Journal article
Angiotensin-(1-7) reduces the perfusion pressure response to angiotensin ii and methoxamine via an endothelial nitric oxide-mediated pathway in cirrhotic rat liver
CB Herath, K Mak, LM Burrell, PW Angus
American Journal of Physiology Gastrointestinal and Liver Physiology | Published : 2013
Abstract
Recent studies have shown that, in cirrhosis, portal angiotensin-(1-7) [Ang-(1-7)] levels are increased and hepatic expression of angiotensin converting enzyme 2 (ACE2) and the Mas receptor are upregulated, but the effects of Ang-(1-7) on hepatic hemodynamics in cirrhosis have not been studied. This study investigated the effects of Ang-(1-7) on vasoconstrictor-induced perfusion pressure increases in cirrhotic rat livers. Ang II or the alpha 1 agonist methoxamine (MTX) were injected in the presence or absence of Ang-(1-7), and the perfusion pressure response was recorded. Denudation of vascular endothelial cells with sodium deoxycholate was used to investigate the contribution of endothelium..
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Funding Acknowledgements
This work was supported by the National Health and Medical Research Council of Australia.