Pechanova Olga, Paulis Ludovit, Simko Fedor
Institute of Normal and Pathological Physiology and Centre of Excellence for Nitric Oxide Research, Slovak Academy of Sciences, Bratislava 81371, Slovak Republic.
Department of Pathophysiology, Faculty of Medicine, Comenius University, Bratislava 81371, Slovak Republic.
Int J Mol Sci. 2014 Oct 8;15(10):17920-37. doi: 10.3390/ijms151017920.
The pineal hormone, melatonin (N-acetyl-5-methoxytryptamine), shows potent receptor-dependent and -independent actions, which participate in blood pressure regulation. The antihypertensive effect of melatonin was demonstrated in experimental and clinical hypertension. Receptor-dependent effects are mediated predominantly through MT1 and MT2 G-protein coupled receptors. The pleiotropic receptor-independent effects of melatonin with a possible impact on blood pressure involve the reactive oxygen species (ROS) scavenging nature, activation and over-expression of several antioxidant enzymes or their protection from oxidative damage and the ability to increase the efficiency of the mitochondrial electron transport chain. Besides the interaction with the vascular system, this indolamine may exert part of its antihypertensive action through its interaction with the central nervous system (CNS). The imbalance between the sympathetic and parasympathetic vegetative system is an important pathophysiological disorder and therapeutic target in hypertension. Melatonin is protective in CNS on several different levels: It reduces free radical burden, improves endothelial dysfunction, reduces inflammation and shifts the balance between the sympathetic and parasympathetic system in favor of the parasympathetic system. The increased level of serum melatonin observed in some types of hypertension may be a counter-regulatory adaptive mechanism against the sympathetic overstimulation. Since melatonin acts favorably on different levels of hypertension, including organ protection and with minimal side effects, it could become regularly involved in the struggle against this widespread cardiovascular pathology.
松果体激素褪黑素(N-乙酰-5-甲氧基色胺)具有强大的受体依赖性和非依赖性作用,参与血压调节。褪黑素的降压作用已在实验性和临床高血压中得到证实。受体依赖性作用主要通过MT1和MT2 G蛋白偶联受体介导。褪黑素具有多效性的受体非依赖性作用,可能对血压产生影响,包括清除活性氧(ROS)的特性、激活和过度表达几种抗氧化酶或保护它们免受氧化损伤以及提高线粒体电子传递链效率的能力。除了与血管系统相互作用外,这种吲哚胺可能通过与中枢神经系统(CNS)相互作用发挥其部分降压作用。交感神经系统和副交感神经系统之间的失衡是高血压的一种重要病理生理紊乱和治疗靶点。褪黑素在中枢神经系统的多个不同层面具有保护作用:它减轻自由基负担、改善内皮功能障碍、减轻炎症并使交感神经系统和副交感神经系统之间的平衡向有利于副交感神经系统的方向转变。在某些类型的高血压中观察到的血清褪黑素水平升高可能是针对交感神经过度刺激的一种反调节适应性机制。由于褪黑素在高血压的不同层面均发挥有益作用,包括器官保护且副作用最小,它可能会经常参与对抗这种广泛存在的心血管疾病的斗争。