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Investigating the influence of perinatal nicotine exposure on genetic profiles of neurons in the sub-regions of the VTA
Chronic nicotine exposure during pregnancy has been shown to induce physiological and anatomical alterations in offspring. Previously, we investigated the complexity of dopamine (DA) neuron firing in the sub-regions of the ventral tegmental area (VTA) following perinatal nicotine exposure. Using app...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016121/ https://www.ncbi.nlm.nih.gov/pubmed/32051445 http://dx.doi.org/10.1038/s41598-020-59248-0 |
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author | Kazemi, Tina Avci, Naze G. Keller, Renee F. Akay, Yasemin M. Akay, Metin |
author_facet | Kazemi, Tina Avci, Naze G. Keller, Renee F. Akay, Yasemin M. Akay, Metin |
author_sort | Kazemi, Tina |
collection | PubMed |
description | Chronic nicotine exposure during pregnancy has been shown to induce physiological and anatomical alterations in offspring. Previously, we investigated the complexity of dopamine (DA) neuron firing in the sub-regions of the ventral tegmental area (VTA) following perinatal nicotine exposure. Using approximate entropy, we found that within the middle sub-region, the parainterfascicular nucleus (PIF), there was higher complexity indicating more random neural firing and a less homogeneous neuron population. Therefore, we sought to investigate the neuron populations within the sub-regions of the VTA following perinatal nicotine exposure. We used real time PCR in order to find the relative quantity of glutamate to γ-aminobutyric acid (GABA), DA, and glutamate neurons within three sub-regions: the parabrachial pigmented nucleus (PBP), parainterfascicular nucleus (PIF), and paranigral nucleus (PN). Our results showed that the PIF region of the VTA contained a more diverse population of neurons resulting in a more complex system. In addition, we found that DA neurons are more activated in PN sub-region of the VTA, which mediates the rewarding effects of drugs including nicotine. Lastly, using immunohistochemistry, we observed an overall decrease in DA neurons following perinatal nicotine exposure. |
format | Online Article Text |
id | pubmed-7016121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70161212020-02-21 Investigating the influence of perinatal nicotine exposure on genetic profiles of neurons in the sub-regions of the VTA Kazemi, Tina Avci, Naze G. Keller, Renee F. Akay, Yasemin M. Akay, Metin Sci Rep Article Chronic nicotine exposure during pregnancy has been shown to induce physiological and anatomical alterations in offspring. Previously, we investigated the complexity of dopamine (DA) neuron firing in the sub-regions of the ventral tegmental area (VTA) following perinatal nicotine exposure. Using approximate entropy, we found that within the middle sub-region, the parainterfascicular nucleus (PIF), there was higher complexity indicating more random neural firing and a less homogeneous neuron population. Therefore, we sought to investigate the neuron populations within the sub-regions of the VTA following perinatal nicotine exposure. We used real time PCR in order to find the relative quantity of glutamate to γ-aminobutyric acid (GABA), DA, and glutamate neurons within three sub-regions: the parabrachial pigmented nucleus (PBP), parainterfascicular nucleus (PIF), and paranigral nucleus (PN). Our results showed that the PIF region of the VTA contained a more diverse population of neurons resulting in a more complex system. In addition, we found that DA neurons are more activated in PN sub-region of the VTA, which mediates the rewarding effects of drugs including nicotine. Lastly, using immunohistochemistry, we observed an overall decrease in DA neurons following perinatal nicotine exposure. Nature Publishing Group UK 2020-02-12 /pmc/articles/PMC7016121/ /pubmed/32051445 http://dx.doi.org/10.1038/s41598-020-59248-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kazemi, Tina Avci, Naze G. Keller, Renee F. Akay, Yasemin M. Akay, Metin Investigating the influence of perinatal nicotine exposure on genetic profiles of neurons in the sub-regions of the VTA |
title | Investigating the influence of perinatal nicotine exposure on genetic profiles of neurons in the sub-regions of the VTA |
title_full | Investigating the influence of perinatal nicotine exposure on genetic profiles of neurons in the sub-regions of the VTA |
title_fullStr | Investigating the influence of perinatal nicotine exposure on genetic profiles of neurons in the sub-regions of the VTA |
title_full_unstemmed | Investigating the influence of perinatal nicotine exposure on genetic profiles of neurons in the sub-regions of the VTA |
title_short | Investigating the influence of perinatal nicotine exposure on genetic profiles of neurons in the sub-regions of the VTA |
title_sort | investigating the influence of perinatal nicotine exposure on genetic profiles of neurons in the sub-regions of the vta |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016121/ https://www.ncbi.nlm.nih.gov/pubmed/32051445 http://dx.doi.org/10.1038/s41598-020-59248-0 |
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