Imaging correlates of brain function in monkeys and rats isolates a hippocampal subregion differentially vulnerable to aging

被引:230
作者
Small, SA
Chawla, MK
Buonocore, M
Rapp, PR
Barnes, CA
机构
[1] Columbia Univ Coll Phys & Surg, Ctr Neurobiol & Behav, Taub Inst Res Alzheimers Dis & Aging Brain, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Dept Neurol, New York, NY 10032 USA
[3] Mt Sinai Sch Med, Kastor Neurobiol Aging Labs, New York, NY 10029 USA
[4] Mt Sinai Sch Med, Fishberg Res Ctr Neurobiol, New York, NY 10029 USA
[5] Mt Sinai Sch Med, Arizona Res Lab, Div Neural Syst Memory & Aging, New York, NY 10029 USA
关键词
D O I
10.1073/pnas.0400285101
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The hippocampal formation contains a distinct population of neurons organized into separate anatomical subregions. Each hippocampal subregion expresses a unique molecular profile accounting for their differential vulnerability to mechanisms of memory dysfunction. Nevertheless, it remains unclear which hippocampal subregion is most sensitive to the effects of advancing age. Here we investigate this question by using separate imaging techniques, each assessing different correlates of neuronal function. First, we used MRI to map cerebral blood volume, an established correlate of basal metabolism, in the hippocampal subregions of young and old rhesus monkeys. Second, we used in situ hybridization to map Arc expression in the hippocampal subregions of young and old rats. Arc is an immediate early gene that is activated in a behavior-dependent manner and is correlated with spike activity. Results show that the dentate gyrus is the hippocampal subregion most sensitive to the effects of advancing age, which together with prior studies establishes a cross-species consensus. This pattern isolates the locus of age-related hippocampal dysfunction and differentiates normal aging from Alzheimer's disease.
引用
收藏
页码:7181 / 7186
页数:6
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