Memory deficits are associated with impaired ability to modulate neuronal excitability in middle-aged mice

被引:87
|
作者
Kaczorowski, Catherine C. [1 ,2 ]
Disterhoft, John F. [1 ,2 ]
机构
[1] Northwestern Univ, Interdepartmental Neurosci Program, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Dept Physiol M211, Chicago, IL 60611 USA
基金
美国国家卫生研究院;
关键词
CA1 PYRAMIDAL NEURONS; LONG-TERM POTENTIATION; CONCENTRATION-DEPENDENT MANNER; ALZHEIMERS-DISEASE; SLOW AFTERHYPERPOLARIZATION; HIPPOCAMPAL-NEURONS; AGING RABBITS; INTRINSIC EXCITABILITY; DORSAL HIPPOCAMPUS; CALCIUM-CURRENTS;
D O I
10.1101/lm.1365609
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Normal aging disrupts hippocampal neuroplasticity and learning and memory. Aging deficits were exposed in a subset (30%) of middle-aged mice that performed below criterion on a hippocampal-dependent contextual fear conditioning task. Basal neuronal excitability was comparable in middle-aged and young mice, but learning-related modulation of the post-burst afterhyperpolarization (AHP)-a general mechanism engaged during learning-was impaired in CA1 neurons from middle-aged weak learners. Thus, modulation of neuronal excitability is critical for retention of context fear in middle-aged mice. Disruption of AHP plasticity may contribute to contextual fear deficits in middle-aged mice-a model of age-associated cognitive decline (AACD).
引用
收藏
页码:362 / 366
页数:5
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