Keyword search (4,163 papers available)

"Schoettner K" Authored Publications:

Title Authors PubMed ID
1 Effects of chronodisruption and alcohol consumption on gene expression in reward-related brain areas in female rats Meyer C; Schoettner K; Amir S; 39624490
PSYCHOLOGY
2 The effects of circadian desynchronization on alcohol consumption and affective behavior during alcohol abstinence in female rats Meyer C; Schoettner K; Amir S; 36620855
CSBN
3 Characterization of Affective Behaviors and Motor Functions in Mice With a Striatal-Specific Deletion of Bmal1 and Per2 Schoettner K; Alonso M; Button M; Goldfarb C; Herrera J; Quteishat N; Meyer C; Bergdahl A; Amir S; 35755440
HKAP
4 Bmal1 in the striatum influences alcohol intake in a sexually dimorphic manner de Zavalia N; Schoettner K; Goldsmith JA; Solis P; Ferraro S; Parent G; Amir S; 34702951
PSYCHOLOGY

 

Title:Bmal1 in the striatum influences alcohol intake in a sexually dimorphic manner
Authors:de Zavalia NSchoettner KGoldsmith JASolis PFerraro SParent GAmir S
Link:https://pubmed.ncbi.nlm.nih.gov/34702951/
DOI:10.1038/s42003-021-02715-9
Publication:Communications biology
Keywords:
PMID:34702951 Category: Date Added:2021-10-27
Dept Affiliation: PSYCHOLOGY
1 Center for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, Canada. nuria.dezavalia@concordia.ca.
2 Center for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, Canada.
3 Center for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, Canada. shimon.amir@concordia.ca.

Description:

Alcohol consumption has been strongly associated with circadian clock gene expression in mammals. Analysis of clock genes revealed a potential role of Bmal1 in the control of alcohol drinking behavior. However, a causal role of Bmal1 and neural pathways through which it may influence alcohol intake have not yet been established. Here we show that selective ablation of Bmal1 (Cre/loxP system) from medium spiny neurons of the striatum induces sexual dimorphic alterations in alcohol consumption in mice, resulting in augmentation of voluntary alcohol intake in males and repression of intake in females. Per2mRNA expression, quantified by qPCR, decreases in the striatum after the deletion of Bmal1. To address the possibility that the effect of striatal Bmal1 deletion on alcohol intake and preference involves changes in the local expression of Per2, voluntary alcohol intake (two-bottle, free-choice paradigm) was studied in mice with a selective ablation of Per2 from medium spiny neurons of the striatum. Striatal ablation of Per2 increases voluntary alcohol intake in males but has no effect in females. Striatal Bmal1 and Per2 expression thus may contribute to the propensity to consume alcohol in a sex -specific manner in mice.





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