Cargando…

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

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-HT(2A)R) is involved in the effects of prenatal alcohol exp...

Descripción completa

Detalles Bibliográficos
Autores principales: Ji, Ming-li, Wu, Yun-hong, Qian, Zhi-bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4541240/
https://www.ncbi.nlm.nih.gov/pubmed/26330832
http://dx.doi.org/10.4103/1673-5374.160101
_version_ 1782386357516107776
author Ji, Ming-li
Wu, Yun-hong
Qian, Zhi-bin
author_facet Ji, Ming-li
Wu, Yun-hong
Qian, Zhi-bin
author_sort Ji, Ming-li
collection PubMed
description 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-HT(2A)R) 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-HT(2A)R 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-HT(2A)R protein and mRNA levels.
format Online
Article
Text
id pubmed-4541240
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Medknow Publications & Media Pvt Ltd
record_format MEDLINE/PubMed
spelling pubmed-45412402015-09-01 Neurotoxicity of prenatal alcohol exposure on medullary pre-Bötzinger complex neurons in neonatal rats Ji, Ming-li Wu, Yun-hong Qian, Zhi-bin Neural Regen Res Research Article 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-HT(2A)R) 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-HT(2A)R 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-HT(2A)R protein and mRNA levels. Medknow Publications & Media Pvt Ltd 2015-07 /pmc/articles/PMC4541240/ /pubmed/26330832 http://dx.doi.org/10.4103/1673-5374.160101 Text en Copyright: © Neural Regeneration Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ji, Ming-li
Wu, Yun-hong
Qian, Zhi-bin
Neurotoxicity of prenatal alcohol exposure on medullary pre-Bötzinger complex neurons in neonatal rats
title Neurotoxicity of prenatal alcohol exposure on medullary pre-Bötzinger complex neurons in neonatal rats
title_full Neurotoxicity of prenatal alcohol exposure on medullary pre-Bötzinger complex neurons in neonatal rats
title_fullStr Neurotoxicity of prenatal alcohol exposure on medullary pre-Bötzinger complex neurons in neonatal rats
title_full_unstemmed Neurotoxicity of prenatal alcohol exposure on medullary pre-Bötzinger complex neurons in neonatal rats
title_short Neurotoxicity of prenatal alcohol exposure on medullary pre-Bötzinger complex neurons in neonatal rats
title_sort neurotoxicity of prenatal alcohol exposure on medullary pre-bötzinger complex neurons in neonatal rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4541240/
https://www.ncbi.nlm.nih.gov/pubmed/26330832
http://dx.doi.org/10.4103/1673-5374.160101
work_keys_str_mv AT jimingli neurotoxicityofprenatalalcoholexposureonmedullaryprebotzingercomplexneuronsinneonatalrats
AT wuyunhong neurotoxicityofprenatalalcoholexposureonmedullaryprebotzingercomplexneuronsinneonatalrats
AT qianzhibin neurotoxicityofprenatalalcoholexposureonmedullaryprebotzingercomplexneuronsinneonatalrats