Enriched environment experience overcomes the memory deficits and depressive-like behavior induced by early life stress

被引:130
作者
Cui, Minghu
Yang, Ya
Yang, Jianli
Zhang, Jichuan
Han, Huili
Ma, Wenpei
Li, Hongbin
Mao, Rongrong
Xu, Lin
Hao, Wei [1 ]
Cao, Jun
机构
[1] Cent S Univ, Hosp 2, Mental Hlth Inst, Changsha 410011, Peoples R China
[2] Cent S Univ, Hosp 2, WHO Collaborating Ctr Psychosocial Factors, Changsha 410011, Peoples R China
[3] Chinese Acad Sci, Kunming Inst Zool, Key Lab Anim Models & Human Dis Mechanisms, Kunming 650223, Peoples R China
[4] Chinese Acad Sci, Kunming Inst Zool, Lab Learning & Memory, Kunming 650223, Peoples R China
[5] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
[6] Kunming Med Coll, Dept Physiol, Kunming 650031, Peoples R China
基金
中国国家自然科学基金;
关键词
enriched environment; memory; long-term potentiation; hippocampus; forced swim; stress; Morris water maze;
D O I
10.1016/j.neulet.2006.05.048
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Stress in early life is believed to cause cognitive and affective disorders, and to disrupt hippocampal synaptic plasticity in adolescence into adult, but it is unclear whether exposure to enriched environment (EE) can overcome these effects. Here, we reported that housing rats in cages with limited nesting/bedding materials on postnatal days 2-21 reduced body weight gain, and this type of early life stress impaired spatial learning and memory of the Morris water maze and increased depressive-like behavior of the forced swim test in young adult rats (postnatal days 53-57). Early life stress also impaired long-term potentiation in hippocampal CA I area of slices of young adult rats. Remarkably, EE experience on postnatal days 22-52 had no effect on spatial learning/memory and depressive-like behavior, but it significantly facilitated UP in control rats, and completely overcame the effects of early life stress on young adult rats. These findings suggest that EE experience may be useful for clinical intervention in preventing cognitive and affective disorders during development. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:208 / 212
页数:5
相关论文
共 30 条
[1]  
ALEISA AM, 2005, IN PRESS INT J NEURO, P1
[2]   Long-lasting modulation of the induction of LTD and LTP in rat hippocampal CA1 by behavioural stress and environmental enrichment [J].
Artola, A ;
von Frijtag, JC ;
Fermont, PCJ ;
Gispen, WH ;
Schrama, LH ;
Kamal, A ;
Spruijt, BM .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2006, 23 (01) :261-272
[3]   Altered regulation of gene and protein expression of hypothalamic-pituitary-adrenal axis components in an immature rat model of chronic stress [J].
Avishai-Eliner, S ;
Gilles, EE ;
Eghbal-Ahmadi, M ;
Bar-El, Y ;
Baram, TZ .
JOURNAL OF NEUROENDOCRINOLOGY, 2001, 13 (09) :799-807
[4]   Rapid induction of intraneuronal neurofibrillary tangles in apolipoprotein E-deficient mice [J].
Bi, XN ;
Yong, AP ;
Zhou, J ;
Ribak, CE ;
Lynch, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (15) :8832-8837
[5]   A SYNAPTIC MODEL OF MEMORY - LONG-TERM POTENTIATION IN THE HIPPOCAMPUS [J].
BLISS, TVP ;
COLLINGRIDGE, GL .
NATURE, 1993, 361 (6407) :31-39
[6]   Stress and the developing hippocampus [J].
Brunson, KL ;
Chen, YC ;
Avishai-Eliner, S ;
Baram, TZ .
MOLECULAR NEUROBIOLOGY, 2003, 27 (02) :121-136
[7]   Stress and glucocorticoids impair retrieval of long-term spatial memory [J].
de Quervain, DJF ;
Roozendaal, B ;
McGaugh, JL .
NATURE, 1998, 394 (6695) :787-790
[8]   Preclinical research on stress, memory, and the brain in the development of pharmacotherapy for depression [J].
Diamond, DM ;
Campbell, A ;
Park, CR ;
Vouimba, RM .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 2004, 14 :S491-S495
[9]   Environmental enrichment modifies the PKA-dependence of hippocampal LTP and improves hippocampus-dependent memory [J].
Duffy, SN ;
Craddock, KJ ;
Abel, T ;
Nguyen, PV .
LEARNING & MEMORY, 2001, 8 (01) :26-34
[10]   Environmental enrichment reverses cognitive and molecular deficits induced by developmental lead exposure [J].
Guilarte, TR ;
Toscano, CD ;
McGlothan, JL ;
Weaver, SA .
ANNALS OF NEUROLOGY, 2003, 53 (01) :50-56