Improved cardiovascular autonomic modulation in transgenic rats expressing an Ang-(1-7)-producing fusion protein

Tools

Item Type:	Article
Title:	Improved cardiovascular autonomic modulation in transgenic rats expressing an Ang-(1-7)-producing fusion protein
Creators Name:	Dartora, D.R., Irigoyen, M.C., Casali, K.R., Moraes-Silva, I.C., Bertagnolli, M., Bader, M. and Santos, R.
Abstract:	Angiotensin-(1-7) counterbalances Angiotensin II cardiovascular effects. However, it has yet to be determined how cardiovascular autonomic modulation may be affected by chronic and acute elevation of Ang-(1-7). Hemodynamics and cardiovascular autonomic profile were evaluated in male Sprague-Dawley (SD) and transgenic rats (TGR) overexpressing Ang-(1-7) [TGR(A1-7)3292]. Blood pressure (BP) was directly measured while cardiovascular autonomic modulation was evaluated by spectral analysis. TGR received A-779 or vehicle and SD rats received Ang-(1-7) or vehicle and were monitored for 5 hours after i.v. administration. In another set of experiments with TGR, A-779 was infused for 7 days using osmotic mini pumps. Although at baseline no differences were observed, acute administration of A-779 in TGR produced a marked long lasting increase in BP accompannied by increased BP variability (BPV) and sympathetic modulation to the vessels. Likewise, chronic administration of A-779 with osmotic mini pumps in TGR increased heart rate, sympathovagal balance, BPV and sympathetic modulation to the vessels. Administration of Ang-(1-7) to SD rats increased HRV values in 88% accompannied by 8% of vagal modulation increase and 18% of mean BP reduction. These results show that both acute and chronic alteration in the Ang-(1-7)-Mas receptor axis may lead to important changes in the autonomic control of circulation, impacting either sympathetic and/or parasympathetic systems.
Keywords:	Renin-Angiotensin System, Angiotensin-(1-7), A-779, Blood Pressure, Autonomic Nervous System, Heart Rate Variability, Spectral Analysis, Animals, Rats
Source:	Canadian Journal of Physiology and Pharmacology
ISSN:	0008-4212
Publisher:	National Research Council Press
Volume:	95
Number:	9
Page Range:	993-998
Date:	September 2017
Additional Information:	Copyright © The Author(s) 2017.
Official Publication:	https://doi.org/10.1139/cjpp-2016-0557
External Fulltext:	View full text on external repository or document server
PubMed:	View item in PubMed

Repository Staff Only: item control page