Amyloid, cholinesterase, melatonin, and metals and their roles in aging and neurodegenerative diseases

被引:33
作者
Lahiri, DK
Chen, DM
Lahiri, P
Bondy, S
Greig, NH
机构
[1] Indiana Univ, Sch Med, Dept Psychiat, Inst Psychiat Res, Indianapolis, IN 46202 USA
[2] Banaras Hindu Univ, Womens Coll, Dept Chem, Varanasi 221005, Uttar Pradesh, India
[3] Univ Calif Irvine, Dept Community & Environm Med, Irvine, CA 92697 USA
[4] NIA, Neurosci Lab, Baltimore, MD 21224 USA
来源
NATURAL PRODUCTS AND MOLECULAR THERAPY | 2005年 / 1056卷
关键词
aging; acetylcholinesterase; amyloid; amyloid precursor protein; brain; cholinergic; cobalt; copper; diet; iron; melatonin; mercury; metalloprotease; metals; mouse; neurodegeneration; neuroprotection; synaptic proteins; zinc;
D O I
10.1196/annals.1352.008
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
The aging brain shows selective neurochemical changes involving several neural cell populations. Increased brain metal levels have been associated with normal aging and a variety of diseases, including Alzheimer's disease (AD). Melatonin levels are decreased in aging, particularly in AD subjects. The loss of melatonin, which is synthesized by the pineal gland, together with the degeneration of cholinergic neurons of the basal forebrain and the deposition of aggregated proteins, such as the amyloid beta peptides (A beta), are believed to contribute to the development of cognitive symptoms of dementia. Aging and its variants, such as AD, should be viewed as the result of multiple "hits," including alterations in the levels of A beta, metals, cholinesterase enzymes, and neuronal gene expression. Herein, we present evidence in support of this theory, based on several studies. We discuss melatonin's neuroprotective function, which plays an important role in aging, prolongation of life span, and health in the aged individual. It interacts with metals and, in some cases, neutralizes their toxic effects. Dietary supplementation of melatonin restores its age-related loss. In mice, an elevated brain melatonin significantly reduced levels of potentially toxic A beta peptides. Thus, compensation of melatonin loss in aging by dietary supplementation could well be beneficial in terms of reducing metal-induced toxicity, lipid peroxidation, and losses in cholinergic signaling. We propose that certain cholinesterase inhibitors and the NMDA partial antagonist memantine, which are FDA-approved drugs for AD and useful to boost central nervous system functioning, can be made more effective by their combination with melatonin or other neuroprotectants. Herein, we highlight studies elucidating the role of the amyloid pathway, metals, melatonin, and the cholinergic system in the context of aging and AD. Finally, melatonin is present in edible plants and walnuts, and consuming foodstuffs containing melatonin would be beneficial by enhancing the antioxidative capacity of the organisms.
引用
收藏
页码:430 / 449
页数:20
相关论文
共 82 条
[1]   ADAMs family members as amyloid precursor protein α-secretases [J].
Allinson, TMJ ;
Parkin, ET ;
Turner, AJ ;
Hooper, NM .
JOURNAL OF NEUROSCIENCE RESEARCH, 2003, 74 (03) :342-352
[2]   Mitochondria as a target for neurotoxins and neuroprotective agents [J].
Bachurin, SO ;
Shevtsova, EP ;
Kireeva, EG ;
Oxenkrug, GF ;
Sablin, SO .
NEUROPROTECTIVE AGENTS, 2003, 993 :334-344
[3]   Melatonin modulates cholinergic transmission by blocking nicotinic channels in the guinea-pig submucous plexus [J].
BarajasLopez, C ;
Peres, AL ;
EspinosaLuna, R ;
ReyesVazquez, C ;
PrietoGomez, B .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1996, 312 (03) :319-325
[4]   The fetal basis of amyloidogenesis:: Exposure to lead and latent overexpression of amyloid precursor protein and β-amyloid in the aging brain [J].
Basha, MR ;
Wei, W ;
Bakheet, SA ;
Benitez, N ;
Siddiqi, HK ;
Ge, YW ;
Lahiri, DK ;
Zawia, NH .
JOURNAL OF NEUROSCIENCE, 2005, 25 (04) :823-829
[5]   Copper depletion down-regulates expression of the Alzheimer's disease amyloid-β precursor protein gene [J].
Bellingham, SA ;
Lahiri, DK ;
Maloney, B ;
La Fontaine, S ;
Multhaup, G ;
Camakaris, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (19) :20378-20386
[6]   AGE-RELATED AND PEROXIDATIVE STRESS-RELATED MODIFICATIONS OF THE CEREBRAL ENZYMATIC-ACTIVITIES LINKED TO MITOCHONDRIA AND THE GLUTATHIONE SYSTEM [J].
BENZI, G ;
MORETTI, A .
FREE RADICAL BIOLOGY AND MEDICINE, 1995, 19 (01) :77-101
[7]   Retardation of brain aging by chronic treatment with melatonin [J].
Bondy, SC ;
Lahiri, DK ;
Perreau, VM ;
Sharman, KZ .
PROTECTIVE STRATEGIES FOR NEURODEGENERATIVE DISEASES, 2004, 1035 :197-215
[8]   Dietary modulation of age-related changes in cerebral pro-oxidant status [J].
Bondy, SC ;
Yang, YE ;
Walsh, TJ ;
Gie, YW ;
Lahiri, DK .
NEUROCHEMISTRY INTERNATIONAL, 2002, 40 (02) :123-130
[9]   Monozygotic twins with Alzheimer's disease treated with melatonin:: case report [J].
Brusco, LI ;
Márquez, M ;
Cardinali, DP .
JOURNAL OF PINEAL RESEARCH, 1998, 25 (04) :260-263
[10]   Genomic profiling of short- and long-term caloric restriction effects in the liver of aging mice [J].
Cao, SX ;
Dhahbi, JM ;
Mote, PL ;
Spindler, SR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (19) :10630-10635