Impact of melatonin on central blood pressure regulation

被引:0
作者
Pechanova, Olga [1 ,2 ]
Paulis, Ludovit [1 ,2 ]
Simko, Fedor [3 ]
机构
[1] Slovak Acad Sci, Inst Normal & Pathol Physiol, Sienkiewiczova 1, Bratislava 81371, Slovakia
[2] Slovak Acad Sci, Ctr Excellence Nitr Oxide Res, Bratislava, Slovakia
[3] Comenius Univ, Fac Med, Dept Pathophysiol, Bratislava 81371, Slovakia
来源
ACTIVITAS NERVOSA SUPERIOR REDIVIVA | 2016年 / 58卷 / 04期
关键词
melatonin; hypertension; CNS; nitric oxide; ROS;
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The dysbalance between the sympathetic and parasympathetic vegetative system and increased free radical burden in the central nervous system (CNS) are the important pathophysiological disorders and therapeutic targets in hypertension. Besides the effects on cardiovascular system, the pineal hormone, melatonin (N-acetyl-5-methoxytryptamine) may exert part of its antihypertensive action just through its interaction with the CNS. Melatonin may be protective in CNS on several different levels: it reduces production of reactive oxygen species, improves endothelial dysfunction, reduces inflammation and shifts the balance between the sympathetic and parasympathetic system in favor of the parasympathetic system. Increased level of serum melatonin observed in some types of hypertension may represent a counterregulatory adaptive mechanism against the sympathetic overstimulation. All these effects of melatonin may include increased production of nitric oxide in their mechanisms of protection. In different experimental models of hypertension upregulation of nitric oxide synthase (NOS) activity and NOS isoform expression in different parts of brain after melatonin treatment have been documented. Thus, it is supposed that the correction of absolute or relative melatonin deficiency by exogenous melatonin administration in conditions of increased blood pressure, may help to attenuate the excessive catecholamine outflow providing a rational background for therapeutic application of melatonin in hypertension treatment.
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页码:99 / 104
页数:6
相关论文
共 88 条
[1]   Melatonin, mitochondria, and cellular bioenergetics [J].
Acuña-Castroviejo, D ;
Martín, M ;
Macías, M ;
Escames, G ;
León, J ;
Khaldy, H ;
Reiter, RJ .
JOURNAL OF PINEAL RESEARCH, 2001, 30 (02) :65-74
[2]   Melatonin ameliorates low-grade inflammation and oxidative stress in young Zucker diabetic fatty rats [J].
Agil, Ahmad ;
Reiter, Russel J. ;
Jimenez-Aranda, Aroa ;
Iban-Arias, Ruth ;
Navarro-Alarcon, Miguel ;
Antonio Marchal, Juan ;
Adem, Abdu ;
Fernandez-Vazquez, Gumersindo .
JOURNAL OF PINEAL RESEARCH, 2013, 54 (04) :381-388
[3]   Effects of melatonin an vascular reactivity, catecholamine levels, and blood pressure in healthy men [J].
Arangino, S ;
Cagnacci, A ;
Angiolucci, M ;
Vacca, AMB ;
Longu, G ;
Volpe, A ;
Melis, GB .
AMERICAN JOURNAL OF CARDIOLOGY, 1999, 83 (09) :1417-+
[4]  
Barta A, 2012, ACT NERV SUPER REDIV, V54, P25
[5]  
Barta A, 2012, CIRCULATION, V125, pE913
[6]  
BENITEZKING G, 1993, EXPERIENTIA, V49, P635
[7]   Effect of L-NAME-induced hypertension on melatonin receptors and melatonin levels in the pineal gland and the peripheral organs of rats [J].
Benova, Miroslava ;
Herichova, Iveta ;
Stebelova, Katarina ;
Paulis, Ludovit ;
Krajcirovicova, Kristina ;
Simko, Fedor ;
Zeman, Michal .
HYPERTENSION RESEARCH, 2009, 32 (04) :242-247
[8]   Melatonin and its analogs in insomnia and depression [J].
Cardinali, Daniel P. ;
Srinivasan, Venkataramanujan ;
Brzezinski, Amnon ;
Brown, Gregory M. .
JOURNAL OF PINEAL RESEARCH, 2012, 52 (04) :365-375
[9]   Renin-angiotensin system-regulating aminopeptidase activities are modified in the pineal gland of rats with breast cancer induced by N-methyl-nitrosourea [J].
Carrera, MP ;
Ramírez-Expósito, MJ ;
Valenzuela, MT ;
Dueñas, B ;
García, MJ ;
Mayas, MD ;
Martínez-Martos, JM .
CANCER INVESTIGATION, 2006, 24 (02) :149-153
[10]   DAILY VARIATION OF CONSTITUTIVELY ACTIVATED NUCLEAR FACTOR KAPPA B (NFKB) IN RAT PINEAL GLAND [J].
Cecon, Erika ;
Fernandes, Pedro A. ;
Pinato, Luciana ;
Ferreira, Zulma S. ;
Markus, Regina P. .
CHRONOBIOLOGY INTERNATIONAL, 2010, 27 (01) :52-67