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Dopamine D(2) gene expression interacts with environmental enrichment to impact lifespan and behavior
Aging produces cellular, molecular, and behavioral changes affecting many areas of the brain. The dopamine (DA) system is known to be vulnerable to the effects of aging, which regulate behavioral functions such as locomotor activity, body weight, and reward and cognition. In particular, age-related...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991369/ https://www.ncbi.nlm.nih.gov/pubmed/26992232 http://dx.doi.org/10.18632/oncotarget.8088 |
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author | Thanos, Panayotis K. Hamilton, John O'Rourke, Joseph R. Napoli, Anthony Febo, Marcelo Volkow, Nora D. Blum, Kenneth Gold, Mark |
author_facet | Thanos, Panayotis K. Hamilton, John O'Rourke, Joseph R. Napoli, Anthony Febo, Marcelo Volkow, Nora D. Blum, Kenneth Gold, Mark |
author_sort | Thanos, Panayotis K. |
collection | PubMed |
description | Aging produces cellular, molecular, and behavioral changes affecting many areas of the brain. The dopamine (DA) system is known to be vulnerable to the effects of aging, which regulate behavioral functions such as locomotor activity, body weight, and reward and cognition. In particular, age-related DA D(2) receptor (D2R) changes have been of particular interest given its relationship with addiction and other rewarding behavioral properties. Male and female wild-type (Drd(2) +/+), heterozygous (Drd(2) +/−) and knockout (Drd(2) −/−) mice were reared post-weaning in either an enriched environment (EE) or a deprived environment (DE). Over the course of their lifespan, body weight and locomotor activity was assessed. While an EE was generally found to be correlated with longer lifespan, these increases were only found in mice with normal or decreased expression of the D(2) gene. Drd(2) +/+ EE mice lived nearly 16% longer than their DE counterparts. Drd(2) +/+ and Drd(2) +/− EE mice lived 22% and 21% longer than Drd(2) −/− EE mice, respectively. Moreover, both body weight and locomotor activity were moderated by environmental factors. In addition, EE mice show greater behavioral variability between genotypes compared to DE mice with respect to body weight and locomotor activity. |
format | Online Article Text |
id | pubmed-4991369 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-49913692016-09-01 Dopamine D(2) gene expression interacts with environmental enrichment to impact lifespan and behavior Thanos, Panayotis K. Hamilton, John O'Rourke, Joseph R. Napoli, Anthony Febo, Marcelo Volkow, Nora D. Blum, Kenneth Gold, Mark Oncotarget Research Paper: Gerotarget (Focus on Aging) Aging produces cellular, molecular, and behavioral changes affecting many areas of the brain. The dopamine (DA) system is known to be vulnerable to the effects of aging, which regulate behavioral functions such as locomotor activity, body weight, and reward and cognition. In particular, age-related DA D(2) receptor (D2R) changes have been of particular interest given its relationship with addiction and other rewarding behavioral properties. Male and female wild-type (Drd(2) +/+), heterozygous (Drd(2) +/−) and knockout (Drd(2) −/−) mice were reared post-weaning in either an enriched environment (EE) or a deprived environment (DE). Over the course of their lifespan, body weight and locomotor activity was assessed. While an EE was generally found to be correlated with longer lifespan, these increases were only found in mice with normal or decreased expression of the D(2) gene. Drd(2) +/+ EE mice lived nearly 16% longer than their DE counterparts. Drd(2) +/+ and Drd(2) +/− EE mice lived 22% and 21% longer than Drd(2) −/− EE mice, respectively. Moreover, both body weight and locomotor activity were moderated by environmental factors. In addition, EE mice show greater behavioral variability between genotypes compared to DE mice with respect to body weight and locomotor activity. Impact Journals LLC 2016-03-15 /pmc/articles/PMC4991369/ /pubmed/26992232 http://dx.doi.org/10.18632/oncotarget.8088 Text en Copyright: © 2016 Thanos et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper: Gerotarget (Focus on Aging) Thanos, Panayotis K. Hamilton, John O'Rourke, Joseph R. Napoli, Anthony Febo, Marcelo Volkow, Nora D. Blum, Kenneth Gold, Mark Dopamine D(2) gene expression interacts with environmental enrichment to impact lifespan and behavior |
title | Dopamine D(2) gene expression interacts with environmental enrichment to impact lifespan and behavior |
title_full | Dopamine D(2) gene expression interacts with environmental enrichment to impact lifespan and behavior |
title_fullStr | Dopamine D(2) gene expression interacts with environmental enrichment to impact lifespan and behavior |
title_full_unstemmed | Dopamine D(2) gene expression interacts with environmental enrichment to impact lifespan and behavior |
title_short | Dopamine D(2) gene expression interacts with environmental enrichment to impact lifespan and behavior |
title_sort | dopamine d(2) gene expression interacts with environmental enrichment to impact lifespan and behavior |
topic | Research Paper: Gerotarget (Focus on Aging) |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4991369/ https://www.ncbi.nlm.nih.gov/pubmed/26992232 http://dx.doi.org/10.18632/oncotarget.8088 |
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