刘薇

个人信息Personal Information

教授

博士生导师

硕士生导师

主要任职:环境学院副院长

其他任职:环境学院教工党支部副书记

性别:女

毕业院校:大连理工大学

学位:博士

所在单位:环境学院

联系方式:Email:Liu_wei@dlut.edu.cn

电子邮箱:liu_wei@dlut.edu.cn

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Effect of gestational and lactational exposure to perfluorooctanesulfonate on calcium-dependent signaling molecules gene expression in rats' hippocampus

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论文类型:期刊论文

发表时间:2010-01-01

发表刊物:ARCHIVES OF TOXICOLOGY

收录刊物:PubMed、SCIE、Scopus

卷号:84

期号:1

页面范围:71-79

ISSN号:0340-5761

关键字:Developmental neurotoxicity; Gestation; Lactation; PFOS; Hippocampus

摘要:Perfluorooctanesulfonate (PFOS) is an environmental contaminant found in human and animal tissues worldwide. The developing nervous system is thought to be particularly sensitive to PFOS by the fact that PFOS can cross blood-brain and placental barriers. Effect of gestational and lactational exposure to PFOS on central nervous system (CNS) in Wistar rats was investigated by the cross-foster model built with PFOS at 0 or 3.2 mg/kg food. Real-time reverse transcription-polymerase chain reaction was employed to evaluate the gene expression of calcium-dependent signaling molecules in rats' hippocampus which are critical to the function of CNS. The expression of calcium-related signaling molecules, such as N-methyl-d-aspartate receptor subtype-2B (NR2B), calmodulin (CaM), Ca(2+)/calmodulin-dependent kinase II alpha (CaMKII alpha) and cAMP-response element-binding (CREB) were increased in the PFOS exposure group at postnatal day 1 (PND 1). The decreased NR2B in the prenatal PFOS exposure group, the decreased CaM in the pre-/postnatal PFOS exposure group, the increased CaMKII alpha in the whole-life PFOS exposure group and the increased CREB in the prenatal/whole-life PFOS exposure group was observed at PND 7. At PND 35, rats exhibited the decreased NR2B in the pre-/postnatal and the whole-life PFOS exposure group, and the decreased CaM in the postnatal PFOS group. The results indicate that perinatal exposure to PFOS during the critical period of development of the brain may have neurotoxic effect on CNS by mediating the molecules of calcium signaling pathway.