Opiate regulation of IL-1β and TNF-α in cultured human articular chondrocytes

被引:10
作者
Andjelkov, N [1 ]
Elvenes, J
Martin, J
Johansen, O
机构
[1] Univ Hosp No Norway, Dept Orthopaed, N-9038 Tromso, Norway
[2] Univ Iowa, Dept Orthopaed Surg, Iowa City, IA 52242 USA
关键词
cytokines; beta-endorphin; cartilage; mu-opioid receptor;
D O I
10.1016/j.bbrc.2005.06.035
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In order to investigate if beta-endorphins anti-inflammatory effect in cartilage-damaging states is mediated via tumor necrosis factor-alpha (TNF-alpha) and interleukin-1 beta (IL-1 beta), we examined its influence on these two cytokines in vitro. Human articular chondrocytes were obtained from patients undergoing total knee arthroplasty and stimulated with beta-endorphin (60-6000 ng/ml). Protein levels of TNF-alpha and IL-1 beta were measured by ELISA in supernatants from articular chondrocyte cultures. beta-Endorphin significantly increased the levels of IL-1 beta for all concentrations used after 15 min incubation, and when stimulated with 600 and 6000 ng/ml after 24 h incubation. The opioid-induced increase in IL-1 beta was blocked by naltrexone in the group tested. TNF-alpha expression was also significantly stimulated by 60 and 600 ng/ml beta-endorphin after 15 trim, an effect blocked by naltrexone in the group tested. These findings indicate that the mechanism of beta-endorphins anti-inflammatory influence in cartilage-damaging states is not apparently mediated via these two cytokines modulation. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1295 / 1299
页数:5
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