Cargando…
Sex-differences in anxiety, neuroinflammatory markers, and enhanced fear learning following chronic heroin withdrawal
Post-traumatic stress disorder (PTSD) and opioid use disorder (OUD) are comorbid in clinical populations. However, both pre-clinical and clinical studies of these co-occurring disorders have disproportionately represented male subjects, limiting the applicability of these findings. Our previous work...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879843/ https://www.ncbi.nlm.nih.gov/pubmed/36633660 http://dx.doi.org/10.1007/s00213-023-06310-0 |
_version_ | 1784878777823657984 |
---|---|
author | Parekh, Shveta V. Adams, Lydia O. Barkell, Gillian A. Lysle, Donald T. |
author_facet | Parekh, Shveta V. Adams, Lydia O. Barkell, Gillian A. Lysle, Donald T. |
author_sort | Parekh, Shveta V. |
collection | PubMed |
description | Post-traumatic stress disorder (PTSD) and opioid use disorder (OUD) are comorbid in clinical populations. However, both pre-clinical and clinical studies of these co-occurring disorders have disproportionately represented male subjects, limiting the applicability of these findings. Our previous work has identified chronic escalating heroin administration and withdrawal can produce enhanced fear learning. This behavior is associated with an increase in dorsal hippocampal (DH) interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), and glial fibrillary acidic protein (GFAP) immunoreactivity. Further, we have shown that these increases in IL-1β and TNF-α are mechanistically necessary for the development of enhanced fear learning. Although these are exciting findings, this paradigm has only been studied in males. The current studies aim to examine sex differences in the behavioral and neuroimmune effects of chronic heroin withdrawal and future enhanced fear learning. In turn, we determined that chronic escalating heroin administration can produce withdrawal in female rats comparable to male rats. Subsequently, we examined the consequence of heroin withdrawal on future enhanced fear learning and IL-1β, TNF-α, and GFAP immunoreactivity. Strikingly, we identified sex differences in these neuroimmune measures, as chronic heroin administration and withdrawal does not produce enhanced fear learning or immunoreactivity changes in females. Moreover, we determined whether heroin withdrawal produces short-term and long-term anxiety behaviors in both female and males. Collectively, these novel experiments are the first to test whether heroin withdrawal can sensitize future fear learning, produce neurobiological changes, and cause short-term and long-term anxiety behaviors in female rats. |
format | Online Article Text |
id | pubmed-9879843 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-98798432023-01-28 Sex-differences in anxiety, neuroinflammatory markers, and enhanced fear learning following chronic heroin withdrawal Parekh, Shveta V. Adams, Lydia O. Barkell, Gillian A. Lysle, Donald T. Psychopharmacology (Berl) Original Investigation Post-traumatic stress disorder (PTSD) and opioid use disorder (OUD) are comorbid in clinical populations. However, both pre-clinical and clinical studies of these co-occurring disorders have disproportionately represented male subjects, limiting the applicability of these findings. Our previous work has identified chronic escalating heroin administration and withdrawal can produce enhanced fear learning. This behavior is associated with an increase in dorsal hippocampal (DH) interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α), and glial fibrillary acidic protein (GFAP) immunoreactivity. Further, we have shown that these increases in IL-1β and TNF-α are mechanistically necessary for the development of enhanced fear learning. Although these are exciting findings, this paradigm has only been studied in males. The current studies aim to examine sex differences in the behavioral and neuroimmune effects of chronic heroin withdrawal and future enhanced fear learning. In turn, we determined that chronic escalating heroin administration can produce withdrawal in female rats comparable to male rats. Subsequently, we examined the consequence of heroin withdrawal on future enhanced fear learning and IL-1β, TNF-α, and GFAP immunoreactivity. Strikingly, we identified sex differences in these neuroimmune measures, as chronic heroin administration and withdrawal does not produce enhanced fear learning or immunoreactivity changes in females. Moreover, we determined whether heroin withdrawal produces short-term and long-term anxiety behaviors in both female and males. Collectively, these novel experiments are the first to test whether heroin withdrawal can sensitize future fear learning, produce neurobiological changes, and cause short-term and long-term anxiety behaviors in female rats. Springer Berlin Heidelberg 2023-01-12 2023 /pmc/articles/PMC9879843/ /pubmed/36633660 http://dx.doi.org/10.1007/s00213-023-06310-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Investigation Parekh, Shveta V. Adams, Lydia O. Barkell, Gillian A. Lysle, Donald T. Sex-differences in anxiety, neuroinflammatory markers, and enhanced fear learning following chronic heroin withdrawal |
title | Sex-differences in anxiety, neuroinflammatory markers, and enhanced fear learning following chronic heroin withdrawal |
title_full | Sex-differences in anxiety, neuroinflammatory markers, and enhanced fear learning following chronic heroin withdrawal |
title_fullStr | Sex-differences in anxiety, neuroinflammatory markers, and enhanced fear learning following chronic heroin withdrawal |
title_full_unstemmed | Sex-differences in anxiety, neuroinflammatory markers, and enhanced fear learning following chronic heroin withdrawal |
title_short | Sex-differences in anxiety, neuroinflammatory markers, and enhanced fear learning following chronic heroin withdrawal |
title_sort | sex-differences in anxiety, neuroinflammatory markers, and enhanced fear learning following chronic heroin withdrawal |
topic | Original Investigation |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9879843/ https://www.ncbi.nlm.nih.gov/pubmed/36633660 http://dx.doi.org/10.1007/s00213-023-06310-0 |
work_keys_str_mv | AT parekhshvetav sexdifferencesinanxietyneuroinflammatorymarkersandenhancedfearlearningfollowingchronicheroinwithdrawal AT adamslydiao sexdifferencesinanxietyneuroinflammatorymarkersandenhancedfearlearningfollowingchronicheroinwithdrawal AT barkellgilliana sexdifferencesinanxietyneuroinflammatorymarkersandenhancedfearlearningfollowingchronicheroinwithdrawal AT lysledonaldt sexdifferencesinanxietyneuroinflammatorymarkersandenhancedfearlearningfollowingchronicheroinwithdrawal |