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非甾体抗炎药对体外及体内软骨细胞代谢的影响。

Effects of nonsteroidal anti-inflammatory drugs on chondrocyte metabolism in vitro and in vivo.

作者信息

Brandt K D

机构信息

Department of Medicine, Indiana University School of Medicine, Indianapolis 46223.

出版信息

Am J Med. 1987 Nov 20;83(5A):29-34. doi: 10.1016/0002-9343(87)90848-5.

Abstract

Salicylates and several other nonsteroidal anti-inflammatory drugs (NSAIDs) that are commonly employed in the treatment of osteoarthritis effectively decrease joint pain and increase mobility. Results from in vitro studies indicate that, in addition, some of these compounds affect proteoglycan metabolism of articular cartilage. Data from in vivo studies suggest that salicylate administration may accelerate articular cartilage damage in several animal models of osteoarthritis. At in vitro concentrations comparable to those that are achieved in the synovial fluid of patients treated with the drug, several NSAIDs suppress proteoglycan synthesis by the chondrocyte. Salicylate has been shown to inhibit the enzymes involved in the early stages of chondroitin sulfate biosynthesis. These NSAID-related effects on chondrocyte metabolism appear unrelated to inhibition of prostaglandin synthetase, and are much more profound in osteoarthritic cartilage than in normal cartilage, due to enhanced uptake of NSAIDs by the osteoarthritic cartilage. Depletion of matrix proteoglycans appears to be a major factor in the increased vulnerability of chondrocytes in degenerating cartilage to effects of NSAIDs. Some NSAIDs may be bound to matrix components. If similar changes occur in the cartilage of patients with arthritis treated with NSAIDs, despite the symptomatic improvement that these drugs produce, cartilage degeneration could be accelerated.

摘要

水杨酸盐和其他几种常用于治疗骨关节炎的非甾体抗炎药(NSAIDs)能有效减轻关节疼痛并提高关节活动度。体外研究结果表明,此外,这些化合物中的一些还会影响关节软骨的蛋白聚糖代谢。体内研究数据表明,在几种骨关节炎动物模型中,服用水杨酸盐可能会加速关节软骨损伤。在与服用该药物的患者滑液中所达到的浓度相当的体外浓度下,几种NSAIDs会抑制软骨细胞的蛋白聚糖合成。水杨酸盐已被证明能抑制硫酸软骨素生物合成早期阶段所涉及的酶。这些NSAIDs对软骨细胞代谢的相关影响似乎与抑制前列腺素合成酶无关,并且由于骨关节炎软骨对NSAIDs的摄取增加,在骨关节炎软骨中比在正常软骨中更为显著。基质蛋白聚糖的消耗似乎是退变软骨中的软骨细胞对NSAIDs作用更敏感的一个主要因素。一些NSAIDs可能会与基质成分结合。如果在用NSAIDs治疗的关节炎患者的软骨中发生类似变化,尽管这些药物能产生症状改善,但软骨退变可能会加速。

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