alpha-MSH modulates experimental inflammatory bowel disease

被引:95
作者
Rajora, N
Boccoli, G
Catania, A
Lipton, JM
机构
[1] UNIV TEXAS, SW MED CTR, DEPT PHYSIOL, DALLAS, TX 75235 USA
[2] UNIV TEXAS, SW MED CTR, DEPT ANESTHESIOL, DALLAS, TX 75235 USA
[3] UNIV TEXAS, SW MED CTR, DEPT PAIN MANAGEMENT, DALLAS, TX 75235 USA
[4] OSPED MAGGIORE, IRCCS, DIV INTERNAL MED 3, I-20122 MILAN, ITALY
关键词
alpha-MSH; inflammatory bowel disease; colitis; antiinflammatory; peptide; TNF alpha; nitric oxide; mice;
D O I
10.1016/S0196-9781(96)00345-2
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
The mechanisms underlying inflammatory bowel disease (IBD) remain obscure but the importance of inflammatory processes is clear and most pharmacological therapies inhibit inflammation. The search for more effective agents with low toxicity continues. To test the possibility that the antiinflammatory/anticytokine peptide alpha-MSH can be used to control 1BD, the peptide was administered to a murine colitis model. The peptide treatment had marked salutary effects: it reduced the appearance of fecal blood by over 80%, inhibited weight loss, and prevented disintegration of the general condition of the animals. Mice given alpha-MSH showed markedly lower production of TNF alpha by tissues of the lower colon stimulated with concanavalin A; the inhibitory effect of alpha-MSH on production of inflammatory nitric oxide by lower bowel tissue was even greater. The combined results indicate that alpha-MSH modulates experimental IBD, perhaps by inhibiting production within the gut of the local proinflammatory agents TNF alpha and nitric oxide, or by inhibiting inflammatory processes closely linked to these mediators. (C) 1997 Elsevier Science Inc.
引用
收藏
页码:381 / 385
页数:5
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