Behavioural state differentially engages septohippocampal cholinergic and GABAergic neurons in R6/1 Huntington's disease mice

被引:17
作者
Ransome, Mark I. [1 ]
Hannan, Anthony J. [1 ,2 ]
机构
[1] Univ Melbourne, Melbourne Brain Ctr, Florey Neurosci Inst, Melbourne, Vic 3010, Australia
[2] Univ Melbourne, Dept Anat & Cell Biol, Melbourne, Vic 3010, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
Huntington's disease; Cholinergic; GABAergic; Cognition; Septohippocampal system; c-Fos; Hippocampus; HIPPOCAMPAL THETA RHYTHM; LONG-TERM-MEMORY; SEPTAL NEURONS; SPATIAL MEMORY; SYNAPTIC PLASTICITY; BASAL FOREBRAIN; MEDIAL SEPTUM; GABA; GENE; NEUROGENESIS;
D O I
10.1016/j.nlm.2012.01.004
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Huntington's disease (HD) is a neurodegenerative condition characterised by progressive motor, psychological and cognitive decline. R6/1 HD transgenic mice model the clinical hippocampal-dependent cognitive deficits observed in patients. Cholinergic and GABAergic septohippocampal projections play important roles in hippocampal-dependent cognition. The current study examined neuronal activity of cholinergic and GABAergic septohippocampal projections in response to arousal elicited during differing behavioural states. The different behavioural states examined were; home cage (controls), acute exploration of a novel enriched environment and either spontaneous wakefulness (dark phase) or spontaneous sleep (light phase). We employed triple-label immunohistochemistry using c-Fos as an indirect marker of neuron activation and parvalbumin and choline acetyltransferase (ChAT) to label GABAergic and cholinergic neurons in the basal forebrain, respectively. The Y-maze was used to assess short-term hippocampal-dependent memory independently during either the dark or light phase and revealed a memory deficit in R6/1 HD mice compared to wildtypes that was particularly prominent during the dark phase. Three-way ANOVA of basal forebrain cholinergic and GABAergic activity through co-expression of c-Fos revealed overt responses to differing behavioural states. Both genotypes increased cholinergic neuron activity in response to exploring a novel enriched environment and also an increase during the dark phase compared to the light phase. Novel enriched environment exploration caused a larger response of GABAergic neuron activity in R6/1 HD mice, which also failed to increase the activity of GABAergic neurons during the dark phase compared to the light phase as observed for wildtype mice. Basal levels of c-Fos-positive cells were greatly increased in the hippocampal granule cell layer of R6/1 HD mice during both circadian phases. The differential activation of septohippocampal cholinergic and GABAergic neurons in R6/1 HD mice in response to differing behavioural states may be associated with impaired hippocampal-dependent short-term memory. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:261 / 270
页数:10
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