Fetal exposure to teratogens: Evidence of genes involved in autism

被引:99
作者
Dufour-Rainfray, Diane [1 ,2 ,3 ]
Vourc'h, Patrick [1 ,2 ,3 ]
Tourlet, Sebastien [1 ]
Guilloteau, Denis [1 ,2 ,3 ]
Chalon, Sylvie [1 ,2 ,3 ]
Andres, Christian R. [1 ,2 ,3 ]
机构
[1] Univ Tours, UMR INSERM U930, CNRS ERL 3106, Tours, France
[2] CHRU Tours, Tours, France
[3] IFR135, Tours, France
关键词
Alcohol; Autistic spectrum disorder; Ethanol; Misoprostol; Thalidomide; Valproate; Epigenetics; PRENATAL ALCOHOL EXPOSURE; VALPROIC ACID; ANIMAL-MODEL; SPECTRUM DISORDERS; HISTONE DEACETYLASE; IN-VIVO; SEROTONIN SYNTHESIS; MOOD STABILIZER; MOBIUS SEQUENCE; FRONTAL-CORTEX;
D O I
10.1016/j.neubiorev.2010.12.013
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
Environmental challenges during the prenatal period can result in behavioral abnormalities and cognitive deficits that appear later in life such as autism. Prenatal exposure to valproic acid, ethanol, thalidomide and misoprostol has been shown to be associated with an increased incidence of autism. In addition, rodents exposed in utero to some of these drugs show autism-like abnormalities, including brain changes and lifelong behavior dysfunction. Our aim is to summarize current understanding of the relationship between in utero exposure to these drugs and autism in humans and in autism-like animal model phenotypes. It also highlights the importance of these models to understanding the neurobiology of autism, particularly in the identification of susceptibility genes. These drugs are able to modulate the expression of many genes involved in processes such as proliferation, apoptosis, neuronal differentiation and migration, synaptogenesis and synaptic activity. It seems essential to focus research on genes expressed during early neurodevelopment which may be the target of mutations or affected by drugs such as those included in this review. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1254 / 1265
页数:12
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