Melatonin Therapy in Patients with Alzheimer's Disease

被引:50
|
作者
Cardinali, Daniel P. [1 ]
Vigo, Daniel E. [1 ]
Olivar, Natividad [2 ]
Vidal, Maria F. [2 ]
Brusco, Luis I. [2 ]
机构
[1] Pontificia Univ Catolica Argentina, Fac Ciencias Medi, Dept Docencia Investigac, RA-1007 Buenos Aires, DF, Argentina
[2] Univ Buenos Aires, Hosp Clin Jos San Martin, Centro Neuropsiquiatria Neurol Conducta, RA-1121 Buenos Aires, DF, Argentina
来源
ANTIOXIDANTS | 2014年 / 3卷 / 02期
关键词
melatonin; Alzheimer's disease; neurodegeneration; free radicals; oxidative stress; aging; mild cognitive impairment; melatonin analogs;
D O I
10.3390/antiox3020245
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Alzheimer's disease (AD) is a major health problem and a growing recognition exists that efforts to prevent it must be undertaken by both governmental and non-governmental organizations. In this context, the pineal product, melatonin, has a promising significance because of its chronobiotic/cytoprotective properties potentially useful for a number of aspects of AD. One of the features of advancing age is the gradual decrease in circulating melatonin levels. A limited number of therapeutic trials have indicated that melatonin has a therapeutic value as a neuroprotective drug in the treatment of AD and minimal cognitive impairment (which may evolve to AD). Both in vitro and in vivo, melatonin prevented the neurodegeneration seen in experimental models of AD. For these effects to occur, doses of melatonin about two orders of magnitude higher than those required to affect sleep and circadian rhythmicity are needed. More recently, attention has been focused on the development of potent melatonin analogs with prolonged effects, which were employed in clinical trials in sleep-disturbed or depressed patients in doses considerably higher than those employed for melatonin. In view that the relative potencies of the analogs are higher than that of the natural compound, clinical trials employing melatonin in the range of 50-100 mg/day are urgently needed to assess its therapeutic validity in neurodegenerative disorders such as AD.
引用
收藏
页码:245 / 277
页数:33
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