Document Detail


A mineralocorticoid receptor mutation causing human hypertension.
MedLine Citation:
PMID:  11496062     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
In recent years, the study of monogenic forms of hypertension has added greatly to our understanding of the regulatory mechanisms affecting blood pressure. Recently, a novel such form of human hypertension caused by gain-of-function mutation in the mineralocorticoid receptor, the mediator of aldosterone-induced sodium transport in the distal nephron, has been described, with the notable finding being that pregnancy causes a severe worsening of blood pressure. In this review, the mechanism by which the mutation causes hypertension, and the implications these findings have for improved understanding of cardiovascular physiology and mineralocorticoid receptor biology, are discussed.
Authors:
D S Geller
Publication Detail:
Type:  Journal Article; Research Support, U.S. Gov't, P.H.S.; Review    
Journal Detail:
Title:  Current opinion in nephrology and hypertension     Volume:  10     ISSN:  1062-4821     ISO Abbreviation:  Curr. Opin. Nephrol. Hypertens.     Publication Date:  2001 Sep 
Date Detail:
Created Date:  2001-08-09     Completed Date:  2001-12-04     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  9303753     Medline TA:  Curr Opin Nephrol Hypertens     Country:  England    
Other Details:
Languages:  eng     Pagination:  661-5     Citation Subset:  IM    
Affiliation:
Section of Nephrology, Yale University School of Medicine, New Haven, Connecticut 06510, USA. david.geller@yale.edu
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MeSH Terms
Descriptor/Qualifier:
Female
Humans
Hypertension / genetics*
Mutation / physiology*
Pregnancy / physiology
Receptors, Mineralocorticoid / genetics*
Structure-Activity Relationship
Chemical
Reg. No./Substance:
0/Receptors, Mineralocorticoid

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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