Evidence map›Paper›PMID 24324408›Full record

ArticleFrontiers in neural circuits2013

Primate cerebellar granule cells exhibit a tonic GABAAR conductance that is not affected by alcohol: a possible cellular substrate of the low level of response phenotype.

Claudia Mohr, Olena Kolotushkina, Joshua S Kaplan, John Welsh, James B Daunais, Kathleen A Grant, David J Rossi

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neural circuits, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

12 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. The Cerebellar GABAHandbook of experimental pharmacology · 2018
    Article
  5. Transient Hypoxemia Chronically Disrupts Maturation of Preterm Fetal Ovine Subplate Neuron Arborization and Activity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. 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

7 authors at 2 institutions in 1 country.

Claudia MohrDepartment of Behavioral Neuroscience, Oregon Health & Science University Portland, OR, USA.
Olena Kolotushkina
Joshua S Kaplan
John Welsh
James B Daunais
Kathleen A Grant
David J Rossi
Oregon Health & Science University · USWake Forest University · US

Funding

YR 50 PROJ- ROBERTS PRIMATE ISLETP51RR000163 · NCRR · OREGON REGIONAL PRIMATE RESEARCH CENTER · PI PICKER, LOUIS J. · 1985 to 2011
$140.8M
Stress and Ethanol Self-Administration in MonkeysU01AA013510 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI KATHLEEN A GRANT · 2002 to 2026
$11.8M
BIOLOGICAL BASES OF ALCOHOLISMT32AA007468 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Andrey E Ryabinin · 1987 to 2026
$11.3M
Monkey Alcohol Tissue Research Resource (MATRR)R24AA019431 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI Mary Lauren Benton, Verginia Carmella Cuzon Carlson · 2010 to 2026
$10.3M
Ultrastructure and Single Particle Microscopy CoreP30NS061800 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI AICHER, SUE A · 2009 to 2020
$6.6M
NEUROSTEROID MODULATION OF ETHANOL WITHDRAWAL SEVERITYR01AA012439 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI FINN, DEBORAH A., ROSSI, DAVID J · 2000 to 2017
$4.6M
Cerebellar malfunction and damage during ischemiaR01NS051561 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI ROSSI, DAVID J · 2006 to 2010
$1.7M
Cerebellar GABAA receptor contributions to EtOH intoxication and EtOH intakeF31AA022267 · NIAAA · OREGON HEALTH & SCIENCE UNIVERSITY · PI KAPLAN, JOSHUA STEVEN · 2013 to 2014
$81k
NCRR NIH HHS P51 RR000163NCRR NIH HHS P51RR000163NIAAA NIH HHS F31 AA022267NIAAA NIH HHS R01 AA012439NIAAA NIH HHS R01AA012439NIAAA NIH HHS R24 AA019431NIAAA NIH HHS R24 AA109431NIAAA NIH HHS T32 AA007468NIAAA NIH HHS U01 AA013510NINDS NIH HHS P30 NS061800NINDS NIH HHS P30NS061800NINDS NIH HHS R01 NS051561NINDS NIH HHS R01NS051561
6 · The paper itself

Abstract

In many rodent brain regions, alcohol increases vesicular release of GABA, resulting in an increase in the frequency of spontaneous inhibitory postsynaptic currents (sIPSCs) and the magnitude of tonic GABAA receptor (GABAAR) currents. A neglected issue in translating the rodent literature to humans is the possibility that phylogenetic differences alter the actions of alcohol. To address this issue we made voltage-clamp recordings from granule cells (GCs) in cerebellar slices from the non-human primate (NHP), Macaca fascicularis. We found that similar to Sprague Dawley rats (SDRs), NHP GCs exhibit a tonic conductance generated by α6δ subunit containing GABAARs, as evidenced by its blockade by the broad spectrum GABAAR antagonist, GABAzine (10 μM), inhibition by α6 selective antagonist, furosemide (100 μM), and enhancement by THDOC (10-20 nM) and THIP (500 nM). In contrast to SDR GCs, in most NHP GCs (~60%), application of EtOH (25-105 mM) did not increase sIPSC frequency or the tonic GABAAR current. In a minority of cells (~40%), EtOH did increase sIPSC frequency and the tonic current. The relative lack of response to EtOH was associated with reduced expression of neuronal nitric oxide synthase (nNOS), which we recently reported mediates EtOH-induced enhancement of vesicular GABA release in rats. The EtOH-induced increase in tonic GABAAR current was significantly smaller in NHPs than in SDRs, presumably due to less GABA release, because there were no obvious differences in the density of GABAARs or GABA transporters between SDR and NHP GCs. Thus, EtOH does not directly modulate α6δ subunit GABAARs in NHPs. Instead, EtOH enhanced GABAergic transmission is mediated by enhanced GABA release. Further, SDR GC responses to alcohol are only representative of a subpopulation of NHP GCs. This suggests that the impact of EtOH on NHP cerebellar physiology will be reduced compared to SDRs, and will likely have different computational and behavioral consequences.

Indexed as

AnimalsCerebellumEthanolGABA-A Receptor Antagonistsgamma-Aminobutyric AcidInhibitory Postsynaptic PotentialsMacaca fascicularisNeural ConductionNeuronsNitric Oxide Synthase Type IPyridazinesReceptors, GABA-AEthanolGABA-A Receptor Antagonistsgabazinegamma-Aminobutyric AcidNitric Oxide Synthase Type IPyridazinesReceptors, GABA-Aalcohol drinkingcerebellumethanolGABA-A receptorGABA modulatorsprimate

Identifiers

PMID24324408
PMCPMC3840389
OpenAlexW2157045453

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.