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产前接触 1-溴丙烷会导致仔鼠海马 CA1 亚区神经元兴奋性延迟性不良反应。

Prenatal exposure to 1-bromopropane causes delayed adverse effects on hippocampal neuronal excitability in the CA1 subfield of rat offspring.

机构信息

Department of Environmental Management and Control, School of Health Sciences, University of Occupational and Environmental Health.

Department of Occupational Toxicology, University of Occupational and Environmental Health.

出版信息

J Occup Health. 2018 Jan 25;60(1):74-79. doi: 10.1539/joh.17-0009-BR. Epub 2017 Nov 1.

DOI:10.1539/joh.17-0009-BR
PMID:29093363
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5799103/
Abstract

OBJECTIVES

Neurotoxicity of 1-bromopropane (1-BP) has been reported in occupational exposure, but whether the chemical exerts developmental neurotoxicity is unknown. We studied the effects of prenatal 1-BP exposure on neuronal excitability in rat offspring.

METHODS

We exposed dams to 1-BP (700 ppm, 6 h a day for 20 days) and examined hippocampal slices obtained from the male offspring at 2, 5, 8, and 13 weeks of age. We measured the stimulation/response (S/R) relationship and paired-pulse ratios (PPRs) of the population spike (PS) at the interpulse intervals (IPIs) of 5 and 10 ms in the CA1 subfield.

RESULTS

Prenatal 1-BP exposure enhanced S/R relationships of PS at 2 weeks of age; however, the enhancement diminished at 5 weeks of age until it reached control levels. Prenatal 1-BP exposure decreased PPRs of PS at 2 weeks of age. After sexual maturation, however, the PPRs of PS increased at 5-ms IPI in rats aged 8 and 13 weeks.

CONCLUSIONS

Our findings indicate that prenatal 1-BP exposure in dams can cause delayed adverse effects on excitability of pyramidal cells in the hippocampal CA1 subfield of offspring.

摘要

目的

1-溴丙烷(1-BP)在职业暴露中已被报道具有神经毒性,但该化学物质是否具有发育神经毒性尚不清楚。我们研究了产前 1-BP 暴露对大鼠后代神经元兴奋性的影响。

方法

我们使孕鼠暴露于 1-BP(700 ppm,每天 6 小时,共 20 天),并检测雄性后代在 2、5、8 和 13 周龄时获得的海马脑片。我们测量了 CA1 亚区在 5 和 10 ms 内的两个脉冲间隔(IPI)时的群体峰(PS)的刺激/反应(S/R)关系和成对脉冲比(PPR)。

结果

产前 1-BP 暴露增强了 2 周龄时 PS 的 S/R 关系;然而,这种增强在 5 周龄时减弱,直到达到对照水平。产前 1-BP 暴露降低了 2 周龄时 PS 的 PPR。然而,在性成熟后,8 周和 13 周龄大鼠的 5 ms IPI 时 PS 的 PPR 增加。

结论

我们的研究结果表明,母体产前 1-BP 暴露可导致后代海马 CA1 亚区锥体神经元兴奋性出现延迟性不良反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e0/5799103/e1070cf3869d/1348-9585-60-74-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e0/5799103/8555d11e518d/1348-9585-60-74-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e0/5799103/e1070cf3869d/1348-9585-60-74-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e0/5799103/8555d11e518d/1348-9585-60-74-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17e0/5799103/e1070cf3869d/1348-9585-60-74-g002.jpg

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