Lipton J M, Catania A
Department of Physiology, University of Texas Southwestern Medical Center at Dallas 75235-9040, USA.
Ann N Y Acad Sci. 1998 May 1;840:373-80. doi: 10.1111/j.1749-6632.1998.tb09576.x.
The antiinflammatory effects of alpha-melanocyte-stimulating hormone (alpha-MSH) molecules, specifically alpha-MSH(1-13) and its COOH-terminal tripeptide alpha-MSH(11-13), are well established. The peptides have been effective in tests of all major models of inflammation, and more recent tests have been extended to include experimental inflammatory bowel disease, CNS ischemia/reperfusion injury, and bacterial endotoxin-induced inflammation within the brain. The broad effectiveness of alpha-MSH molecules in all major types of inflammation indicates that the peptides exert actions that are very basic to the inflammatory process. Three general mechanisms of antiinflammatory action of alpha-MSH molecules have been identified: inhibition of production of inflammatory mediators by, or inhibition of inflammatory actions of, peripheral host cells; inhibition of peripheral inflammation induced by actions on melanocortin receptors within the brain; inhibition of CNS inflammation by local action of the peptides. It appears that alpha-MSH molecules have multiple actions that modulate the primitive inflammatory response.
α-黑素细胞刺激素(α-MSH)分子,特别是α-MSH(1-13)及其羧基末端三肽α-MSH(11-13)的抗炎作用已得到充分证实。这些肽在所有主要炎症模型的试验中均有效,并且最近的试验已扩展到包括实验性炎症性肠病、中枢神经系统缺血/再灌注损伤以及脑内细菌内毒素诱导的炎症。α-MSH分子在所有主要类型炎症中的广泛有效性表明,这些肽发挥的作用对于炎症过程非常基本。已确定α-MSH分子抗炎作用的三种一般机制:抑制外周宿主细胞产生炎症介质或抑制其炎症作用;通过作用于脑内黑皮质素受体抑制外周炎症;肽的局部作用抑制中枢神经系统炎症。看来α-MSH分子具有多种调节原始炎症反应的作用。