Evidence map›Paper›PMID 35367433›Full record

ArticleBrain research2022

Sex differences and the lack of effects of chemogenetic manipulation of pro-opiomelanocortin (POMC) neurons on alcohol consumption in male and female mice.

Jonna M Leyrer-Jackson, Lauren E Hood, M Foster Olive

Open access · greenAbstract read
In one paragraph

Article in Brain research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

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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

3 authors at 1 institution in 1 country.

Jonna M Leyrer-JacksonDepartment of Psychology, Arizona State University, Tempe, AZ 85281, USA. Electronic address: jmjack22@asu.edu.
Lauren E HoodDepartment of Psychology, Arizona State University, Tempe, AZ 85281, USA.
M Foster OliveDepartment of Psychology, Arizona State University, Tempe, AZ 85281, USA.
Arizona State University · US

Funding

Brain endorphin targets of low dose alcoholR01AA025590 · NIAAA · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI OLIVE, M. FOSTER · 2016 to 2020
$1.8M
The role of pro-opiomelanocortin neuronal circuitry in mediating ethanol consumptionF32AA027962 · NIAAA · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI JACKSON, JONNA M · 2019 to 2021
$195k
NIAAA NIH HHS F32 AA027962NIAAA NIH HHS R01 AA025590
6 · The paper itself

Abstract

The endogenous opioid system has been implicated in the rewarding and reinforcing effects of alcohol. Pro-opiomelanocortin (POMC) neurons located within the arcuate nucleus of the hypothalamus (ArcN) secrete multiple peptides associated with alcohol consumption, including β-endorphin (β-END), α-melanocyte stimulating hormone (α-MSH), and adrenocorticotropic hormone (ACTH). In this study, we utilized chemogenetics to bidirectionally modulate ArcN POMC neurons to determine their role in alcohol and saccharin consumption and regional levels of POMC-derived peptides. Male and female POMC-cre mice were infused with viral vectors designed for cre-dependent expression of either excitatory and inhibitory DREADDs or a control vector into the ArcN. Following recovery, animals were allowed to consume alcohol or saccharin using the drinking-in-the-dark (DID) paradigm of binge-like intake for 4 consecutive days. Prior to the final test session, animals were injected with clozapine-N-oxide (2.5 mg/kg, i.p.) for DREADD activation. Following the last DID session, animals were euthanized and the ArcN, VTA, amygdala and NAc were dissected and assessed for POMC peptide expression utilizing western blotting. We found that female mice consumed more alcohol than males during DID sessions 2-4, and that chemogenetic activation had no effect on alcohol or saccharin consumption in either sex. We found that β-END expression within the ArcN positively correlated with alcohol consumption. Given the molecular and functional heterogeneity of ArcN POMC neurons, future studies are needed to assess the effects of modulation of specific subpopulations of these neurons within the ArcN on consumption of rewarding substances such as alcohol and saccharin.

Indexed as

Pro-OpiomelanocortinSex CharacteristicsAlcohol DrinkingAnimalsbeta-EndorphinEthanolFemaleMaleMiceNeuronsSaccharinbeta-EndorphinEthanolPro-OpiomelanocortinSaccharinAdrenocorticotropic hormoneAlcoholChemogeneticsDrinking-in-the-darkPro-opiomelanocortinSaccharinα-melanocyte stimulating hormoneβ-endorphin

Identifiers

PMID35367433
PMCPMC9126074
OpenAlexW4220876243

What OpenQuestion holds

Textmetadata
LicenceTDM
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.