The intrarenal generation of angiotensin II is required for experimental hypertension

Curr Opin Pharmacol. 2015 Apr:21:73-81. doi: 10.1016/j.coph.2015.01.002. Epub 2015 Jan 21.

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Angiotensin II / metabolism*
  • Animals
  • Humans
  • Hypertension / metabolism*
  • Kidney / metabolism*
  • Peptidyl-Dipeptidase A / metabolism
  • Renin-Angiotensin System / physiology

Substances

  • Angiotensin II
  • Peptidyl-Dipeptidase A