Evidence map›Paper›PMID 28550509›Full record

ArticleJournal of neural transmission (Vienna, Austria : 1996)2017

Possible involvement of ACSS2 gene in alcoholism.

Andrea Frozino Ribeiro, Roseli Boerngen de Lacerda, Diego Correia, Ana Lúcia Brunialti-Godard, Débora Marques de Miranda, Valdir Ribeiro Campos, Valéria Fernandes de Souza, Angela Maria Ribeiro

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neural transmission (Vienna, Austria : 1996), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 57% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
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

8 authors at 2 institutions in 1 country.

Andrea Frozino RibeiroPontifícia Universidade Católica de Minas Gerais, R. do Rosário, 1081, Bairro Angola, Betim, MG, CEP 32604-115, Brazil. andreafron@gmail.com.
Roseli Boerngen de LacerdaDepartment of Pharmacology, Universidade Federal do Paraná, Jardim das Américas, Curitiba, PR, CEP 81531-990, Brazil.
Diego CorreiaDepartment of Pharmacology, Universidade Federal do Paraná, Jardim das Américas, Curitiba, PR, CEP 81531-990, Brazil.
Ana Lúcia Brunialti-GodardDepartment of Geral Biology, Universidade Federal de Minas Gerais, Belo Horizonte, MG, CEP 31270-901, Brazil.
Débora Marques de MirandaDepartment of Pediatric, Faculty of Medicine, Universidade Federal de Minas Gerais, Pampulha, Belo Horizonte, MG, CEP 30130-100, Brazil.
Valdir Ribeiro CamposDepartment of Psychiatry and Neurology, Faculty of Medicine, Universidade Federal de Minas Gerais, Pampulha, Belo Horizonte, MG, CEP 30130-100, Brazil.
Valéria Fernandes de SouzaDepartment of Biochemistry and Immunology, Universidade Federal de Minas Gerais, Pampulha, Belo Horizonte, MG, CEP 31270-901, Brazil.
Angela Maria RibeiroDepartment of Biochemistry and Immunology, Universidade Federal de Minas Gerais, Pampulha, Belo Horizonte, MG, CEP 31270-901, Brazil.
Universidade Federal de Minas Gerais · BRUniversidade Federal do Paraná · BR

Funding

FAPEMIG APQ-00179-08
6 · The paper itself

Abstract

Alcoholism is a psychiatric disorder that composes one of the principal causes of health disabilities in the world population. Furthermore, the available pharmacotherapy is limited. Therefore, this research was carried out to better understand the basis of the underlying neurobiological processes of this disorder and to discover potential therapeutic targets. Real-time PCR analysis was performed in the amygdala nuclei region of the brain of mice exposed to a chronic three-bottle free-choice model (water, 5 and 10% v/v ethanol). Based on individual ethanol intake, the mice were classified into three groups: "compulsive-like" (i.e., ethanol intake not affected by quinine adulteration), "ethanol-preferring" and "ethanol non-preferring". A fourth group had access only to tap water (control group). The candidate gene ACSS2 was genotyped in human alcoholics by real-time polymerase chain reaction using the markers rs6088638 and rs7266550. Seven genes were picked out (Acss2, Acss3, Acat1, Acsl1, Acaa2, Hadh, and Hadhb) and the mRNA level of the Acss2 gene was increased only in the "compulsive-like" group (p = 0.004). The allele frequency of rs6088638 for the gene ACSS2 was higher in the Alcoholic human group (p = 0.03), although sample size was very small. The gene ACSS2 is associated with alcoholism, suggesting that biochemical pathways where it participates may have a role in the biological mechanisms susceptible to the ethanol effects.

Indexed as

Acetate-CoA LigaseAdultAlcoholismAnimalsCentral Nervous System DepressantsChoice BehaviorCompulsive BehaviorDisease Models, AnimalEthanolFemaleGene FrequencyHumansMaleMicePolymorphism, Single NucleotideRNA, MessengerAcetate-CoA LigaseACSS2 protein, humanACSS2 protein, mouseCentral Nervous System DepressantsEthanolRNA, Messengeracyl-coa synthetaseAlcoholismHumanMouseReal-time PCR

Identifiers

PMID28550509
OpenAlexW2616995696

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.