Angiotensin-(1-7)-induced renal vasodilation is reduced in human kidneys with renal artery stenosis

J Hypertens. 2014 Dec;32(12):2428-32; discussion 2432. doi: 10.1097/HJH.0000000000000351.

Abstract

Background: Angiotensin-(1-7) modulates renal blood flow in humans with essential hypertension by inducing vasodilation and counterbalancing angiotensin II-induced vasoconstriction. Little is, however, known about the effects of angiotensin-(1-7) in kidneys with atherosclerotic renal artery stenosis. We previously demonstrated that the effect of angiotensin-(1-7) is reduced in patients with increased activity of the renin-angiotensin system. As the renin-angiotensin system is also activated in kidneys with renal artery stenosis, we hypothesized that the vasodilatory effect of angiotensin-(1-7) is also reduced in such kidneys.

Method: Therefore, we selectively measured mean renal blood flow (¹³³Xenon washout method) before and during local infusion of angiotensin-(1-7) (0.27, 0.9, and 2.7 ng/kg per min) in hypertensive patients who were angiographically evaluated for the presence of renovascular abnormalities. Data were analyzed in three groups: stenotic kidneys, nonstenotic kidneys with renal artery stenosis of the contralateral kidney (contralateral stenotic kidneys), or essentially hypertensive controls without renovascular abnormalities (matched for urinary sodium excretion).

Results: Angiotensin-(1-7) infusion resulted in an increase in renal blood flow in matched controls. In stenotic kidneys however, the effect of angiotensin-(1-7) was significantly reduced as compared to controls. The angiotensin-(1-7) effect in contralateral stenotic kidneys was comparable to controls.

Conclusion: Angiotensin-(1-7)-induced vasodilation is reduced in stenotic kidneys, but not in contralateral stenotic kidneys. This suggests that the altered blood flow regulation in kidneys with atherosclerotic renal artery stenosis is a local phenomenon and not related to generalized atherosclerotic burden. Probably, the renin-angiotensin system activation, bioavailability of nitric oxide, and structural changes in the stenotic kidney play a role in this phenomenon.

Publication types

  • Evaluation Study

MeSH terms

  • Angiotensin I / pharmacology*
  • Case-Control Studies
  • Essential Hypertension
  • Female
  • Humans
  • Hypertension / physiopathology*
  • Kidney / blood supply*
  • Male
  • Middle Aged
  • Peptide Fragments / pharmacology*
  • Renal Artery / drug effects
  • Renal Artery Obstruction / physiopathology*
  • Renal Circulation
  • Renin-Angiotensin System / drug effects
  • Vasodilation / drug effects*

Substances

  • Peptide Fragments
  • Angiotensin I
  • angiotensin I (1-7)