Septo-hippocampal cholinergic and neurotrophin markers in age-induced cognitive decline

被引:61
作者
Sugaya, K
Greene, R
Personett, D
Robbins, M
Kent, C
Bryan, D
Skiba, E
Gallagher, M
McKinney, M
机构
[1] Mayo Clin Jacksonville, Dept Pharmacol, Jacksonville, FL 32224 USA
[2] Johns Hopkins Univ, Dept Psychol, Baltimore, MD 21218 USA
关键词
cognition; spatial learning; messenger RNA; immunoblotting; in situ hybridization histochemistry; aging;
D O I
10.1016/S0197-4580(98)00072-4
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Messenger RNA (mRNA) molecules encoding proteins related to the presynaptic cholinergic and neurotrophin systems were quantitated in the hippocampus and basal forebrain of Long-Evans rats with spatial learning ability assessed in the Morris water maze. The reverse transcriptase-polymerase chain reaction showed that the mRNAs for the low-affinity neurotrophin receptor (p75-NTR) and the growth-associated protein GAP-43 were decreased in level in the basal forebrain of aged-impaired rats. Tn the hippocampus of these aged-impaired rats, the mRNA for VGF, another neurotrophin-inducible gene, also was decreased. In situ hybridization histochemistry revealed that mRNAs for nerve growth factor (NGF) and brain-derived neurotrophic factor increased in level in the aged rat hippocampus; when age effects were removed, NGF mRNA level remained significantly correlated with maze performance. Enzyme-linked immunosorbent assay indicated that NGF protein was expressed at normal levels in the aged rat hippocampus. These mRNA and protein alterations may signify that a defect in neurotrophin signaling exists in the brains of aged Long-Evans rats; underlying reduced plasticity responses in the basal forebrain cholinergic system. (C) 1998 Elsevier Science Inc.
引用
收藏
页码:351 / 361
页数:11
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