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    08 January 2013, Volume 17 Issue 2 Previous Issue    Next Issue
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    Comparing three methods of preparing tissue engineering tracheal matrix
    Wu Fan, Zhang Zhi-pei, Wang Jian, Li Jian-zhong, Jin Yan, Jiang Tao, Han Yong, Li Xiao-fei
    2013, 17 (2):  191-195.  doi: 10.3969/j.issn.2095-4344.2013.02.001
    Abstract ( 394 )   PDF (405KB) ( 576 )   Save

    BACKGROUND: It is a key step to prepare tracheal matrices in tissue engineering for repairing long segment tracheal defects.
    OBJECTIVE: To find the better method for preparing tissue engineering tracheal matrices through comparing and analyzing three different ways of preparing allogeneic acellular tracheal matrices.
    METHODS: Fresh rabbit tracheas were obtained by surgical operation and divided to four groups: untreated group, conventional vitrificational group, detergent-enzymatic group, modified vitrificational group. Hematoxylin-eosin staining and scanning electron microscopy were used to observe the morphology and ultrastructure of the treated tracheal matrices. The biomechanical properties including maximum tensile force, rupture force and tissue elongation of the treated tracheal matrices were measured.
    RESULTS AND CONCLUSION: Histological observations showed that there were epithelial cells in the untreated and conventional vitrificational groups, but there were no epithelial cells in the detergent-enzymatic and modified vitrificational groups. There were abundant extracellular matrices and collagen fibers in the untreated group, conventional vitrificational group, and modified vitrificational group under electromicroscopy. Conversely, no extracellular matrix was found in the detergent-enzymatic group, in which there were only collagen fibers. Finally, no statistical differences were found in the maximum tensile force, rupture force and tissue elongation among all the groups. The method of modified vitrification, by which the antigen can be removed, and the extracellular matrix and biomechanical properties can be maintained effectively, is a more ideal way to prepare tissue engineering tracheal matrix.

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    Tissue-engineered graft for urinary diversion in rabbits
    Liao Wen-biao, Song Chao, Yang Si-xing, Li Yong-wei, Meng Ling-chao, Li Xin-hui
    2013, 17 (2):  196-200.  doi: 10.3969/j.issn.2095-4344.2013.02.002
    Abstract ( 348 )   PDF (401KB) ( 779 )   Save

    BACKGROUND: For muscle invasive bladder cancer, radical cystectomy is the most effective treatment now and urinary diversion is often necessary. The use of intestinal tissue for urinary diversion is frequently associated with complications.
    OBJECTIVE: To study the feasibility of tissue-engineered graft using bladder epithelial cells and bladder acellular matrix (BAM) for urinary diversion in rabbits.
    METHODS: BAM of rabbits was made in vitro. Bladder epithelial cells of rabbits were cultivated and expanded in vitro, then implanted into the BAM and cultured for 7 days before making a 4 cm conduit. In the experimental group, 24 New Zealand rabbits, divided into six groups with four in each, were subjected to excising most of the bladder with bladder trigone retained. Then the retained bladder trigone were anatomized with the conduit which was then wrapped by omentum. In the control group, the conduit was made using unseeded BAM and anatomized with the retained bladder trigone in the four New Zealand rabbits. Specimens of tissue-engineered grafts were obtained at 1, 2, 4, and 8 weeks after surgery respectively and were stained with haematoxylin and eosin. Immunohistochemistry examination was done at 8 weeks postoperatively.
    RESULTS AND CONCLUSION: All animals were alive in the experimental group. Hematoxylin and eosin staining showed epithelial coverage on the lumen of tissue-engineered conduit. With the time going on, grown epithelial cells gradually integrated with the BAM. Immunohistochemistry showed anti-cytokeratin AE1/AE3 antibody and anti-ZO1 antibody were positive, confirming that there were mature and functional epithelial cells on the lumen of conduit. In the control group, four rabbits were all dead within 2 weeks. Scar formation, atresia, and severe hydronephrosis were found in the process of autopsy. It is feasible to prepare tissue-engineered grafts using bladder epithelial cells and BAM for urinary diversion in rabbits.

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    Serum biomarkers related to primary osteoarthritis
    Liu Yuan, Sun Xue-lian, Zhou Hong-hai
    2013, 17 (2):  201-204.  doi: 10.3969/j.issn.2095-4344.2013.02.003
    Abstract ( 481 )   PDF (749KB) ( 657 )   Save

    BACKGROUND: With the continuous development of the molecular biology, studies on laboratory indicators reflecting the pathological changes of early articular cartilage degeneration have become a hot spot.
    OBJECTIVE: To explore clinical significance of type Ⅱ collagen telopeptides and cartilage oligomeric matrix protein in knee osteoarthritis patients, seeking the relativity between them and characteristic rule of primary knee osteoarthrosis.
    METHODS: Seventy patients with primary knee osteoarthrosis were enrolled in the experimental group, and 18 healthy volunteers served as control group. Serum type Ⅱ collagen telopeptides and cartilage oligomeric matrix protein levels were detected by enzyme-linked immunosorbent assay method.
    RESULTS AND CONCLUSION: The serum type Ⅱ collagen telopeptides and cartilage oligomeric matrix protein levels in the experimental group were significantly higher than those in the control group. There were notable differences among different genders, age and X-ray changes. Stroke musculoskeletal patients with different syndromes of traditional Chinese medicine had lower type Ⅱ collagen telopeptides levels than patients with liver and kidney deficiency as well as vital energy retardation and blood stasis, but no difference was found in cartilage oligomeric matrix protein levels. These findings indicate that type Ⅱ collagen telopeptides and cartilage oligomeric matrix protein have a closely related relationship with the occurrence and development of primary knee osteoarthritis. Combination of type Ⅱ collagen telopeptides and cartilage oligomeric matrix protein can play an important role in the pathogenesis of knee osteoarthritis, have a close relationship with cartilage degeneration and reflect the condition and syndromes of traditional Chinese medicine.

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    Intraosseous injection of pure alcohol induces necrosis of the femoral head in a rabbit
    Chen Dong, Hua Wen-bin, Ye Shu-nan, Yang Shu-hua, Chen Chao, Wang Xiao-hong, Yu Qian, Liu Xian-zhe, Suo Jin-ping, Nie Lei
    2013, 17 (2):  205-209.  doi: 10.3969/j.issn.2095-4344.2013.02.004
    Abstract ( 422 )   PDF (456KB) ( 736 )   Save

    BACKGROUND: Currently, it is difficult to prepare an animal model of early osteonecrosis of the femoral head (ONFH).
    OBJECTIVE: To develop a simple and dependable animal model of ONFH that allows the evaluation of different therapeutic approaches.
    METHODS: Pure alcohol was injected into the centre of the right femoral head in New Zealand white rabbits under X-ray fluoroscopy, and the left femoral head with no treatment served as controls. After 2, 4 and 6 weeks, the animals were killed under anesthesia and the femoral heads were harvested.
    RESULTS AND CONCLUSION: Gross and X-ray observations indicated that the articular cartilage in the modeling side of the femoral head was dark in color and had the uneven bone density at the first two weeks after modeling. At 6 weeks, a slight depression was found on the articular surface, and the bone density shadow increased. MRI results showed that line or irregular T1-weighted signals and high T2-weighted signals were seen in the weight-bearing area of the femoral head at 2 weeks; femoral head degeneration, subchondral fracture, articular surface collapse, and crescent formation occurred at 6 weeks after modeling. In addition, there was no abnormality in the control side of the femoral head at 2, 4 and 6 weeks. Histopathological results showed karyopyknosis, degeneration and necrosis of the femoral head at 2 weeks after modeling. These findings verified that partial osteonecrosis was confirmed over a period of 2 weeks in all animals. The morphology of necrosis in combination with intact macrotexture and joint cartilage was similar to the features described in early ONFH in humans. We obtained a good efficacy and similarity animal model of the early stages of ONFH in humans. This model may be compatible to develop new therapeutic methods for ONFH.

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    Effects of compound danshen extract on bone histomorphometry of high-fat rats
    Zhang Xin-le, Wu Tie, Cui Liao, Xu Bi-lian
    2013, 17 (2):  210-216.  doi: 10.3969/j.issn.2095-4344.2013.02.005
    Abstract ( 462 )   PDF (407KB) ( 760 )   Save

    BACKGROUND: Compound danshen extract can inhibit bone resorption and rival bone loss of rats induced by prednisone. However, there are no reports indicating its effectiveness in osteoporosis induced by hyperlipidemia.
    OBJECTIVE:To study the effect of compound danshen extract against tibia and lumbar spine bone loss by using bone histomorphometry through establishing a osteoporosis rat model induced by high-fat emulsion.
    METHODS: Thirty 3-month-old male Sprague-Dawley rats were randomly divided into normal saline group, high-fat emulsion group, compound danshen extract group. Rats were sacrificed after 16 weeks.
    RESULTS AND CONCLUSION: Compared with the high-fat emulsion group, serum total cholesterol decreased and high-density lipoprotein cholesterol increased significantly following treatment with compound danshen extract. In the longitudinal proximal tibial metaphyseal of rats treated with compound danshen extract, %Tb.Ar, Tb.N and %Ob.S.Pm increased (P < 0.05), while Tb.Sp, %Oc.S.Pm and Oc.N/mm decreased (P < 0.01). In the tibial shaft, %Ct.Ar increased (P < 0.01), while %Ma.Ar decreased (P < 0.01). In the fifth lumbar vertebral body, %Tb.Ar, Tb.N and Tb.Th increased (P < 0.05), while Tb.Sp decreased (P < 0.01). Long-term high-fat diets can cause the loss of bone in rats, and compound danshen extract can prevent these changes through stimulating periosteal bone formation.

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    Raloxifene promotes the healing of mandibular fractures in rabbits
    Liu Kai, Shi Chong, Liu Shu-fa, Zhang Hong-kai
    2013, 17 (2):  217-222.  doi: 10.3969/j.issn.2095-4344.2013.02.006
    Abstract ( 583 )   PDF (491KB) ( 625 )   Save

    BACKGROUND: Although raloxifene has been widely applied in the treatment of osteoporosis, its influence on fracture healing is unclear.
    OBJECTIVE: To investigate the effect of raloxifene on the healing of mandibular fractures in rabbits.
    METHODS: Totally 24 New Zealand white rabbits were collected. Model of bilateral mandibular angle bone defect (1.5 mm×10.0 mm) in rabbits was established. All rabbits were randomly divided into experimental and control groups. The rabbits in the experimental group were performed 7.5 mg/(kg•d) raloxifene at day 2 after modeling for 30 days, while those in the control group had no treatment.
    RESULTS AND CONCLUSION: X-ray observation showed that callus formation was not obvious in the two groups after modeling for 1 week. Defect area of the experimental group was indistinct, but that of the control group could be found at week 3. At week 4, callus in the experimental group was increased and medullary cavity passed again. Callus in the control group was more, and medullary cavity did not pass. Compared with control group, bone mineral density and serum bone alkaline phosphatase in the experimental group was increased obviously after modeling for 1, 3 and 4 weeks (P < 0.05), and they both reached the peak. The expression of bone morphogenetic protein 2 in callus was higher than that of the control group after modeling for 3 and 4 weeks (P < 0.01). These results suggest that raloxifene can promote osteoblast differentiation, accelerate bone mineral deposition, and induce bone morphogenetic protein 2 expression at the same time, and thereby accelerate the healing of bone fracture

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    Condensed autologous bone marrow transplantation facilitates the tendon-bone healing
    Zhang Yi-long, Li Ning, Song You-xin, Fang Ya-qun, Zhang Hong, Zhang Jin-yan
    2013, 17 (2):  223-227.  doi: 10.3969/j.issn.2095-4344.2013.02.007
    Abstract ( 455 )   PDF (357KB) ( 599 )   Save

    BACKGROUND: There are a lot of applications of hamstring tendons autografts in the reconstruction of anterior cruciate ligament, which needs a long term for the tendon-bone healing and restricts the early functional activities of patients.
    OBJECTIVE: To evaluate the effect of condensed autologous bone marrow transplantation on the tendon-bone interface in the reconstruction of anterior cruciate ligament.
    METHODS: One knee joint was chosen as the experimental group and the other side as the control group in 32 New Zealand rabbits experiencing the reconstruction of anterior cruciate liagment. The tibial tendon-bone interface was injected with condensed autologous bone marrow in the experimental side and the other side was not injected as the control.
    RESULTS AND CONCLUSION: The histological anatomy showed the tendon-bone interface was filled with granulation tissues that were loose, and there were some activities of bone formation in the control group at     2 weeks after operation; the tendon-bone interface was filled with granulation tissues that were not compact, but there were active activities of bone formation in the experimental group at 2 weeks after operations. The bound between the tendon and bone was becoming obscure, and there were collagen fiber-fibrocartilage-calcified fibrocartilage-bone transitional zones at the interface in the control group at 12 weeks after operation. In the experimental group, there were conspicuous collagen fiber-fibrocartilage-calcified fibrocartilage-bone transitional zones and clear tidal line at the interface. The maximal pull-out loads in the experimental group were higher than those in the control group at 4, 8 and 12 weeks after operation (P < 0.05). These findings indicate that condensed autologous bone marrow transplantation can enhance the tensile strength of tendon-bone interface, and can do good to tendon-bone healing in a bone tunnel.

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    Ultrapulse CO2 fractional laser intervens in situ superficial scar regeneration in a rabbit ear
    Tan Jun, Lei Ying, Li Gao-feng, Ouyang Hua-wei, Zhu Yi, Li Bo
    2013, 17 (2):  228-234.  doi: 10.3969/j.issn.2095-4344.2013.02.008
    Abstract ( 655 )   PDF (603KB) ( 1188 )   Save

    BACKGROUND: The ultrapulse CO2 fractional laser has a good effect on the treatment of superficial scars, but the mechanism is unclear.
    OBJECTIVE: To investigate the effect of ultrapulse CO2 fractional laser on the treatment of superficial scars in rabbit ear and to explore mechanism of wound in situ regeneration and repair.
    METHODS: The superficial scars in rabbit ear were induced with ultrapulse CO2 fractional laser, then traditional iodophor treatment and moist exposed burn ointment treatment methods were used for repairing the wound.
    RESULTS AND CONCLUSION: The wound healing time of moist exposed burn ointment group was shorter than that of iodophor group (P < 0.01). The epidermal stem cells emerged after the superficial scars induced with ultrapulse CO2 fractional laser, and the expression of cytokeratin 19 and P63 protein was observed after induced for 24 hours. The number of cytokeratin 19 and P63 protein in the moist exposed burn ointment was increased after induced for 4 days and reached peak at 7 days and then decreased at 14 days. While the number of cytokeratin 19 and P63 protein in the iodophor group was increased after induced for 4 days, and then decreased after induced for 7 and 14 days. The expression of cytokeratin 19 and P63 protein in the moist exposed burn ointment group was significantly higher than that in the iodophor group (P < 0.05). Ultrapulse CO2 fractional laser combined with moist exposed burn ointment for the treatment of superficial scar in rabbit ear can better activate and protect the epidermal stem cells, and promote wound repair and in situ regeneration.

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    Variation of RhoA/ROCK transduction pathway in the articular cartilages under abnormal stress
    Zhang Hai-xiang, Wang Chen
    2013, 17 (2):  235-240.  doi: 10.3969/j.issn.2095-4344.2013.02.009
    Abstract ( 821 )   PDF (381KB) ( 776 )   Save

    BACKGROUND: In order to confirm whether RhoA/ROCK transduction pathway play an active role in in vivo articular cartilage degeneration or osteoarthritis, we designed this experiment.
    OBJECTIVE: To explore the role of the RhoA/ROCK transduction pathway in the process of articular cartilage degeneration.
    METHODS: Totally 36 New Zealand white rabbits were randomly divided into a control and 2-, 4- and 6-week immobilization groups, and the right hindlimbs of rabbits were immobilized with plaster bandage in extension position except those in the control group. The articular cartilage of the lateral tibial plateau was harvested for hematoxylin-eosin staining and immunohistochemistry to observe the pathological changes and the content of RhoA and ROCK.
    RESULTS AND CONCLUSION: The articular cartilage degenerated with time prolonged, and the Mankin scores showed there were significant differences among groups (P < 0.05). Immunohistochemical results showed that the RhoA/ROCK transduction pathway was motivated mainly in the tangent layer and the middle layer of the cartilage and inhibited with immobilization time prolonged. The RhoA/ROCK transduction pathway takes an important role in the process of articular cartilage degeneration.

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    Effect of radix clematidis extract on viability of knee osteoarthritis chondrocytes
    Xu Yang, Gui Jian-chao, Gao Feng, Xu Yan, Wang Li-ming, Lu Yi-ming, Yin Zhao-wei
    2013, 17 (2):  241-246.  doi: 10.3969/j.issn.2095-4344.2013.02.010
    Abstract ( 592 )   PDF (353KB) ( 752 )   Save

    BACKGROUND: In recent years, studies have shown that excessive apoptosis of articular chondrocytes is the key factor for the start and progress of osteoarthritis. To study the progress in the use of drugs that inhibit apoptosis of chondrocytes to control osteoarthritis has become a hotspot. Clematis has obtained exact effect in the domestic clinical treatment of osteoarthritis, but the specific mechanism underlying 
    inhibition of chondrocytes apoptosis has not been reported.
    OBJECTIVE: To observe the effect of radix clematidis extract on cell viability of the knee osteoarthritis chondrocytes.
    METHODS: Joint cartilage was shredded after harvested from the patients of osteoarthritis undergoing the knee replacements, and chondrocytes were isolated and cultured by the way of enzymatic digestion. The third-passage cells in the logarithmic growth phase were cultured in vitro and randomly divided into six groups after adherence. The experimental groups were cultured in Dulbecco’s modified Eagle’s medium with 0.01, 0.05, 0.1, 0.5, and   1.0 g/L radix clematidis extract, while the control group was given normal medium alone. Live/Dead assay method was adopted to observe the effect of radix clematidis extract with different concentrations on cell viability of the knee osteoarthritis chondrocytes, and TUNEL method was used to assay apoptosis index of the knee osteoarthritis chondrocytes.
    RESULTS AND CONCLUSION: 0.05 and 0.1 g/L radix clematidis extracts increased cell viability of chondrocytes, while 0.5 and 1.0 g/L radix clematidis extracts decreased the cell viability of chondrocytes. There was a significant difference in the cell viability between 0.05, 0.1, 0.5, 1.0 g/L radix clematidis extract groups and the control group (P < 0.05). 0.01, 0.05, 0.1 g/L radix clematidis extracts effectively inhibited apoptosis of chondrocytes, while   1.0 g/L radix clematidis extract promote the apoptosis of chondrocytes. There was a significant difference in the apoptotic index between 0.01, 0.05, 0.1, 1.0 g/L radix clematidis extract groups and the control group (P < 0.05). The appropriate concentration of radix clematidis extract could improve chondrocytes viability and restrain chondrocytes apoptosis, and the peak was at 0.1 g/L group. But excessive concentration of radix clematidis extract could reduce chondrocytes viability and promote chondrocytes apoptosis, representing the toxic effects on human articular chondrocytes.

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    Monosodium iodoacetate induces apoptosis of primary rat chondrocytes
    Jiang Li-ping, Li Long-jie, Gong De-zheng, Geng Cheng-yan, Jiang Li-jie, Zhong Lai-fu
    2013, 17 (2):  247-253.  doi: 10.3969/j.issn.2095-4344.2013.02.011
    Abstract ( 590 )   PDF (475KB) ( 733 )   Save

    BACKGROUND: Recently, monosodium iodoacetate is usually used to cause cartilage degradation resembling the pathological changes of human osteoarthritis. However, rate studies report the mechanisms underlying monosodium iodoacetate-induced chondrocyte apoptosis.  
    OBJECTIVE: To assess the apoptosis of primary rat chondrocytes induced by different concentrations of monosodium iodoacetate and to clarify the underlying mechanism.
    METHODS: The primary rat chondrocytes were treated with monosodium iodoacetate for 24 hours, and the induction of apoptosis was analyzed by flow cytometry and Hoechst 33342/PI staining. The levels of mitochondrial membrane potential were evaluated using fluorescence spectrophotometer and laser scanning confocal microscope. The production of reactive oxygen species was determined by fluorescence spectrophotometer. Apoptosis-related protein cytochrome C and caspase-3 expressions were examined by western blotting.
    RESULTS AND CONCLUSION: Monosodium iodoacetate induced cellular apoptosis in a dose-dependent manner. Significantly increased level of reactive oxygen species was observed in primary rat chondrocytes at higher concentration of monosodium iodoacetate (P < 0.05). Significantly decreased levels of mitochondrial membrane potential were also shown in primary rat chondrocytes (P < 0.05). Western blot assay revealed that monosodium iodoacetate significantly increased the release of cytochrome C and the protein expression of caspase-3, leading to cell apoptosis. Together these observations suggest that the mechanisms of monosodium iodoacetate-induced apoptosis are primarily via the production of reactive oxygen species and mitochondria- mediated caspase-3 activation in primary rat chondrocytes.

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    Paeoniflorin accelerates annulus fibrosus cells proliferation
    Chen Shao-qing, Lin Jian-ping, Wang Shi-zhong, Hong Yu, Chen Le-chun
    2013, 17 (2):  254-258.  doi: 10.3969/j.issn.2095-4344.2013.02.012
    Abstract ( 370 )   PDF (419KB) ( 575 )   Save

    BACKGROUND: Chinese herbaceous peony has been usually used in the treatment of cervical spondylosis in a frequency of over 30%. Paeoniflorin, known as one of the main monomers, has cell-protective abilities against inflammation and apoptosis. Despite these compelling observations, whether paeoniflorin protects annulus fibrosus cells is not reported.
    OBJECTIVE: To explore the proliferative and protective effects of paeoniflorin on intervertebral disc annulus fibrosus cells.
    METHODS: Annulus fibrosus cells derived from the intervertebral disc were digested with trypsin and collagenase type Ⅱ for the further culture in vitro. The third-passage annulus fibrosus cells were selected to establish an apoptosis model in response to Fas ligand (20 μg/L) and were interfered with paeoniflorin. The appropriate concentration of paeoniflorin was detected by the method of MTT. Apoptotic rate was evaluated with Annexin V/FITC double staining.
    RESULTS AND CONCLUSION: The 20.8 and 2.08 μmol/L paeoniflorin significantly promoted the proliferation of annulus fibrosus cells. The apoptotic rate of annulus fibrosus cells in vitro was significantly increased after induction with the 20 μg/L Fas ligand. 20.8 μmol/L paeoniflorin could protect annulus fibrosus cells against Fas ligand-induced apoptosis.

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    Recombinant green fluorescent protein plasmids expressing human telomerase reverse transcriptase transfect normal nucleus pulposus cells in the intervertebral disc
    Wu Jin-feng, Ye Dong-ping, Dai Li-bing, Liang Wei-guo
    2013, 17 (2):  259-263.  doi: 10.3969/j.issn.2095-4344.2013.02.013
    Abstract ( 385 )   PDF (352KB) ( 715 )   Save

    BACKGROUND: Nucleus pulposus cells are difficult to be isolated and cultured from the intervertebral disc, and the cells age rapidly. An urgent standard cell line is required for experimental research.
    OBJECTIVE: To investigate the construction of recombinant green fluorescent protein plasmid expressing human telomerase reverse transcriptase and to assess the feasibility of constructing immortalized human nucleus pulposus cell line.
    METHODS: Target gene cloning, target gene sequencing in eukaryotic expression plasmids, construction of eukaryotic expression plasmids expressing target genes, and transfection of human telomerase reverse transcriptase were performed in order.
    RESULTS AND CONCLUSION: Nucleus pulposus cells transfected with recombinant green fluorescent protein plasmid expressing human telomerase reverse transcriptase have a stable expression. It is anticipated that human telomerase reverse transcriptase can be useful for creating the immortalized nucleus pulposus cells.

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    Influence of soy isoflavone tincture on wound healing of deep partial-thickness scald in mice
    Zhang Li, Chen Juan, Su Wei-sheng, Huang Jia-jun
    2013, 17 (2):  264-269.  doi: 10.3969/j.issn.2095-4344.2013.02.014
    Abstract ( 450 )   PDF (342KB) ( 912 )   Save

    BACKGROUND: Estrogen has a role to promote wound healing, and combination of soy isoflavones and estrogen receptor presents an obvious estrogen-like effect.
    OBJECTIVE: To explore the preparation of soy isoflavone tincture and to study its influence on wound healing in scalded mice.
    METHODS : Soy isoflavone tincture was prepared by cold dipping and the most effective concentration was
    screened. At the beginning of the experiment, all of the mice were used to prepare deep partial-thickness scald models and then randomly divided into soy isoflavone tincture (0.100, 0.361, 1.000, 3.610 g/L), solvent control (75% ethanol) and blank (without treatment) groups. From the 3rd day on, nonhealing rates of wound were assessed every other day. Simultaneously, the histological and morphological changes were observed and analyzed at days 3, 9, 14 after modeling.
    RESULTS AND CONCLUSION: The most effective concentration of soybean isoflavone tincture was 3.61 g/L. On days 5, 7, 9, 11, 13 after injury, the nonhealing rate of wound in the soybean isoflavone tincture group was significantly less than that of the blank group (P < 0.05), as well as that of the solvent control group (P < 0.05). On day 9 post scalded, the histomorphology displayed that there were many more fibroblasts in the granulation tissue in the soy isoflavone tincture group than those of the blank group, also than those of the solvent control group. On day 14 post scalded, the histomorphology showed that the epithelial layer in the soy isoflavone tincture group was thicker than that of the other two groups. It is a viable method that soy isoflavone tincture is prepared in 75% ethanol solution, and its concentration of 3.61 g/L can significantly accelerate the wound healing in scalded mice by local application.

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    Establishment of a rat model of knee osteoarthritis with kidney deficiency and blood stagnation
    Liu Zhen-feng, Fang Rui, Ailijiang•Asila, Hong Han-gang, Deng Ying-jie, Meng Qing-cai
    2013, 17 (2):  270-274.  doi: 10.3969/j.issn.2095-4344.2013.02.015
    Abstract ( 468 )   PDF (317KB) ( 640 )   Save

    BACKGROUND: To establish a model of osteoarthritis with traditional Chinese medicine syndromes is conductive to the syndrome differentiation studies.
    OBJECTIVE: To establish a rat model of knee osteoarthritis with kidney deficiency and blood stagnation.
    METHODS: A total of 30 female Sprague-Dawley rats aged 2 months, SPF grade, were randomly divided into normal group, knee osteoarthritis group and knee osteoarthritis with kidney deficiency and bloods stagnation group (combined group), 10 rats in each group. Knee osteoarthritis models were established using Hulth method, kidney deficiency models were established using ovariectomized method, and blood stagnation models were established by injection of adrenal corticosteroids and epinephrine. Combined models were prepared based on the above-mentioned three models. Kidney deficiency models were prepared first followed by establishment of knee osteoarthritis and bloods stagnation models.
    RESULTS AND CONCLUSION: Rats in the combined group presented listlessness, non-flexible activities and loose stools at 3 weeks after establishment of kidney deficiency models, and coat lackluster, ptosis, obvious weight loss and blue tail at 6 weeks after establishment of bloods stagnation models. Rats in the combined group also showed that the reducing viscosity was significantly up-regulated and the platelet aggregation reinforced, with blood flow slow-moving, circulatory disorder and so on. Meanwhile, the articular cartilage of the knee osteoarthritis group showed cataplasia, but it was slighter compared with the combined group. The rat model of knee osteoarthritis with kidney deficiency and blood stagnation is established successfully, and kidney deficiency and blood stagnation can aggravate articular cartilage degeneration.

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    Protective action of salvianolic acid B on skin photoaging in mice
    Zhou Xiang-jun, Ye Cai-guo, Yang Guang-li, Liu Lin-sheng
    2013, 17 (2):  275-279.  doi: 10.3969/j.issn.2095-4344.2013.02.016
    Abstract ( 447 )   PDF (318KB) ( 757 )   Save

    BACKGROUND: Chinese medicine and its extract can improve skin structure, improve the activity of antioxidant enzymes, inhibit high expression of matrix metalloproteinase, and enhance the immune defense function of the skin, which plays a preventive effect against skin photoaging.
    OBJECTIVE: To observe the protective effect of salvianolic acid B on skin photoaging in mice.
    METHODS: Mouse skin cells were cultured and irradiated in vitro to prepare UV damage models, which were treated with different doses of salvianolic acid B. MTT and single cell electrophoresis were performed to observe the severity of skin injury and protective role of salvianolic acid B on cell injury. Skin photoaging models were prepared through UV irradiation in mice, and then model mice were intragastrically administrated with different doses of salvianolic acid B. Hydroxyproline and superoxide dismutase contents were determined to evaluate whether salvianolic acid B can inhibit skin photoaging.
    RESULTS AND CONCLUSION: UV irradiation could increase malondialdehyde content in the skin, decrease hydroxyproline content as well as superoxide dismutase and glutathione oxidase activity. Salvianolic acid B could effectively protect the cells from UV damage, remarkably reduce malondialdehyde content in the skin, increase hydroxyproline, superoxide dismutase and glutathione oxidase contents, playing an inhibitory effect on skin photoaging. These findings indicate that salvianolic acid B has a protective effect on skin photoaging in mice.

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    Effect of posterior cruciate ligament rupture on histological features of medial collateral ligament
    Yu Fang, Li Kang-hua, Zhang Can, Li Yu-sheng, Gao Shu-guang, Lu Bang-bao
    2013, 17 (2):  280-285.  doi: 10.3969/j.issn.2095-4344.2013.02.017
    Abstract ( 494 )   PDF (346KB) ( 724 )   Save

    BACKGROUND: By comparing the relative quantity of typeⅠ and III collagens and type Ⅰ/Ⅲ collagen ratio, we can determine the ligament histology performance to some extent.
    OBJECTIVE: To explore the histological effect of posterior cruciate ligament injury on the medial collateral ligament under a lower physiological load in rabbits.
    METHODS: Bilateral knees of 24 male rabbits were enrolled for a self-control trial. Posterior cruciate ligaments at the experimental side were transected, and those in the control side were only exposed but not transected. At the 8th, 16th, 24th and 40th weeks after modeling, six rabbits were executed randomly, and then the histological alteration of the medial collateral ligament was observed through hematoxylin-eosin staining and picrosirius-polarization staining.
    RESULTS AND CONCLUSION: (1)Hematoxylin-eosin staining: At the 8th, 16thand 24th weeks, there was no obvious difference in the collagen distribution and arrangement of the medial collateral ligament between experimental group and control group; at the 40th week, the collagen was thinner in the experimental group. (2)Picrosirius-polarization staining: At the 8th, 16th and 24th weeks, the total number of type Ⅰ and Ⅲ collagens in the medial collateral ligament of the experiment group was more than that in the control group (P < 0.05); however, at the 40th week, the total number of type I and III collagens in the medial collateral ligament of the experimental group was much fewer than that of the control group (P < 0.05); at the 8th week, ratio of type Ⅰ/Ⅲ collagen in the medial collateral ligament of the experimental group did not differ from that in the control group (P > 0.05); however, at the 16th, 24th and 40th weeks, the ratio of type Ⅰ/Ⅲ collagen in the experimental group was much fewer than that in the control group (P < 0.05). In short-term, posterior cruciate ligament injury has no significant effect on histological properties of the rabbit medial collateral ligament. However, the histological properties can decrease significantly with time.

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    Monosodium urate monohydrate crystals affect the tight junctions among renal tubular epithelial cells
    Li Hui-juan, Chen Gan, Fu Jun-zhou, Zhou Shan-shan
    2013, 17 (2):  286-290.  doi: 10.3969/j.issn.2095-4344.2013.02.018
    Abstract ( 515 )   PDF (299KB) ( 951 )   Save

    BACKGROUND: Up to now, the relationship of uric acid stones with tight junction proteins and renal interstitial fibrosis is yet unclear.
    OBJECTIVE: To observe the effect of monosodium urate (MSU) monohydrate crystals on the tight junction among NRK-52E cells.
    METHODS: The NRK-52E cells were divided into two groups: control group and MSU group cultured in serum-free medium and MSU crystals, respectively. The protein and mRNA expressions of ZO-1 were investigated by immunofluorescence and reverse transcription-PCR, respectively. 
    RESULTS AND CONCLUSION: Compared with the control group, the protein and mRNA expressions of ZO-1 were down-regulated after the stimulation of MSU at 24, 48, 72 hours (P < 0.05), especially at 72 hours (P < 0.01). Protein expression appeared with redistribution phenomenon. These findings indicate that MSU can damage the structure, function and distribution of tight junction proteins of renal tubular epithelial cells

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    Formation of traumatic deep venous thrombosis and mRNA expression of Hmox-1 in the blood
    Zheng Yan-ke, Li Hong-kun, Tang Shan-hua, Zhao Min, Lü Ren-fa, Chen Rong-jian
    2013, 17 (2):  291-295.  doi: 10.3969/j.issn.2095-4344.2013.02.019
    Abstract ( 1586 )   PDF (809KB) ( 559 )   Save

    BACKGROUND: The diagnosis of deep vein thrombosis is mainly dependent on imaging and laboratory tests, and the most fatal lack is that thrombosis can be confirmed until it has been formed. Accordingly, it is necessary to explore inherent rules using molecular technology.
    OBJECTIVE: To observe the Hmox-1 expression in the process of formation of traumatic deep vein thrombosis in rats and to discuss the feasibility of Hmox-1 as a molecular marker for predictive diagnosis of deep vein thrombosis.
    METHODS: Bilateral femoral veins were clamped and both hind limbs were fixed in rats to prepare traumatic deep venous thrombosis models. According the modeling time and formation of thrombosis, 100 experimental rats were randomized into five groups: normal group, trauma group, pre-thrombosis group, group of thrombosis formation at peak stage, group of non-thrombosis formation at peak stage. Real time-PCR was used to detect blood Hmox-1 mRNA expression. Bilateral femoral veins were isolated for histological observation of thrombosis degree.
    RESULTS AND CONCLUSION: At 25 hours after modeling, the thrombosis rate was 58.46% (38∕65). mRNA expression of Hmox-1 in the pre-thrombosis group and group of thrombosis formation at peak stage was higher than that of the normal group (P < 0.05). There was no significant difference in the Hmox-1 mRNA expression between the normal group and the group of non-thrombosis formation at peak stage. These findings indicate that the variation tendency of Hmox-1 in the blood is consistent with the biological process of thrombosis formation, and Hmox-1 may become a marker for predictive diagnosis of deep venous thrombosis.

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    Notch signal pathway effect on receptor protein regulation by transforming growth factor beta in primary human keratinocytes
    Xue Si-liang, Wang Xiao-shan, Li Dong-chuan, Zhang Jue
    2013, 17 (2):  296-300.  doi: 10.3969/j.issn.2095-4344.2013.02.020
    Abstract ( 454 )   PDF (313KB) ( 596 )   Save

    BACKGROUND: Regulation of the receptor protein tyrosine phosphatase kappa (RPTP-κ) in the skin is essential, while transforming growth factor beta (TGF-β) appears to be an upstream factor of its regulation. As Notch signaling pathway is similar to TGF-β signaling pathway, whether Notch participates in the regulation of RPTP-κ transcription by TGF-β signaling?
    OBJECTIVE: To find out the role of Notch signal in regulation of RPTP-κ transcription by TGF-β.
    METHODS: Jagged-1 and gamma-secretase inhibitors (GSI) were use respectively to activate and inhibit Notch signal followed by addition of TGF-β. Simultaneously, control group was set. Real-time PCR was used to determine RPTP-k mRNA expression in human keratinocytes.
    RESULTS AND CONCLUSION: After adding TGF-β into 40% confluent keratinocytes, the RPTP-κ mRNA expression was higher at different time as compared with the control group. Following Jagged-1 activated Notch signaling pathway, the mRNA expression of RPTP-κ in the keratinocytes was higher when Jagged-1, TGF-β or their combination was added into the cells as compared with the control group (P < 0.05, P < 0.01). Following GSI inhibited Notch signaling pathway, the mRNA expression of RPTP-κ in the keratinocytes was higher only when TGF-β was added into the cells as compared with the control group (P < 0.01), and no significant difference was seen when GSI alone or combination of TGF-β and GSI was added into the cells as compared with the control group (P > 0.05). These findings indicate that the mRNA expression of RPTP-κ in the keratinocytes was increased after TGF-β was added, and following activation or inhibition of Notch signaling, the mRNA expression of RPTP-κ was significantly increased or suppressed. Therefore, Notch signaling is very important and indispensable in the regulation of RPTP-κ by TGF-β.

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    RNA interference inhibits Weibel-Palade body release from endothelial cells
    Yang Shui-xiang, Wei Xiao-fei, Cui Yu-xia, Zhou Yong
    2013, 17 (2):  301-308.  doi: 10.3969/j.issn.2095-4344.2013.02.021
    Abstract ( 483 )   PDF (1030KB) ( 527 )   Save

    BACKGROUND: RNA interference and silent genes have got more and more attention as they can achieve the clinical effect.
    OBJECTIVE: To explore the effect of small hairpin RNA in inhibiting the Weibel-Palade body release in endothelial cell.
    METHODS: A small hairpin RNA mediated with an adenovirus vector was designed depending upon the N-terminal functional area of N-ethylmaleimide sensitive factor which act as a key protein in Weibel-Palade body release in endothelial cell. Being screened and identified, the harvested viruses were transfected into human aortic endothelial cell. The adenovirus vector with N-ethylmaleimide sensitive factor small hairpin RNA was regarded as the experimental group, and the pure adenovirus vector was regarded as negative control group, the blank control group without any treatment.
    RESULTS AND CONCLUSION: There was significant difference of N-ethylmaleimide sensitive factor mRNA expression in the endothelial cell in three groups after transfected with N-ethylmaleimide sensitive factor small hairpin RNA (P < 0.05); the expression of N-ethylmaleimide sensitive factor mRNA in the experimental group was decreased with time prolonged, and there was significant difference of the N-ethylmaleimide sensitive factor mRNA expression in the experimental group at 24, 48 and 72 hours (P=0.048). The expression of N-ethylmaleimide sensitive factor protein in the experimental group was lower than that in the negative control group and blank control group, and the difference was significant (P < 0.05); there was no significant difference between negative control group and blank control group (P=0.249). The immunofluorescence staining showed that the release of Weibel-Palade body in endothelial cell induced with thrombin was inhibited obviously after transfected with N-ethylmaleimide sensitive factor small hairpin RNA. The expression of N-ethylmaleimide sensitive factor mRNA and protein in endothelial cell transfected with harvested adenoviruses which carried the N-ethylmaleimide sensitive factor small hairpin RNA were significantly decreased, and the release of Weibel-Palade Body induced with thrombin was inhibited dramatically.

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    Procyanidins effects on apoptosis-related proteins in the gastrocnemius after heavy load training in rats
    Min Zhu, Liu Wen-jie, Geng Xiao, Su Quan-sheng
    2013, 17 (2):  309-314.  doi: 10.3969/j.issn.2095-4344.2013.02.022
    Abstract ( 355 )   PDF (424KB) ( 602 )   Save

    BACKGROUND: It will bring a variety of negative effects to the body after heavy load training, which is related to delayed onset muscle soreness and exercise fatigue.
    OBJECTIVE: To observe the effect of procyanidins on metabolism of free radicals, apoptosis-related protein FAS, and tumor necrosis factor in the gastrocnemius after heavy load training in rats.
    METHODS: Totally 48 adult female Sprague-Dawley rats were randomly divided into placebo group and medication group, and each group was divided into three subgroups, including static control group, instantly post-exercise group and 24-hour post-exercise group. Rats of the medication group were fed with 10 g/L procyanidins by intragastric administration, and those in the placebo group were given equal volume of distilled water as placebo. After 2 weeks, in all groups expect two static control groups, a heavy load running with a slope of -10° at 20 m/min was performed. Rats were decapitated before exercise, instantly and 24 hours after exercise, respectively, and then gastrocnemius from the left hind limb was taken off for detection.
    RESULTS AND CONCLUSION: (1) The gastrocnemius superoxide dismutase activity had a decrease tendency in the two instantly post-exercise groups, and the decline in superoxide dismutase activity was slighter in the medication group than the placebo group. The content of malondialdehyde increased significantly in the two instantly post-exercise groups, but the increase was smaller in the medication group than the placebo group. The ratio of superoxide dismutase and malondialdehyde decreased significantly after exercise, but compared with the placebo group, the decrease of the medication group was lower at every phase after exercise. (2) The expression of FAS protein in both groups increased significantly after exercise, and the increase of the placebo group was higher than the medication group. (3) The expression of tumor necrosis factor α was higher in the placebo group than the medication group at different phase after exercise. These findings indicate that to a certain extent, procyanidins could relieve the injury of gastrocnemius and restrain cell apoptosis after a heavy load exercise in rats.

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    Construction and identification of a mutated-Cdh1 eukaryotic expressing vector
    Li Li, Shi Xiao-yun, Zhang Deng-wen, Zhang Chuan-han, Yao Wen-long
    2013, 17 (2):  315-319.  doi: 10.3969/j.issn.2095-4344.2013.02.023
    Abstract ( 512 )   PDF (402KB) ( 693 )   Save

    BACKGROUND: The activity of anaphase promoting complex-Cdh1 is regulated by phosphorylation.
    Phosphorylated Cdh1 cannot be combined with anaphase promoting complex, thereby inhibiting the activity
    of the anaphase promoting complex.
    OBJECTIVE: To construct and identify a mutated-Cdh1 eukaryotic expressing vector.
    METHODS: The entire coding sequence of the Cdh1 gene was amplified from rat hippocampal mRNA by reverse transcription-PCR. Then the PCR product of Cdh1 was cloned into pBluescript plasmid by double digestion with restriction endonucleases EcoR1 and Xba1, and ligation. Based on site-directed mutagenesis, the pBluescript-Cdh1 plasmid containing Cdh1 coding sequence was used as a template. The 40, 151, 163 serine (S) and 121 threonine (T) in Cdh1 gene was mutated to alanine (A) by multiple PCR with four pairs of mutated primers. The mutated Cdh1 vector was identified by DNA sequencing.
    RESULTS AND CONCLUSION: The PCR product was about 1 500 bp by electrophoresis, including the entire coding sequence of Cdh1, restriction sites at both ends of Cdh1 and KOZAK sequence. The recombinant pBluescript-Cdh1 plasmid was identified by digestion with restriction endonuclease EcoR1 and Xba1, which was consistent with the expected results. DNA sequencing showed that A at the 930th base of Cdh1 (BC162059.1)   coding sequence was mutated to G in the recombinant plasmid of pBluescript-Cdh1. But the sequence of amino acids was not affected. The 40, 121, 151, 163 amino acids in pBluescript-Cdh1-4A40, 121, 151, 163 mutant plasmids were all mutated to alanine. The mutated Cdh1 gene expressing plasmid at phosphorylation site was successfully constructed, which provides a good foundation for further studies of Cdh1 gene function.

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    Anatomical structure of human maxillary sinus: Cone-beam CT analysis
    Li Ming-xia, Wang Guang-ping, Wang Hu
    2013, 17 (2):  320-324. 
    Abstract ( 1056 )   PDF (605KB) ( 1014 )   Save

    BACKGROUND: In order to avoid related complications and to facilitate the choice of surgical approaches, it is particularly important to understand the anatomic characteristics of the maxillary sinus before maxillary sinus augmentation.
    OBJECTIVE: To investigate the anatomic characteristics of human maxillary sinus based on cone-beam CT imaging for providing some reference related to sinus floor elevation and implant insertion.  
    METHODS: Cone-beam CT imaging data from 249 adults were selected and analyzed. The length (internal wall) and width of the maxillary sinus were measured, and the incidence of maxillary sinus septa and the characteristics of the maxillary sinus vessels were investigated and analyzed preliminarily.
    RESULTS AND CONCLUSION: The mean length (internal wall) and width of maxillary sinus were (32.0±3.81) and (21.70±5.16) mm, respectively. No significant differences were noted in the length and width of maxillary sinus based on sex or age (P > 0.05). The incidence of maxillary sinus septa was 33% (78/249). Moreover, the distribution and characteristics of the maxillary sinus vessels could be seen clearly and accurately on cone-beam CT three-dimensional images. These findings indicate that cone-beam CT images can show anatomical structures of the maxillary sinus fully and accurately, and the use of cone-beam CT is advantageous and mandatory to determine surgical indications and approaches, and avoid or reduce the incidence of surgical complications of maxillary sinus floor elevation.

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    Non-genetic influential factors for the healthy life of Yao Nationality in Bama Yao Autonomous County
    He Jiang-chuan, Yang Fang
    2013, 17 (2):  325-330.  doi: 10.3969/j.issn.2095-4344.2013.02.025
    Abstract ( 473 )   PDF (313KB) ( 528 )   Save

    BACKGROUND: A health and life quality survey in the minority populations of South China is of practical and political significance for the improvement of the domestic public health system. Non-genetic influential factor analysis for human healthy life is a typical representative.
    OBJECTIVE: Through a correlation analysis of living environment and eating habits of the residents from the longevity area and non-longevity area of Bama Yao Autonomous County, Guangxi Zhuang Autonomous Region, to attempt to provide the reference of longevity and health for populations from other regions of China.
    METHODS: Three townships from the longevity area and two townships form the non-longevity area of Bama Yao Autonomous County were selected as study sites. Statistical software SPSS 17.0 for Windows was used for sample descriptive statistical analysis, independent sample hypothesis testing, factor analysis and comprehensive evaluation.
    RESULTS AND CONCLUSION: There are five main factors as the non-genetic factors for the healthy life of Yao Nationality from Bama area: Ethnic habits as the main influence factor, with a contribution rate accounting for 37%, and second is the body form, with a contribution rate of 22.97%, followed by family health, education level, and fitness awareness.

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    Mechanism underlying interaction between estrogen and runt-related transcription factor 2 in osteoblasts
    Wang Hui, Sun Hui-qiang
    2013, 17 (2):  331-336.  doi: 10.3969/j.issn.2095-4344.2013.02.026
    Abstract ( 1078 )   PDF (506KB) ( 845 )   Save

    BACKGROUND: It is widely believed that estrogen and runt-related transcription factor 2 (Runx2) are important regulatory factors in the formation and maintenance of bone.
    OBJECTIVE: To summarize the recent research progresses and to elaborate the molecular mechanism of interaction between estrogen and Runx2 in osteoblasts.
    METHODS: “Estrogen”, “runt-related transcription factor 2 (Runx2)” and “osteoblast” were used as search terms in Chinese and English to retrieve PubMed, China Biology Medicine disc, VIP journal full-text database, WanFang database. Repeatability studies and irrelevant researches were excluded. Totally 62 literatures were obtained with preliminary retrieval and 22 were reserved after further study and analysis.
    RESULTS AND CONCLUSION: A mass of scientific researchers have found that estrogen and Runx2 do not function independently in osteoblasts but interact with each other through multiple patterns to co-regulate osteoblasts. There exist a complex mechanism of interaction between estrogen and Runx2. Various pathways are involved besides the direct action between estrogen/estrogen receptor and Runx2, such as transforming growth factor-β pathway, Wnt/β-catenin pathway, Fas/Fas ligand pathway and nuclear factor kappa B pathway.

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    Progress in Dickkopf-1-mediated bone metabolism
    Wang Lu-fei, Bai Ding, Han Xiang-long
    2013, 17 (2):  337-341.  doi: 10.3969/j.issn.2095-4344.2013.02.027
    Abstract ( 466 )   PDF (390KB) ( 1205 )   Save

    BACKGROUND: Dickkopf-1 is a soluble inhibitor of canonical Wnt/β-catenin signaling pathway. It blocks Wnt/β-catenin signaling by competitively binding with Wnt protein co-receptor LRP5/6 and then mediates downstream target gene transcription.
    OBJECTIVE: To review the research progress of Dickkopf-1-mediated bone metabolism, and to provide theoretical foundation of anti-Dickkopf-1 therapy for bone disease.
    METHODS: A computer-based online search was conducted in Medline and CBM databases from 1995-2012. Articles focusing on Dickkopf-1-mediated bone metabolism were collected using the keywords of “Dkk1; bone remodeling; bone diseases” in English and Chinese, respectively. High-quality studies were included, while repetitive studies were excluded.
    RESULTS AND CONCLUSION: 118 articles were obtained initially, and after screening procedure 36 literatures were selectively included in this review finally. Bone tissue is always in dynamic remodeling process. The interaction between osteoblasts and osteoclasts determines the dynamic balance between bone formation and bone resorption. Dickkopf-1 not only inhibits bone formation by blocking Wnt/β-catenin pathway, but also promotes osteoclast differentiation and maturation through the crosstalk with osteoprotegerin/receptor activator of nuclear factor-kappa B ligand/receptor activator of nuclear factor-kappa B axis. Promoting bone formation and inhibiting bone resorption is the biological mechanism of anti- Dickkopf-1 for preventing bone loss which occurs in bone metabolic diseases, and the clinical results are favorable. Therefore, Dickkopf-1 should be a potential target in the treatment of bone disease.

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    Effect of bone morphogenetic protein 2 signal transduction pathway on osteogenesis, bone development and damage repair
    Hou Bo, Wang Yi, Shen Yu-hui
    2013, 17 (2):  342-348.  doi: 10.3969/j.issn.2095-4344.2013.02.028
    Abstract ( 292 )   PDF (383KB) ( 563 )   Save

    BACKGROUND: Bone morphogenetic proteins play an important role in bone formation, fracture healing and bone induction after bone destruction, and it can be used as a start regulating factor to promote the new bone formation with other signal paths. The regulation of endogenous bone morphogenetic protein 2 can be used as a new target in the future field of bone repair.
    OBJECTIVE: Through analyzing and summarizing the mechanism of the bone morphogenetic protein signal transduction pathway in endochondral ossification reported from 1988 to now, adult bone growth and development, to explore the role of the bone morphogenetic protein signal pathways in the bone growth and damage repair.
    METHODS: A computer-based search was performed to search relevant articles about bone morphogenetic protein signaling pathways and its function from VIP and PubMed databases (1998-01/2009-12), respectively by using the key words of “bone morphogenetic protein, endochondral ossification, bone repair” in Chinese and “bone reduction” in English. Literatures irrelevant to research purpose or containing a similar content were eliminated. Finally, 34 articles were chosen for further analysis.
    RESULTS AND CONCLUSION: Because of its osteoinductive, bone morphogenetic protein signal pathway has become a hot spot in spinal surgery, fracture healing and bone induction after bone destruction. During the bone formation, the bone morphogenetic protein also serves as a start regulating factor to promote the new bone formation with other signal paths. In the bone micro environment, the bone morphogenetic protein and other signal paths that influence bone dynamic balance offer a new target for anabolic therapy that induces the bone formation, which provides a new thought on bone morphogenetic protein control to the formation of new bone following bone repair.

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    Parathyroid hormone regulation for related protein and receptor activator of nuclear factor-kappa B in bone metabolism
    Wang Dan, Bao Jie, Wang Guo-xiang
    2013, 17 (2):  347-352.  doi: 10.3969/j.issn.2095-4344.2013.02.029
    Abstract ( 361 )   PDF (403KB) ( 578 )   Save

    BACKGROUND: Parathyroid hormone is the most important factor to influence the axis of bone metabolism. Meanwhile, parathyroid hormone is the important hormone to regulate osteoprotegerin and receptor activator of nuclear factor-kappa B ligand expression.
    OBJECTIVE: To review the articles related to the effect of parathyroid hormone on the regulation of osteoprotegerin and receptor activator of nuclear factor-kappa B ligand.
    METHODS: An online search of CNKI and HighWire databases was performed for articles related to “parathyroid hormone, osteoprotegerin, receptor activator of nuclear factor-kappa B and its ligand in bone metabolism”. The keywords of “parathyroid hormone, osteoprotegerin, receptor activator of nuclear factor-kappa B ligand” were used in Chinese and English. Articles related to the effects of parathyroid hormone on the signaling pathways were selected and those published recently or in the authorized journals were of priority. A total of 175 articles were collected in the initial research, and 31 of them were retained according to inclusion and exclusion criteria.
    RESULTS AND CONCLUSION: Parathyroid hormone is one of the most important hormones in the regulation of bone metabolism through strengthening osteoclast activity. Receptor activator of nuclear factor-kappa B ligand is the key factor to regulating bone absorption, and functions a role in combination with r eceptor activator of nuclear factor-kappa B to start the receptor activator of nuclear factor-κB factor ligand signal transduction. After that, there is a competition between osteoprotegerin and receptor activator of nuclear factor-kappa B ligand binding with receptor activator of nuclear factor-κB factor. The ratio of receptor activator of nuclear factor-κB factor ligand/osteoprotegerin influences the differentiation, maturation and function of osteoclasts. However, whether the variations of parathyroid hormone in the body during exercise can influence osteoprotegerin and receptor activator of nuclear factor-kappa B ligand to adjust bone absorption and synthesis needs further studies.

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    Latest transgenic technology in bone and cartilage defect repair
    Ru Jia, Li Qiang
    2013, 17 (2):  353-257.  doi: 10.3969/j.issn.2095-4344.2013.02.030
    Abstract ( 309 )   PDF (409KB) ( 587 )   Save

    BACKGROUND: Tissue engineering technology has made a great progress in bone and cartilage repair, and the introduction of transgenic technology in recent years also has caused widespread concern.
    OBJECTIVE: To summarize the development of transgenic technology in the repair of bone and cartilage defects in the past 5 years.
    METHODS: Relevant articles about transgenic technology in bone and cartilage defect which were published from January 2007 to March 2012 were retrieved in CNKI and PubMed with the key words of “gene, therapy, bone, cartilage, defect” in Chinese and English, respectively. Finally, 22 articles that met the inclusive criterion were included.
    RESULTS AND CONCLUSION: Gene therapy introduces a new treatment concept for bone and cartilage regeneration, which can induce genes into targeted cells with specific expression. Genes for bone and cartilage defects include bone morphogenetic protein, transforming growth factor, basic fibroblast growth factor, insulin-like growth factor, vascular endothelial growth factor, and Bcl-xl gene. Gene therapy can induce bone and cartilage formation, and provides a new approach for bone and cartilage repairing.

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    wnt signal pathway in neurogenesis
    Cao Min
    2013, 17 (2):  358-362.  doi: 10.3969/j.issn.2095-4344.2013.02.031
    Abstract ( 509 )   PDF (391KB) ( 869 )   Save

    BACKGROUND: As an open, multi-link and multi-site pathway, wnt signaling pathway plays a very important role in the nervous system. Therefore, it is very important to understand the effects and possible mechanisms for neurogenesis research.
    OBJECTIVE: To summarize the effect and possible mechanism of wnt signaling pathway in the process of neurogenesis.
    METHODS: The literatures about the wnt signaling pathway in neurogenesis both at home and abroad were searched, which were published from January 2001 to December 2011, and 19 articles considered to be representative were selected, and then summarized and analyzed.
    RESULTS AND CONCLUSION: The wnt signaling pathway is involved in embryonic and adult neurogenesis, cortex model and synapse formation. But the role of wnt signaling pathway in these processes is not always consistent. The characteristics and microenvironment of neural stem cells as well as different downstream target genes can cause different effects. Meanwhile, the wnt signaling pathway may interact with a variety of signaling pathways, so the final effect on the nervous system is very specific. However, the clear cellular or molecular mechanisms are still not very sure.

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    Transplantation of tissue-engineered corneal endothelium
    Li Shan-yi, Chen Jian-su
    2013, 17 (2):  363-368.  doi: 10.3969/j.issn.2095-4344.2013.02.032
    Abstract ( 320 )   PDF (390KB) ( 555 )   Save

    BACKGROUND: Tissue-engineered corneal endothelium can overcome the shortages of donor corneas for transplantation and also improve the quality of corneal endothelial cells. Finding a kind of ideal reconstructed corneal endothelium is very important in the field of tissue-engineered cornea.
    OBJECTIVE: To review and discuss the current research in the reconstruction of tissue-engineered corneal endothelium.
    METHODS: The PubMed database (http://www.ncbi.nlm.nih.gov/PubMed) was retrieved by computer to search the relevant literature published between 2000 and 2012 using the key words of “corneal endothelial cell, transplantation, tissue engineering” in English. Then, the paper was further analyzed and reviewed in line with the theme.
    RESULTS AND CONCLUSION: A total of 163 papers were searched. At last, 44 papers were selected according to the titles and objectives. So far, many kinds of biomaterials and methods have been used for reconstruction of tissue-engineered corneal endothelium. But many difficulties and problems must be solved in the clinical practice of tissue-engineered corneal endothelium. Every material and method for tissue-engineered corneal endothelium has its own advantages and disadvantages, so further research is to improve this disadvantage and investigate the long-term effects in vivo.

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    Neurotrophic factors and spinal cord injury
    Xu Wei, Cheng Li-ming
    2013, 17 (2):  369-374.  doi: 10.3969/j.issn.2095-4344.2013.02.033
    Abstract ( 285 )   PDF (393KB) ( 714 )   Save

    BACKGROUND: Neurotrophic factors can effectively suppress neuronal apoptosis and promote neural regeneration and differentiation after spinal cord injuries. But the short half-life, poor ability to pass through the blood-spinal cord-barrier and limitation for space reconstruction severely obstruct the applications of neurotrophic factors.
    OBJECTIVE: To review the neurotrophic factor research progress and to find out more effective application methods providing assistance for both science and clinical research.
    METHODS: Papers about neurotrophic factors for spinal cord injuries published from 2001-01 to 2011-12 in CNKI, WanFang, and PubMed databases were reviewed. “Neurotrophic factor; neurotrophin; spinal cord injuries; stem cell; bioengineer, tissue engineering” in Chinese and English served as the search term in the title and abstract retrieval. All the papers closely related to the neurotrophic factor applications were selected and those recently published or in the prestigious journals were selected in the same field. We got 379 initial papers and 41 were reviewed according to the inclusion criteria.
    RESULTS AND CONCLUSION: A series of improvements and optimizations have been made for the deficient application of neurotrophic factors. Combined applications of neurotrophins to repair spinal cord injuries have a synergistic effect. Stem cells secrete neurotrophic factors continuously to help injured spinal cord reconstruction involved in stem cell differentiation by gene transfer technology. In addition, through bio-engineering techniques, hydrogel nanofiber scaffolds with neurotrophic factor are made to provide space and channels for neural pathway rebuild after spinal cord injuries. But the best combinations of neurotrophic factors, stem cells and biomaterials need further studies.

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    Revealing the near-infrared pulsed light in the breast
    Deng Yan-qiong, Li Wen-ke, Wan Ying-wen, Li Kai-yang
    2013, 17 (2):  375-380.  doi: 10.3969/j.issn.2095-4344.2013.02.034
    Abstract ( 438 )   PDF (661KB) ( 805 )   Save

    BACKGROUND: The existing traditional diagnosis methods of breast diseases are mostly harmful and expensive to the human body. In recent years, diagnosis of breast diseases depends on the optical properties of the breast tissue, which has attracted more attention because of some advantages, such as safe, economical and practical condition.
    OBJECTIVE: To study the clinical application of the optical properties of the breast tissue irradiated by near-infrared pulse light.
    METHODS: 760 nm and 850 nm wavelength near-infrared pulsed lights irradiated the breast tissue, and the wavelength of these two kinds of transmitted lights was analyzed using power spectrum and cross-correlation analysis.
    RESULTS AND CONCLUSION: There were differences between the healthy breast and unhealthy breast, the cross-correlation coefficient of normal, benign and malignant breast turned to reduce. Clinical studies have shown that the near-infrared pulsed light in the optical properties of breast tissue is useful to the differential diagnosis of breast disease.

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