Objective： To investigate the effect of Ermiao Recipe （二妙方, EMR） with medicinal guide Angelicae Pubescentis Radix （APR） on the homing of bone marrow stem cells （BMSCs） to focal zone in osteoarthritis （OA） ...Objective： To investigate the effect of Ermiao Recipe （二妙方, EMR） with medicinal guide Angelicae Pubescentis Radix （APR） on the homing of bone marrow stem cells （BMSCs） to focal zone in osteoarthritis （OA） rats. Methods： Forty-eight Sprague-Dawley rats were randomly assigned to the sham-operated, model, EMR, and EMR plus APR groups （12 rats in each group）. The OA rat model was induced by anterior cruciate ligament transection and medial meniscus resection. All rats were injected with recombinant human granulocyta colony- stimulating factor [rhG-CSF, 30 μg/（kg.d） for continuous 7 days], and rats in the EMR and EMR plus APR groups were treated with EMR or EMR plus APR at 1.6 or 1.9 g/（kg.d） for 3 or 6 weeks, respectively. Cartilage histopathologic changes were observed by hematoxylin and eosin staining. Chondrocytes apoptosis and cartilage matrix components were tested by transferase-mediated deoxyuridine triphosphate-biotin nick end labeling assay and special staining. Interleukin-1β （IL-1 β）, tumor necrosis factor α （TNF-α）, bone morphogenetic protein 2 （BMP-2）, and transforming growth factor beta-1 （TGF-β1） in serum were detected by enzyme-linked immunosorbent assay or radioimmunoassay assay. Matrix metalloproteinase （MMP）-13, tissue inhibitors of metalloproteinase （TIMP）-1, bromodeoxyuridine （BrdU）, cluster of differentiation 34 （CD34）, and stromal cell derived factor 1 （SDF-1） were measured by immunohistochemistry assay. Results： EMR and EMR plus APR significantly inhibited articular cartilage damage and synovium inflammation in OA rats at 3 or 6 weeks of treatment, the most obvious changes in these parameters were found in the EMR plus APR group. At 6 weeks, compared with EMR treatment, EMR plus APR remarkably inhibited chondrocytes apoptosis and the release of IL-1β and TNF- a, obviously decreased MMP-13 expression, and significantly increased expressions of proteoglycan, collagen, type 11 collagen and TIMP-1, serum levels of B展开更多
基金Supported by National Natural Science Foundation of China(No.81072900)
文摘Objective： To investigate the effect of Ermiao Recipe （二妙方, EMR） with medicinal guide Angelicae Pubescentis Radix （APR） on the homing of bone marrow stem cells （BMSCs） to focal zone in osteoarthritis （OA） rats. Methods： Forty-eight Sprague-Dawley rats were randomly assigned to the sham-operated, model, EMR, and EMR plus APR groups （12 rats in each group）. The OA rat model was induced by anterior cruciate ligament transection and medial meniscus resection. All rats were injected with recombinant human granulocyta colony- stimulating factor [rhG-CSF, 30 μg/（kg.d） for continuous 7 days], and rats in the EMR and EMR plus APR groups were treated with EMR or EMR plus APR at 1.6 or 1.9 g/（kg.d） for 3 or 6 weeks, respectively. Cartilage histopathologic changes were observed by hematoxylin and eosin staining. Chondrocytes apoptosis and cartilage matrix components were tested by transferase-mediated deoxyuridine triphosphate-biotin nick end labeling assay and special staining. Interleukin-1β （IL-1 β）, tumor necrosis factor α （TNF-α）, bone morphogenetic protein 2 （BMP-2）, and transforming growth factor beta-1 （TGF-β1） in serum were detected by enzyme-linked immunosorbent assay or radioimmunoassay assay. Matrix metalloproteinase （MMP）-13, tissue inhibitors of metalloproteinase （TIMP）-1, bromodeoxyuridine （BrdU）, cluster of differentiation 34 （CD34）, and stromal cell derived factor 1 （SDF-1） were measured by immunohistochemistry assay. Results： EMR and EMR plus APR significantly inhibited articular cartilage damage and synovium inflammation in OA rats at 3 or 6 weeks of treatment, the most obvious changes in these parameters were found in the EMR plus APR group. At 6 weeks, compared with EMR treatment, EMR plus APR remarkably inhibited chondrocytes apoptosis and the release of IL-1β and TNF- a, obviously decreased MMP-13 expression, and significantly increased expressions of proteoglycan, collagen, type 11 collagen and TIMP-1, serum levels of B
