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纸质出版:2010
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徐兴欣,马金龙,高彦丽,安风仙,朱永方.高温致金黄地鼠神经管畸形中p38MAPK、Bax的表达变化[J].陆军军医大学学报(原第三军医大学学报),2010,32(18):1958-1961.
Xu Xingxin,Ma Jinlong,Gao Yanli,An Fengxian,Zhu Yongfang.Expressions of p38 mitogen-activated protein kinase and Bax in hyperthermia induced neural tube defects in golden hamsters[J].J Amry Med Univ (J Third Mil Med Univ),2010,32(18):1958-1961.
徐兴欣,马金龙,高彦丽,安风仙,朱永方.高温致金黄地鼠神经管畸形中p38MAPK、Bax的表达变化[J].陆军军医大学学报(原第三军医大学学报),2010,32(18):1958-1961. DOI:
Xu Xingxin,Ma Jinlong,Gao Yanli,An Fengxian,Zhu Yongfang.Expressions of p38 mitogen-activated protein kinase and Bax in hyperthermia induced neural tube defects in golden hamsters[J].J Amry Med Univ (J Third Mil Med Univ),2010,32(18):1958-1961. DOI:
目的 探讨p38MAPK蛋白激酶及Bax在高温致神经管畸形中的分子机制。 方法 将雌性金黄地鼠72只按完全随机设计分组法分为正常对照组和高温致神经管畸形实验组,每组36只。孕鼠于妊娠第8天进行高温水浴,并分别于高温后2、8、16、24、48、72 h取出胚胎。Western blot法对p38MAPK、P-p38MAPK及Bax活性进行分析。 结果 ① Bax在正常对照组胚胎稳定表达,且无明显量的改变(P0.05);Bax的表达在高温后8~48 h明显升高,与正常对照组相比差异有统计学意义(P0.05),于8、16 h时表达增加最为显著(P0.01)。② p38MAPK及P-p38MAPK在正常组中稳定低表达;而在高温致畸组中,p38MAPK的表达无明显变化(P0.05),P-p38MAPK的表达在高温后8~48 h均明显高于相应时间点的正常组(P0.05),于16 h时表达增加最为显著(P0.01)。 结论 高温能促进p38MAPK蛋白激酶及其凋亡蛋白Bax的表达,诱发胚胎的细胞凋亡,导致神经管畸形的发生。
Objective To explore the molecular mechanism of p38 mitogen-activated protein kinase and Bax in the development of neural tube defects induced by hyperthermia. Methods Totally 72 pregnant golden hamsters were randomly divided into 2 groups
group 1 (normal control) and group 2 (hyperthermiainduced neural tube defects). Water bath at 37 or 42 ℃ for 20 min was respectively given to the hamsters of group 1 or group 2 at gestational day 8. The pregnant golden hamsters were sacrificed at 2
8
16
24
48
and 72 h after water bath (n=6 for each time point)
and the embryos were taken out for brain tissues. Changes in p38MAPK
P-p38MAPK and Bax expression were detected by Western blot analyses using special antibodies directed against p38MAPK and Bax. Results Bax was steadily expressed in control group at all time points. The expression was obviously increased in the hyperthermia group at 8 to 48 h after water bath
with a significant difference with the corresponding control groups (P0.05)
and the peak appeared at 8 and 16 h (P0.01). P-p38MAPK activity was increased compared with the control group in the hyperthermia group at 8 to 48 h (P0.05)
and the peak appeared at 16 h (P0.01). In contrast
the level of total p38MAPK was not changed in the whole course of experiment. Conclusion Hyperthermia may promote the expressions of p38MAPK and Bax during development
induce excessive apoptosis in embryo
and thereby result in the development of neural tube defects.
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