کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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2786008 | 1568405 | 2013 | 7 صفحه PDF | دانلود رایگان |

In utero exposure to valproic acid (VPA) may cause symptoms related to autism spectrum disorder (ASD). An abnormal serotonergic (5-HT) system has been implicated in the etiology of ASD. In the present study, we have examined the expression and distribution of two early inducers of 5-HT neurons in rat embryos, to elucidate the prenatal development of 5-HT neurons after VPA exposure at embryonic day (E) 9.5. Whole-embryo in situ hybridization at E11.5 showed that the expression of sonic hedgehog, one of the early inducers of 5-HT neurons, was reduced around the isthmus in the VPA-exposed group. Furthermore, whole-mount immunohistochemistry of the hindbrain and quantitative analysis of 5-HT neurons in the rostral raphe nucleus (rRN) revealed that neuronal distribution in the caudal part of the rRN was narrower at E15.5 in the VPA-exposed group than in controls. Thus, the early development of 5-HT neurons was altered after VPA exposure in utero. The observed prenatal alteration may be significant in the etiology of autism.
► We examined 5-HT neurons in a model of autism based on prenatal VPA exposure.
► Prenatal VPA exposure attenuated the expression of Shh at E11.5.
► The distribution of 5-HT neurons at E15.5 was altered.
► The expansion of caudal 5-HT neurons was suppressed.
► These prenatal alterations might contribute to the etiology of autism.
Journal: International Journal of Developmental Neuroscience - Volume 31, Issue 3, May 2013, Pages 202–208