Back to Search Start Over

Effects of intrarenal angiotensin 1-7 infusion on renal haemodynamic and excretory function in anaesthetised two-kidney one-clip and deoxycorticosterone acetate-salt hypertensive rats.

Authors :
Barry EF
Abdulla MH
O'Neill J
AlMarabeh S
Beshara J
Parna-Gile E
Johns EJ
Source :
Experimental physiology [Exp Physiol] 2023 Feb; Vol. 108 (2), pp. 268-279. Date of Electronic Publication: 2022 Dec 01.
Publication Year :
2023

Abstract

New Findings: What is the central question of this study? Are renal functional responses to intrarenal angiotensin 1-7 (Ang (1-7)) infusion dependent on the level of the endogenous renin-angiotensin system (RAS) in the two-kidney one-clip (2K1C) and deoxycorticosterone acetate (DOCA)-salt animal models of hypertension? What is the main finding and its importance? The renal actions of Ang (1-7) are dependent on the relative endogenous levels of each arm of the classical angiotensin II-angiotensin II type 1 receptor (AT <subscript>1</subscript> R) axis and those of the Ang (1-7)-Mas receptor axis. These findings support the hypothesis that a balance exists between the intrarenal classical and novel arms of the RAS, and in particular the relative abundance of AT <subscript>1</subscript> R to Mas receptor, which may to a large extent determine the renal excretory response to Ang (1-7) infusion.<br />Abstract: This study investigated the action of angiotensin 1-7 (Ang (1-7)) on renal haemodynamic and excretory function in the two-kidney one-clip (2K1C) and deoxycorticosterone acetate (DOCA)-salt rat models of hypertension, in which the endogenous renin-angiotensin system (RAS) activity was likely to be raised or lowered, respectively. Rats were anaesthetised and prepared for the measurement of mean arterial pressure and kidney function during renal interstitial infusion of Ang (1-7) or saline. Kidney tissue concentrations of angiotensin II (Ang II) and Ang (1-7) were determined. Intrarenal infusion of Ang (1-7) into the clipped kidney of 2K1C rats increased urine flow (UV), absolute (U <subscript>Na</subscript> V) and fractional sodium (FE <subscript>Na</subscript> ) excretions by 110%, 214% and 147%, respectively. Renal Ang II concentrations of the clipped kidney were increased with no major changes in Ang (1-7) concentration. By contrast, Ang (1-7) infusion decreased UV, U <subscript>Na</subscript> V, and FE <subscript>Na</subscript> by 27%, 24% and 21%, respectively in the non-clipped kidney in which tissue Ang (1-7) concentrations were increased, but renal Ang II concentrations were unchanged compared to sham animals. Ang (1-7) infusion in DOCA-salt rats had minimal effects on glomerular filtration rate but significantly decreased UV, U <subscript>Na</subscript> V and FE <subscript>Na</subscript> by ∼30%. Renal Ang (1-7) concentrations were higher and Ang II concentrations were lower in DOCA-salt rats compared to sham rats. These findings demonstrate that the intrarenal infusion of exogenous Ang (1-7) elicits different renal excretory responses the magnitude of which is dependent on the balance between the endogenous renal Ang II-AT <subscript>1</subscript> receptor axis and Ang (1-7)-Mas receptor axis.<br /> (© 2022 The Authors. Experimental Physiology published by John Wiley & Sons Ltd on behalf of The Physiological Society.)

Details

Language :
English
ISSN :
1469-445X
Volume :
108
Issue :
2
Database :
MEDLINE
Journal :
Experimental physiology
Publication Type :
Academic Journal
Accession number :
36454195
Full Text :
https://doi.org/10.1113/EP090791