Prenatal exposure to alcohol does not affect radial maze learning and hippocampal mossy fiber sizes in three inbred strains of mouse
被引:8
|
作者:
Sluyter, Frans
论文数: 0引用数: 0
h-index: 0
机构:
Kings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Res Ctr, London WC2R 2LS, EnglandKings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Res Ctr, London WC2R 2LS, England
Sluyter, Frans
[1
]
Jamot, Laure
论文数: 0引用数: 0
h-index: 0
机构:
Trophos SA, F-13288 Marseille 09, FranceKings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Res Ctr, London WC2R 2LS, England
Jamot, Laure
[2
]
Bertholet, Jean-Yves
论文数: 0引用数: 0
h-index: 0
机构:
Univ Paris 05, Ctr Henri Pieron, Inst Psychol, F-92100 Boulogne, FranceKings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Res Ctr, London WC2R 2LS, England
Bertholet, Jean-Yves
[3
]
Crusio, Wim E.
论文数: 0引用数: 0
h-index: 0
机构:
CNRS, UMR 5106, Cognit Neurosci Lab, Ave Fac, F-33405 Talence, FranceKings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Res Ctr, London WC2R 2LS, England
Crusio, Wim E.
[4
]
机构:
[1] Kings Coll London, Inst Psychiat, Social Genet & Dev Psychiat Res Ctr, London WC2R 2LS, England
[2] Trophos SA, F-13288 Marseille 09, France
[3] Univ Paris 05, Ctr Henri Pieron, Inst Psychol, F-92100 Boulogne, France
[4] CNRS, UMR 5106, Cognit Neurosci Lab, Ave Fac, F-33405 Talence, France
Background: The aim of this study was to investigate the effects of prenatal alcohol exposure on radial- maze learning and hippocampal neuroanatomy, particularly the sizes of the intra- and infrapyramidal mossy fiber (IIPMF) terminal fields, in three inbred strains of mice (C57BL/6J, BALB/cJ, and DBA/2J). Results: Although we anticipated a modification of both learning and IIPMF sizes, no such effects were detected. Prenatal alcohol exposure did, however, interfere with reproduction in C57BL/6J animals and decrease body and brain weight (in interaction with the genotype) at adult age. Conclusion: Prenatal alcohol exposure influenced neither radial maze performance nor the sizes of the IIPMF terminal fields. We believe that future research should be pointed either at different targets when using mouse models for Fetal Alcohol Syndrome (e.g. more complicated behavioral paradigms, different hippocampal substructures, or other brain structures) or involve different animal models.