Cognitive aging as an extension of brain development: A model linking learning, brain plasticity, and neurodegeneration

被引:34
作者
de Magalhaes, JP
Sandberg, A
机构
[1] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[2] Royal Inst Technol, Dept Numer Anal & Comp Sci, S-10044 Stockholm, Sweden
关键词
longevity; mind; neuroplasticity; senescence; synaptic plasticity;
D O I
10.1016/j.mad.2005.04.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Differences in cognitive aging rates among mammals suggest that the pace of brain aging is genetically determined. In this work, we investigate the possibility that brain aging is an extension of brain development. It is possible that a subset of developmental mechanisms are extreme cases of antagonistic pleiotropy in that they are necessary for reaching adulthood and yet later cause age-related diseases. We derive a model linking development and brain aging in which childhood events essential for brain development later result in neurodegeneration. The hypothesis presented herein involves brain plasticity in which the same mechanisms that shape the adult phenotype continue at later ages contributing to cognitive dysfunction and eventually dementia. The same genetic program that decreases brain plasticity at early ages to focus our mind to the surrounding environment may continue in adulthood resulting in cognitive aging. Experimental implications for understanding neurodegeneration in this context are also discussed. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:1026 / 1033
页数:8
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