期刊文献+

孕哺期双酚A暴露对雄性仔鼠海马即早基因表达的影响

Effects of Exposure to Bisphenol A on the Expression of Immediate Early Genes in the Hippocampus of Male Offspring Rats
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摘要 目的探讨孕哺期双酚A暴露对雄性仔鼠海马即早基因c-fos、c-jun、egr-1和Arc表达的影响。方法低、中、高剂量双酚A组孕鼠分别灌胃染毒2mg/kg、10mg/kg、50mg/kg双酚A,对照组孕鼠用同体积的玉米油灌胃,至哺乳期结束,检测雄性仔鼠的学习记忆能力以及海马c-los、c-jun、egr-1和Arc水平。结果双酚A组雄性仔鼠在水迷宫中的逃离潜伏期明显高于对照组,海马c-los、c-jun和egr-1水平显著低于对照组,具有一定的剂量一反应关系。结论孕哺期双酚A暴露损害雄性仔鼠学习记忆能力的机制可能与海马c-fos、c-jull和egr-1表达降低有关。 Objective To study the effects of exposure to bisphenol A (BPA) on the expression of immediate early genes including c-fos, c-jun, egr-1 and Arc in the hippocampus of male offspring rats. Methods Low-, middle-, and high- dose BPA groups were administrated with 2, 10, 50 mg/kg BPA, respectively, and control group was given to corn oil of same volume by gavage during prenancy and lactation. Learning, memory and c-fos, c-jun, egr-1 and Arc expression were measured. Results Escape latency of BPA groups in the water maze test were higher significantly than that of control group, and c-fos, c-jun and egr-1 expression levels in the hippocampus of BPA groups were lower significantly than those of control group, presenting dose-effect relationship. Conclusion Exposure to BPA injured learning and memory of male offsprings rats, which was associated with low levels of c-fos, c-jun and egr-1 in the hippocampus.
出处 《中国实用乡村医生杂志》 2012年第4期33-36,共4页 Chinese Practical Journal of Rural Doctor
关键词 双酚A·海马 即早基因 表达 Bisphenol A hippocampus immediate early genes
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参考文献8

  • 1Masuo Y, Ishido M. Neurotoxicity of endocrine disruptors: possible involvement in brain development and neurodegeneration[J]. J Toxicol Environ Health B Crit Rev, 2011, 14(5-7): 346-369.
  • 2Wolstenholme JT, Rissman EF, Connelly JJ. The role of Bisphenol A in shaping the brain, epigenome and behavior[J]. Horm Behav, 2011, 59(3): 296-305.
  • 3Xu XH, Zhang J, Wang YM, et al. Perinatal exposure to bisphenol-A impairs learning-memory by concomitant down-regulation of N-methyl-D-aspartate receptors of hippocampus in male offspring mice[J]. Horm Behav, 2010, 58(2): 326-333.
  • 4Kubik S, Miyashita T, Guzowski JF. Using immediateearly genes to map hippocampal subregional functions[J]. Learning and Memory, 2007, 14(11): 758-770.
  • 5Kim K, Son TG, Park HR, et al. Potencies of bisphenol A on the neuronal differentiation and hippocampal neurogenesis[J]. J Toxicol Environ Health A, 2009, 72(21-22): 1343-1351.
  • 6Xu X, Tian D, Hong X, ct al. Sex-specific influence of exposure to bisphonol-A between adolescence and young adulthood on mouse behaviors[J]. Neuropharmacology, 2011, 61(4): 565-573.
  • 7Miyamoto E. Molecular mechanism of neuronal plasticity: induction and maintenance of long-term potentiation in the hippocampus[J]. Pharmacol Sci, 2006, 100(5): 433-442.
  • 8Jones MW, Errington ML, French PJ, otal. A requirement for the immcdiato oarly gone Zif268 in the expression of late LTP and the consolidation of long-term memories[J]. Nature Ncurosci, 2001, 4(3): 289-296.

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