| Literature DB >> 25616034 |
Jorge F Giani1, Kandarp H Shah1, Zakir Khan1, Ellen A Bernstein1, Xiao Z Shen1, Alicia A McDonough2, Romer A Gonzalez-Villalobos3, Kenneth E Bernstein4.
Abstract
Hypertension is a major risk factor for cardiovascular disease. While the cause of hypertension is multifactorial, renal dysregulation of salt and water excretion is a major factor. All components of the renin-angiotensin system are produced locally in the kidney, suggesting that intrarenal generation of angiotensin II plays a key role in blood pressure regulation. Here, we show that two mouse models lacking renal angiotensin converting enzyme (ACE) are protected against angiotensin II and l-NAME induced hypertension. In response to hypertensive stimuli, mice lacking renal ACE do not produce renal angiotensin II. These studies indicate that the intrarenal renin-angiotensin system works as an entity separate from systemic angiotensin II generation. Renal ACE appears necessary for experimental hypertension.Entities:
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Year: 2015 PMID: 25616034 PMCID: PMC4380835 DOI: 10.1016/j.coph.2015.01.002
Source DB: PubMed Journal: Curr Opin Pharmacol ISSN: 1471-4892 Impact factor: 5.547