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Regulation of angiotensin-(1-7) and angiotensin II type 1 receptor by telmisartan and losartan in adriamycin-induced rat heart failure.

Authors :
Zong, Wen-na
Yang, Xiao-hui
Chen, Xiu-mei
Huang, Hong-juan
Zheng, Hong-jian
Qin, Xiao-yi
Yong, Yong-hong
Cao, Kejiang
Huang, Jun
Lu, Xin-zheng
Source :
Acta Pharmacologica Sinica; Nov2011, Vol. 32 Issue 11, p1345-1350, 6p
Publication Year :
2011

Abstract

Aim:To investigate the possible effects of telmisartan and losartan on cardiac function in adriamycin (ADR)-induced heart failure in rats, and to explore the changes in plasma level of angiotensin-(1-7)[Ang-(1-7)] and myocardial expression of angiotensin II type 1/2 receptors (AT1R / AT2R) and Mas receptor caused by the two drugs.Methods:Male Sprague-Dawley rats were randomly divided into 4 groups: the control group, ADR-treated heart failure group (ADR-HF), telmisartan plus ADR-treated group (Tel+ADR) and losartan plus ADR-treated group (Los+ADR). ADR was administrated (2.5 mg/kg, ip, 6 times in 2 weeks). The rats in the Tel+ADR and Los+ADR groups were treated orally with telmisartan (10 mg/kg daily po) and losartan (30 mg/kg daily), respectively, for 6 weeks. The plasma level of Ang-(1-7) was determined using ELISA. The mRNA and protein expression of myocardial Mas receptor, AT<subscript>1</subscript>R and AT<subscript>2</subscript>R were measured using RT-PCR and Western blotting, respectively.Results:ADR significantly reduced the plasma level of Ang-(1-7) and the expression of myocardial Mas receptor and myocardial AT<subscript>2</subscript>R, while significantly increased the expression of myocardial AT1R. Treatment with telmisartan and losartan effectively increased the plasma level of Ang-(1-7) and suppressed myocardial AT1R expression, but did not influence the expression of Mas receptor and AT<subscript>2</subscript>R.Conclusion:The protective effects of telmisartan and losartan in ADR-induced heart failure may be partially due to regulation of circulating Ang-(1-7) and myocardial AT1R expression. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16714083
Volume :
32
Issue :
11
Database :
Complementary Index
Journal :
Acta Pharmacologica Sinica
Publication Type :
Academic Journal
Accession number :
67042540
Full Text :
https://doi.org/10.1038/aps.2011.96