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阿米洛利抑制关节软骨细胞中的酸感应离子通道可减轻佐剂关节炎大鼠的关节软骨破坏。

Inhibition of acid-sensing ion channels in articular chondrocytes by amiloride attenuates articular cartilage destruction in rats with adjuvant arthritis.

机构信息

College of Pharmacy, Anhui Medical University, Hefei, Anhui, People's Republic of China.

出版信息

Inflamm Res. 2010 Nov;59(11):939-47. doi: 10.1007/s00011-010-0206-4. Epub 2010 May 8.

Abstract

OBJECTIVE

The aim of this study was to examine whether drugs such as amiloride that block acid sensing ion channels (ASICs) could attenuate articular cartilage destruction in adjuvant-induced arthritis (AA).

METHODS

Articular chondrocytes were isolated from the normal rats, and intracellular calcium ([Ca(2+)]i) was analyzed with laser scanning confocal microscopy. The cell injury was analyzed with lactate dehydrogenase release assay and electron microscopy. Amiloride or phosphate buffered saline was administered daily to AA rats for 1 week from the time of arthritis onset. Morphology of the articular cartilage was examined by hematoxylin and eosin staining, and Mankin score was calculated. The expression level of type II collagen (COII) and aggrecan mRNA and proteins in the articular cartilage was evaluated by real-time PCR and Western blotting, respectively.

RESULTS

The rapid decrease in extracellular pH (6.0) induced a conspicuous increase in [Ca(2+)]i in the articular chondrocytes. Amiloride reduced this increase in [Ca(2+)]i, and inhibited acid-induced articular chondrocyte injury. Amiloride significantly decreased Mankin scores in the articular cartilage in AA rats. COII and aggrecan mRNA and protein expression in the articular cartilage was significantly increased by amiloride.

CONCLUSION

These findings represent some experimental evidence of a potential role for ASICs in the pathogenesis of articular cartilage destruction in rheumatoid arthritis.

摘要

目的

本研究旨在探讨阿米洛利等阻断酸感应离子通道(ASICs)的药物是否能减轻佐剂性关节炎(AA)中的关节软骨破坏。

方法

从正常大鼠中分离关节软骨细胞,并用激光共聚焦扫描显微镜分析细胞内钙离子([Ca(2+)]i)。通过乳酸脱氢酶释放试验和电子显微镜分析细胞损伤。从关节炎发病时起,用阿米洛利或磷酸盐缓冲盐水每天给 AA 大鼠治疗 1 周。用苏木精和伊红染色检查关节软骨的形态,并用 Mankin 评分计算。通过实时 PCR 和 Western blot 分别评估关节软骨中 II 型胶原(COII)和聚集蛋白聚糖 mRNA 和蛋白的表达水平。

结果

细胞外 pH 值(6.0)的快速下降导致关节软骨细胞中[Ca(2+)]i的显著增加。阿米洛利减少了这种[Ca(2+)]i的增加,并抑制了酸诱导的关节软骨细胞损伤。阿米洛利显著降低了 AA 大鼠关节软骨中的 Mankin 评分。阿米洛利显著增加了关节软骨中的 COII 和聚集蛋白聚糖 mRNA 和蛋白的表达。

结论

这些发现为 ASICs 在类风湿关节炎关节软骨破坏发病机制中的潜在作用提供了一些实验证据。

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