SORA

Advancing, promoting and sharing knowledge of health through excellence in teaching, clinical practice and research into the prevention and treatment of illness

Environmental enrichment enhances ethanol preference over social reward in male swiss mice: Involvement of oxytocin-dopamine interactions.

Rae, M; Gomes, I; Spelta, LEW; Bailey, A; Marcourakis, T; Devi, L; Camarini, R (2024) Environmental enrichment enhances ethanol preference over social reward in male swiss mice: Involvement of oxytocin-dopamine interactions. Neuropharmacology, 253. p. 109971. ISSN 1873-7064 https://doi.org/10.1016/j.neuropharm.2024.109971
SGUL Authors: Bailey, Alexis

[img] PDF Accepted Version
Restricted to Repository staff only until 4 May 2025.
Available under License Creative Commons Attribution Non-commercial No Derivatives.

Download (13MB)

Abstract

The impact of environmental enrichment (EE) on natural rewards, including social and appetitive rewards, was investigated in male Swiss mice. EE, known for providing animals with various stimuli, was assessed for its effects on conditioned place preference (CPP) associated with ethanol and social stimuli. We previously demonstrated that EE increased the levels of the prosocial neuropeptide oxytocin (OT) in the hypothalamus and enhanced ethanol rewarding effects via an oxytocinergic mechanism. This study also investigated the impact of EE on social dominance and motivation for rewards, measured OT-mediated phospholipase C (PLC) activity in striatal membranes, and assessed OT expression in the hypothalamus. The role of dopamine in motivating rewards was considered, along with the interaction between OT and D1 receptors (DR) in the nucleus accumbens (NAc). Results showed that EE mice exhibited a preference for ethanol reward over social reward, a pattern replicated by the OT analogue Carbetocin. EE mice demonstrated increased social dominance and reduced motivation for appetitive taste stimuli. Higher OT mRNA levels in the hypothalamus were followed by diminished OT receptor (OTR) signaling activity in the striatum of EE mice. Additionally, EE mice displayed elevated D1R expression, which was attenuated by the OTR antagonist (L-368-889). The findings underscore the reinforcing effect of EE on ethanol and social rewards through an oxytocinergic mechanism. Nonetheless, they suggest that mechanisms other than the prosocial effect of EE may contribute to the ethanol pro-rewarding effect of EE and Carbetocin. They also point towards an OT-dopamine interaction potentially underlying some of these effects.

Item Type: Article
Additional Information: © 2024. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/
Keywords: Carbetocin, Motivation, Nucleus accumbens, Phospholipase C, Social dominance, Striatum, Carbetocin, Motivation, Nucleus accumbens, Phospholipase C, Social dominance, Striatum, 1109 Neurosciences, 1115 Pharmacology and Pharmaceutical Sciences, 1701 Psychology, Neurology & Neurosurgery
SGUL Research Institute / Research Centre: Academic Structure > Institute of Medical & Biomedical Education (IMBE)
Academic Structure > Institute of Medical & Biomedical Education (IMBE) > Centre for Biomedical Education (INMEBE)
Journal or Publication Title: Neuropharmacology
ISSN: 1873-7064
Language: eng
Dates:
DateEvent
5 May 2024Published
4 May 2024Published Online
25 April 2024Accepted
Publisher License: Creative Commons: Attribution-Noncommercial-No Derivative Works 4.0
Projects:
Project IDFunderFunder ID
2018/05038–0São Paulo Research FoundationUNSPECIFIED
2021/04816–1São Paulo Research FoundationUNSPECIFIED
408228/2016–4National Council for Scientific and Technological DevelopmentUNSPECIFIED
DA008863National Institutes of Healthhttp://dx.doi.org/10.13039/100000002
1R03TR003647-0National Institutes of Healthhttp://dx.doi.org/10.13039/100000002
PubMed ID: 38705568
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/116483
Publisher's version: https://doi.org/10.1016/j.neuropharm.2024.109971

Actions (login required)

Edit Item Edit Item