Sabbatini Maria Eugenia
Department of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI 48109-5622, United States.
Regul Pept. 2009 Apr 10;154(1-3):5-15. doi: 10.1016/j.regpep.2009.02.009. Epub 2009 Feb 20.
Atrial natriuretic peptide (ANP) and C-type natriuretic peptide (CNP) are members of the natriuretic peptide family best known for their role in blood pressure regulation. However, in recent years all the natriuretic peptides and their receptors have been described in the gastrointestinal tract, digestive glands and central nervous system, as well as implicated in the regulation of digestive gland functions. The current review highlights the regulatory role of ANP and CNP in pancreatic and other digestive secretions. ANP and CNP stimulate basal as well as induced pancreatic secretion and modify bicarbonate and chloride secretions. Whereas ANP and CNP exert effects directly on pancreatic cells, CNP also acts through a vago-vagal reflex. At high doses both peptides attenuate pancreatic secretion induced by high doses of secretin through the PLC/PKC pathway. With regards to other digestive secretions, ANP and CNP decrease bile secretion in the rat. ANP does not induce salivation by itself but enhances stimulated salivary secretion and modifies salivary composition in rat parotid as well as submandibular glands. In rat pancreatic, hepatic, parotid and submandibular tissues, the NPR-C receptor mediates mostly peripheral responses whereas NPR-A and NPR-B receptors, which are coupled to guanylate cyclase, likely mediate the central response. In addition, ANP modulates gastric acid secretion via a vagal-dependent mechanism. In the intestine, ANP and CNP decrease water and sodium chloride absorption through an increase in cGMP levels. Overall, these findings indicate that ANP and CNP are members of the large group of regulatory peptides affecting digestive secretions.
心房利钠肽(ANP)和C型利钠肽(CNP)是利钠肽家族的成员,以其在血压调节中的作用而闻名。然而,近年来,所有利钠肽及其受体已在胃肠道、消化腺和中枢神经系统中被描述,并且与消化腺功能的调节有关。本综述重点介绍了ANP和CNP在胰腺及其他消化液分泌中的调节作用。ANP和CNP刺激基础及诱导的胰腺分泌,并改变碳酸氢盐和氯化物分泌。虽然ANP和CNP直接作用于胰腺细胞,但CNP也通过迷走-迷走反射发挥作用。高剂量时,两种肽均通过PLC/PKC途径减弱高剂量促胰液素诱导的胰腺分泌。关于其他消化液分泌,ANP和CNP可减少大鼠胆汁分泌。ANP本身不诱导唾液分泌,但可增强刺激的唾液分泌,并改变大鼠腮腺及下颌下腺的唾液成分。在大鼠胰腺、肝脏、腮腺和下颌下组织中,NPR-C受体主要介导外周反应,而与鸟苷酸环化酶偶联的NPR-A和NPR-B受体可能介导中枢反应。此外,ANP通过迷走神经依赖机制调节胃酸分泌。在肠道中,ANP和CNP通过增加cGMP水平减少水和氯化钠的吸收。总体而言,这些发现表明ANP和CNP是影响消化液分泌的一大类调节肽的成员。