Department of Rehabilitation Medicine, Health School of Fujian Medical University, Fuzhou, China.
Department of Cellular and Integrative, Physiology of University of Nebraska Medical Center, Omaha, Nebraska.
J Appl Physiol (1985). 2022 Jun 1;132(6):1460-1467. doi: 10.1152/japplphysiol.00459.2021. Epub 2022 May 12.
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 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, gene (SHR-ACE2), and gene combined with ExT (SHR-ACE2-ExT). Wistar-Kyoto (WKY) rats were used as a control. gene or ExT significantly delayed the elevation of blood pressure, and the combined effect prevented the development and progression of prehypertension. Either 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. Angiotensin-converting enzyme 2 () 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.
血管紧张素转换酶 2 (ACE2) 或运动训练 (ExT) 有益于高血压,但它们的联合作用尚不清楚。在这项研究中,携带增强型绿色荧光蛋白 (eGFP) 和 的慢病毒被微注射到年轻雄性自发性高血压大鼠 (SHR) 的室旁核 (PVN) 中,然后将 SHR 分为五组:安静组 (SHR)、SHR-ExT、SHR-eGFP、ACE2 基因 (SHR-ACE2) 和 ACE2 基因与 ExT 联合 (SHR-ACE2-ExT)。Wistar-Kyoto (WKY) 大鼠被用作对照。ACE2 过表达或 ExT 显著延缓了血压升高,联合作用防止了高血压前期的发展和进展。无论是 ACE2 过表达还是 ExT 都改善了动脉压力反射敏感性 (BRS),而联合作用则使 SHR 的 BRS 恢复正常。与 SHR 相比,SHR-ACE2 和 SHR-ExT 显示出更高水平的 ACE2 蛋白,但 PVN 中的血浆去甲肾上腺素 (NE) 和血管紧张素 II (AngII) 以及血管紧张素 II 型 1 受体 (AT1) 蛋白表达水平较低。SHR-ACE2-ExT 显示出 AngII 和 AT1 蛋白表达的最大减少。SHR-ACE2-ExT 组 PVN 中的活性氧 (ROS) 水平和 NADPH 氧化酶 (NOX2 和 NOX4) 蛋白表达也低于 SHR-ACE2 和 SHR-ExT 组。结论是,联合作用有效地防止了 SHR 高血压前期的进展和压力反射功能障碍,这与 PVN 中 AngII/AT1 轴功能和氧化应激的降低有关。血管紧张素转换酶 2 (ACE2) 基因与运动训练 (ExT) 的联合作用通过使压力反射敏感性 (BRS) 减弱和抑制交感神经活性 (SNA) 正常化来延缓高血压的进展。其潜在机制可能与抑制高血压前期大鼠室旁核 (PVN) 中 AngII/AT1 轴功能和中枢氧化应激有关。