Broglio Fabio, Papotti Mauro, Muccioli Giampiero, Ghigo Ezio
Division of Endocrinology and Metabolism, Department of Internal Medicine, University of Turin, corso Dogliotti 14, 10126 Turin, Italy.
Trends Endocrinol Metab. 2007 Aug;18(6):246-51. doi: 10.1016/j.tem.2007.06.004. Epub 2007 Jul 13.
Although cortistatin (CST) shares great structural homology with somatostatin (SST) and binds to all SST receptor subtypes with similar affinity, these neurohormones have divergent biological roles, as evidenced by their different patterns of tissue expression and biological actions. Moreover, CST, but not SST, can bind to the proadrenomedullin N-terminal peptide (PAMP) receptor MrgX2 and type 1a growth hormone secretagogue (GHS) receptor (GHSR-1a), also known as the 'ghrelin' receptor. These findings suggest that CST-specific actions could be mediated by the GHSR-1a and CST might represent a link between the ghrelin and the SST systems. Here, we review the data leading to this working hypothesis and discuss the in vitro, in vivo and clinical implications of potential SST-receptor-independent, GHSR-1a-mediated neuroendocrine and metabolic effects of CST.
虽然皮质抑素(CST)与生长抑素(SST)具有高度的结构同源性,且以相似的亲和力与所有SST受体亚型结合,但这些神经激素具有不同的生物学作用,这从它们不同的组织表达模式和生物学作用中得到了证明。此外,CST而非SST能够与肾上腺髓质素原N端肽(PAMP)受体MrgX2和1a型生长激素促分泌素(GHS)受体(GHSR-1a,也称为“胃饥饿素”受体)结合。这些发现表明,CST的特异性作用可能由GHSR-1a介导,并且CST可能代表胃饥饿素和SST系统之间的一种联系。在此,我们回顾了得出这一工作假设的数据,并讨论了CST潜在的不依赖SST受体、由GHSR-1a介导的神经内分泌和代谢作用在体外、体内及临床方面的意义。