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胃饥饿素作为食欲主要调节剂的作用及其在神经内分泌学中的其他功能。

Ghrelin's role as a major regulator of appetite and its other functions in neuroendocrinology.

机构信息

Centre for Endocrinology, William Harvey Research Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.

出版信息

Prog Brain Res. 2010;182:189-205. doi: 10.1016/S0079-6123(10)82008-4.

Abstract

Ghrelin is a circulating growth-hormone-releasing and appetite-inducing brain-gut peptide. It is a known natural ligand of the growth hormone secretagogue receptor (GHS-R). Ghrelin is acylated on its serine 3 residue by ghrelin O-acyltransferase (GOAT). The acylation is essential for its orexigenic and adipogenic effects. Ghrelin exerts its central orexigenic effect through activation of various hypothalamic and brain stem neurons. Several new intracellular targets/mediators of the appetite-inducing effect of ghrelin in the hypothalamus have recently been identified, including the AMP-activated protein kinase, its upstream kinase calmodulin kinase kinase 2, components of the fatty acid pathway and the uncoupling protein 2. The ghrelin/GOAT/GHS-R system is now recognised as a potential target for the development of anti-obesity treatment. Ghrelin regulates the function of the anterior pituitary through stimulation of secretion not only of growth hormone, but also of adrenocorticotrophin and prolactin. The implication of ghrelin and its receptor in the pathogenesis of the neuroendocrine tumors will also be discussed in this review.

摘要

胃饥饿素是一种循环生长激素释放和食欲诱导的脑肠肽。它是生长激素促分泌素受体(GHS-R)的已知天然配体。胃饥饿素在其丝氨酸 3 残基上被胃饥饿素 O-酰基转移酶(GOAT)酰化。酰化对于其食欲和脂肪生成作用是必不可少的。胃饥饿素通过激活各种下丘脑和脑干神经元发挥其中枢食欲作用。最近,在下丘脑,已经确定了胃饥饿素食欲诱导作用的几个新的细胞内靶标/介质,包括 AMP 激活蛋白激酶、其上游激酶钙调蛋白激酶激酶 2、脂肪酸途径的组成部分和解偶联蛋白 2。胃饥饿素/GOAT/GHS-R 系统现在被认为是开发抗肥胖治疗的潜在靶点。胃饥饿素通过刺激生长激素、促肾上腺皮质激素和催乳素的分泌来调节垂体前叶的功能。本综述还将讨论胃饥饿素及其受体在神经内分泌肿瘤发病机制中的作用。

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