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1.
China Journal of Orthopaedics and Traumatology ; (12): 804-808, 2014.
Article in Chinese | WPRIM | ID: wpr-345305

ABSTRACT

<p><b>OBJECTIVE</b>To explore the technique and therapeutic effect of bridge wire splint fixation with ankle dorsiflexion for the treatment of femoral shaft fractures in young children. Methods:From June 2006 to June 2012,45 young children with femoral shaft fractures were treated by bridge wire splint fixation with ankle dorsiflexion,which was designed according to arch bridge mechanical principle and structure. There were 31 males and 14 females with an average age of 3.2 years old ranging from 8 months to 5.5 years old; 14 cases were upper 1/3 femoral fractures,26 cases were middle 1/3 femoral fractures,5 cases were lower 1/3 femoral fractures; 20 cases were transverse fractures, 14 cases were oblique fractures,6 cases were spiral frac- tures, and 5 cases were comminuted fractures. X-ray, follow-up imaging changes,clinical curative effect and complications were assessed.</p><p><b>RESULTS</b>Forty-five patients were followed up for 6 to 21 months (averaged 12 months). All fractures were reached clinical bone healing after 5 to 7 weeks (averaged 6 weeks) fixation. Seven cases appearred limb soft tissue complications, including buttocks bedsore,dorsal foot and Achilles tendon epidermal necrosis, and healed after dressing and removal of external fixation. During follow-up,the original overlap angle and lateral displacement were remodeled, and limbs were restored to the normal line of force and bone structure. According to Flynn standard, 35 cases got excellent results, 8 cases good, 2 cases fair.</p><p><b>CONCLUSION</b>The bridge wire splint fixation with ankle dorsiflexion for the treatment of femoral. shaft fractures in young children (less than 6 years old) is safe,feasible, simple,and has raliable effect, which can be applied in primary hospitals.</p>


Subject(s)
Child , Child, Preschool , Female , Humans , Infant , Male , Ankle , General Surgery , Bone Wires , Femoral Fractures , General Surgery , Femur , General Surgery , Follow-Up Studies , Fracture Fixation, Intramedullary , Treatment Outcome
2.
Chinese Journal of Plastic Surgery ; (6): 298-303, 2011.
Article in Chinese | WPRIM | ID: wpr-246935

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of pyrroloquinoline quinine (PQQ) on proliferation and expression of c-fos, c-jun, CREB and PCNA in cultured Schwann cells.</p><p><b>METHODS</b>Schwann cells were cultured and purified in vitro. The purity of Schwann cells was identified by immunofluorescence of S-100. After synchronization of cell cycle by serum-free medium, different concentration of PQQ (0,1, 10, 100, 1,000, 10,000 nmol/L) were added into culture medium for 72 h. Flow cytometry was used to determine cell cycle. The content of c-fos, c-jun, and CREB mRNA were detected by RT-PCR, and the expression of PCNA protein was detected by Western blot.</p><p><b>RESULTS</b>After PQQ treatment, the percentage of cells in G0/G1 phase decreased and the percentage of cells in S and G2/M phase increased. After treated by PQQ at concentration of 1-10,000nmol/L, content of c-fos,c-jun,CREB mRNA was increased by 0.33,0.42 and 0. 52 fold (P < 0. 05). However, at concentration of 1 000 nmol/L, there was no difference in mRNAs content when compare to control (P >0.05). And it showed a decline at concentration of 10,000 nmol/L (P < 0.05). PCNA protein expression was up-regulated at PQQ concentration of 1-100 nmol/L. At 100 nmol/L, the expression increased by 1.17 fold (P < 0.05); However, at 1,000 nmol/L, there was no difference in PCNA expression when compared to control. And 10,000 nmol/L of PQQ inhibited the expression of PCNA (P < 0.05).</p><p><b>CONCLUSIONS</b>When treated with PQQ at concentration of 10-100 nmol/L, the proliferation of Schwann cells increased and the expression of c-fos,c-jun, CREB and PCNA was up-regulated.</p>


Subject(s)
Animals , Rats , Cell Proliferation , Cells, Cultured , Cyclic AMP Response Element-Binding Protein , Metabolism , Genes, fos , Genes, jun , PQQ Cofactor , Pharmacology , Proliferating Cell Nuclear Antigen , Metabolism , Rats, Sprague-Dawley , Schwann Cells , Cell Biology , Metabolism
3.
China Journal of Orthopaedics and Traumatology ; (12): 851-853, 2011.
Article in Chinese | WPRIM | ID: wpr-347049

ABSTRACT

<p><b>OBJECTIVE</b>To explore the effects of debridement combined with vacuum sealing drainage (VSD) technique in treatment of high-pressure paint injection injuries of hand.</p><p><b>METHODS</b>From April 2005 to August 2010,14 patients with high-pressure paint injection injuries of hand were treated with debridement and VSD technique within 6 hours after injury. All the patients were male,ranging in age from 23 to 47 years with an average of 36.5 years. All injuries occurred left hand,thumb injured in 5 cases,index finger in 3 cases, middle finger in 2 cases and palm in 4 cases. Injured hands swelled obviously with poor blood circulation. When the wounds were covered with fresh granulation tissue without inflammatory effusion after operation of 3-4 times, the skingrafting (9 cases) or transfer flap (5 cases) were done on the wounds.</p><p><b>RESULTS</b>All the patients were followed up from 8 to 16 months with an average of 12 months. All the wounds obtained good healing. Therapeutic effects were estimated according to TAM criteria, 7 cases were excellent,6 good and 1 fair.</p><p><b>CONCLUSION</b>In high-pressure paint injection injuries of hands,debridement combined with VSD technique can avoid wound infection,promote the growth of granulation tissue. It is beneficial to wound healing.</p>


Subject(s)
Adult , Humans , Male , Middle Aged , Debridement , Methods , Drainage , Methods , Hand Injuries , General Surgery , Injections , Paint
4.
Chinese Journal of Plastic Surgery ; (6): 53-56, 2010.
Article in Chinese | WPRIM | ID: wpr-328633

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the roles of PI3K/Akt signal pathway in Schwann cells proliferation promoted by pyrroloquinoline quinone (PQQ).</p><p><b>METHODS</b>Schwann cells were cultured and purified in vitro. The purity was identified by immunofluorescence of S-100; the expression of Akt and phosphorylated-Akt (p-Akt) were detected by western blot, and the expression of p-Akt after blocking the PI3K signal transduction pathway by PI3K inhibitor wortmannin was detected by western blot.</p><p><b>RESULTS</b>Morphological change was observed in PQQ-treated Schwann cells, p-Akt was detected 30 min after PQQ treated, reached the peak at 4 h, and disappeared 12 h later. 1-100 nmol/L PQQ could up-regulate the expression of p-Akt; this up-regulated expression of p-Akt was inhibited by wortmannin (P<0.05).</p><p><b>CONCLUSIONS</b>PQQ could affect morphology of Schwann cells and activation of Akt. It indicates that PI3K/Akt signal pathway might be involved in Schwann cells proliferation promoted by PQQ.</p>


Subject(s)
Animals , Rats , Androstadienes , Pharmacology , Cell Proliferation , Cells, Cultured , PQQ Cofactor , Pharmacology , Phosphatidylinositol 3-Kinases , Metabolism , Protein Kinase Inhibitors , Pharmacology , Proto-Oncogene Proteins c-akt , Metabolism , Rats, Sprague-Dawley , Schwann Cells , Cell Biology , Metabolism , Signal Transduction
5.
Chinese Journal of Plastic Surgery ; (6): 444-447, 2010.
Article in Chinese | WPRIM | ID: wpr-268660

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of mitogen-activated protein kinase (MEK) kinase cascade, extracellular signal-regulated kinase (ERK1/2) signal pathway on Schwann cells proliferation promoted by Pyrroloquinoline Quinine (PQQ) and its molecular mechanisms.</p><p><b>METHODS</b>Schwann cells were cultured and purified in vitro. The purity was identified by S-100. Different time and concentration of PQQ was added into culture medium. The expression of ERK1/2 and phosphorylated-ERK1/2 was detected by western blot. The expression of p-ERK1/2 after blocking of MEK signal pathway by specific inhibitor PD98059 was detected by western blot.</p><p><b>RESULTS</b>Morphological change was observed in PQQ treated Schwann cells. 1-500 nmol/L PQQ could up-regulate the expression of p-ERK1/2, and 1000 nmol/L had no effects, while 10 000 nmol/L exhibited inhibitory effect (P < 0.05). p-ERK1/2 increased to peak 1 h after PQQ added, and this up-regulation of p-ERK1/2 was inhibited by PD98059 (P < 0.05).</p><p><b>CONCLUSIONS</b>PQQ could affect morphology of Schwann cells and activation of ERK1/2. MEK inhibitor PD98059 could, block this activation. It suggests that MEK/ERK signal pathway should be involved in Schwann cells proliferation promoted by PQQ.</p>


Subject(s)
Animals , Rats , Cell Proliferation , Cells, Cultured , Extracellular Signal-Regulated MAP Kinases , Metabolism , Physiology , Mitogen-Activated Protein Kinases , Metabolism , Physiology , Pyrroles , Pharmacology , Quinolines , Pharmacology , Rats, Sprague-Dawley , Schwann Cells , Cell Biology , Signal Transduction
6.
Yonsei Medical Journal ; : 832-837, 2009.
Article in English | WPRIM | ID: wpr-178452

ABSTRACT

PURPOSE: The purpose of this study was to study the protective effect and influence of sodium hyaluronate (Na-HA) on mRNA expression of peroxisome proliferators-activated receptor gamma (PPAR-gamma) in cartilage of rabbit osteoarthritis (OA) model. MATERIALS AND METHODS: Forty eight white rabbits were randomly divided into A, B, and C groups. Group A was normal control group, B and C groups underwent unilateral anterior cruciate ligament transection (ACLT). The rabbits in group B were injected normal saline after ACLT; and Group C received intraarticular1% sodium hyaluronate (HA) injection 5 weeks after surgery, 0.3 mL once a week. At 11th week after surgery, all the rabbits were sacrificed. The cartilage changes on the medial femoral condyles were graded separately. Cartilage sections were stained with safranin-O and HE, and messenger RNA (mRNA) expression of PPAR-gamma was detected by using real time polymerase chain reaction (Real Time-PCR). RESULTS: Cartilage degeneration in group B was significantly more severe than in A and C injection group. The grey value of Safranin-O of B group was higher than A and C groups. Expression of PPAR-gamma mRNA in group B was higher than group A and C. CONCLUSION: This study shows that Na-HA has a protective effect on articular cartilage degeneration, and the inhibitory effect on the PPAR-gamma mRNA expression may be one of therapeutic mechanism of Na-HA.


Subject(s)
Animals , Rabbits , Cartilage/drug effects , Gene Expression/drug effects , Hyaluronic Acid/pharmacology , Microscopy , Osteoarthritis/drug therapy , PPAR gamma/genetics , RNA, Messenger/genetics , Random Allocation , Reverse Transcriptase Polymerase Chain Reaction , Viscosupplements/pharmacology
7.
Chinese Journal of Plastic Surgery ; (6): 67-70, 2008.
Article in Chinese | WPRIM | ID: wpr-314157

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effects of rhVEGF on autologous free granular fat grafts in rats.</p><p><b>METHODS</b>Forty-eight Sprague-Dawley rats were randomly divided into three groups, sixteen of each. After the autologous free granular fat transplantation, all groups were treated with the plasmid DNA containing cDNA encoding rhVEGF, the blank plasmid DNA and normal saline respectively as the experimental group, the negative group and the saline group. After 3, 7, 15, 30 days, the rats were sacrificed and the grafts were weighted accurately. Histological pathology was evaluated. Micro-vessel count and the expression of vascular endothelial growth factor (VEGF) were examined by immunohistochemical staining.</p><p><b>RESULTS</b>The weights of the two latter groups were significantly reduced on the 7, 15, 30 day compared with the experimental group. The expression of VEGF and the micro-vessel count in the experimental group were significantly higher than the other two groups during the latter periods.</p><p><b>CONCLUSION</b>The cDNA encoding VEGF can induce the expression of VEGF in fat graft, angiogenesis and reduce the free fat graft absorption.</p>


Subject(s)
Animals , Female , Male , Rats , Adipose Tissue , Transplantation , Gene Transfer Techniques , Graft Survival , Rats, Sprague-Dawley , Recombinant Proteins , Genetics , Transplantation, Autologous , Vascular Endothelial Growth Factor A , Genetics
8.
Chinese Journal of Traumatology ; (6): 28-33, 2008.
Article in English | WPRIM | ID: wpr-236739

ABSTRACT

<p><b>OBJECTIVE</b>To observe the effect of tissue engineered nerves in repairing peripheral nerve defects (about 1.5 cm in length) in rats to provide data for clinical application.</p><p><b>METHODS</b>Glycerinated sciatic nerves (2 cm in length) from 10 Sprague Dawley (SD) rats (aged 4 months) were used to prepare homologous dermal acellular matrix. Other 10 neonate SD rats (aged 5-7 days) were killed by neck dislocation. After removing the epineurium, the separated sciatic nerve tracts were cut into small pieces, then digested by 2.5 g/L trypsin and 625 U/ml collagenase and cultured in Dulbecco's modified Eagle's medium (DMEM) for 3 weeks. After proliferation, the Schwann cells (SCs) were identified and prepared for use. And other 40 female adult SD rats (weighing 200 g and aged 3 months) with sciatic nerve defects of 1.5 cm in length were randomly divided into four groups: the defects of 10 rats bridged with proliferated SCs and homologous dermal acellular matrix (the tissue engineered nerve group, Group A), 10 rats with no SCs but homologous dermal acellular matrix with internal scaffolds (Group B), 10 with autologous nerves (Group C), and the other 10 with nothing (the blank control group, Group D). The general status of the rats was observed, the wet weight of triceps muscle of calf was monitored, and the histological observation of the regenerated nerves were made at 12 weeks after operation.</p><p><b>RESULTS</b>The wounds of all 40 rats healed after operation and no death was found. No foot ulceration was found in Groups A, B and C, but 7 rats suffered from foot ulceration in Group D. The triceps muscles of calf were depauperated in the experimental sides in all the groups compared with the uninjured sides, which was much more obvious in Group D. The wet weight of triceps muscle of calf and nerve electrophysiologic monitoring showed no statistical difference between Group A and Group C, but statistical difference was found between Groups A and B and Groups B and D. And significant statistical difference was found between Group B and Group D. Obvious compound muscle (or motor) action potential (CMAP) could be evoked in Group A and Group C, but the evoked amplitude was very low in Group B and Group D. The axons of regenerated nerves penetrated through the whole graft in Group A and Group C, and partly penetrated through the graft in Group B, but did not penetrate in Group D. The two tips of the separated sciatic nerves of Groups A , B , and C were connected together, without formation of neuroma. But those of Group D were not connected together and neuroma formed in 6 rats.</p><p><b>CONCLUSIONS</b>Tissue engineered nerves can be used for repairing long defects of the peripheral nerves of rats and ideal repairing effects can be obtained.</p>


Subject(s)
Animals , Female , Rats , Animals, Newborn , Nerve Regeneration , Peripheral Nerve Injuries , Rats, Sprague-Dawley , Sciatic Nerve , Wounds and Injuries , Tissue Engineering , Methods
9.
Chinese Journal of Traumatology ; (6): 42-44, 2008.
Article in English | WPRIM | ID: wpr-236736

ABSTRACT

<p><b>OBJECTIVE</b>To compare the clinical efficacy of percutaneous vertebroplasty (PVP) with percutaneous kyphoplasty (PKP) in the treatment of vertebral compression fracture (VCF).</p><p><b>METHODS</b>Ninety-eight patients with VCF were treated by PVP (n=42) or PKP (n=56). The anterior midline and posterior heights of vertebrae body, preoperative and postoperative visual analogue scale (VAS), operation time and amount of blood loss were compared between 2 groups.</p><p><b>RESULTS</b>There was statistical difference in vertebral height between two groups (P < 0.01). No significant difference was seen in VAS, operation time and blood loss between two groups (P < 0.05).</p><p><b>CONCLUSIONS</b>PKP and PVP have the similar therapeutic efficacy in treatment of VCF with minimal invasion, less operation time and blood loss. However, PKP is superior in the recovery of vertebral height.</p>


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Bone Cements , Fractures, Compression , General Surgery , Injections , Spinal Fractures , General Surgery , Vertebroplasty , Methods
10.
Chinese Journal of Traumatology ; (6): 49-53, 2008.
Article in English | WPRIM | ID: wpr-236734

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of recombinant human vascular endothelial growth factor (rhVEGF) on autologous free granular fat grafts in rats.</p><p><b>METHODS</b>Forty-eight Sprague Dawley (SD) rats, weighing 190-280 g and regardless sex, were randomly divided into three groups, sixteen in each. After fat transplantation, the rats were treated with plasmid DNA encoding rhVEGF protein (the experimental group), plasmid DNA (the negative group) and normal saline (the blank control group), respectively. At 3, 7, 15 and 30 days after transplantation, the rats were killed and the grafts were weighed, respectively. Histopathological changes were evaluated. Microvessel density and the expression of VEGF were examined by immunohistochemical staining and Western blotting.</p><p><b>RESULTS</b>The weights of the negative and blank control groups were significantly reduced on the 7th, 15th and 30th days compared with those of the experimental group. The expression of VEGF and the microvessel density in the experimental group were significantly higher than the other two groups during the latter periods.</p><p><b>CONCLUSION</b>The plasmid encoding VEGF can induce expression of VEGF and angiogenesis in fat grafts and reduce the absorption of free fat grafts.</p>


Subject(s)
Animals , Female , Male , Rats , Adipose Tissue , Transplantation , Graft Survival , Physiology , Random Allocation , Rats, Sprague-Dawley , Transduction, Genetic , Transplantation, Autologous , Vascular Endothelial Growth Factor A , Genetics
11.
Chinese Journal of Traumatology ; (6): 94-97, 2008.
Article in English | WPRIM | ID: wpr-236725

ABSTRACT

<p><b>OBJECTIVE</b>To study the regularity of migration and distribution of bone marrow stromal cells (BMSCs) in injured spinal cord with intradural space transplantation.</p><p><b>METHODS</b>Forty Wistar rats were randomly assigned into 4 groups. The spinal cord injury model was prepared according to the modified Allen method. BMSCs were labeled by CM-Dil. And 5.0 multiply 10(6) cells were transplanted by different channels including intraventricular injection (Group A),injured spinal cord intrathecally injection (Group B), remote intrathecally injection at the L(3)-L(4) level (Group C), and intravenous injection (Group D). Spinal cord was dissected at 24 hours, 1, 2, 3 and 4 weeks after transplantation. Sections of 4 micromolar were cut on a cryostat and observed under fluorescence microscopy.</p><p><b>RESULTS</b>No fluorescence was observed 24 hours after transplantation in spinal cord injury parenchyma except Group B. One week later, BMSCs in Groups A and C began to migrate to the injured parenchyma; 2-4 weeks later, BMSCs penetrated into the injured parenchyma except Group D. The number of BMSCs decreased at 3-4 weeks after transplantation. The number of cells in Group B decreased faster than that of Groups A and C.</p><p><b>CONCLUSIONS</b>BMSCs transplanted through intraventricular injection, injured spinal cord intrathecally injection and remote intrathecal injection could migrate to the injured parenchyma of spinal cord effectively. The number of BMSCs migrated into injured spinal cord parenchyma is rare by intravenous injection.</p>


Subject(s)
Animals , Male , Rats , Bone Marrow Cells , Cell Biology , Bone Marrow Transplantation , Methods , Cell Movement , Physiology , Random Allocation , Rats, Wistar , Spinal Cord Injuries , Pathology , General Surgery , Stromal Cells , Cell Biology , Transplantation
12.
Chinese Journal of Traumatology ; (6): 293-296, 2008.
Article in English | WPRIM | ID: wpr-239832

ABSTRACT

<p><b>OBJECTIVE</b>To observe the influence of intra-articular injection of sodium hyaluronate (SH) on the expression of inducible nitric oxide synthase (iNOS) in the synovium and nitric oxide (NO) content in synovial fluid of rabbits with traumatic osteoarthritis (OA).</p><p><b>METHODS</b>Sixteen white rabbits underwent unilateral anterior cruciate ligament transection and were randomly divided into 2 groups 5 weeks after the operation. Rabbits in the experimental group received intra-articular injection of 0.3 ml of 1% SH, once a week for 5 weeks. Animals in the control group were treated under the same conditions using physiological saline. All the animals were sacrificed at the 10th week after surgery. The mRNA expression of iNOS in the synovium was analyzed using reverse transcription-polymerase chain reaction. The content of NO in the synovial fluid was assayed.</p><p><b>RESULTS</b>The level of iNOS expression of the synovium in the experimental group was lower than that in control group (0.47+/-0.09 vs. 0.65+/-0.12, t equal to 3.45, P less than 0.01). Compared with control group, the content of NO decreased significantly in synovial fluid of SH injection group (134.11 micromolar/L +/- 12.47 micromolar/L vs. 152.17 micromolar/L +/- 15.69 micromolar/L, t equal to 2.55, P less than 0.05).</p><p><b>CONCLUSIONS</b>SH significantly decreases the content of NO in the synovial fluid of rabbits with traumatic OA. SH may exert the effect on synovial fluid NO level as a result of the suppression of iNOS expression in the synovium. It may be one of the mechanisms of the therapeutic effect of SH on early traumatic OA.</p>


Subject(s)
Animals , Rabbits , Anterior Cruciate Ligament Injuries , Hyaluronic Acid , Pharmacology , Therapeutic Uses , Nitric Oxide , Nitric Oxide Synthase Type II , Osteoarthritis , Drug Therapy , Metabolism , Random Allocation , Synovial Fluid , Chemistry , Synovial Membrane
13.
Chinese Journal of Traumatology ; (6): 339-344, 2007.
Article in English | WPRIM | ID: wpr-236754

ABSTRACT

<p><b>OBJECTIVE</b>To study the effect of allograft compound vertebra on vertebral reconstruction in rabbits so as to provide biomechanical direction for manufacturing and selecting vertebral reconstruction materials.</p><p><b>METHODS</b>Twenty-five healthy New Zealand white rabbits were divided randomly into three groups: normal group (Group A, n equal to 5),iliac bone graft group (Group B, n equal to 10) and allograft compound vertebra group (Group C, equal to 10). After C4 was resected, iliac bone implantation and allograft bone cage transplantation were fulfilled in Group B and Group C, respectively. Every 5 rabbits from Group B and Group C were selected to test the biomechanical strength and biological activity one and two months postoperatively.</p><p><b>RESULTS</b>No significant statistical difference was found between Group A and Group C one and two months postoperatively (P larger than 0.05). The biomechanical strength of Group B was much weaker than that of Group A and Group C one month postoperatively (P less than 0.05), but at two months postoperatively, no statistical difference was found among the three groups. The biological activity and vertebral moulding ability of Group C were better than those of Group B at one and two months postoperatively.</p><p><b>CONCLUSIONS</b>Compound vertebra, which is made up of allograft cortical bone cage and autogenous cancellous bone, shows instantaneous and permanent biomechanical stability and biological activity, therefore, it is an ideal material for vertebral reconstruction.</p>


Subject(s)
Animals , Rabbits , Biomechanical Phenomena , Bone Substitutes , Bone Transplantation , Ilium , Transplantation , Models, Animal , Plastic Surgery Procedures , Spinal Neoplasms , General Surgery , Transplantation, Homologous
14.
Chinese Journal of Plastic Surgery ; (6): 55-59, 2006.
Article in Chinese | WPRIM | ID: wpr-240384

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of tissue-engineering bone on repair of segmental bone defects.</p><p><b>METHODS</b>Segmental bone defect of 21mm was created at sheep left metatarsus, which was then implanted with tissue-engineering bone (the experimental group) and pure porous beta-TCP (the control group) respectively. The bone defect in the blank group was left without treatment. After the sheep were sacrificed at the 1st, 3rd, or 6th month postoperatively, the samples were taken and examined by radiological, histological and biomechanical methods as well as scanning electron microscopy. The sheep in the blank group were sacrificed at the 6th month postoperatively.</p><p><b>RESULTS</b>The osteoid tissue, woven bone and lamellar bone in the defect of the experimental group occurred earlier than in the control group. The new bone formed directly without through a cartilaginous intermediate in the experimental group, while the defect was repaired in a "creep substitution" way in the control group. At the 6th month, radiological and biomechanical tests revealed nearly complete repair of the bone defect of the experimental group, partial repair in the control group and non-healing in the blank group.</p><p><b>CONCLUSIONS</b>Tissue-engineering bone can repair bone defect, accelerating healing and without "creep substitution", which is a good option in repair of critical segmental bone defects. This study set up a basis for clinical applications in the future.</p>


Subject(s)
Animals , Biocompatible Materials , Bone Diseases , General Surgery , Bone Marrow Cells , Cell Biology , Bone Regeneration , Calcium Phosphates , Therapeutic Uses , Cell Culture Techniques , Cells, Cultured , Mesenchymal Stem Cells , Cell Biology , Sheep , Tissue Engineering , Methods , Transplantation, Autologous
15.
Chinese Journal of Traumatology ; (6): 8-12, 2005.
Article in English | WPRIM | ID: wpr-338654

ABSTRACT

<p><b>OBJECTIVE</b>To observe the influence of intra-articular injection of sodium hyaluronate (HA) on the mRNA expressions of matrix metalloproteinase-1,-3 (MMP-1,-3) and tissue inhibitor of metalloproteinase-1 (TIMP-1) in cartilage and synovium of traumatic osteoarthritis (OA).</p><p><b>METHODS</b>Sixteen white rabbits underwent unilateral anterior cruciate ligament transection (ACLT) were divided into 2 groups randomly 5 weeks after transection. The experimental group rabbits received 0.3 ml of 1% HA by intra-articular injection once a week. Animals in the control group were treated under the same conditions using physiological saline. Ten weeks following surgery, cartilage and synovium were harvested. The mRNA expressions of MMP-1, MMP-3 and TIMP-1 were analyzed using reverse transcription-polymerase chain reaction (RT-PCR).</p><p><b>RESULTS</b>In synovium, the mRNA expression of MMP-3 was suppressed in the HA injection group. HA treatment had no effect on the MMP-3 expression in cartilage. No significant difference of MMP-1 and TIMP-1 expressions in cartilage and synovium was found between the HA injection group and the control group.</p><p><b>CONCLUSIONS</b>One of the mechanisms of the therapeutic effect of HA may be the inhibition of expression of MMP-3 in synovium during early stage of traumatic OA.</p>


Subject(s)
Animals , Rabbits , Anterior Cruciate Ligament , Metabolism , Cartilage, Articular , Metabolism , Hyaluronic Acid , Pharmacology , Matrix Metalloproteinase 3 , Genetics , Osteoarthritis, Knee , Metabolism , Pathology , RNA, Messenger , Genetics , Reverse Transcriptase Polymerase Chain Reaction , Synovial Membrane , Metabolism , Tissue Inhibitor of Metalloproteinase-1 , Genetics
16.
Chinese Journal of Traumatology ; (6): 216-219, 2005.
Article in English | WPRIM | ID: wpr-338610

ABSTRACT

<p><b>OBJECTIVE</b>To detect the concentration of monocyte chemoattractant protein-1 (MCP-1) in the serum of patients with incomplete spinal cord injury and evaluate its relation with the pathologic classification of the spinal cord injury.</p><p><b>METHODS</b>MCP-1 concentration in the serum of patients with incomplete spinal cord injury (iSCI), single spine compression and healthy subjects were detected by ELISA, respectively in the present study and the magnetic resonance imaging data of these patients were studied at the same time on a blind base.</p><p><b>RESULTS</b>Serum level of MCP-1 in iSCI patients was 428 pg/ml +/- 11 pg/ml by ELISA, which was higher than both that of the patients with single spine compression and of controls, with the concentration of 184 pg/ml +/- 21 pg/ml and 124 pg/ml +/- 15 pg/ml, respectively. There was significant difference between any two groups (P < 0.01). iSCI patients with normal MRI showed a lower serum level of MCP-1 as 312 pg/ml+/- 30 pg/ml. Pathological classification of spinal cord edema and hematoma corresponded to 390 pg/ml +/- 16 pg/ml and 508 pg/ml+/- 24 pg/ml in the concentration of MCP-1.</p><p><b>CONCLUSIONS</b>MCP-1 may induce secondary inflammatory response by recruiting inflammatory cells to the injury site and thus affect the prognosis of spinal cord injury.</p>


Subject(s)
Adult , Aged , Humans , Middle Aged , Acute Disease , Chemokine CCL2 , Blood , Enzyme-Linked Immunosorbent Assay , Magnetic Resonance Imaging , Spinal Cord Injuries , Blood , Pathology
17.
Chinese Journal of Traumatology ; (6): 225-229, 2005.
Article in English | WPRIM | ID: wpr-338608

ABSTRACT

<p><b>OBJECTIVE</b>To investigate the effect of pyrroloquinoline quinone (PQQ) on nerve regeneration of transected sciatic nerve in animal models.</p><p><b>METHODS</b>Forty SD rats weighing 220-240 g were randomized into a PQQ group (n = 20) and a control group (n = 20). Each animal underwent sciatic nerve transection operation. After the operation, PQQ 0.5 ml (250 microg/Kg) was injected at the operation site in the PQQ group, while the same volume of normal saline was delivered in the control group. Nerve functional evaluation, electrophysiological index recording were carried out according to the experimental design. Newly generated nerve specimens were harvested 12 weeks postoperatively for morphological studies.</p><p><b>RESULTS</b>In the PQQ group there was a good nerve regeneration and the sciatic nerve function, sciatic nerve function index, electrophysiological index and morphological appearance were superior to the control group (P < 0.05).</p><p><b>CONCLUSIONS</b>PQQ has a remarkable effect in enhancing nerve regeneration of transected peripheral nerve.</p>


Subject(s)
Animals , Male , Rats , Nerve Regeneration , PQQ Cofactor , Pharmacology , Rats, Sprague-Dawley , Sciatic Nerve , Wounds and Injuries , Pathology , Physiology
18.
Chinese Journal of Physical Medicine and Rehabilitation ; (12)2003.
Article in Chinese | WPRIM | ID: wpr-682802

ABSTRACT

Objective To evaluate the preventative effects of rehabilitation training(RT)on deep venous thrombosis(DVT)after arthroplasty.Methods Fifty-six patients with articulatio coxae or knee arthroplasty were randomly divided into a control group and an experiment group(E group).RT,including active movement of the foot and ankle,isometric contraction of the quadriceps fexoris and deep breathing training,was administered to the E group after arthroplasty.Negative cheirapsis was applied in the control group.Peak and average blood flow velocities (PABFVs)in the femoral vein,as well as DVT,were detected and measured using color ultrasound Doppler imaging before and 7 d after arthroplasty.Results PABFVs in the E group were higher than those in the control group (P

19.
Chinese Journal of Rheumatology ; (12)2001.
Article in Chinese | WPRIM | ID: wpr-683084

ABSTRACT

Objective To observe the expression of matrix metalloproteinases(MMP)-1,MMP-3 and iNOS in cartilage of experimental rabbit osteoarthritis at different time intervals after anterior cruciate ligament transection(ACLT)operation.The aim of this study is to provide the theoritical evidence for using ACLT rabbit model in Osteoarthritis(OA)research.Methods Unilateral ACLT was performed on 27 randomly selected while rabbits and underwent unilateral arthrotomy was performed on the other 9 white rabbits as the control group.Nine randomly selected white rabbits in experimental group were killed and 3 white rabbits in the control group at 4th,8th and 12th week respectively.Cartilage degradation of femoral condyles was evaluated macr-oscopically,mRNA expression level and protein expression level of MMP-1,MMP-3 and iNOS was measured by reverse transcription-polymerase chain reaction(RT-PCR)and immunohistochemistry respectively.Results Forepart OA cartilage degradation was observed at the 4th week and became more severe at the 8th week after ACLF.Afterpart cartilage degradation was evident at the 12th week after ACLT while cartilage still remained normal in the control group,mRNA expression level and protein expression level of MMP-1.MMP-3 and iNOS were increased at the 4th week and became higher gradually at the 8th,12th week after ACLT compared with the control group.Expression distribution of MMP-1,MMP-3 and iNOS bad different patterns respectively.Conclusion It is suggested that the process of OA cartilage degradation can be simulated by ACLT model and MMP-1,MMP-3 and iNOS may be good markers in therapeutical research of OA.

20.
Chinese Journal of Rheumatology ; (12)2000.
Article in Chinese | WPRIM | ID: wpr-682653

ABSTRACT

Objective To investigate the effect of intra-articular carboxymethylated ehitosan(CM- CTS)injection on inducible nitric oxide synthase(iNOS)expression in cartilage at the early stage of os- teoarthfitis(OA).Methods Thirty-two white rabbits were underwent unilateral anterior cruciate ligament transection(ACLT)and were randomly divided into 4 groups 5 weeks after transection.Rabbits of group A re- ceived 0.3 ml of 2% high molecular weight CMCTS(H-CMCTS)once every two weeks.Rabbits in group B were treated using 2% low molecular weight(L-CMCTS)CMCTS at:the same intervals.Group C rabbits were injected intra-articularly with 0.3 ml of 1% sodium hyaluronate(Na-HA)once a week.Animals of group D were not injected.At sacrifice,11 weeks following surgery,the expression of iNOS in cartilages was analyzed by immunohistochemistry and reverse transcription-polymerase chain reaction(RT-PCR)methods.Results Both immunohistochemistry and RT-PCR showed that the level of iNOS expression of cartilage in CMCTS in- jection groups was lower than that in Na-HA injection group and the untreated group.There was no significant difference in iNOS expression between the two different molecular weight CMCTS injection groups. No signifi- cant difference of iNOS expression in cartilage was found between Na-HA injection group and the untreated group.Conclusion CMCTS suppresses iNOS expression in cartilage during the early stage of OA.Na-HA treatment has no effect on iNOS expression in cartilage.

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