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Ghrelin and Metabolic Disorders

机译:Ghrelin和代谢紊乱

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Ghrelin is a gut-brain peptide that has somatotropic, food intake increasing and adipogenic effects. Ghrelin is involved in modulating insulin and glucose metabolism in rodents according to recent studies. In humans acylated ghrelin reduces insulin sensitivity while unacylated ghrelin has opposite effects. In general, ghrelin seems to have diabetogenic effects. Obese, in particular abdominally obese, subjects have low ghrelin levels and decreased total ghrelin levels have been associated with metabolic syndrome and Type 2 diabetes. Most of the human studies in Type 1 diabetes have reported low ghrelin levels probably as a compensatory mechanism against hyperglycaemia. The data on obestatin in the regulation of energy balance is extremely contradictory. Interestingly, ghrelin receptor antagonists may improve glucose tolerance in rats without inducing weight gain by increasing insulin secretion. Antagonism of ghrelin function to treat diabetes is thus a fascinating idea. This review concentrates on recent findings on the orexigenic peptide ghrelin and its derivatives in metabolic disorders with emphasis put on human studies.
机译:生长激素释放肽是一种肠脑肽,具有促生长作用,食物摄入增加和成脂作用。根据最近的研究,Ghrelin参与调节啮齿动物中的胰岛素和葡萄糖代谢。在人类中,酰化的生长素释放肽降低了胰岛素敏感性,而未酰化的生长素释放肽则具有相反的作用。通常,生长素释放肽似乎具有促糖尿病作用。肥胖,特别是腹部肥胖,受试者的生长素释放肽水平低,总生长素释放肽水平降低与代谢综合征和2型糖尿病有关。人类在1型糖尿病中的大多数研究都报告低生长素释放肽水平可能是针对高血糖的一种补偿机制。肥胖抑制素在调节能量平衡方面的数据极为矛盾。有趣的是,生长素释放肽受体拮抗剂可以改善大鼠的葡萄糖耐量,而不会通过增加胰岛素分泌而引起体重增加。生长激素释放肽功能拮抗以治疗糖尿病因此是一个令人着迷的想法。这篇综述集中在关于致代谢肽ghrelin及其衍生物在代谢性疾病中的最新发现,重点放在人体研究上。

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