Aged Non-Human Primates: An Animal Model of Age-Associated Neurodegenerative Disease

被引:66
作者
Price, Donald L. [1 ,2 ,4 ]
Martin, Lee J. [1 ,2 ]
Sisodia, Sangram S. [1 ,2 ]
Wagster, Molly V. [1 ,2 ]
Koo, Edward H. [1 ,2 ,3 ,5 ]
Walker, Lary C. [1 ,2 ]
Koliatsos, Vassilis E. [1 ,2 ,3 ,5 ]
Cork, Linda C. [1 ,2 ,5 ]
机构
[1] Johns Hopkins Univ, Sch Med, Neuropathol Lab, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pathol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Div Comparat Med, Baltimore, MD 21205 USA
关键词
D O I
10.1111/j.1750-3639.1991.tb00672.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Aged non-human primates develop age-associated behavioral and brain abnormalities similar to those that occur in aged humans and, to a greater extent, in individuals with Alzheimer's disease. Declines in performance on cognitive and memory tasks begin at the monkey equivalent of late-middle life. As occurs in elderly humans, significant differences have been demonstrated in levels of performance between animals within older age groups. The brains of old monkeys show degenerative changes in neurons, abnormal axons and neurites (particularly in telencephalic areas), and deposits of amyloid in senile plaques and around blood vessels. Moreover, in some older animals, decrements occur in markers of specific neurotransmitter circuits, including the basal forebrain cholinergic system. It has been suggested that alterations in these cholinergic neurons contribute to the memory deficits that occur in older individuals. Because axotomy-induced retrograde degeneration of these neurons can be prevented by the administration of nerve growth factor, we have begun studies to determine whether administration of nerve growth factor improves performance of aged animals on memory tasks. This review describes the complementary nature of studies of non-human primates and human subjects, illustrating how these investigations can clarify factors that influence behavior and brain biology in age-associated diseases.
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收藏
页码:287 / 296
页数:10
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