The aging hippocampus: A multi-level analysis in the rat

被引:167
作者
Driscoll, I.
Howard, S. R.
Stone, J. C.
Monfils, M. H.
Tomanek, B.
Brooks, W. M.
Sutherland, R. J.
机构
[1] NIA, GEC, IRP, NIH, Baltimore, MD 21224 USA
[2] Univ Lethbridge, Canadian Ctr Behav Neurosci, Lethbridge, AB T1K 3M4, Canada
[3] Univ Calgary, Expt Imaging Ctr, Calgary, AB, Canada
[4] Univ Kansas, Med Ctr, Hoglund Brain Imaging Ctr, Kansas City, KS 66103 USA
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
FBNF1; Morris water task; transverse patterning; MRI; MRS; neurogenesis;
D O I
10.1016/j.neuroscience.2006.01.040
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
In the current experiment we conducted a multi-level analysis of age-related characteristics in the hippocampus of young adult (3 months), middle-aged (12 months), and old (24 months) Fisher 344 x Brown Norway hybrid (FBNF1) rats. We examined the relationships between aging, hippocampus, and memory using a combination of behavioral, non-invasive magnetic resonance imaging and spectroscopy, and postmortem neuroanatomical measures in the same rats. Aging was associated with functional deficits on hippocampus-dependent memory tasks, accompanied by structural alterations observed both in vivo (magnetic resonance imaging-hippocampal volume) and postmortem (dentate gyrus neuronal density and neurogenesis). Neuronal metabolic integrity, assessed by levels of N-acetylaspartate with magnetic resonance spectroscopy, was however, preserved. Further, our results suggest that neurogenesis (doublecortin) seems to be related to both performance deficits on hippocampus-dependent tasks and hippocampal volume reduction. The observed pattern of age-related alterations closely resembles that previously reported in humans and suggests FBNF1 rats to be a useful model of normal human aging. (c) 2006 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1173 / 1185
页数:13
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