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实验性骨关节炎中中性蛋白聚糖酶引起的软骨降解。类固醇的抑制作用。

Cartilage degradation by neutral proteoglycanases in experimental osteoarthritis. Suppression by steroids.

作者信息

Pelletier J P, Martel-Pelletier J

出版信息

Arthritis Rheum. 1985 Dec;28(12):1393-401. doi: 10.1002/art.1780281212.

Abstract

In this study, we sought to determine the role of neutral proteases in cartilage matrix proteoglycan degradation, which occurs during the early stages of experimental osteoarthritis. The anterior cruciate ligament was transected in the right knees of 33 dogs. Their left knees served as sham operated controls. The animals were killed 2, 4, 8, and 12 weeks after surgery. Six dogs were treated with oral prednisone and then killed 4 weeks after surgery. Cartilage specimens from medial and lateral tibial plateaus were analyzed for DNA, proteoglycan content, and neutral proteoglycan degrading activity. No significant differences in cartilage DNA and proteoglycan content were observed among the dogs that had surgery, the controls, and the prednisone-treated animals. Total neutral metalloproteoglycan-degrading enzyme (NMPE) activity, determined by direct tissue assay, was significantly higher at all time points in osteoarthritic cartilage than in control cartilage. The active form of NMPE was significantly higher in osteoarthritic cartilage than in control cartilage at 2, 4, and 8 weeks in lateral plateaus and at 2 and 4 weeks in medial plateaus. Treatment for 4 weeks with prednisone (0.20-0.25 mg/kg/day) blocked the increased NMPE activity in osteoarthritic cartilage. The increase in the total and active neutral proteoglycanases supports the hypothesis that these enzymes are involved in early osteoarthritis. The synthesis of NMPE appears to be controlled by stimulating factors released by the synovium.

摘要

在本研究中,我们试图确定中性蛋白酶在实验性骨关节炎早期软骨基质蛋白聚糖降解过程中的作用。对33只犬的右膝前交叉韧带进行横断。它们的左膝作为假手术对照。术后2、4、8和12周处死动物。6只犬口服泼尼松后,于术后4周处死。分析内侧和外侧胫骨平台的软骨标本的DNA、蛋白聚糖含量和中性蛋白聚糖降解活性。在接受手术的犬、对照犬和泼尼松治疗的动物之间,未观察到软骨DNA和蛋白聚糖含量有显著差异。通过直接组织测定确定的总中性金属蛋白酶(NMPE)活性,在骨关节炎软骨的所有时间点均显著高于对照软骨。在外侧平台的2、4和8周以及内侧平台的2和4周时,骨关节炎软骨中NMPE的活性形式显著高于对照软骨。用泼尼松(0.20 - 0.25mg/kg/天)治疗4周可阻断骨关节炎软骨中NMPE活性的增加。总中性蛋白聚糖酶和活性中性蛋白聚糖酶的增加支持了这些酶参与早期骨关节炎的假说。NMPE的合成似乎受滑膜释放的刺激因子控制。

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