Early-Life Exposure to Fibroblast Growth Factor-2 Facilitates Context-Dependent Long-Term Memory in Developing Rats

被引:15
作者
Graham, Bronwyn M. [1 ]
Richardson, Rick [1 ]
机构
[1] Univ New S Wales, Sch Psychol, Sydney, NSW 2052, Australia
基金
澳大利亚研究理事会;
关键词
fibroblast growth factor-2; developing rat; contextual fear; extinction; renewal; HIPPOCAMPAL-NEURONS; PROTEIN-KINASE; FEAR; EXTINCTION; ADULT; FGF-2; DIFFERENTIATION; PROLIFERATION; REINSTATEMENT; NEUROGENESIS;
D O I
10.1037/a0019582
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
Fibroblast growth factor-2 (FGF2) is a potent neurotrophic factor that is involved in brain development and the formation of long-term memory. It has recently been shown that acute FGF2, administered at the time of learning, enhances long-term memory for contextual fear conditioning as well as extinction of conditioned fear in developing rats. As other research has shown that administering FGF2 on the first day of life leads to long-term morphological changes in the hippocampus, in the present study we investigated whether early life exposure to FGF2 affects contextual fear conditioning, and renewal following extinction, later in life. Experiment I demonstrated that a single injection of FGF2 on Postnatal Day (PND) 1 did not lead to any detectable changes in contextual fear conditioning in PND 16 or PND 23 rats. Experiments 2 and 3 demonstrated that 5 days of injections of FGF2 (from PND 1-5) facilitated contextual fear conditioning in PND 16 and PND 23 rats. Experiment 4 demonstrated that the observed facilitation of memory was not due to FGF2 increasing rats' sensitivity to foot shock. Experiment 5 showed that early life exposure to FGF2 did not affect learning about a discrete conditioned stimulus, but did allow PND 16 rats to use contextual information in more complex ways, leading to context-dependent extinction of conditioned fear. These results further implicate FGF2 as a critical signal involved in the development of learning and memory.
引用
收藏
页码:337 / 345
页数:9
相关论文
共 42 条
[1]   Sustained phosphorylation of mitogen-activated protein kinase is required for basic fibroblast growth factor-mediated axonal branch formation in cultured rat hippocampal neurons [J].
Abe, K ;
Aoyagi, A ;
Saito, H .
NEUROCHEMISTRY INTERNATIONAL, 2001, 38 (04) :309-315
[2]  
ALTMAN J, 1968, Developmental Psychobiology, V1, P10, DOI 10.1002/dev.420010104
[3]  
Anagnostaras SG, 1999, J NEUROSCI, V19, P1106
[4]   CHARACTERIZATION OF BASIC FIBROBLAST GROWTH FACTOR-MEDIATED ACCELERATION OF AXONAL BRANCHING IN CULTURED RAT HIPPOCAMPAL-NEURONS [J].
AOYAGI, A ;
NISHIKAWA, K ;
SAITO, H ;
ABE, K .
BRAIN RESEARCH, 1994, 661 (1-2) :117-126
[5]   Is extinction of fear erasure or inhibition? Why both, of course [J].
Barad, M .
LEARNING & MEMORY, 2006, 13 (02) :108-109
[6]   ROLE OF CONDITIONED CONTEXTUAL STIMULI IN REINSTATEMENT OF EXTINGUISHED FEAR [J].
BOUTON, ME ;
BOLLES, RC .
JOURNAL OF EXPERIMENTAL PSYCHOLOGY-ANIMAL BEHAVIOR PROCESSES, 1979, 5 (04) :368-378
[7]   Hippocampal granule neuron production and population size are regulated by levels of bFGF [J].
Cheng, YH ;
Black, IB ;
DiCicco-Bloom, E .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2002, 15 (01) :3-12
[8]  
Cheng YH, 2001, J NEUROBIOL, V46, P220, DOI 10.1002/1097-4695(20010215)46:3<220::AID-NEU1004>3.0.CO
[9]  
2-P
[10]   Hippocampal inactivation disrupts contextual retrieval of fear memory after extinction [J].
Corcoran, KA ;
Maren, S .
JOURNAL OF NEUROSCIENCE, 2001, 21 (05) :1720-1726