Trovato Letizia, Gallo Davide, Settanni Fabio, Gesmundo Iacopo, Ghigo Ezio, Granata Riccarda
Division of Endocrinology, Diabetology and Metabolism, Department of Medical Sciences, University of Turin, Turin, Italy.
Front Horm Res. 2014;42:175-85. doi: 10.1159/000358346. Epub 2014 Apr 7.
Obestatin was identified in 2005 by Zhang and colleagues as a ghrelin-associated peptide, derived from posttranslational processing of the prepro-ghrelin gene. Initially, obestatin was reported to activate the G-protein-coupled receptor GPR39 and to reduce food intake and gastric emptying. However, obestatin remains a controversial peptide, as these findings have been questioned and its receptor is still a matter of debate, as well as its effects on feeding behavior. Recently, interaction with the glucagon-like peptide 1 receptor has been suggested, in line with obestatin-positive effects on glucose and lipid metabolism. In addition, obestatin displays a variety of cellular effects, by regulating metabolic cell functions, increasing cell survival and proliferation, and inhibiting apoptosis and inflammation in different cell types. Finally, like ghrelin, obestatin is produced in the gastrointestinal tract, including the pancreas and adipose tissue, and exerts both local actions in peripheral tissues, and distant effects at the central level. Therefore, obestatin may indeed be considered a hormone, although additional studies are required to clarify its physiopathological role and to definitely identify its receptor.
2005年,张及其同事将肥胖抑制素鉴定为一种与胃饥饿素相关的肽,它来源于前胃饥饿素基因的翻译后加工。最初,据报道肥胖抑制素可激活G蛋白偶联受体GPR39,并减少食物摄入量和胃排空。然而,肥胖抑制素仍然是一种有争议的肽,因为这些发现受到了质疑,其受体仍然存在争议,其对摄食行为的影响也存在争议。最近,有人提出它与胰高血糖素样肽1受体相互作用,这与肥胖抑制素对葡萄糖和脂质代谢的积极作用一致。此外,肥胖抑制素通过调节代谢细胞功能、增加细胞存活和增殖以及抑制不同细胞类型的凋亡和炎症,表现出多种细胞效应。最后,与胃饥饿素一样,肥胖抑制素在胃肠道(包括胰腺和脂肪组织)中产生,在外周组织中发挥局部作用,并在中枢水平产生远距离效应。因此,肥胖抑制素确实可以被认为是一种激素,尽管还需要更多的研究来阐明其生理病理作用并明确鉴定其受体。