Evidence map›Paper›PMID 17591544›Full record

ReviewAlcohol (Fayetteville, N.Y.)2007

Ethanol acts directly on extrasynaptic subtypes of GABAA receptors to increase tonic inhibition.

Vijayalakshmi Santhakumar, Martin Wallner, Thomas S Otis

Erratum issuedAbstract readReview
In one paragraph

Review in Alcohol (Fayetteville, N.Y.), 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

56 citing papers in PubMed, 129 citations in OpenAlex.

  1. The neurobiological markers of acute alcohol's subjective effects in humans.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Trial
  2. Trial
  3. Trial
  4. Neurobiological Bases of Alcohol Consumption After Social Stress.Current topics in behavioral neurosciences · 2022
    Article
  5. Article
  6. Humulone Modulation of GABAFrontiers in neuroscience · 2020
    Article
  7. Mechanisms of GABAScientific reports · 2019
    Article
  8. Article
  9. Direction of action of presynaptic GABAJournal of neurophysiology · 2019
    Article
  10. Article
  11. Article
  12. GABANeuropharmacology · 2018
    Review
  13. Article
  14. The Cerebellar GABAHandbook of experimental pharmacology · 2018
    Article
  15. Article
  16. Review
  17. Intraperitoneal Administration of Ethanol as a Means of Euthanasia for Neonatal Mice (Journal of the American Association for Laboratory Animal Science : JAALAS · 2017
    Article
  18. Sigma Receptors and Alcohol Use Disorders.Handbook of experimental pharmacology · 2017
    Review
  19. Review
  20. Sigma Receptors and Substance Use Disorders.Advances in experimental medicine and biology · 2017
    Review
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Vijayalakshmi SanthakumarDepartment of Neurology, David Geffen School of Medicine, University of California, Box 951763, 63-314 CHS, Los Angeles, CA 90095-1763, USA.
Martin Wallner
Thomas S Otis
University of California, Los Angeles · US

Funding

ZINC AND GABAA RECEPTOR PLASTICITYP01NS035985 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI MODY, ISTVAN · 1998 to 2009
$7.9M
NINDS NIH HHS P01 NS035985
6 · The paper itself

Abstract

Based on the similarity of ethanol intoxication to the behavioral effects of drugs known to target gamma-aminobutyric acid type A (GABAA) receptors (GABARs), it has been suspected for decades that ethanol facilitates the activity of GABA. Even so, it has been surprisingly difficult to identify molecular targets of ethanol. Research conducted over the past several years suggests that a subclass of GABARs (those containing delta subunits) responds in a relevant concentration range to ethanol. Although delta subunit-containing GABARs are not ubiquitously expressed at inhibitory synapses like their gamma subunit-containing, synaptic counterparts, they are found in many neurons in extrasynaptic locations. Here, they give rise to a tonic form of inhibition that can potently suppress neuronal excitability. Studies have shown that both recombinant and native delta subunit-containing GABARs (1) are modulated by behaviorally relevant (i.e., low millimolar) concentrations of ethanol, (2) directly bind ethanol over the same concentration range, (3) show altered function upon single amino substitutions linked to changes in behavioral responsiveness to ethanol, and (4) are a site of action of Ro15-4513, a competitive antagonist of ethanol binding and a drug which prevents many of the behavioral aspects of ethanol intoxication. Despite such comprehensive evidence, however, the field is not free from controversy. This review evaluates published data for and against a central role of delta subunit-containing GABARs in ethanol actions and suggests future directions that might help settle points of controversy.

Indexed as

Amino Acid SubstitutionAnimalsBrainCentral Nervous System DepressantsEthanolHumansNeuronsReceptors, GABA-ACentral Nervous System DepressantsEthanolReceptors, GABA-A

Identifiers

PMID17591544
PMCPMC2040048
OpenAlexW2104021021

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.