Cerra M C
Department of Cellular Biology and of Pharmaco Biology, University of Calabria, Italy.
Cardioscience. 1994 Dec;5(4):215-24.
Natriuretic peptides are hormones that play an important role in the cardiovascular control of mammalian and non-mammalian vertebrates. They have been classified into four groups. Of these, ANP (atrial natriuretic peptide), BNP (brain atriuretic peptides), CNP (C-type natriuretic peptide) are detected in cardiac and non cardiac tissues of all vertebrates; while VNP (ventricular natriuretic peptide) has been isolated only from the fish ventricle. All peptides have shown a high degree of sequence homology. The expression of the three principal types of natriuretic peptide (ANP, BNP and CNP) in cardiac tissues is developmentally and functionally regulated in a highly tissue-specific manner. Three types of natriuretic peptide receptors have been identified in numerous target tissues. Two receptors are transmembrane guanylyl cyclases (ANPR-A and ANPR-B) that mediate biological effects of natriuretic peptides; the third one (ANPR-C) has no guanylyl cyclase and is called "clearance receptor." The presence of natriuretic peptide binding sites in the heart suggests new aspects of paracrine control of cardiac function. A relevant localization of natriuretic peptide receptors was found in those cardiac regions particularly suitable for monitoring blood volume and pressure oscillations such as the inflow tract and the outflow tract. For example, in birds (quail) the highest levels of natriuretic peptide receptors were detected in the inflow tract represented by the vena cava. In both fish and birds, the outflow chamber, the bulbus cordis, had a high number of natriuretic peptide binding sites. In mammals, a remarkable concentration of natriuretic peptide receptors was also observed in the coronary vessels. This zoning of cardiac natriuretic peptide receptors indicates an intracardiac action of the hormones and adds a humoral dimension to the morphofunctional design of the vertebrate heart.
利钠肽是一类激素,在哺乳动物和非哺乳动物脊椎动物的心血管控制中发挥着重要作用。它们已被分为四类。其中,心房利钠肽(ANP)、脑利钠肽(BNP)、C型利钠肽(CNP)在所有脊椎动物的心脏和非心脏组织中均有检测到;而心室利钠肽(VNP)仅从鱼类心室中分离得到。所有肽类均表现出高度的序列同源性。心脏组织中三种主要类型的利钠肽(ANP、BNP和CNP)的表达在发育和功能上以高度组织特异性的方式受到调节。在众多靶组织中已鉴定出三种类型的利钠肽受体。两种受体是跨膜鸟苷酸环化酶(ANPR - A和ANPR - B),介导利钠肽的生物学效应;第三种(ANPR - C)没有鸟苷酸环化酶,被称为“清除受体”。心脏中利钠肽结合位点的存在提示了心脏功能旁分泌控制的新方面。在那些特别适合监测血容量和压力波动的心脏区域,如流入道和流出道,发现了利钠肽受体的相关定位。例如,在鸟类(鹌鹑)中,在以腔静脉为代表的流入道中检测到最高水平的利钠肽受体。在鱼类和鸟类中,流出腔室——动脉圆锥,都有大量的利钠肽结合位点。在哺乳动物中,在冠状血管中也观察到利钠肽受体的显著浓度。心脏利钠肽受体的这种分区表明了激素的心脏内作用,并为脊椎动物心脏的形态功能设计增添了体液维度。