ACE2 gene combined with exercise training attenuates central AngII/AT1 axis function and oxidative stress in a prehypertensive rat model

• Published in: Journal of applied physiology (1985) Vol. 132; no. 6; pp. 1460 - 1467
• Main Authors: Chen, Xiu-Yun, Lin, Cheng, Liu, Guo-Ying, Pei, Chun, Xu, Gui-Qing, Gao, Lie, Wang, Shi-Zhong, Pan, Yan-Xia
• Format: Journal Article
• Language: English
• Published: United States American Physiological Society 01.06.2022
• Series: Physical Activity and the Brain
• Subjects: ACE2; ACE2 gene; Angiotensin; Angiotensin I - metabolism; Angiotensin II; Angiotensin II - metabolism; Angiotensin-converting enzyme 2; Angiotensin-Converting Enzyme 2 - metabolism; Animal models; Animals; Baroreceptors; Blood Pressure; CYBB protein; Fitness training programs; Fluorescence; Green fluorescent protein; Hypertension; Hypertension - metabolism; Hypertension - therapy; Male; NAD(P)H oxidase; Norepinephrine; NOX4 protein; Oxidative stress; Oxidative Stress - physiology; Paraventricular Hypothalamic Nucleus; Paraventricular nucleus; Peptidyl-dipeptidase A; Physical Conditioning, Animal - physiology; Physical training; Prehypertension - metabolism; Pressure effects; Protein expression; Proteins; Rats; Rats, Inbred SHR; Rats, Inbred WKY; Reactive oxygen species; Reflexes; baroreflex; hypertension; renin-angiotensin system; exercise training; paraventricular nucleus
• ISSN: 8750-7587; 1522-1601; 1522-1601
• DOI: 10.1152/japplphysiol.00459.2021

Angiotensin-converting enzyme 2 (ACE2) gene in combination with exercise training (ExT) delayed the progression of hypertension via normalizing the blunted baroreflex sensitivity (BRS) and inhibiting sympathetic nerve activity (SNA). Its underlying mechanism may be related to the inhibition of AngII/AT1 axis function and central oxidative stress in the paraventricular nucleus (PVN) of prehypertensive rats. Angiotensin-converting enzyme 2 (ACE2) or exercise training (ExT) is beneficial to hypertension, but their combined effects remain unknown. In this study, lentivirus containing enhanced green fluorescent protein (eGFP) and ACE2 were microinjected into the paraventricular nucleus (PVN) of young male spontaneous hypertensive rats (SHRs), and SHRs were assigned into five groups: sedentary (SHR), SHR-ExT, SHR-eGFP, ACE2 gene (SHR-ACE2), and ACE2 gene combined with ExT (SHR-ACE2-ExT). Wistar–Kyoto (WKY) rats were used as a control. ACE2 gene or ExT significantly delayed the elevation of blood pressure, and the combined effect prevented the development and progression of prehypertension. Either ACE2 overexpression or ExT improved arterial baroreflex sensitivity (BRS), whereas the combined effect normalized BRS in SHR. Compared with SHR, SHR-ACE2 and SHR-ExT displayed a significantly higher level of ACE2 protein but had lower plasma norepinephrine (NE) and angiotensin II (AngII) as well as angiotensin II type 1 receptor (AT1) protein expression in the PVN. SHR-ACE2-ExT showed the largest decrease in AngII and AT1 protein expression. Reactive oxygen species (ROS) level and NADPH oxidase (NOX2 and NOX4) protein expression in PVN were also decreased in SHR-ACE2-ExT group than in SHR-ACE2 and SHR-ExT groups. It was concluded that the combined effect has effectively prevented prehypertension progression and baroreflex dysfunction in SHR, which is associated with the reduction in AngII/AT1 axis function and oxidative stress in the PVN. NEW & NOTEWORTHY Angiotensin-converting enzyme 2 ( ACE2) gene in combination with exercise training (ExT) delayed the progression of hypertension via normalizing the blunted baroreflex sensitivity (BRS) and inhibiting sympathetic nerve activity (SNA). Its underlying mechanism may be related to the inhibition of AngII/AT1 axis function and central oxidative stress in the paraventricular nucleus (PVN) of prehypertensive rats.