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α-黑素细胞刺激素可减轻内毒素诱导的肝脏炎症。

Alpha-melanocyte-stimulating hormone reduces endotoxin-induced liver inflammation.

作者信息

Chiao H, Foster S, Thomas R, Lipton J, Star R A

机构信息

Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas 75235, USA.

出版信息

J Clin Invest. 1996 May 1;97(9):2038-44. doi: 10.1172/JCI118639.

Abstract

Alpha-Melanocyte-stimulating hormone (MSH) is a potent anti-inflammatory agent in many models of inflammation, suggesting that it inhibits a critical step common to different forms of inflammation. We showed previously that alpha-MSH inhibits nitric oxide (NO) production in cultured macro-phages. To determine how alpha-MSH acts in vivo, we induced acute hepatic inflammation by administering endotoxin (LPS) to mice pretreated with Corynebacterium parvum, alpha-MSH prevented liver inflammation even when given 30 min after LPS administration. To determine the mechanisms of action of alpha-MSH, we tested its influence on NO, infiltrating inflammatory cells, cytokines, and chemokines. Alpha-MSH inhibited systemic NO production, hepatic neutrophil infiltration, and increased hepatic mRNA abundance for TNF alpha, and the neutrophil and monocyte chemokines (KC/IL-8 and MCP-1). We conclude that alpha-MSH prevents LPS-induced hepatic inflammation by inhibiting production of chemoattractant chemokines which then modulate infiltration of inflammatory cells. Thus, alpha-MSH has an effect very early in the inflammatory cascade.

摘要

α-黑素细胞刺激素(α-MSH)在许多炎症模型中都是一种有效的抗炎剂,这表明它能抑制不同形式炎症所共有的关键步骤。我们之前表明,α-MSH可抑制培养的巨噬细胞中一氧化氮(NO)的产生。为了确定α-MSH在体内的作用方式,我们通过向经微小棒状杆菌预处理的小鼠注射内毒素(LPS)来诱导急性肝炎症,即使在LPS注射30分钟后给予α-MSH,它也能预防肝脏炎症。为了确定α-MSH的作用机制,我们测试了它对NO、浸润性炎症细胞、细胞因子和趋化因子的影响。α-MSH抑制全身NO的产生、肝脏中性粒细胞浸润,并增加肝脏中TNFα、中性粒细胞趋化因子和单核细胞趋化因子(KC/IL-8和MCP-1)的mRNA丰度。我们得出结论,α-MSH通过抑制趋化性趋化因子的产生来预防LPS诱导的肝脏炎症,进而调节炎症细胞的浸润。因此,α-MSH在炎症级联反应的早期就发挥作用。

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