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通过体外放射自显影观察心房利钠肽和血管紧张素II受体的重叠分布:生理拮抗作用的形态学基础。

Overlapping distributions of receptors for atrial natriuretic peptide and angiotensin II visualized by in vitro autoradiography: morphological basis of physiological antagonism.

作者信息

Mendelsohn F A, Allen A M, Chai S Y, Sexton P M, Figdor R

机构信息

University of Melbourne, Department of Medicine, Austin Hospital, Heidelberg, Victoria, Australia.

出版信息

Can J Physiol Pharmacol. 1987 Aug;65(8):1517-21. doi: 10.1139/y87-239.

Abstract

Atrial natriuretic peptides exert actions on many key organs involved in blood pressure and water and electrolyte balance. Many of these actions result in a physiological antagonism of angiotensin. To investigate the morphological basis of this interaction, we have mapped the distribution of receptors for atrial natriuretic peptide and angiotensin II in a number of target organs, using 125I-labelled rat atrial natriuretic peptide (99-126) and 125I-labelled [Sar1,Ile8]angiotensin II. In the kidney both atrial natriuretic peptide and angiotensin II receptors were observed overlying glomeruli, vasa recta bundles (high densities), and the outer cortex (moderate density). In the other tissues studied, atrial natriuretic peptide and angiotensin II receptors were codistributed in the adrenal zona glomerulosa, cerebral circumventricular organs including the subfornical organ, organum vasculosum of the lamina terminalis and area postrema, and the external plexiform layer of the olfactory bulb. The concurrent distribution of specific receptors for both peptides at these sites provides the basis for atrial natriuretic peptide to exert a functional antagonism of the actions of angiotensin II on blood pressure and water and electrolyte homeostasis at multiple sites.

摘要

心房利钠肽对许多参与血压及水盐平衡的关键器官发挥作用。其中许多作用导致对血管紧张素的生理性拮抗。为研究这种相互作用的形态学基础,我们使用125I标记的大鼠心房利钠肽(99 - 126)和125I标记的[Sar1,Ile8]血管紧张素II,在多个靶器官中绘制了心房利钠肽和血管紧张素II受体的分布图。在肾脏中,肾小球、直小血管束(高密度)和肾皮质外层(中等密度)均观察到心房利钠肽和血管紧张素II受体。在其他研究的组织中,心房利钠肽和血管紧张素II受体共分布于肾上腺球状带、包括穹窿下器官、终板血管器和最后区在内的脑室内器官,以及嗅球的外丛状层。这两种肽的特异性受体在这些部位的同时分布,为心房利钠肽在多个部位对血管紧张素II在血压及水盐稳态方面的作用发挥功能性拮抗提供了基础。

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