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Simvastatin Reduces Pressor Response to Centrally Administered Angiotensin II

Authors :
Mariusz Sikora
Tymoteusz Zera
Marcin Ufnal
Ewa Szczepanska-Sadowska
Source :
American Journal of Hypertension. 23:956-959
Publication Year :
2010
Publisher :
Oxford University Press (OUP), 2010.

Abstract

Background Angiotensin II (Ang II) plays a pivotal role in regulation of the circulatory system. Activation of angiotensin type 1 (AT1) receptors in several brain regions leads to an increase in blood pressure. Accumulating data suggest that statins affect the peripheral action of Ang II; however, their central effects are poorly recognized. The study was aimed to determine whether simvastatin interferes with the brain angiotensin system in rats. Methods Twelve-week-old, Sprague-Dawley rats were divided into two groups. Untreated group was maintained on tap water, whereas simvastatin group received water containing simvastatin for the following 12 weeks. Later, both groups were subjected to experiments in which mean arterial blood pressure (MABP) and heart rate (HR) were recorded during baseline conditions and after intracerebroventricular (ICV) infusion of either saline, Ang II, or losartan. Results ICV infusion of Ang II elicited a significant increase in MABP in both groups. However, the pressor response in the simvastatin group was significantly smaller than that in the untreated group. There was no significant change in MABP after ICV infusion of saline or losartan. ICV infusion of Ang II elicited a significant increase in HR in the untreated group but not in the simvastatin group. There was no significant change in HR after ICV infusion of saline or losartan. Conclusions The results show that simvastatin reduces the pressor response to ICV-infused Ang II in rats. This implies that statins may affect the central regulation of the circulatory system, especially when the brain angiotensin system is stimulated.

Details

ISSN :
19417225 and 08957061
Volume :
23
Database :
OpenAIRE
Journal :
American Journal of Hypertension
Accession number :
edsair.doi.dedup.....24e3c13a6b0fc2297e5cd160c3446363
Full Text :
https://doi.org/10.1038/ajh.2010.103