Non-associative learning in larval zebrafish

被引:166
作者
Best, Jonathan D. [1 ]
Berghmans, Stephane [1 ]
Hunt, Julia J. F. G. [1 ]
Clarke, Samantha C. [1 ]
Fleming, Angeleen [1 ]
Goldsmith, Paul [1 ]
Roach, Alan G. [1 ]
机构
[1] DanioLabs Ltd, Unit 7330, Cambridge CB25 9TN, England
基金
英国生物技术与生命科学研究理事会;
关键词
zebrafish; non-associative learning; cholinergic; rolipram; cognition; NMDA;
D O I
10.1038/sj.npp.1301489
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Habituation, where a response is reduced when exposed to a continuous stimulus is one of the simplest forms of non-associative learning and has been shown in a number of organisms from sea slugs to rodents. However, very little has been reported in the zebrafish, a model that is gaining popularity for high-throughput compound screens. Furthermore, since most of the studies involving learning and memory in zebrafish have been conducted in adults, we sought to determine if zebrafish larvae could display non-associative learning and whether it could be modulated by compounds identified in previous rodent studies. We demonstrated that zebrafish larvae (7 days post fertilization) exhibit iterative reduction in a startle response to a series of acoustic stimuli. Furthermore, this reduction satisfied criteria for habituation: spontaneous recovery, more rapid reductions in startle to shorter intertrial intervals and dishabituation. We then investigated the pathways mediating this behavior using established compounds in learning and memory. Administration of rolipram (PDE4 inhibitor), donepezil (acetylcholinesterase inhibitor), and memantine (N-methyl-D-aspartic acid (NMDA) receptor antagonist) all increased the acoustic startle response and decreased habituation in the larvae, similar to previous rodent studies. Further studies demonstrated that NMDA blocked the memantine response and the effect of donepezil was blocked by mecamylamine but not atropine suggesting that the donepezil response was mediated by nicotinic rather than muscarinic receptors. Zebrafish larvae possess numerous advantages for medium to high-throughput screening; the model described herein therefore offers the potential to screen for additional compounds for further study on cognition function.
引用
收藏
页码:1206 / 1215
页数:10
相关论文
共 55 条
[1]   High-throughput behavioral screening method for detecting auditory response defects in zebrafish [J].
Bang, PI ;
Yelick, PC ;
Malicki, JJ ;
Sewell, WF .
JOURNAL OF NEUROSCIENCE METHODS, 2002, 118 (02) :177-187
[2]   Rolipram, a type IV-specific phosphodiesterase inhibitor, facilitates the establishment of long-lasting long-term potentiation and improves memory [J].
Barad, M ;
Bourtchouladze, R ;
Winder, DG ;
Golan, H ;
Kandel, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (25) :15020-15025
[3]   Nonassociative learning processes affecting swimming probability in the seaslug Tritonia diomedea:: habituation, sensitization and inhibition [J].
Brown, GD .
BEHAVIOURAL BRAIN RESEARCH, 1998, 95 (02) :151-165
[4]   The effects of donepezil in Alzheimer's disease -: Results from a multinational trial [J].
Burns, A ;
Rossor, M ;
Hecker, J ;
Gauthier, S ;
Petit, H ;
Möller, HJ ;
Rogers, SL ;
Friedhoff, LT .
DEMENTIA AND GERIATRIC COGNITIVE DISORDERS, 1999, 10 (03) :237-244
[5]   Clock mechanisms in zebrafish [J].
Cahill, GM .
CELL AND TISSUE RESEARCH, 2002, 309 (01) :27-34
[6]   Ethanol effects on the developing zebrafish: neurobehavior and skeletal morphogenesis [J].
Carvan, MJ ;
Loucks, E ;
Weber, DN ;
Williams, FE .
NEUROTOXICOLOGY AND TERATOLOGY, 2004, 26 (06) :757-768
[7]   Habituation of an odorant-induced startle response in Drosophila [J].
Cho, W ;
Heberlein, U ;
Wolf, FW .
GENES BRAIN AND BEHAVIOR, 2004, 3 (03) :127-137
[8]   Molecular characterization and embryonic expression of the family of N-methyl-D-aspartate receptor subunit genes in the zebrafish [J].
Cox, JA ;
Kucenas, S ;
Voigt, MM .
DEVELOPMENTAL DYNAMICS, 2005, 234 (03) :756-766
[9]  
Easter SS, 1996, DEV BIOL, V180, P646
[10]   Zebrafish as a pharmacological tool: the how, why and when [J].
Goldsmith, P .
CURRENT OPINION IN PHARMACOLOGY, 2004, 4 (05) :504-512