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Social learning promotes nicotine self-administration by facilitating the extinction of conditioned aversion in isogenic strains of rats
Both social environment and genetic factors are critical for smoking initiation and nicotine addiction. We reported that rats developed conditioned flavor (i.e., taste and odor) aversion to intravenously self-administered (IVSA) nicotine, and that social learning promoted nicotine IVSA with flavor c...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556091/ https://www.ncbi.nlm.nih.gov/pubmed/28808247 http://dx.doi.org/10.1038/s41598-017-08291-5 |
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author | Han, Wenyan Wang, Tengfei Chen, Hao |
author_facet | Han, Wenyan Wang, Tengfei Chen, Hao |
author_sort | Han, Wenyan |
collection | PubMed |
description | Both social environment and genetic factors are critical for smoking initiation and nicotine addiction. We reported that rats developed conditioned flavor (i.e., taste and odor) aversion to intravenously self-administered (IVSA) nicotine, and that social learning promoted nicotine IVSA with flavor cues. We thus tested the hypothesis that socially acquired nicotine IVSA is a heritable trait by using female rats of six inbred strains and six F1 hybrids. Each strain was tested for 10 daily IVSA sessions. We found that the intake of nicotine (15 and 30 μg/kg/inf) varied among these strains by 33.7–56.6-fold. The heritability of nicotine intake was estimated to be 0.54–0.65. Further, there was a strong correlation in nicotine intake (R(2) = 0.85, p < 0.0001) between the two nicotine doses. Another cohort of rats was given three daily IVSA sessions followed by five sessions that tested conditioned flavor aversion. Nicotine intake was highly correlated with the extinction of the conditioned aversion (R(2) = 0.58, p < 0.005). These data showed that nicotine intake in the socially acquired nicotine self-administration model is controlled by genetic factors and that the role of social learning is likely in facilitating the extinction of conditioned aversive response to nicotine. |
format | Online Article Text |
id | pubmed-5556091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55560912017-08-16 Social learning promotes nicotine self-administration by facilitating the extinction of conditioned aversion in isogenic strains of rats Han, Wenyan Wang, Tengfei Chen, Hao Sci Rep Article Both social environment and genetic factors are critical for smoking initiation and nicotine addiction. We reported that rats developed conditioned flavor (i.e., taste and odor) aversion to intravenously self-administered (IVSA) nicotine, and that social learning promoted nicotine IVSA with flavor cues. We thus tested the hypothesis that socially acquired nicotine IVSA is a heritable trait by using female rats of six inbred strains and six F1 hybrids. Each strain was tested for 10 daily IVSA sessions. We found that the intake of nicotine (15 and 30 μg/kg/inf) varied among these strains by 33.7–56.6-fold. The heritability of nicotine intake was estimated to be 0.54–0.65. Further, there was a strong correlation in nicotine intake (R(2) = 0.85, p < 0.0001) between the two nicotine doses. Another cohort of rats was given three daily IVSA sessions followed by five sessions that tested conditioned flavor aversion. Nicotine intake was highly correlated with the extinction of the conditioned aversion (R(2) = 0.58, p < 0.005). These data showed that nicotine intake in the socially acquired nicotine self-administration model is controlled by genetic factors and that the role of social learning is likely in facilitating the extinction of conditioned aversive response to nicotine. Nature Publishing Group UK 2017-08-14 /pmc/articles/PMC5556091/ /pubmed/28808247 http://dx.doi.org/10.1038/s41598-017-08291-5 Text en © The Author(s) 2017 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 Han, Wenyan Wang, Tengfei Chen, Hao Social learning promotes nicotine self-administration by facilitating the extinction of conditioned aversion in isogenic strains of rats |
title | Social learning promotes nicotine self-administration by facilitating the extinction of conditioned aversion in isogenic strains of rats |
title_full | Social learning promotes nicotine self-administration by facilitating the extinction of conditioned aversion in isogenic strains of rats |
title_fullStr | Social learning promotes nicotine self-administration by facilitating the extinction of conditioned aversion in isogenic strains of rats |
title_full_unstemmed | Social learning promotes nicotine self-administration by facilitating the extinction of conditioned aversion in isogenic strains of rats |
title_short | Social learning promotes nicotine self-administration by facilitating the extinction of conditioned aversion in isogenic strains of rats |
title_sort | social learning promotes nicotine self-administration by facilitating the extinction of conditioned aversion in isogenic strains of rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556091/ https://www.ncbi.nlm.nih.gov/pubmed/28808247 http://dx.doi.org/10.1038/s41598-017-08291-5 |
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