Nussdorfer G G, Rossi G P, Mazzocchi G
Department of Anatomy, University of Padua, Italy. ggnanatipdunidx.unipd.it
Peptides. 1997;18(7):1079-89. doi: 10.1016/s0196-9781(97)00046-6.
Adrenomedullin (ADM) is a hypotensive peptide, originally isolated from human pheochromocytomas, and then found to be widely distributed in the various body systems. ADM derives from preproadrenomedullin, a 185-amino acid residue prohormone, containing at its N-terminal a 20-amino acid sequence, named proadrenomedullin N-terminal 20 peptide (PAMP). ADM and PAMP immunoreactivities have been detected in the hypothalamo-pituitary-adrenal (HPA) axis of humans, rats, and pigs. Adrenal glands possess binding sites for both ADM and PAMP, the former being mainly of the subtype 1 of calcitonin gene-related peptide (CGRP) receptors. ADM exerts a direct inhibitory action on angiotensin II- or potassium-stimulated aldosterone secretion of zona glomerulosa cells. This effect is mediated by the CGRP1 receptor and its mechanism probably involves the blockade of Ca2+ influx. In contrast, ADM enhances aldosterone production by in situ perfused rat adrenals and human adrenal slices (containing medullary chromaffin cells), again through the activation of CGRP1 receptors. This aldosterone secretagogue effect of ADM is blocked by the beta-adrenoceptor antagonist l-alprenolol, thereby suggesting that it is indirectly mediated by the release of catecholamines by chromaffin cells. The effects of ADM on adrenal glucocorticoid release are doubtful and probably mediated by the increase in adrenal blood flow rate and the inhibition of ACTH release by pituitary corticotropes. The concentrations reached by ADM and PAMP in the blood rule out the possibility that they act on the HPA axis as circulating hormones. Conversely, their content in both adrenal and hypothalamo-pituitary complex is consistent with a paracrine mechanism of action, which may play a potentially important role in the regulation of fluid and electrolyte homeostasis.
肾上腺髓质素(ADM)是一种降压肽,最初从人嗜铬细胞瘤中分离出来,随后发现它广泛分布于人体各个系统。ADM由前肾上腺髓质素衍生而来,前肾上腺髓质素是一种含185个氨基酸残基的前体激素,其N端含有一个20个氨基酸的序列,称为肾上腺髓质素N端20肽(PAMP)。在人类、大鼠和猪的下丘脑-垂体-肾上腺(HPA)轴中已检测到ADM和PAMP的免疫反应性。肾上腺具有ADM和PAMP的结合位点,前者主要是降钙素基因相关肽(CGRP)受体的1型亚型。ADM对血管紧张素II或钾刺激的肾小球带细胞醛固酮分泌具有直接抑制作用。这种作用由CGRP1受体介导,其机制可能涉及阻断Ca2+内流。相反,ADM通过激活CGRP1受体,增强原位灌注大鼠肾上腺和人肾上腺切片(含髓质嗜铬细胞)的醛固酮生成。ADM的这种醛固酮促分泌作用被β-肾上腺素能受体拮抗剂l-阿普洛尔阻断,因此表明它是由嗜铬细胞释放儿茶酚胺间接介导的。ADM对肾上腺糖皮质激素释放的影响尚不确定,可能是由肾上腺血流速度增加和垂体促肾上腺皮质激素细胞释放促肾上腺皮质激素(ACTH)受抑制介导的。ADM和PAMP在血液中达到的浓度排除了它们作为循环激素作用于HPA轴的可能性。相反,它们在肾上腺和下丘脑-垂体复合体中的含量与旁分泌作用机制一致,这可能在体液和电解质稳态调节中发挥潜在重要作用。