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Protective Effects of Human Placenta Extract on Cartilage Degradation in Experimental Osteoarthritis

机译:人胎盘提取物对实验性骨关节炎软骨降解的保护作用

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This study investigated the effect of human placenta extract (HPE) on cartilage degradation in vitro MG-63 cells, articular cartilage explants, and in vivo monoiodoacetate (MIA)-induced osteoarthritis (OA). Matrix metalloproteinase (MMP)-2 activity was measured in HPE-treated osteoblastic MG-63 cells. Articular cartilage explants in rabbit were cultured, and the degree of proteoglycan (PG) degradation was assessed by measuring the amount of glycosaminoglycan (GAG) released into the culture medium. Experimental osteoarthritis was induced by intra-articular injection of 3mg MIA in rats. Beginning 14 d post-MIA injection, HPE was administered intra-articularly once. a day for 14 d. The knee joints were assessed by roentgenography, histology, and gelatinase activity. HPE inhibited PG degradation in articular cartilage explants. HPE significantly reduced deformity of knee joints and suppressed the histological change in MIA-induced OA. HPE inhibited MMP-2 activity in MG-63 cells. MMP-2 and-9 activities were also reduced in the cartilages of HPE-treated knee, joints. Our results indicate that HPE has therapeutic effects on OA by protecting cartilage.
机译:这项研究调查了人胎盘提取物(HPE)对体外MG-63细胞,关节软骨外植体和体内单碘乙酸(MIA)诱导的骨关节炎(OA)软骨降解的影响。在HPE处理的成骨细胞MG-63细胞中测量基质金属蛋白酶(MMP)-2活性。培养兔的关节软骨外植体,并通过测量释放到培养基中的糖胺聚糖(GAG)的量来评估蛋白聚糖(PG)的降解程度。通过关节内注射3mg MIA诱导大鼠实验性骨关节炎。 MIA注射后14天开始,HPE关节内给药一次。每天14天。通过放射线照相术,组织学和明胶酶活性评估膝关节。 HPE抑制了关节软骨外植体中的PG降解。 HPE显着减少了膝关节畸形,并抑制了MIA诱导的OA的组织学变化。 HPE抑制MG-63细胞中的MMP-2活性。 HPE治疗的膝关节的软骨中MMP-2和9的活性也降低了。我们的结果表明,HPE通过保护软骨对OA具有治疗作用。

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