Adult hippocampal neurogenesis and aging

被引:107
作者
Klempin, Friederike
Kempermann, Gerd
机构
[1] Univ Med Berlin, Dept Expt Neurol, Volkswagen Res Grp, Charite, D-10117 Berlin, Germany
[2] Max Delbruck Ctr Mol Med, D-13125 Berlin, Germany
关键词
environmental enrichment; physical activity; depression; dentate gyrus; stem cell; precursor cell; AGE-RELATED DECLINE; GENERATED GRANULE CELLS; PITUITARY-ADRENAL AXIS; NEWLY BORN CELLS; DENTATE GYRUS; NEURONAL DIFFERENTIATION; SUBVENTRICULAR ZONE; BRAIN NEUROGENESIS; PHYSICAL-ACTIVITY; INDUCED INCREASES;
D O I
10.1007/s00406-007-0731-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The demographic changes in the foreseeable future stress the need for research on successful cognitive aging. Advancing age constitutes a primary risk factor for disease of the central nervous system most notably neurodegenerative disorders. The hippocampus is one of the brain regions that is prominently affected by neurodegeneration and functional decline even in what is still considered "normal aging". Plasticity is the basis for how the brain adapts to changes over time. The discovery of adult hippocampal neurogenesis has added a whole new dimension to research on structural plasticity in the adult and aging hippocampus. In this article, we briefly summarize and discuss recent findings on the regulation of adult neurogenesis with relevance to aging. Aging is an important co-variable for many regulatory mechanisms affecting adult neurogenesis but so far, only few studies have specifically addressed this interaction. We hypothesize that adult neurogenesis contributes to a neural reserve, i.e. the maintained potential for structural plasticity that allows compensation in situations of functional losses with aging. As such we propose that adult neurogenesis might contribute to the structural correlates of successful aging.
引用
收藏
页码:271 / 280
页数:10
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