Impaired spatial learning ln aged rats is associated with loss of p75-positive neurons in the basal forebrain

被引:34
作者
Greferath, U
Bennie, A
Kourakis, A
Barrett, GL [1 ]
机构
[1] Univ Melbourne, Dept Physiol, Parkville, Vic 3052, Australia
[2] Royal Melbourne Hosp, Walter & Eliza Hall Inst Med Res, Parkville, Vic 3050, Australia
关键词
basal forebrain; p75 neurotrophin receptor; spatial learning; aging; apoptosis; cholinergic neuron;
D O I
10.1016/S0306-4522(00)00260-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We investigated age-related changes in the number and size of neurons positive for the p75 neurotrophin receptor in the cholinergic basal forebrain of female Dark Agouti rats. Since the integrity of these neurons is known to be closely associated with performance in tests of spatial learning ability, we also investigated the incidence of age-related spatial learning impairments, using the Barnes maze. Spatial learning impairments occurred with increasing frequency with age. No rats showed impairment at six months, but 50% were impaired at 14 months and 71% at 26 months. There was no correlation between age and decreased number of p75-positive neurons in the rostral basal forebrain, which consists of the medial septum and vertical limb of the diagonal band of Broca. In the caudal basal forebrain, which consists of the horizontal limb and the nucleus of Meynert, there was a 13% reduction in the number of p75-positive neurons at 17 months compared to six months, and a 30% reduction at 26 months. There was a strong correlation between the presence of spatial learning impairment and a reduction in the number of p75-positive neurons. This correlation was most evident in the rostral basal forebrain, but was also present in the caudal basal forebrain. In the rostral basal forebrain, all learning impaired rats had fewer p75-positive neurons than the average number in unimpaired rats. A close correspondence between the presence of p75 and choline acetyltransferase was evident in basal forebrain neurons of learning-impaired and unimpaired rats. Gross pathological changes to the morphology of p75-positive neurons were relatively frequent in learning-impaired rats. These changes consisted of hypertrophy, appearance of vacuoles, and marginalisation of the cytoplasm. The results indicate the susceptibility of p75-positive neurons to degenerative changes with aging, and show that the loss of these neurons in the basal forebrain was strongly correlated with impairment in spatial learning. (C) 2000 IBRO. Published by Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:363 / 373
页数:11
相关论文
共 48 条
[11]   Hippocampal grafts of acetylcholine-producing cells are sufficient to improve behavioural performance following a unilateral fimbria-fornix lesion [J].
Dickinson-Anson, H ;
Aubert, I ;
Gage, FH ;
Fisher, LJ .
NEUROSCIENCE, 1998, 84 (03) :771-781
[12]   Comparison of site specific injections into the basal forebrain on water maze and radial arm maze performance in the male rat after immunolesioning with 192 IgG saporin [J].
Dornan, WA ;
McCampbell, AR ;
Tinkler, GP ;
Hickman, LJ ;
Bannon, AW ;
Decker, MW ;
Gunther, KL .
BEHAVIOURAL BRAIN RESEARCH, 1997, 86 (02) :181-189
[13]   NEURON ATROPHY DURING AGING - PROGRAMMED OR SPORADIC [J].
FINCH, CE .
TRENDS IN NEUROSCIENCES, 1993, 16 (03) :104-110
[14]   PROGRESSIVE DECLINE IN SPATIAL-LEARNING AND INTEGRITY OF FOREBRAIN CHOLINERGIC NEURONS IN RATS DURING AGING [J].
FISCHER, W ;
CHEN, KS ;
GAGE, FH ;
BJORKLUND, A .
NEUROBIOLOGY OF AGING, 1992, 13 (01) :9-23
[15]   DEGENERATIVE CHANGES IN FOREBRAIN CHOLINERGIC NUCLEI CORRELATE WITH COGNITIVE IMPAIRMENTS IN AGED RATS [J].
FISCHER, W ;
GAGE, FH ;
BJORKLUND, A .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1989, 1 (01) :34-45
[16]  
Flavell DJ, 1998, CURR TOP MICROBIOL, V234, P57
[17]  
Frade JM, 1996, NATURE, V383, P166
[19]   AGING - THE CHOLINERGIC HYPOTHESIS OF COGNITIVE DECLINE [J].
GALLAGHER, M ;
COLOMBO, PJ .
CURRENT OPINION IN NEUROBIOLOGY, 1995, 5 (02) :161-168
[20]   Impairment of basal forebrain cholinergic neurons associated with aging and long-term loss of ovarian function [J].
Gibbs, RB .
EXPERIMENTAL NEUROLOGY, 1998, 151 (02) :289-302