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产前酒精暴露对新生大鼠延髓前包钦格复合体神经元的神经毒性作用。

Neurotoxicity of prenatal alcohol exposure on medullary pre-Bötzinger complex neurons in neonatal rats.

作者信息

Ji Ming-Li, Wu Yun-Hong, Qian Zhi-Bin

机构信息

Department of Physiology, Xinxiang Medical University, Xinxiang, Henan Province, China.

Department of Functional Laboratory, Xinxiang Medical University, Xinxiang, Henan Province, China.

出版信息

Neural Regen Res. 2015 Jul;10(7):1095-100. doi: 10.4103/1673-5374.160101.

DOI:10.4103/1673-5374.160101
PMID:26330832
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4541240/
Abstract

Prenatal alcohol exposure disrupts the development of normal fetal respiratory function, but whether it perturbs respiratory rhythmical discharge activity is unclear. Furthermore, it is unknown whether the 5-hydroxytryptamine 2A receptor (5-HT2AR) is involved in the effects of prenatal alcohol exposure. In the present study, pregnant female rats received drinking water containing alcohol at concentrations of 0%, 1%, 2%, 4%, 8% or 10% (v/v) throughout the gestation period. Slices of the medulla from 2-day-old neonatal rats were obtained to record respiratory rhythmical discharge activity. 5-HT2AR protein and mRNA levels in the pre-Bötzinger complex of the respiratory center were measured by western blot analysis and quantitative RT-PCR, respectively. Compared with the 0% alcohol group, respiratory rhythmical discharge activity in medullary slices in the 4%, 8% and 10% alcohol groups was decreased, and the reduction was greatest in the 8% alcohol group. Respiratory rhythmical discharge activity in the 10% alcohol group was irregular. Thus, 8% was the most effective alcohol concentration at attenuating respiratory rhythmical discharge activity. These findings suggest that prenatal alcohol exposure attenuates respiratory rhythmical discharge activity in neonatal rats by downregulating 5-HT2AR protein and mRNA levels.

摘要

产前酒精暴露会干扰正常胎儿呼吸功能的发育,但它是否会扰乱呼吸节律性放电活动尚不清楚。此外,5-羟色胺2A受体(5-HT2AR)是否参与产前酒精暴露的影响也未知。在本研究中,怀孕的雌性大鼠在整个妊娠期饮用含0%、1%、2%、4%、8%或10%(v/v)酒精的饮用水。获取2日龄新生大鼠的延髓切片以记录呼吸节律性放电活动。分别通过蛋白质印迹分析和定量逆转录-聚合酶链反应测量呼吸中枢前包钦格复合体中5-HT2AR蛋白和mRNA水平。与0%酒精组相比,4%、8%和10%酒精组延髓切片中的呼吸节律性放电活动降低,且在8%酒精组中降低幅度最大。10%酒精组的呼吸节律性放电活动不规则。因此,8%是减弱呼吸节律性放电活动最有效的酒精浓度。这些发现表明,产前酒精暴露通过下调5-HT2AR蛋白和mRNA水平减弱新生大鼠的呼吸节律性放电活动。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fc7/4541240/9db4be5296d6/NRR-10-1095-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fc7/4541240/715a20e4599b/NRR-10-1095-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fc7/4541240/9b852a6a3e69/NRR-10-1095-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fc7/4541240/3342cd39f6b9/NRR-10-1095-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fc7/4541240/9db4be5296d6/NRR-10-1095-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fc7/4541240/715a20e4599b/NRR-10-1095-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fc7/4541240/9b852a6a3e69/NRR-10-1095-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fc7/4541240/3342cd39f6b9/NRR-10-1095-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fc7/4541240/9db4be5296d6/NRR-10-1095-g005.jpg

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