Bridging Neurocognitive Aging and Disease Modification: Targeting Functional Mechanisms of Memory Impairment

被引:23
作者
Gallagher, M. [1 ]
Bakker, A. [1 ]
Yassa, M. A. [2 ,3 ]
Stark, C. E. L. [2 ,3 ]
机构
[1] Johns Hopkins Univ, Dept Psychol & Brain Sci, Baltimore, MD 21218 USA
[2] Univ Calif Irvine, Dept Neurobiol & Behav, Irvine, CA USA
[3] Univ Calif Irvine, Ctr Neurobiol Learning & Memory, Irvine, CA 92717 USA
关键词
Memory; mild cognitive impairment; hippocampus; dentate gyrus/CA3; pattern separation; pattern completion; animal models; neuroimaging; MILD COGNITIVE IMPAIRMENT; MEDIAL TEMPORAL-LOBE; ALZHEIMERS-DISEASE; HIPPOCAMPAL ACTIVATION; PATTERN SEPARATION; DENTATE GYRUS; AGED RATS; CA3; DEMENTIA; DEFICITS;
D O I
10.2174/156720510791050867
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Risk for Alzheimer's disease escalates dramatically with increasing age in the later decades of life. It is widely recognized that a preclinical condition in which memory loss is greater than would be expected for a person's age, referred to as amnestic mild cognitive impairment, may offer the best opportunity for intervention to treat symptoms and modify disease progression. Here we discuss a basis for age-related memory impairment, first discovered in animal models and recently isolated in the medial temporal lobe system of man, that offers a novel entry point for restoring memory function with the possible benefit in slowing progression to Alzheimer's disease.
引用
收藏
页码:197 / 199
页数:3
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