Back to Search
Start Over
Corticotropin releasing hormone receptor 1 in the medial prefrontal cortex mediates aversion resistant alcohol intake.
- Source :
-
Psychopharmacology [Psychopharmacology (Berl)] 2024 Dec; Vol. 241 (12), pp. 2539-2550. Date of Electronic Publication: 2024 Oct 28. - Publication Year :
- 2024
-
Abstract
- Rationale: Alcohol consumption despite negative consequences is a core symptom of Alcohol Use Disorder. In animal models, this is studied by pairing aversive stimuli with alcohol access, and continuation of drinking under these conditions is known as aversion resistance. Previously, we found that female mice are more aversion resistant than males. Corticotropin releasing hormone (Crh) and the Crh receptor 1 (Crhr1) regulate stress-induced reinstatement, alcohol dependence, and binge-like drinking. However, the role of the Crh system in aversion resistance has not been assessed.<br />Objectives: We aimed to identify sex differences in the Crh system during quinine-adulterated alcohol intake.<br />Methods: We used two-bottle choice and adulterated the alcohol solution with quinine. Next, we measured Crh and Crhr1 levels in brain tissue using real-time polymerase chain reaction (RT-qPCR) and RNAscope in situ hybridization. We then infused a Crhr1 antagonist into the medial prefrontal cortex (mPFC) prior to quinine-alcohol intake.<br />Results: After quinine-alcohol consumption, females exhibited increased mPFC Crhr1 mRNA levels as measured by RT-qPCR. This was confirmed with greater anatomical specificity using RNAscope, with females exhibiting an increased number of Crhr1 + cells in the dorsomedial PFC and the ventromedial PFC. mPFC Crhr1 antagonist treatment reduced quinine-alcohol consumption in females but did not impact consumption in males. Quinine-free alcohol intake was unaffected by Crhr1 antagonist treatment.<br />Conclusions: Our findings suggest that Crhr1 in mPFC plays a role in aversion resistant alcohol intake in females. Future experiments will examine the sources of Crh innervation to the mPFC and their distinct roles in alcohol seeking.<br />Competing Interests: Declarations Conflict of interest On behalf of all authors, the corresponding author states that there is no conflict of interest.<br /> (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
- Subjects :
- Animals
Male
Female
Mice
Ethanol administration & dosage
Ethanol pharmacology
Sex Factors
Receptors, Corticotropin-Releasing Hormone metabolism
Prefrontal Cortex metabolism
Prefrontal Cortex drug effects
Alcohol Drinking metabolism
Corticotropin-Releasing Hormone metabolism
Mice, Inbred C57BL
Quinine pharmacology
Quinine administration & dosage
Subjects
Details
- Language :
- English
- ISSN :
- 1432-2072
- Volume :
- 241
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Psychopharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 39466414
- Full Text :
- https://doi.org/10.1007/s00213-024-06707-5