Evidence map›Paper›PMID 36175550›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2023

Overexpression of wild type glycine alpha 1 subunit rescues ethanol sensitivity in accumbal receptors and reduces binge drinking in mice.

Anibal Araya, Scarlet Gallegos, Adolfo Maldonado, Mario Rivera-Meza, Ramesh Chandra, Mary Kay Lobo, Luis G Aguayo

Open access · greenAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 46% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Review
  3. 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 3 institutions in 2 countries.

Anibal ArayaLaboratory of Neurophysiology, Department of Physiology, Universidad de Concepción, Concepcion, Chile.
Scarlet GallegosLaboratory of Neurophysiology, Department of Physiology, Universidad de Concepción, Concepcion, Chile.
Adolfo MaldonadoLaboratory of Experimental Pharmacology, Department of Pharmacological and Toxicological Chemistry, Faculty of Chemical Sciences and Pharmacy, Universidad de Chile, Santiago, Chile.
Mario Rivera-MezaLaboratory of Experimental Pharmacology, Department of Pharmacological and Toxicological Chemistry, Faculty of Chemical Sciences and Pharmacy, Universidad de Chile, Santiago, Chile.
Ramesh ChandraDepartment of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Mary Kay LoboDepartment of Anatomy and Neurobiology, University of Maryland School of Medicine, Baltimore, MD, USA.ORCID 0000-0002-9419-2079
Luis G AguayoLaboratory of Neurophysiology, Department of Physiology, Universidad de Concepción, Concepcion, Chile. laguayo@udec.cl.
University of Concepción · CLUniversity of Chile · CLUniversity of Maryland, Baltimore · US

Funding

Mechanisms for potentiation of glycine receptors by ethanol.R01AA025718 · NIAAA · UNIVERSITY OF CONCEPCION · PI AGUAYO, LUIS GERARDO · 2017 to 2021
$1.1M
NIAAA NIH HHS R01 AA025718
6 · The paper itself

Abstract

The nucleus accumbens (nAc) is a critical region in the brain reward system since it integrates abundant synaptic inputs contributing to the control of neuronal excitability in the circuit. The presence of inhibitory α1 glycine receptor (GlyRs) subunits, sensitive to ethanol, has been recently reported in accumbal neurons suggesting that they are protective against excessive binge consumption. In the present study, we used viral vectors (AAV) to overexpress mutant and WT α1 subunits in accumbal neurons in D1 Cre and α1 KI mice. Injection of a Cre-inducible AAV carrying an ethanol insensitive α1 subunit in D1 Cre neurons was unable to affect sensitivity to ethanol in GlyRs or affect ethanol drinking. On the other hand, using an AAV that transduced WT α1 GlyRs in GABAergic neurons in the nAc of high-ethanol consuming mice caused a reduction in ethanol intake as reflected by lowered drinking in the dark and reduced blood ethanol concentration. As expected, the AAV increased the glycine current density by 5-fold without changing the expression of GABA

Indexed as

Binge DrinkingGlycineAnimalsEthanolGABAergic NeuronsMiceNucleus AccumbensReceptors, GlycineEthanolGlra1 protein, mouseGlycineReceptors, Glycine

Identifiers

PMID36175550
PMCPMC10353986
OpenAlexW4297980387

What OpenQuestion holds

Textmetadata
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.