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Control of left ventricular mass by moxonidine involves reduced DNA synthesis and enhanced DNA fragmentation

Authors :
Jolanta Gutkowska
Bogdan A. Danalache
P-A Paquette
Suhayla Mukaddam-Daher
David Duguay
Ahmed Menaouar
R El Ayoubi
Denis deBlois
Source :
British Journal of Pharmacology. 153:459-467
Publication Year :
2008
Publisher :
Wiley, 2008.

Abstract

Background and purpose: Left ventricular hypertrophy (LVH) is a maladaptive process associated with increased cardiovascular risk. Regression of LVH is associated with reduced complications of hypertension. Moxonidine is an antihypertensive imidazoline compound that reduces blood pressure primarily by central inhibition of sympathetic outflow and by direct actions on the heart to release atrial natriuretic peptide, a vasodilator and an antihypertrophic cardiac hormone. This study investigated the effect of moxonidine on LVH and the mechanisms involved in this effect. Experimental approach: Spontaneously hypertensive rats were treated with several doses of moxonidine (s.c.) over 4 weeks. Blood pressure and heart rate were continuously monitored by telemetry. Body weight and water and food intake were measured weekly. Measurements also included left ventricular mass, DNA content, synthesis, fragmentation, and apoptotic/ anti-apoptotic pathway proteins. Key results: The decrease in mean arterial pressure stabilized at B � 10 mm Hg after 1 week of treatment and thereafter. Compared to vehicle-treated rats (100%), left ventricular mass was dose- and time-dependently reduced by treatment. This reduction remained significantly lower after normalizing to body weight. Moxonidine reduced left ventricular DNA content and inhibited DNA synthesis. DNA fragmentation transiently, but significantly increased at 1 week of moxonidine treatment and was paralleled by elevated active caspase-3 protein. The highest dose significantly decreased the apoptotic protein Bax and all doses stimulated anti-apoptotic Bcl-2 after 4 weeks of treatment. Conclusions and implications: These studies implicate the modulation of cardiac DNA dynamics in the control of left ventricular mass by moxonidine in a rat model of hypertension. British Journal of Pharmacology (2008) 153, 459–467; doi:10.1038/sj.bjp.0707588; published online 3 December 2007

Details

ISSN :
00071188
Volume :
153
Database :
OpenAIRE
Journal :
British Journal of Pharmacology
Accession number :
edsair.doi...........010819867b398a08f3cf67e7ff6cf73f
Full Text :
https://doi.org/10.1038/sj.bjp.0707588