NITRIC-OXIDE MEDIATES INTERLEUKIN-1 INDUCED-INHIBITION OF GLYCOSAMINOGLYCAN SYNTHESIS IN RAT ARTICULAR-CARTILAGE

被引:66
作者
JARVINEN, TAH
MOILANEN, T
JARVINEN, TLN
MOILANEN, E
机构
[1] UNIV TAMPERE,SCH MED,SF-33101 TAMPERE,FINLAND
[2] TAMPERE UNIV HOSP,DEPT SURG,SF-33521 TAMPERE,FINLAND
[3] TAMPERE UNIV HOSP,DEPT CLIN PHARMACOL,SF-33521 TAMPERE,FINLAND
关键词
ARTHRITIS; CARTILAGE; CHONDROCYTE; GLUCOCORTICOID; GLYCOSAMINOGLYCAN SYNTHESIS; INTERLEUKIN-1-BETA; NITRIC OXIDE;
D O I
10.1155/S0962935195000184
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
INTERLEUKIN-1 beta (IL-1) is a key mediator of cartilage matrix degradation in osteoarthritis and rheumatoid arthritis. It was found that the IL-1-induced suppression of glycosaminoglycan (GAG) synthesis in rat articular cartilage occurred simultaneously with the accumulation of nitrite (a metabolite of nitric oxide (NO) in aqueous milieu) in the culture medium. NO-synthase inhibitors, L-NMMA and L-NIO, inhibited both these IL-1 effects. Dexamethasone suppressed GAG synthesis additively to IL-1, but did not alter nitrite accumulation. Three NO-donors (GEA 3175, SNAP and SIN-1) also had an inhibitory effect on cartilage GAG synthesis. Therefore, it is concluded that IL-1 induced suppression of GAG synthesis in rat articular cartilage is mediated by the production of NO.
引用
收藏
页码:107 / 111
页数:5
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