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Neurogenesis and learning: Acquisition and asymptotic performance predict how many new cells survive in the hippocampus
被引:59
作者:
Dalla, Christina
Bangasser, Debra A.
Edgecomb, Carol
Shors, Tracey J.
机构:
[1] Rutgers State Univ, Dept Psychol, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Ctr Collaborat Neurosci, Piscataway, NJ 08854 USA
关键词:
Neurogenesis;
BrdU;
dentate gyrus;
hippocampus;
associative learning;
trace conditioning;
time;
D O I:
10.1016/j.nlm.2007.02.003
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:
Previous research has shown that some associative learning tasks prevent the death of new neurons in the adult hippocampus. However, it is unclear whether it is mere exposure to the training stimuli that rescues neurons or whether successful learning of the task is required for enhanced neuronal survival. If learning is the important variable, then animals that learn better given the same amount of training should retain more of the new cells after learning than animals that do not learn as well, Here, we examined the effects of training versus learning on cell survival in the adult hippocampus. Animals were injected with BrdU to label a population of cells and trained one week later on one of two trace conditioning tasks, one of which depends on the hippocampus and one that does not. Increases in cell number occurred only in animals that acquired the learned response, irrespective of the task. There were significant correlations between acquisition and cell number, as well as between asymptotic performance and cell number. These data support the idea that learning and not simply training increases the survival of the new cells in the hippocampus. (c) 2007 Elsevier Inc. All rights reserved.
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页码:143 / 148
页数:6
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