Impairment in long-term memory formation and learning-dependent synaptic plasticity in mice lacking glycogen synthase in the brain

被引:113
|
作者
Duran, Jordi [1 ,2 ]
Saez, Isabel [1 ,3 ]
Gruart, Agnes [4 ]
Guinovart, Joan J. [1 ,2 ,3 ]
Delgado-Garcia, Jose M. [4 ]
机构
[1] IRB Barcelona, Barcelona, Spain
[2] Ctr Invest Biomed Red Diabet & Enfermedades Metab, Barcelona, Spain
[3] Univ Barcelona, Dept Biochem & Mol Biol, Barcelona, Spain
[4] Pablo de Olavide Univ, Div Neurosci, Seville 41013, Spain
来源
关键词
brain glycogen; hippocampus; long-term potentiation; mice; operant conditioning; NERVOUS-SYSTEM; BEHAVING MICE; POTENTIATION; HIPPOCAMPUS; SYNAPSES; CONSOLIDATION; ACCUMULATION; STIMULATION; METABOLISM; EXPRESSION;
D O I
10.1038/jcbfm.2012.200
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glycogen is the only carbohydrate reserve of the brain, but its overall contribution to brain functions remains unclear. Although it has traditionally been considered as an emergency energetic reservoir, increasing evidence points to a role of glycogen in the normal activity of the brain. To address this long-standing question, we generated a brain-specific Glycogen Synthase knockout (GYS1(Nestin-KO)) mouse and studied the functional consequences of the lack of glycogen in the brain under alert behaving conditions. These animals showed a significant deficiency in the acquisition of an associative learning task and in the concomitant activity-dependent changes in hippocampal synaptic strength. Long-term potentiation (LTP) evoked in the hippocampal CA3-CA1 synapse was also decreased in behaving GYS1(Nestin-KO) mice. These results unequivocally show a key role of brain glycogen in the proper acquisition of new motor and cognitive abilities and in the underlying changes in synaptic strength. Journal of Cerebral Blood Flow & Metabolism (2013) 33, 550-556; doi:10.1038/jcbfm.2012.200; published online 2 January 2013
引用
收藏
页码:550 / 556
页数:7
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