Use of ghrelin as a treatment for inflammatory bowel disease: mechanistic considerations.

International Journal of Peptides Pub Date : 2011-01-01 Epub Date: 2011-08-09 DOI:10.1155/2011/189242
Mark D Deboer
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引用次数: 34

Abstract

Inflammatory bowel diseases (IBD)-and in particular Crohn's disease-are immune-mediated processes that result in denuded intestinal mucosa and can produce decreased appetite, weight loss, and systemic inflammation. Current treatments include anti-inflammatory medications, immunomodulators, and feeding interventions. Ghrelin is an endogenous orexigenic hormone that directly stimulates growth hormone release, increases gut motility, and has cardiovascular and anti-inflammatory properties. Although ghrelin levels are elevated in active IBD, administration of ghrelin in most (but not all) animal models of colitis has produced improvements in disease activity and systemic inflammation. The mechanism for these effects is not known but may relate to decreased inflammation, increased motility, increased appetite, and increased colonic blood flow. Human trials have not been performed, however, and more research is clearly needed.

使用胃饥饿素治疗炎症性肠病:机制考虑。
炎症性肠病(IBD)——尤其是克罗恩病——是免疫介导的过程,导致肠黏膜脱落,并可导致食欲下降、体重减轻和全身性炎症。目前的治疗方法包括抗炎药物、免疫调节剂和喂养干预。胃饥饿素是一种内源性促氧激素,直接刺激生长激素的释放,增加肠道动力,并具有心血管和抗炎特性。虽然生长素水平在活动性IBD中升高,但在大多数(但不是全部)结肠炎动物模型中给予生长素可以改善疾病活动性和全身性炎症。这些作用的机制尚不清楚,但可能与减少炎症、增加运动性、增加食欲和增加结肠血流量有关。然而,人体试验尚未进行,显然需要更多的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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