Sheikh S P
University Department of Clinical Biochemistry, Rigshospitalet, Copenhagen, Denmark.
Am J Physiol. 1991 Nov;261(5 Pt 1):G701-15. doi: 10.1152/ajpgi.1991.261.5.G701.
The present paper reviews the chemistry, distribution, and release of neuropeptide Y (NPY) and peptide YY (PYY) and evaluates their role as neuronal and hormonal regulators in gastrointestinal physiology. In addition, the current concepts of receptors for NPY and PYY, the Y1 and Y2 receptor subtypes and their localization, characterization by ligand binding studies, and structural analysis by affinity-labeling experiments, are presented and discussed. NPY is present in both central and peripheral neurons, whereas PYY is mainly expressed in endocrine cells in the lower bowel. PYY and NPY inhibit gut motility, gastric emptying and acid secretion, and pancreatic exocrine secretion and are potent vasoconstrictors in many vascular beds. It is suggested that these peptides regulate gastrointestinal function by effects on blood flow, by modulating neural control mechanism, and in some cases by direct effects on differential functional cells such as enterocytes. Multiple receptors for NPY and PYY probably exist, and these appear to fall into Y1 and Y2 types by their specificity for a long COOH-terminal fragment, NPY-(13-36) and an NPY analogue, [Leu31,Pro34]NPY. The latter is specific for Y1 receptors, whereas the COOH-terminal fragment preferentially binds to Y2 receptors. Furthermore, affinity-labeling experiments have shown that the Y1 and Y2 receptors are structurally distinct glycoproteins. It is concluded that the herein characterized Y1 and Y2 receptors may be the structural proteins that mediate the physiological actions of NPY and PYY.
本文综述了神经肽Y(NPY)和肽YY(PYY)的化学、分布及释放情况,并评估了它们在胃肠生理学中作为神经元和激素调节剂的作用。此外,还介绍并讨论了目前关于NPY和PYY受体的概念,即Y1和Y2受体亚型及其定位、通过配体结合研究进行的表征以及通过亲和标记实验进行的结构分析。NPY存在于中枢和外周神经元中,而PYY主要在下消化道的内分泌细胞中表达。PYY和NPY可抑制肠道蠕动、胃排空和胃酸分泌以及胰腺外分泌,并且在许多血管床中是强效血管收缩剂。有人提出,这些肽通过影响血流、调节神经控制机制以及在某些情况下直接作用于诸如肠上皮细胞等不同功能细胞来调节胃肠功能。NPY和PYY可能存在多种受体,根据它们对长COOH末端片段NPY-(13 - 36)和一种NPY类似物[Leu31,Pro34]NPY的特异性,这些受体似乎可分为Y1和Y2类型。后者对Y1受体具有特异性,而COOH末端片段优先与Y2受体结合。此外,亲和标记实验表明Y1和Y2受体是结构不同的糖蛋白。得出的结论是,本文所表征的Y1和Y2受体可能是介导NPY和PYY生理作用的结构蛋白。