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Published on: November 6, 2018
Morphine reduces the interest for natural rewards
Alessandro Piccin1,2, Gilles Courtand1,2, Angelo Contarino3,4
1Université de Bordeaux, INCIA, UMR 5287, Bordeaux, France.
Opioid use disorder (OUD) in mice shows reduced interest in social interaction and food. Both rewarding and non-rewarding morphine doses decreased motivation for natural rewards, suggesting brain reward systems are sensitive to drug effects.
Area of Science:
- Neuroscience
- Pharmacology
- Addiction Research
Background:
- Substance use disorder (SUD) is characterized by excessive motivation for drugs and reduced interest in natural rewards.
- Pre-clinical evidence for these SUD features, particularly anhedonia, is limited and inconsistent.
Purpose of the Study:
- Investigate the effects of rewarding and non-rewarding morphine doses on social behavior, food motivation, and intake in male and female mice.
- Assess sex differences in response to morphine's rewarding and anhedonic effects.
Main Methods:
- Conditioned place preference (CPP) assessed rewarding effects of morphine (1.25 and 2.5 mg/kg).
- Three-chamber social interaction test, operant behavior for food motivation, and palatable food preference tests evaluated social behavior and anhedonia.
- Effects were examined independently of cognitive function and locomotor activity.
Main Results:
- Morphine (2.5 mg/kg) induced CPP in both sexes; 1.25 mg/kg induced CPP only in females.
- Both morphine doses reduced sociability, food motivation, and intake in male and female mice.
- These effects were independent of cognitive function or locomotor activity.
Conclusions:
- Female mice exhibit higher sensitivity to morphine's rewarding effects compared to males.
- Both rewarding and non-rewarding morphine doses impair motivation for natural rewards, suggesting heightened sensitivity of reward systems to drug-induced deficits.
- Findings highlight the complex impact of opioids on reward pathways and potential sex differences in addiction vulnerability.
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