Abstract

BackgroundExercise training (T) blunts functional deficits and renin-angiotensin system (RAS) hyperactivity in hypertensive individuals. There is no information on T-induced temporal changes of brain RAS. We evaluate now the simultaneous effects of T on functional responses and time course changes in the expression/activity of brain RAS components in autonomic cardiovascular-controlling areas.Methods and ResultsSpontaneously hypertensive rats (SHR) and age-matched normotensive controls (WKY) were trained for 0, 1, 2, 4, 8 and 12 weeks. Sedentary (S) groups served as time-controls. After arterial pressure (AP) and heart rate (HR) recordings at rest, fresh and fixed brains were harvested for qPCR and immunofluorescence assays. SHR-S vs. WKY-S exhibited higher mean AP (MAP) and HR, increased pressure variability and sympathetic activity, elevated AT1 receptor (AT1) expression in nucleus tractus solitarii (NTS) and higher Mas receptor expression in the rostroventrolateral medulla (RVLM). In SHR, T promptly (T2 on) reduced sympathetic variability to heart/vessels and largely decreased angiotensinogen expression in the paraventricular hypothalamic nucleus (PVN) and NTS, with a late RVLM reduction (T4). AT1 expression was only reduced at T12 (PVN and NTS) with transient, not maintained Mas receptor changes in PVN and RVLM. These responses were accompanied by baseline MAP and HR reduction in the SHR-T (from T4 on). In the SHR group, PVN angiotensinogen expression correlated positively with sympathetic activity, resting MAP and HR. In WKY-T, a precocious (T2-T12) RVLM AT1 decrease preceded the appearance of resting bradycardia (from T8 on).ConclusionsEarly and maintained reduction of angiotensinogen content in autonomic areas of the SHR is the most prominent effect of training on brain RAS. Down-regulation of PVN RAS expression is an essential factor to drive cardiovascular benefits in SHR-T, while resting bradycardia in WKY-T is correlated to RVLM AT1 reduction.

Highlights

  • Chronic hypertension is closely related to overactivity of the pressor axis of the renin-angiotensin system (RAS) [1,2,3]

  • Down-regulation of paraventricular hypothalamic nucleus (PVN) RAS expression is an essential factor to drive cardiovascular benefits in Spontaneously hypertensive rats (SHR)-T, while resting bradycardia in WKY-T is correlated to rostroventrolateral medulla (RVLM) angiotensin type 1 receptor (AT1) reduction

  • Time course changes on baseline arterial pressure and heart rate and autonomic balance At the beginning of the experiments, SHR-S exhibited higher mean AP (MAP) and HR levels than agematched WKY

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Summary

Introduction

Chronic hypertension is closely related to overactivity of the pressor axis of the renin-angiotensin system (RAS) [1,2,3]. The increased expression of angiotensinogen (Aogen), angiotensin converting enzyme (ACE) and angiotensin type 1 receptor (AT1) and the elevated Ang II content in autonomic brain areas, reduce baroreceptor reflex control, alter the sympatho-vagal balance to the heart and cause a robust increase in sympathetic nerve activity[4, 6, 7]. These observations confirmed the involvement of brain ACE-Ang II-AT1 axis in the pathophysiology of hypertension. We evaluate the simultaneous effects of T on functional responses and time course changes in the expression/activity of brain RAS components in autonomic cardiovascular-controlling areas.

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