Januszewicz A
Department of Hypertension and Angiology, Academy of Medicine, Warsaw, Banacha, Poland.
Curr Opin Cardiol. 1995 Sep;10(5):495-500. doi: 10.1097/00001573-199509000-00009.
The natriuretic peptide family consists of three members: atrial natriuretic peptide, brain natriuretic peptide, and C-type natriuretic peptide. Atrial and brain natriuretic peptides possess similar effects, causing natriuresis, vasodilation, and suppression of the renin-angiotensin-aldosterone system. C-type natriuretic peptide has been suggested to exert its predominant effect on the vasculature, eliciting vasodilation and inhibiting the proliferation of vascular smooth muscle cells. Numerous studies have broadened our current knowledge of the regulation of natriuretic peptide gene expression, biosynthesis, and secretion, as well as structure of specific receptors. This has led to a better understanding of the renal, cardiovascular, and endocrine actions of natriuretic peptides in both normal and pathophysiological states, including hypertensive disease. Development of nonpeptide neutral endopeptidase inhibitors and antagonists for natriuretic peptide receptors may reveal the range of potential therapeutic application of atrial and other natriuretic peptides in hypertension.
心房利钠肽、脑利钠肽和C型利钠肽。心房利钠肽和脑利钠肽具有相似的作用,可引起利钠、血管舒张,并抑制肾素-血管紧张素-醛固酮系统。有人提出,C型利钠肽对血管系统发挥主要作用,引起血管舒张并抑制血管平滑肌细胞增殖。众多研究拓展了我们目前对利钠肽基因表达调控、生物合成、分泌以及特定受体结构的认识。这使我们能更好地理解利钠肽在正常和病理生理状态(包括高血压疾病)下对肾脏、心血管和内分泌的作用。开发非肽类中性内肽酶抑制剂和利钠肽受体拮抗剂,可能会揭示心房利钠肽和其他利钠肽在高血压治疗中的潜在应用范围。