Evidence map›Paper›PMID 34702951›Full record

ArticleCommunications biology2021

Bmal1 in the striatum influences alcohol intake in a sexually dimorphic manner.

Nuria de Zavalia, Konrad Schoettner, Jory A Goldsmith, Pavel Solis, Sarah Ferraro, Gabrielle Parent, Shimon Amir

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Bmal1 Modulates Striatal cAMP Signaling and Motor Learning.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Review
  10. Core clock gene,Animal cells and systems · 2023
    Article
  11. Article
  12. Haploinsufficiency of a Circadian Clock GeneInternational journal of molecular sciences · 2022
    Article
  13. International journal of molecular sciences · 2022
    Article
  14. Article
  15. Article
  16. Article
  17. Frontiers in behavioral neuroscience · 2021
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Nuria de ZavaliaCenter for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, Canada. nuria.dezavalia@concordia.ca.ORCID 0000-0002-4865-7752
Konrad SchoettnerCenter for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, Canada.ORCID 0000-0001-5656-8170
Jory A GoldsmithCenter for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, Canada.
Pavel SolisCenter for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, Canada.
Sarah FerraroCenter for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, Canada.
Gabrielle ParentCenter for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, Canada.
Shimon AmirCenter for Studies in Behavioral Neurobiology, Department of Psychology, Concordia University, Montreal, Canada. shimon.amir@concordia.ca.ORCID 0000-0003-1919-5023
Concordia University · CA

Funding

CIHR
6 · The paper itself

Abstract

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.

Indexed as

Alcohol DrinkingAnimalsARNTL Transcription FactorsCorpus StriatumEthanolFemaleMaleMiceMice, KnockoutSex CharacteristicsARNTL Transcription FactorsBmal1 protein, mouseEthanol

Identifiers

PMID34702951
PMCPMC8548330
OpenAlexW3211185894

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.