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[胃饥饿素对食欲的调节——肠-脑轴中的一种新型神经内分泌胃肽激素]

[Appetite regulation by ghrelin - a novel neuro-endocrine gastric peptide hormone in the gut-brain-axis].

作者信息

Hagemann D, Meier J J, Gallwitz B, Schmidt W E

机构信息

Medizinische Klinik I, St.-Josef-Hospital Bochum, Klinikum der Ruhr-Universität Bochum, Germany.

出版信息

Z Gastroenterol. 2003 Sep;41(9):929-36. doi: 10.1055/s-2003-41853.

Abstract

Ghrelin a novel peptide consisting of 28 amino acids was first identified in the stomach in 1999. It is mainly produced in endocrine cells of the human gastric mucosa, but it was also found in several other tissues e. g. in the pituitary, the hypothalamus and the pancreas. The functional receptor belongs to the family of the 7-transmembrane G-protein receptors and is predominantly detected in the pituitary and at lower levels in hypothalamic nuclei, the stomach, heart, lungs, kidneys, gut, the adipose and many other tissues. According to the widespread distribution of the peptide and its receptor, ghrelin has multiple biological effects: it stimulates the release of growth hormone in the pituitary and induces a rise in the serum concentration of ACTH, cortisol, catecholamines and prolactin. Ghrelin causes an increase of food intake and body weight by stimulating the production of neuropeptide Y (NPY) and agouti-related protein (AGP) in the nucleus arcuatus. It further leads to elevated concentrations of plasma glucose. A physiological antagonism between ghrelin and GLP-1 in the hypothalamic regulation of appetite is being discussed. The basic serum level of ghrelin depends on the state of nutrition and is negatively correlated with the body-mass-index. It shows a certain pattern of variation before and after food intake with a preprandial increase and a postprandial decrease. Ghrelin modulates gastric acid secretion and the gastrointestinal motility via vagal cholinergic pathways. The discovery of ghrelin definitely contributes to the understanding of the growth-hormone secretion and of the regulation of appetite and food intake.

摘要

胃饥饿素是一种由28个氨基酸组成的新型肽,于1999年首次在胃中被发现。它主要由人胃黏膜的内分泌细胞产生,但也在其他几种组织中被发现,例如垂体、下丘脑和胰腺。其功能性受体属于7跨膜G蛋白受体家族,主要在垂体中被检测到,在下丘脑核、胃、心脏、肺、肾脏、肠道、脂肪组织和许多其他组织中的水平较低。根据该肽及其受体的广泛分布,胃饥饿素具有多种生物学效应:它刺激垂体中生长激素的释放,并导致促肾上腺皮质激素、皮质醇、儿茶酚胺和催乳素的血清浓度升高。胃饥饿素通过刺激弓状核中神经肽Y(NPY)和刺鼠相关蛋白(AGP)的产生,导致食物摄入量和体重增加。它还会导致血浆葡萄糖浓度升高。目前正在讨论胃饥饿素与胰高血糖素样肽-1在下丘脑食欲调节中的生理拮抗作用。胃饥饿素的基础血清水平取决于营养状况,与体重指数呈负相关。它在进食前后呈现一定的变化模式,进食前升高,进食后降低。胃饥饿素通过迷走胆碱能途径调节胃酸分泌和胃肠蠕动。胃饥饿素的发现无疑有助于对生长激素分泌以及食欲和食物摄入调节的理解。

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