Document Detail


Influence of estrogen depletion and salt loading on renal angiotensinogen expression in the mRen(2).Lewis strain.
MedLine Citation:
PMID:  20462965     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The mRen(2).Lewis (mRen2) strain is an ANG II-dependent model of hypertension expressing marked sex differences in blood pressure and tissue injury that also exhibits estrogen and salt sensitivity. Because estrogen and salt influence angiotensinogen (AGT), circulating and renal expression of the protein were assessed in the mRen2 using a sensitive and specific ELISA. Hemizygous female and male mRen2 were placed on normal (1% NaCl, NS)- or high (8% NaCl, HS)-salt diets from 5 to 15 wk of age while a separate NS cohort was ovariectomized (OVX). The OVX mRen2 exhibited higher blood pressure (184 +/- 6 vs. 149 +/- 5 mmHg, n = 6), a 16-fold increase in urinary AGT (uAGT) (0.2 +/- 0.02 vs. 0.01 +/- 0.01 microg x kg(-1) x day(-1), P < 0.01), but no change in proteinuria (PROT). Excretion of AGT was correlated with blood pressure and PROT in the female groups. The HS diet led to higher blood pressure (224 +/- 8 mmHg), a 180-fold increase in uAGT (1.8 +/- 0.2 microg x kg(-1) x day(-1)), and increased PROT (98 +/- 9 vs. 7 +/- 1 mg x kg(-1) x day(-1)). Compared with females, NS males expressed higher excretion of uAGT (3.0 +/- 0.4 microg x kg(-1) x day(-1)) and PROT (32 +/- 5 mg x kg(-1) x day(-1)); both were increased eightfold with HS (uAGT: 23 +/- 3 microg x kg(-1) x day(-1); PROT: 285 +/- 28 mg x kg(-1) x day(-1)) without a change in blood pressure. Although uAGT was markedly higher in the OVX and HS groups, neither renal cortical AGT mRNA or protein expression was increased. Moreover, AGT release in cortical slices was similar for the NS and HS females. We conclude that the increase in uAGT with estrogen depletion or HS likely may be a biomarker for glomerular damage reflecting filtration of the circulating protein in the mRen2.
Authors:
Jonathan A Cohen; Sarah H Lindsey; Nancy T Pirro; K Bridget Brosnihan; Patricia E Gallagher; Mark C Chappell
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, N.I.H., Extramural     Date:  2010-05-12
Journal Detail:
Title:  American journal of physiology. Renal physiology     Volume:  299     ISSN:  1522-1466     ISO Abbreviation:  Am. J. Physiol. Renal Physiol.     Publication Date:  2010 Jul 
Date Detail:
Created Date:  2010-06-18     Completed Date:  2010-07-13     Revised Date:  2013-05-29    
Medline Journal Info:
Nlm Unique ID:  100901990     Medline TA:  Am J Physiol Renal Physiol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  F35-42     Citation Subset:  IM    
Affiliation:
Hypertension and Vascular Research Center, Wake Forest University Health Sciences, Winston-Salem, North Carolina 27157-1095, USA.
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MeSH Terms
Descriptor/Qualifier:
Angiotensinogen / blood,  genetics,  metabolism*,  urine
Animals
Biological Markers / metabolism
Blood Pressure
Disease Models, Animal
Enzyme-Linked Immunosorbent Assay
Estrogens / deficiency*
Female
Hypertension / etiology,  genetics,  metabolism*,  physiopathology
Kidney / metabolism*
Male
Mice
Ovariectomy*
Proteinuria / genetics,  metabolism
RNA, Messenger / metabolism
Rats
Rats, Inbred Lew
Rats, Transgenic
Renin / genetics*
Sex Factors
Sodium Chloride, Dietary / adverse effects*
Time Factors
Up-Regulation
Grant Support
ID/Acronym/Agency:
HL-51952/HL/NHLBI NIH HHS; HL-56973/HL/NHLBI NIH HHS; T32-RR-07009/RR/NCRR NIH HHS
Chemical
Reg. No./Substance:
0/Biological Markers; 0/Estrogens; 0/RNA, Messenger; 0/Ren2 protein, mouse; 0/Sodium Chloride, Dietary; 11002-13-4/Angiotensinogen; EC 3.4.23.15/Renin
Comments/Corrections

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