Department of Clinical Sciences and Laboratory Medicine, Kansai Medical University, Hirakata City, Osaka, Japan.
Hypertens Res. 2011 Nov;34(11):1147-60. doi: 10.1038/hr.2011.105. Epub 2011 Aug 4.
The central nervous system has a key role in regulating the circulatory system by modulating the sympathetic and parasympathetic nervous systems, pituitary hormone release, and the baroreceptor reflex. Digoxin- and ouabain-like immunoreactive materials were found >20 years ago in the hypothalamic nuclei. These factors appeared to localize to the paraventricular and supraoptic nuclei and the nerve fibers at the circumventricular organs and supposed to affect electrolyte balance and blood pressure. The turnover rate of these materials increases with increasing sodium intake. As intracerebroventricular injection of ouabain increases blood pressure via sympathetic activation, an endogenous digitalis-like factor (EDLF) was thought to regulate cardiovascular system-related functions in the brain, particularly after sodium loading. Experiments conducted mainly in rats revealed that the mechanism of action of ouabain in the brain involves sodium ions, epithelial sodium channels (ENaCs) and the renin-angiotensin-aldosterone system (RAAS), all of which are affected by sodium loading. Rats fed a high-sodium diet develop elevated sodium levels in their cerebrospinal fluid, which activates ENaCs. Activated ENaCs and/or increased intracellular sodium in neurons activate the RAAS; this releases EDLF in the brain, activating the sympathetic nervous system. The RAAS promotes oxidative stress in the brain, further activating the RAAS and augmenting sympathetic outflow. Angiotensin II and aldosterone of peripheral origin act in the brain to activate this cascade, increasing sympathetic outflow and leading to hypertension. Thus, the brain Na(+)-ENaC-RAAS-EDLF axis activates sympathetic outflow and has a crucial role in essential and secondary hypertension. This report provides an overview of the central mechanism underlying hypertension and discusses the use of antihypertensive agents.
中枢神经系统通过调节交感和副交感神经系统、垂体激素释放和压力感受器反射,在调节循环系统方面起着关键作用。二十多年前,人们在下丘脑核中发现了洋地黄和哇巴因样免疫反应物质。这些因素似乎定位于室旁核和视上核以及室周器官的神经纤维,它们可能影响电解质平衡和血压。这些物质的周转率随着钠摄入量的增加而增加。由于向脑室内注射哇巴因通过交感神经激活来升高血压,因此认为内源性洋地黄样因子(EDLF)可调节大脑中与心血管系统相关的功能,尤其是在钠负荷后。主要在大鼠中进行的实验表明,哇巴因在大脑中的作用机制涉及钠离子、上皮钠离子通道(ENaC)和肾素-血管紧张素-醛固酮系统(RAAS),所有这些都受钠负荷的影响。高盐饮食的大鼠会在其脑脊液中产生升高的钠水平,从而激活 ENaC。激活的 ENaC 和/或神经元内增加的钠离子激活 RAAS;这会在大脑中释放 EDLF,激活交感神经系统。RAAS 在大脑中引发氧化应激,进一步激活 RAAS 并增加交感神经输出。外周来源的血管紧张素 II 和醛固酮在大脑中作用以激活该级联反应,增加交感神经输出并导致高血压。因此,大脑 Na(+)-ENaC-RAAS-EDLF 轴激活交感神经输出,在原发性和继发性高血压中起着至关重要的作用。本报告概述了高血压的中枢机制,并讨论了降压药物的应用。