Abstract
Genetically-selected Marchigian Sardinian alcohol-preferring (msP) rats display comorbid symptoms of increased alcohol preference and elevated anxiety-like behavior. Heightened stress sensitivity in msPs is influenced by genetic polymorphisms of the corticotropin-releasing factor receptor in the central nucleus of the amygdala (CeA), as well as reduced influence of anti-stress mechanisms that normally constrain the stress response. Given this propensity for stress dysregulation, in this study, we expand on the possibility that msPs may display differences in neuroendocrine processes that normally terminate the stress response. We utilized behavioral, biochemical, and molecular assays to compare basal and restraint stress-induced changes in the hypothalamic–pituitary–adrenal (HPA) axis of male and female msPs relative to their nonselected Wistar counterparts. The results showed that msPs display deficits in marble-burying behavior influenced by environmental factors and procedures that modulate arousal states in a sex-dependent manner. Whereas male msPs display evidence of dysregulated neuroendocrine function (higher adrenocorticotropic hormone levels and subthreshold reductions in corticosterone), females display restraint-induced elevations in corticosterone levels that were persistently higher in msPs. A dexamethasone challenge reduced the circulation of these stress hormones, although the reduction in corticosterone was generally attenuated in msP versus Wistar rats. Finally, we found evidence of diminished stress-induced glucocorticoid receptor (GR) phosphorylation in the hypothalamic paraventricular nucleus of msPs, as well as innate increases in phosphorylated GR levels in the CeA of male msPs. Collectively, these findings suggest that negative feedback processes regulating HPA responsiveness are diminished in msP rats, possibly underlying differences in the expression of anxiety-like behaviors.
| Original language | English |
|---|---|
| Article number | e12978 |
| Journal | Addiction Biology |
| Volume | 26 |
| Issue number | 3 |
| DOIs | |
| State | Published - May 2021 |
Bibliographical note
Publisher Copyright:© 2020 Society for the Study of Addiction
Funding
We are grateful for the support provided by the National Institute on Alcohol Abuse and Alcoholism via the following mechanisms: R37‐AA017447, R01‐AA015566, P60‐AA006420, AA027700, AA021491, AA013498, K99/R00‐AA025393, R01‐AA025996, T32‐AA007456, and the Pearson Center for Alcoholism and Addiction Research. This is Scripps manuscript number 30002. We sincerely appreciate the technical assistance from Caleigh Hasenfluck and Delaney Gaither for the behavioral analyses. We are grateful for the support provided by the National Institute on Alcohol Abuse and Alcoholism via the following mechanisms: R37-AA017447, R01-AA015566, P60-AA006420, AA027700, AA021491, AA013498, K99/R00-AA025393, R01-AA025996, T32-AA007456, and the Pearson Center for Alcoholism and Addiction Research. This is Scripps manuscript number 30002. We sincerely appreciate the technical assistance from Caleigh Hasenfluck and Delaney Gaither for the behavioral analyses.
| Funders | Funder number |
|---|---|
| Pearson Center for Alcoholism and Addiction Research | 30002 |
| National Institute on Alcohol Abuse and Alcoholism | R37‐AA017447, R01‐AA025996, AA013498, AA027700, P60‐AA006420, T32‐AA007456, AA021491, R01‐AA015566, K99AA025393 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- HPA axis
- corticosterone
- phosphorylation
ASJC Scopus subject areas
- Medicine (miscellaneous)
- Pharmacology
- Psychiatry and Mental health
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