Reduction of Excitatory Synaptic Transmission Efficacy in the Infralimbic Prefrontal Cortex Potentially Contributes to Impairment of Contextual Fear Memory Extinction in Aged Mice

被引:3
|
作者
Shan, Qiang [1 ]
Yu, Xiaoxuan [1 ]
Tian, Yao [2 ]
机构
[1] Shantou Univ, Lab Synapt Plast, Med Coll, 22 Xinling Rd, Shantou 515041, Guangdong, Peoples R China
[2] Nankai Univ, Chern Inst Math, Tianjin, Peoples R China
基金
中国国家自然科学基金;
关键词
Aging-related cognitive decline; Contextual fear memory; Infralimbic prefrontal cortex; Memory extinction; Synaptic plasticity; LONG-TERM POTENTIATION; DISSOCIABLE ROLES; AMYGDALA; CONSOLIDATION; DEPRESSION; PLASTICITY; NEURONS; RECALL;
D O I
10.1093/gerona/glac137
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Human beings are living longer than ever before and the cognitive decline experienced by aged adults, such as compromise in cognitive flexibility, has been attracting more and more attention. One such example is the aging-related impairment of memory extinction. However, its underlying neural basis, especially its functional basis at the synapse level, is largely unknown. This study verifies that Pavlovian contextual fear memory extinction is impaired in aged mice. A large body of previous studies has shown that the infralimbic prefrontal cortex (ilPFC) plays a pivotal role in memory extinction. Correspondingly, this study reveals an aging-related reduction in the efficacy of excitatory synaptic transmission onto the ilPFC pyramidal neurons via electrophysiology recordings. This study further suggests that this reduced excitation potentially contributes to the aging-related impairment of contextual fear memory extinction: chemogenetically suppressing the activity of the ilPFC pyramidal neurons in young mice impairs contextual fear memory extinction, whereas chemogenetically compensating for the reduced excitation of the ilPFC pyramidal neurons in aged mice restores contextual fear memory extinction. This study identifies a functional synaptic plasticity in the ilPFC pyramidal neurons that potentially contributes to the aging-related impairment of contextual fear memory extinction, which would potentially help to develop a therapy to treat related cognitive decline in aged human adults.
引用
收藏
页码:930 / 937
页数:8
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