Targeting Adult Neurogenesis to Optimize Hippocampal Circuits in Aging

被引:32
|
作者
McAvoy, Kathleen M. [1 ,2 ,3 ]
Sahay, Amar [1 ,2 ,3 ,4 ]
机构
[1] Massachusetts Gen Hosp, Ctr Regenerat Med, Boston, MA 02114 USA
[2] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[3] Harvard Med Sch, Massachusetts Gen Hosp, Dept Psychiat, Boston, MA 02114 USA
[4] BROAD Inst Harvard & MIT, Cambridge, MA 02142 USA
基金
美国国家卫生研究院;
关键词
Aging; Neurogenesis; Dentate gyrus; Hippocampus; Memory; Pattern separation; AGE-RELATED DECLINE; ENHANCED SYNAPTIC PLASTICITY; NEURAL PROGENITOR CELLS; DENTATE GRANULE CELLS; PATTERN SEPARATION; SPATIAL MEMORY; COGNITIVE FUNCTION; OLDER-ADULTS; RECOGNITION MEMORY; CRITICAL PERIOD;
D O I
10.1007/s13311-017-0539-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Millions of individuals suffer from age-related cognitive decline, defined by impaired memory precision. Increased understanding of hippocampal circuit mechanisms underlying memory formation suggests a role for computational processes such as pattern separation and pattern completion in memory precision. We describe evidence implicating the dentate gyrus-CA3 circuit in pattern separation and completion, and examine alterations in dentate gyrus-CA3 circuit structure and function with aging. We discuss the role of adult hippocampal neurogenesis in memory precision in adulthood and aging, as well as the circuit mechanisms underlying the integration and encoding functions of adult-born dentate granule cells. We posit that understanding these circuit mechanisms will permit generation of circuit-based endophenotypes that will edify new therapeutic strategies to optimize hippocampal encoding during aging.
引用
收藏
页码:630 / 645
页数:16
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