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PMID: 8993855 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Presence of angiotensin II AT2 receptor binding sites in the adventitia of human kidney vasculature.

Clinical and experimental pharmacology & physiology. Supplement ·Vol. 3 ·1996-00-00 ·Pages S147-54

Zhuo J, Dean R, MacGregor D, Alcorn D, Mendelsohn FA

Abstract

1. Angiotensin II (AngII) receptor subtypes in adult human kidney were pharmacologically characterized by in vitro autoradiography using the AngII receptor subtype-selective antagonists, losartan and PD 123319, and the sensitivity to the reducing agent, dithiothreitol. 2. High densities of AngII AT1 receptor binding occur in the glomeruli and the inner stripe of the outer medulla, while a moderate AT1 receptor binding is localized in the proximal convoluted tubules. 3. AT2 receptor binding is observed predominantly in the intrarenal large blood vessels, including the arcuate, inter- and intra-lobular arteries, and in the renal capsule. 4. In the major renal artery, AT1 receptor binding is abundant in the media and adventitia, while AT2 receptor binding is observed mainly in the adventitia. 5. At the light microscopic level using emulsion autoradiography, AT1 receptors are localized in the glomeruli and juxtaglomerular apparatus, as expected. However, in larger renal blood vessels, including the arcuate arteries, inter- and intra-lobular arteries, intense AT2 receptor labelling occurs primarily in the adventitia, while the endothelium and vascular smooth muscle layers contain only low levels of AngII receptor binding. 6. These results indicate that the adult human kidney displays two pharmacologically distinct AngII receptor subtypes, with AT1 predominating in the glomeruli, juxtaglomerular apparatus, proximal tubules and the inner stripe of the outer medulla, while AT2 predominates in the adventitia of the arcuate and interlobular arteries and the renal capsule. The functional significance of AT2 receptor binding sites in the adventitia of adult human kidney vessels remains to be elucidated.

MeSH Terms
Adult Angiotensin II/blood,metabolism Angiotensin Receptor Antagonists Autoradiography Binding, Competitive Biphenyl Compounds/metabolism,pharmacology Carcinoma, Renal Cell/pathology Humans Imidazoles/metabolism,pharmacology Kidney/blood supply,metabolism Kidney Glomerulus/drug effects,metabolism Kidney Tubules, Proximal/drug effects,metabolism Losartan Pyridines/metabolism,pharmacology Tetrazoles/metabolism,pharmacology Tunica Media/metabolism
Chemicals
Angiotensin Receptor Antagonists Biphenyl Compounds Imidazoles Pyridines Tetrazoles Angiotensin II PD 123319 Losartan
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Zhuo J
Department of Medicine, University of Melbourne, Victoria, Australia.
Dean R
MacGregor D
Alcorn D
Mendelsohn F A
Article Info
Journal
Clinical and experimental pharmacology & physiology. Supplement
Abbr.
Clin Exp Pharmacol Physiol Suppl
ISSN
0143-9294
Published
1996-00-00
Pages
S147-54
Language
English
Region
Australia
NLM ID
7611484
Subset
IM
External Links
PubMed source
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