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Glucosamine sulfate modulates dysregulated activities of human osteoarthritic chondrocytes in vitro.

机译:硫酸葡萄糖胺在体外调节人骨关节炎软骨细胞的失调活性。

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OBJECTIVE: The efficacy of glucosamine sulfate (GS) in the symptomatic treatment of patients with osteoarthritis (OA) is suggested to be mediated by still unknown effects on the altered OA cartilage. DESIGN: Using human OA chondrocytes in culture, the effects of GS on protein synthesis, caseinase, collagenase, phospholipase A2 (PLA2) and protein kinase C (PKC) activities as well as production of nitric oxide and cyclic AMP were studied in both cells and culture medium. RESULTS: GS significantly reduced PLA2 activity, and more modestly collagenase activity, in the OA chondrocytes in a dose-dependent manner. By contrast, PLA2 and collagenase activity of the culture medium was not modified. No effects on caseinase activity was seen. GS significantly and dose-dependently increased protein synthesis. GS did not modify nitric oxide and cAMP production but significantly increased PKC production. CONCLUSION: GS modified cultured OA chondrocyte metabolism by acting on PKC, cellular PLA2, protein synthesis and possibly collagenase activation. Extrapolation of the effect to the in-vivo situation remains hypothetical but they might represent some possible mechanisms of action of the drug in human.
机译:目的:硫酸氨基葡萄糖(GS)在对症治疗骨关节炎(OA)的对症治疗中的功效可能是由对骨软骨变化的影响尚不清楚。设计:使用培养的人OA软骨细胞,研究了GS对蛋白质合成,酪蛋白酶,胶原酶,磷脂酶A2(PLA2)和蛋白激酶C(PKC)活性以及一氧化氮和环状AMP产生的影响。培养基。结果:GS以剂量依赖的方式显着降低了OA软骨细胞中的PLA2活性,并适度降低了胶原酶的活性。相反,培养基的PLA2和胶原酶活性未改变。没有发现对酪蛋白酶活性的影响。 GS显着且剂量依赖性地增加了蛋白质合成。 GS不会改变一氧化氮和cAMP的产生,但会显着增加PKC的产生。结论:GS通过作用于PKC,细胞PLA2,蛋白质合成以及可能的胶原酶活化来修饰培养的OA软骨细胞代谢。对体内作用的推断仍是假设的,但它们可能代表药物在人体内的某些可能作用机制。

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