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Social rank-associated stress vulnerability predisposes individuals to cocaine attraction
Studies of personality have suggested that dissimilarities in ability to cope with stressful situations results in differing tendency to develop addictive behaviors. The present study used selectively bred stress-resilient, socially-dominant (Dom) and stress-vulnerable, socially-submissive (Sub) mic...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789078/ https://www.ncbi.nlm.nih.gov/pubmed/29379100 http://dx.doi.org/10.1038/s41598-018-19816-x |
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author | Yanovich, Chen Kirby, Michael L. Michaelevski, Izhak Yadid, Gal Pinhasov, Albert |
author_facet | Yanovich, Chen Kirby, Michael L. Michaelevski, Izhak Yadid, Gal Pinhasov, Albert |
author_sort | Yanovich, Chen |
collection | PubMed |
description | Studies of personality have suggested that dissimilarities in ability to cope with stressful situations results in differing tendency to develop addictive behaviors. The present study used selectively bred stress-resilient, socially-dominant (Dom) and stress-vulnerable, socially-submissive (Sub) mice to investigate the interaction between environmental stress and inbred predisposition to develop addictive behavior to cocaine. In a Conditioned Place Preference (CPP) paradigm using cocaine, Sub mice displayed an aversion to drug, whereas Dom mice displayed drug attraction. Following a 4-week regimen of Chronic Mild Stress (CMS), Sub mice in CPP displayed a marked increase (>400%) in cocaine attraction, whereas Dom mice did not differ in attraction from their non-stressed state. Examination of hippocampal gene expression revealed in Sub mice, exposure to external stimuli, stress or cocaine, increased CRH expression (>100%), which was evoked in Dom mice only by cocaine exposure. Further, stress-induced decreases in DRD1 (>60%) and DRD2 (>50%) expression in Sub mice differed markedly from a complete lack of change in Dom mice. From our findings, we propose that social stratification dictates vulnerability to stress-induced attraction that may lead to addiction via differential regulation of hippocampal response to dopaminergic input, which in turn may influence differing tendency to develop addictive behaviors. |
format | Online Article Text |
id | pubmed-5789078 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57890782018-02-08 Social rank-associated stress vulnerability predisposes individuals to cocaine attraction Yanovich, Chen Kirby, Michael L. Michaelevski, Izhak Yadid, Gal Pinhasov, Albert Sci Rep Article Studies of personality have suggested that dissimilarities in ability to cope with stressful situations results in differing tendency to develop addictive behaviors. The present study used selectively bred stress-resilient, socially-dominant (Dom) and stress-vulnerable, socially-submissive (Sub) mice to investigate the interaction between environmental stress and inbred predisposition to develop addictive behavior to cocaine. In a Conditioned Place Preference (CPP) paradigm using cocaine, Sub mice displayed an aversion to drug, whereas Dom mice displayed drug attraction. Following a 4-week regimen of Chronic Mild Stress (CMS), Sub mice in CPP displayed a marked increase (>400%) in cocaine attraction, whereas Dom mice did not differ in attraction from their non-stressed state. Examination of hippocampal gene expression revealed in Sub mice, exposure to external stimuli, stress or cocaine, increased CRH expression (>100%), which was evoked in Dom mice only by cocaine exposure. Further, stress-induced decreases in DRD1 (>60%) and DRD2 (>50%) expression in Sub mice differed markedly from a complete lack of change in Dom mice. From our findings, we propose that social stratification dictates vulnerability to stress-induced attraction that may lead to addiction via differential regulation of hippocampal response to dopaminergic input, which in turn may influence differing tendency to develop addictive behaviors. Nature Publishing Group UK 2018-01-29 /pmc/articles/PMC5789078/ /pubmed/29379100 http://dx.doi.org/10.1038/s41598-018-19816-x Text en © The Author(s) 2018 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 Yanovich, Chen Kirby, Michael L. Michaelevski, Izhak Yadid, Gal Pinhasov, Albert Social rank-associated stress vulnerability predisposes individuals to cocaine attraction |
title | Social rank-associated stress vulnerability predisposes individuals to cocaine attraction |
title_full | Social rank-associated stress vulnerability predisposes individuals to cocaine attraction |
title_fullStr | Social rank-associated stress vulnerability predisposes individuals to cocaine attraction |
title_full_unstemmed | Social rank-associated stress vulnerability predisposes individuals to cocaine attraction |
title_short | Social rank-associated stress vulnerability predisposes individuals to cocaine attraction |
title_sort | social rank-associated stress vulnerability predisposes individuals to cocaine attraction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5789078/ https://www.ncbi.nlm.nih.gov/pubmed/29379100 http://dx.doi.org/10.1038/s41598-018-19816-x |
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