Blood pressure-independent ETA and AT1 receptor blocker effects on the coronaries of rats harboring human renin and angiotensinogen genes

Item Type:	Article
Title:	Blood pressure-independent ETA and AT1 receptor blocker effects on the coronaries of rats harboring human renin and angiotensinogen genes
Creators Name:	Gerbaulet, S.P. and Kraemer, J. and Bohlender, J. and Dietz, R. and Gross, C.M.
Abstract:	Background:Blood pressure-independent (BP) effects of angiotensin (Ang) II and endothelin (ET) on coronaries (remodeling) in high renin hypertension are incompletely understood. Methods:We studied the effects of subdepressor doses of Ang II receptor (AT1) blockade with losartan (10 mg/kg/day gavage) and endothelin A receptor (ETA) blockade with LU135252 (30 mg/kg/day) on the coronaries of rats harboring human renin and angiotensinogen genes (dTGR). Nontransgenic Sprague-Dawley rats were controls. The rats were treated between the ages of 6 and 10 weeks. Coronary cross-sectional area [CSA; 0.79 × (external diameter2 – internal diameter2)], cell proliferation, and infiltration of monocytes/macrophages were determined. Results:Monotherapy did not lower BP while combination treatment did (p < 0.05). All treatments reduced mortality (p < 0.01). CSA was decreased by all treatments compared to vehicle, independent of blood pressure (p < 0.05). Extensive proliferation by PCNA staining and infiltration of ED-1-positive cells was diminished by both treatment and the combination. Conclusions:The data show that Ang II promotes coronary inflammation and remodeling, in part independent of blood pressure but dependent upon ET signaling. Combination treatment directed at both pathways may improve outcome, independent of blood pressure reduction.
Keywords:	Angiotensin II, Hypertrophy, Transgenic rats, Inflammation, Coronary arteries, Remodeling, Animals, Rats
Source:	Kidney and Blood Pressure Research
ISSN:	1420-4096
Volume:	28
Page Range:	134-143
Date:	1 January 2005
Official Publication:	https://doi.org/10.1159/000085956
PubMed:	View item in PubMed

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