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Influence of dopamine D3 receptor knockout on age-related decline of spatial memory
被引:24
|作者:
Xing, Bo
[1
,2
,3
]
Meng, Xia
[1
,2
,3
]
Wei, Shuguang
[1
,2
,3
]
Li, Shengbin
[1
,2
,3
]
机构:
[1] Xi An Jiao Tong Univ, Sch Med, Dept Forens Sci, Xian 710061, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Minist Forens Sci, Key Lab Hlth, Xian 710061, Shaanxi, Peoples R China
[3] Xi An Jiao Tong Univ, Minist Educ, Key Lab Environm & Gene Related Dis, Xian 710061, Shaanxi, Peoples R China
关键词:
D-3;
receptor;
Aging;
Spatial memory;
CREB;
Morris water maze;
LONG-TERM-MEMORY;
CREB PHOSPHORYLATION;
PREFRONTAL CORTEX;
WORKING-MEMORY;
PROTEIN-KINASE;
HIPPOCAMPUS;
DEFICITS;
RATS;
MICE;
DYSREGULATION;
D O I:
10.1016/j.neulet.2010.06.071
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
There is evidence indicating that the brain's dopaminergic system is involved in age-associated memory impairment. However, specific roles in this process for the different dopamine receptor subtypes have not been elucidated. The cAMP-response element binding protein (CREB) is one of the cellular molecules that have been strongly implicated in the synaptic plasticity deficits occurring in age-related memory and cognitive impairment. In the present study, dopamine D-3 receptor mutant mice were tested in the Morris water maze task. We found that aged D3 receptor mutant mice perform comparatively better than their even-aged wild-type counterparts in both spatial learning training and a subsequent memory test. The degree of hippocampal CREB phosphorylation is significantly higher in aged D-3 receptor mutants compared to aged wild-type mice, whereas no difference in CREB activation was observed in the prefrontal cortex. These results suggest that blockade of D-3 receptors ameliorates age-related memory decline and that D-3 receptor-regulated CREB signaling in the hippocampus may be involved in these age-associated alterations. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
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页码:149 / 153
页数:5
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