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作 者:潘亮[1,2] 于涛[1] 刘艳华[1] 肖莎[1] 李丹丹[1] 逯晓波[1]
机构地区:[1]中国医科大学公共卫生学院卫生毒理教研室,辽宁沈阳110001 [2]沈阳市第九人民医院,辽宁沈阳110024
出 处:《中国工业医学杂志》2012年第2期97-99,共3页Chinese Journal of Industrial Medicine
基 金:辽宁省教育厅科学技术项目(批准号L2010703)
摘 要:目的通过邻苯二甲酸二(2-乙基己基)酯(DEHP)胚胎期暴露,评价其对子代大鼠神经行为的影响,初步探讨DEHP所致子鼠神经毒性的机制。方法雌性Wistar大鼠从妊娠日起用10、100、500 mg/(kg.d)DEHP连续灌胃染毒19 d,观察子代大鼠的神经行为学指标。于子鼠出生第7天和第21天测定海马神经细胞凋亡率,不同剂量的DEHP染毒对海马组织bcl-2、bax基因的表达的影响。结果于子鼠出生6周后,进行水迷宫测试。结果显示,随着DEHP剂量增加,中、高剂量组错误次数增加和潜伏期延长十分明显(F=8.058,P<0.05;F=11.221,P<0.05)。电穿梭测试显示,中、高剂量组电击次数增加和主动逃避时间延长较为明显(F=6.984,P<0.05;F=9.841,P<0.05)。出生后7 d子代大鼠海马神经元的细胞凋亡率高于出生21 d,高剂量组尤为显著。RT-PCR检测表明,与对照组相比,bcl-2和bax基因表达增高(F=253.78,P<0.05;F=66.67,P<0.05),且随着DEHP暴露剂量的升高,表达亦增加。结论 DEHP对子代大鼠神经系统具有明显的毒性作用,存在着剂量-反应关系,其可能通过干扰bcl-2和bax基因的表达而影响子代大鼠神经系统发育。Objective The purpose of this s tudy is to observe the effect of embryon ic exposure to DEHP on nervous behavior in offspring rats,and explore the primar y mechanism of neurotoxicity induced by DEHP.Methods The mature female Wistar ra ts were consecutively lavaged with 10 mg /(kg·d),100 mg/(kg·d) and 500 mg/(kg·d) of DEH P respectively from the first day until t he 19 th day of pregnancy,and observation was made on the nervous beh avior of offspring rats.The apoptosis rates in hippocampus of the offspring rats at the 7 th and 2 1 st postnatal day(PND)were detecte d respectively by flow cytometer(FCM).Me antime,the influence of different doses of DEHP on gene expression of bcl-2 an d bax were also analysed.Results The water maze test showed that both false time and latency were increased in DEHP groups and was dose-dependent,especially in the 100 mg/(kg·d) an d 500 mg/(kg·d) groups(F=8.058,P〈0.05;F=11.221,P〈0.05).Meanwhile,electricity shutt led test also showed that both shocked t ime and active elusion time were inc reased in DEHP groups,especially 100 mg/(kg·d) and 500 mg/(kg·d) groups(F=6.984,P〈0. 05;F=9.841,P〈0.05).While the apoptosis r ate in hippocampus of PND7 was higher th an that of PND21,especially in 500 mg/(k g·d)group.In addition,there were statist ical significance between DEHP groups an d the controls in gene expression of bcl-2 and bax(F=253.78,P〈0.05;F=66.67,P〈0.0 5), and the increase of bcl-2 and bax gene e xpressions were dose dependent.Conclusio n DEHP shows obvious toxicity on the of fspring nervous system of DEHP exposed r ats,the possible mechanism might be the interference on the expression of bcl-2 and bax,thereby affecting nervous system development.
关 键 词:邻苯二甲酸二(2-乙基己基)酯(DEHP) 神经行为学 细胞凋亡 bcl-2 bax
分 类 号:R114[医药卫生—卫生毒理学]
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