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衰老和关节炎疾病对人关节软骨细胞一氧化氮产生的影响。

Effects of ageing and arthritic disease on nitric oxide production by human articular chondrocytes.

作者信息

Min B H, Kim H J, Lim H, Park C S, Park S R

机构信息

Department of Orthopaedic surgery, Ajou University, Woncheon-Dong, Suwon, Korea.

出版信息

Exp Mol Med. 2001 Dec 31;33(4):299-302. doi: 10.1038/emm.2001.48.

Abstract

Nitric oxide (NO) has been considered as an important mediator in inflammatory phases and in loss of cartilage. In inflammatory arthritis, NO levels are correlated with disease activity and articular cartilage is able to produce large amounts of NO with the appropriate inducing factor such as cytokines. The old animals are shown to have a greater sensitivity to NO than young animals. This study evaluated the basal production of NO in normal and OA-affected chondroyctes from young and old patients and compared the levels of NO formation in response to IL-1beta. The results showed that the basal levels were 7-fold higher in old chondrocytes than those of young cells. However, the IL-1beta induced NO production was seen to decrease with age. Aminoguianidine (AG), a competitive inhibitor of iNOS, inhibited NO formation completely in both chondrocytes from young and old individuals. However, at the same concentration of AG it caused partial inhibition of NO and iNOS formation in chondrocytes from OA-affected individuals. In addition, although the IL-1beta induced NO production was much lesser than that of young chondrocytes, the inhibition of collagen production by IL-1beta was prominent in old chondrocytes and OA-affected chondrocytes. These results suggest that age-related differences in the regulation of NO production and collagen production, which may affect the ageing cells and osteoarthritic changes in some way.

摘要

一氧化氮(NO)被认为是炎症阶段和软骨损伤中的一种重要介质。在炎症性关节炎中,NO水平与疾病活动相关,并且关节软骨能够在诸如细胞因子等适当诱导因子的作用下产生大量NO。研究表明,老年动物对NO的敏感性高于幼年动物。本研究评估了年轻和老年患者正常及骨关节炎(OA)相关软骨细胞中NO的基础生成情况,并比较了它们对白细胞介素-1β(IL-1β)反应时NO的生成水平。结果显示,老年软骨细胞中的基础水平比年轻细胞高7倍。然而,IL-1β诱导的NO生成量随年龄增长而减少。氨基胍(AG),一种诱导型一氧化氮合酶(iNOS)的竞争性抑制剂,能完全抑制年轻和老年个体软骨细胞中的NO生成。然而,在相同浓度的AG作用下,它只能部分抑制OA相关个体软骨细胞中的NO和iNOS生成。此外,尽管IL-1β诱导的NO生成量比年轻软骨细胞少得多,但IL-1β对老年软骨细胞和OA相关软骨细胞中胶原蛋白生成的抑制作用却很显著。这些结果表明,NO生成和胶原蛋白生成调节方面的年龄相关差异可能以某种方式影响衰老细胞和骨关节炎的变化。

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