Cargando…
Insidious Transmission of a Stress-Related Neuroadaptation
Stress is highly pervasive in humans, impacting motivated behaviors with an enormous toll on life quality. Many of the effects of stress are orchestrated by neuropeptides such as corticotropin-releasing factor (CRF). It has previously been shown that in stress-naïve male mice, CRF acts in the core o...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7571264/ https://www.ncbi.nlm.nih.gov/pubmed/33132859 http://dx.doi.org/10.3389/fnbeh.2020.564054 |
_version_ | 1783597136447799296 |
---|---|
author | Steger, Jennifer S. Land, Benjamin B. Lemos, Julia C. Chavkin, Charles Phillips, Paul E. M. |
author_facet | Steger, Jennifer S. Land, Benjamin B. Lemos, Julia C. Chavkin, Charles Phillips, Paul E. M. |
author_sort | Steger, Jennifer S. |
collection | PubMed |
description | Stress is highly pervasive in humans, impacting motivated behaviors with an enormous toll on life quality. Many of the effects of stress are orchestrated by neuropeptides such as corticotropin-releasing factor (CRF). It has previously been shown that in stress-naïve male mice, CRF acts in the core of the nucleus accumbens (NAc) to produce appetitive effects and to increase dopamine release; yet in stress-exposed male mice, CRF loses its capacity to modulate NAc dopamine release and is aversive. In the current research, we tested whether this effect is comparable in females to males and whether the neuroadaptation is susceptible to social transmission. We found that, like in males, CRF increased dopamine release in stress-naïve but not stress-exposed female mice. Importantly, this persistent physiological change was not accompanied by overt behavioral changes that would be indicative of depression- or anxiety-like phenotype. Nonetheless, when these mice were housed for 7 days with stress-naïve conspecifics, the cage mates also exhibited a loss of dopamine potentiation by CRF. These data demonstrate the asymptomatic, yet pervasive transmission of stress-related neuroadaptations in the population. |
format | Online Article Text |
id | pubmed-7571264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75712642020-10-30 Insidious Transmission of a Stress-Related Neuroadaptation Steger, Jennifer S. Land, Benjamin B. Lemos, Julia C. Chavkin, Charles Phillips, Paul E. M. Front Behav Neurosci Behavioral Neuroscience Stress is highly pervasive in humans, impacting motivated behaviors with an enormous toll on life quality. Many of the effects of stress are orchestrated by neuropeptides such as corticotropin-releasing factor (CRF). It has previously been shown that in stress-naïve male mice, CRF acts in the core of the nucleus accumbens (NAc) to produce appetitive effects and to increase dopamine release; yet in stress-exposed male mice, CRF loses its capacity to modulate NAc dopamine release and is aversive. In the current research, we tested whether this effect is comparable in females to males and whether the neuroadaptation is susceptible to social transmission. We found that, like in males, CRF increased dopamine release in stress-naïve but not stress-exposed female mice. Importantly, this persistent physiological change was not accompanied by overt behavioral changes that would be indicative of depression- or anxiety-like phenotype. Nonetheless, when these mice were housed for 7 days with stress-naïve conspecifics, the cage mates also exhibited a loss of dopamine potentiation by CRF. These data demonstrate the asymptomatic, yet pervasive transmission of stress-related neuroadaptations in the population. Frontiers Media S.A. 2020-10-05 /pmc/articles/PMC7571264/ /pubmed/33132859 http://dx.doi.org/10.3389/fnbeh.2020.564054 Text en Copyright © 2020 Steger, Land, Lemos, Chavkin and Phillips. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Behavioral Neuroscience Steger, Jennifer S. Land, Benjamin B. Lemos, Julia C. Chavkin, Charles Phillips, Paul E. M. Insidious Transmission of a Stress-Related Neuroadaptation |
title | Insidious Transmission of a Stress-Related Neuroadaptation |
title_full | Insidious Transmission of a Stress-Related Neuroadaptation |
title_fullStr | Insidious Transmission of a Stress-Related Neuroadaptation |
title_full_unstemmed | Insidious Transmission of a Stress-Related Neuroadaptation |
title_short | Insidious Transmission of a Stress-Related Neuroadaptation |
title_sort | insidious transmission of a stress-related neuroadaptation |
topic | Behavioral Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7571264/ https://www.ncbi.nlm.nih.gov/pubmed/33132859 http://dx.doi.org/10.3389/fnbeh.2020.564054 |
work_keys_str_mv | AT stegerjennifers insidioustransmissionofastressrelatedneuroadaptation AT landbenjaminb insidioustransmissionofastressrelatedneuroadaptation AT lemosjuliac insidioustransmissionofastressrelatedneuroadaptation AT chavkincharles insidioustransmissionofastressrelatedneuroadaptation AT phillipspaulem insidioustransmissionofastressrelatedneuroadaptation |