffold materials in tissue-engineered meniscus repair.
    METHODS: A computer-based search of CNKI and PubMed was performed for articles related to tissue-engineered meniscus repair published from 1996 to 2015. The keywords were "meniscal repair, meniscal injury, tissue engineering, tissue-engineered meniscus, biomaterials, stem cells" in Chinese and English, respectively.
    RESULTS AND CONCLUSION: Tissue-engineered meniscus reconstruction is a more viable method for repair of meniscus injury. Mesenchymal stem cells are pluripotent cells that are ideal seed cells for tissue-engineered meniscus reconstruction. Scaffolds are one of important factors for meniscus repair, and natural meniscal scaffolds play an important role. Selection and development of scaffold materials for meniscus tissue engineering have experienced a rapid development period from a single material to composite materials. Composite materials make up a lot of shortcomings and deficiencies that a single material has, and open up new ideas for developing new materials. Meniscal tissues with geometric shapes can be constructed using tissue engineering technology. However, the long-term observation of the biological properties of meniscal tissues is necessary, and from basic to clinic, there is still a lack of reliable data to prove the effect of tissue engineering technology in the meniscus repair. 

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    Anterolateral ligament of the knee: anatomy, biomechanics and functional recovery
    Wu Jiang, Huang Jing-min, Zhao Bin, Cao Jian-gang, Chen Xiao
    2016, 20 (11):  1658-1665.  doi: 10.3969/j.issn.2095-4344.2016.11.021
    Abstract ( 301 )   PDF (537KB) ( 826 )   Save

    BACKGROUND: Anterior cruciate ligament injury accompanied by unstable rotation is a hotspot in sports medicine. Further understanding of the anatomy and biomechanics of the anterolateral ligament can play a guiding significance for the recovery of knee joint rotational stability.
    OBJECTIVE: To systematically review current literature on the anterolateral ligament of the knee and to understand the incidence, anatomy, morphology and histology of the anterolateral ligament as well as mechanism of anterolateral ligament injury.
    METHODS: The first author searched the PubMed, Medline, CNKI, Wanfang, VIP databases for articles specifically addressing the anterolateral ligament. Data extraction related to the incidence, anatomy, morphometry, biomechanics, and histology of the anterolateral ligament and its relation to the “Segond” fracture was performed. The retrieve time ranged from 1878 to 2015. Totally 362 literatures were retrieved, including 342 articles in English and 20 in Chinese. According to inclusive and exclusive criteria, 42 articles were included in result analysis.
    RESULTS AND CONCLUSION: The occurrence rate of the anterolateral ligament ranges from 83% to 100%, and this range occurs because of small discrepancies in the definition of the bony insertions of the anterolateral ligament. The anterolateral ligament originates anterior and distal to the femoral attachment of the lateral collateral ligament. It spans the joint in an oblique fashion and inserts between the fibular head and Gerdy tubercle of the tibia. Exact anatomic and morphometric descriptions vary in the literature, and there are discrepancies regarding the anterolateral ligament attachment to the capsule and lateral meniscus. The anterolaterial ligament is a contributor to the stability of tibial internal rotation, and histologically, it exhibits parallel, crimped fibers consistent with a ligamentous microstructure. The footprint of the anterolateral ligament has been shown to be at the exact location of the Segond fracture. The anterolateral ligament is a distinct ligamentous structure at the anterolateral plane of the knee, and it is likely involved in the control of excessive tibial internal rotation that can cause the Segond fracture. 

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    Core strength training in the elderly with chronic low back pain
    Xie En-li, Zhan Jian-guo
    2016, 20 (11):  1666-1672.  doi: 10.3969/j.issn.2095-4344.2016.11.022
    Abstract ( 281 )   PDF (581KB) ( 732 )   Save

    BACKGROUND: Numerous studies have confirmed the effectiveness of core strength training, most of which focus on the adult rather than the elderly.
     OBJECTIVE: To review the relevant literatures targeting the elderly with low back pain and to explore the mechanism of core strength training in the treatment of elderly low back pain as well as different training methods and precautions, in order to provide theoretical basis for treatment of elderly patients with chronic low back pain.
    METHODS: Studies on the application of core strength training in the elderly with low back pain were retrospectively reviewed using bibliometrics method. The keywords were “chronic low back pain, core strength training, elderly person” in English and Chinese, respectively.
    RESULTS AND CONCLUSION: A large number of scholars have focused on the non-pathological therapy for elderly patients with chronic lower back pain. Core strength training for treatment of low back pain is characterized as a simple operation, low cost, significant effectiveness and few side effects, which is basically applicable in different groups. Combination of two or more exercise therapies can enhance the core strength training effect. In addition, correct health concept education, psychological and behavioral interventions are necessary to o eliminate the fear of pain and improve patient compliance, thereby increasing the effectiveness of exercise therapy. During the core strength training, we also should pay attention to distinguish the severity of diseases, degree of urgency, stage of disease, age, and individual physical differences, and take targeted exercises.
      

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