Aging, neurodegenerative disease and the brain

被引:7
作者
McGeer, EG [1 ]
McGeer, PL [1 ]
机构
[1] UNIV BRITISH COLUMBIA, KINSMEN LAB NEUROL RES, VANCOUVER, BC V6T 1Z3, CANADA
来源
CANADIAN JOURNAL ON AGING-REVUE CANADIENNE DU VIEILLISSEMENT | 1997年 / 16卷 / 02期
关键词
inflammation; Alzheimer Disease; neurotransmitters; dopamine; Parkinson's disease; Pick's disease; Diffuse Lewy Body Disease; complement;
D O I
10.1017/S071498080001432X
中图分类号
R4 [临床医学]; R592 [老年病学];
学科分类号
1002 ; 100203 ; 100602 ;
摘要
The brain undergoes many changes in chemistry and structure during normal aging. For example, it dries and shrinks. Neurons are lost from some regions and there is also neuronal atrophy and loss of synaptic branching. The extent of such losses remains controversial for all but a few subcortical regions of the brain. Decreases in glucose metabolism and in some pre- and post-synaptic neurotransmitter indices have also been reported. Many systems, however, remain entirely unexplored. The evidence to date also indicates that there is great regional specificity in the effects, and that humans show considerable variability between individuals. Of interest is the fact that some of the changes most clearly demonstrated in normal aging - such as loss of dopaminergic neurons of the substantia nigra and cholinergic neurons of the medial basal forebrain - also occur in a much accentuated form in neurodegenerative diseases such as Parkinson's disease and Alzheimer disease. The small loss of these systems in normal aging may account for the shuffling gait, stooped posture and memory loss in the elderly. A phenomenon seen in neurodegenerative diseases, but not in normal aging, is the appearance of chronic inflammation in the brain. The suggestion that the progress of such diseases might be slowed by treatment with anti-inflammatory agents has, in the case of Alzheimer disease, gained some support from 19 epidemiological studies and one very small clinical trial. Clearly more detailed clinical trials are required, and caution must be used because of the undesirable side effects of currently available anti-inflammatory agents.
引用
收藏
页码:218 / 236
页数:19
相关论文
共 88 条
[1]   EARLY RESPONSE OF BRAIN RESIDENT MICROGLIA TO KAINIC ACID-INDUCED HIPPOCAMPAL-LESIONS [J].
AKIYAMA, H ;
TOOYAMA, I ;
KONDO, H ;
IKEDA, K ;
KIMURA, H ;
MCGEER, EG ;
MCGEER, PL .
BRAIN RESEARCH, 1994, 635 (1-2) :257-268
[2]   BRAIN MICROGLIA CONSTITUTIVELY EXPRESS BETA-2 INTEGRINS [J].
AKIYAMA, H ;
MCGEER, PL .
JOURNAL OF NEUROIMMUNOLOGY, 1990, 30 (01) :81-93
[3]   OXIDANTS, ANTIOXIDANTS, AND THE DEGENERATIVE DISEASES OF AGING [J].
AMES, BN ;
SHIGENAGA, MK ;
HAGEN, TM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (17) :7915-7922
[4]   DO NONSTEROIDAL ANTIINFLAMMATORY DRUGS DECREASE THE RISK FOR ALZHEIMERS-DISEASE - THE ROTTERDAM STUDY [J].
ANDERSEN, K ;
LAUNER, LJ ;
OTT, A ;
HOES, AW ;
BRETELER, MMB ;
HOFMAN, A .
NEUROLOGY, 1995, 45 (08) :1441-1445
[5]   THE CHOLINERGIC HYPOTHESIS OF GERIATRIC MEMORY DYSFUNCTION [J].
BARTUS, RT ;
DEAN, RL ;
BEER, B ;
LIPPA, AS .
SCIENCE, 1982, 217 (4558) :408-417
[6]   RHEUMATOID-ARTHRITIS AND SUSCEPTIBILITY TO ALZHEIMERS-DISEASE [J].
BEARD, CM ;
KOKMAN, E ;
KURLAND, LT .
LANCET, 1991, 337 (8754) :1426-1426
[7]   THE SUPEROXIDE-FORMING ENZYMATIC SYSTEM OF PHAGOCYTES [J].
BELLAVITE, P .
FREE RADICAL BIOLOGY AND MEDICINE, 1988, 4 (04) :225-261
[8]   RESEARCH AND ALZHEIMERS-DISEASE - AN EPIDEMIOLOGIC PERSPECTIVE [J].
BRAYNE, C .
PSYCHOLOGICAL MEDICINE, 1993, 23 (02) :287-296
[9]   DELAYED-ONSET OF ALZHEIMERS-DISEASE WITH NONSTEROIDAL ANTIINFLAMMATORY AND HISTAMINE-H2 BLOCKING-DRUGS [J].
BREITNER, JCS ;
WELSH, KA ;
HELMS, MJ ;
GASKELL, PC ;
GAU, BA ;
ROSES, AD ;
PERICAKVANCE, MA ;
SAUNDERS, AM .
NEUROBIOLOGY OF AGING, 1995, 16 (04) :523-530
[10]   INVERSE ASSOCIATION OF ANTIINFLAMMATORY TREATMENTS AND ALZHEIMERS-DISEASE - INITIAL RESULTS OF A COTWIN CONTROL STUDY [J].
BREITNER, JCS ;
GAU, BA ;
WELSH, KA ;
PLASSMAN, BL ;
MCDONALD, WM ;
HELMS, MJ ;
ANTHONY, JC .
NEUROLOGY, 1994, 44 (02) :227-232