Diz Debra I, Varagic Jasmina, Groban Leanne
Wake Forest University School of Medicine, The Hypertension & Vascular Research Center, Medical Center Boulevard, Winston-Salem, NC 27157-1032, USA.
Future Cardiol. 2008 May;4(3):237-45. doi: 10.2217/14796678.4.3.237.
This article discusses evidence that impairments in control of autonomic outflow mediated by the brain renin-angiotensin system (RAS) contribute to the decline in baroreceptor reflex function and the development of insulin resistance that accompany hypertension and excess salt intake, especially during aging. Imbalances in the regulation of the sympathetic and parasympathetic limbs of the autonomic nervous system observed in older subjects underlie changes in heart-rate variability and play a role in the regulation of overall cardiac function. Age-related alterations in autonomic nervous system function may also explain the age-associated alterations in metabolism. Reduced heart-rate variability is linked to increased mortality in patients with cardiovascular disorders and, coupled with information that is known about local changes in the cardiac and brain RAS during aging, the evidence reveals potential mechanisms for the protective effects of systemic blockade of the RAS against age-related changes that impact the heart.
由脑肾素-血管紧张素系统(RAS)介导的自主神经输出控制受损,会导致压力感受器反射功能下降以及胰岛素抵抗的发展,而这与高血压和高盐摄入相关,尤其是在衰老过程中。在老年受试者中观察到的自主神经系统交感神经和副交感神经调节失衡,是心率变异性变化的基础,并在整体心脏功能调节中发挥作用。自主神经系统功能的年龄相关改变,也可能解释了与年龄相关的代谢变化。心率变异性降低与心血管疾病患者死亡率增加有关,再结合已知的衰老过程中心脏和脑RAS的局部变化信息,这些证据揭示了RAS系统阻断对影响心脏的年龄相关变化具有保护作用的潜在机制。