Evidence map›Paper›PMID 20181584›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2010

Diverse voltage-sensitive dyes modulate GABAA receptor function.

Steven Mennerick, Mariangela Chisari, Hong-Jin Shu, Amanda Taylor, Michael Vasek, Lawrence N Eisenman, Charles F Zorumski

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 citing papers in PubMed, 69 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Studying Synaptically Evoked Cortical ResponsesFrontiers in neuroscience · 2021
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Rapid Throughput Analysis of GABAMolecular pharmacology · 2017
    Article
  17. Article
  18. Article
  19. Article
  20. 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.

Steven MennerickDepartment of Psychiatry, Washington University School of Medicine, St. Louis, Missouri 63110, USA. menneris@psychiatry.wustl.edu.
Mariangela Chisari
Hong-Jin Shu
Amanda Taylor
Michael Vasek
Lawrence N Eisenman
Charles F Zorumski
Washington University in St. Louis · USNeurology, Inc · US

Funding

STRUCTURE/ACTIVITY STUDIES OF NEUROSTEROID ANALOGUESP01GM047969 · NIGMS · WASHINGTON UNIVERSITY · PI ZORUMSKI, CHARLES F · 1992 to 2011
$18.7M
CONTROL OF SYNAPTIC GLUTAMATE RELEASER01MH078823 · NIMH · WASHINGTON UNIVERSITY · PI MENNERICK, STEVEN J · 2006 to 2015
$3.2M
MODULATION OF HIPPOCAMPAL SYNAPTIC PLASTICITYR01MH077791 · NIMH · WASHINGTON UNIVERSITY · PI ZORUMSKI, CHARLES F · 2007 to 2013
$2.4M
ETHANOL, NEUROSTEROIDS & HIPPOCAMPAL PLASTICITYR01AA017413 · NIAAA · WASHINGTON UNIVERSITY · PI ZORUMSKI, CHARLES F · 2009 to 2013
$1.8M
Axonal Signaling in the HippocampusR01NS054174 · NINDS · WASHINGTON UNIVERSITY · PI MENNERICK, STEVEN J · 2006 to 2010
$1.5M
Pregnenolone Sulfate Inhibition of GABA CurrentK08NS044041 · NINDS · WASHINGTON UNIVERSITY · PI EISENMAN, LAWRENCE N · 2004 to 2008
$797k
NIAAA NIH HHS AA017413NIAAA NIH HHS R01 AA017413NIGMS NIH HHS GM47969NIGMS NIH HHS P01 GM047969NIMH NIH HHS MH77791NIMH NIH HHS R01 MH077791NIMH NIH HHS R01 MH078823NINDS NIH HHS K08 NS044041NINDS NIH HHS NS44041NINDS NIH HHS R01 NS054174
6 · The paper itself

Abstract

Voltage-sensitive dyes are important tools for assessing network and single-cell excitability, but an untested premise in most cases is that the dyes do not interfere with the parameters (membrane potential, excitability) that they are designed to measure. We found that popular members of several different families of voltage-sensitive dyes modulate GABA(A) receptor with maximum efficacy and potency similar to clinically used GABA(A) receptor modulators. Di-4-ANEPPS and DiBAC4(3) potentiated GABA function with micromolar and high nanomolar potency, respectively, and yielded strong maximum effects similar to barbiturates and neurosteroids. Newer blue oxonols had biphasic effects on GABA(A) receptor function at nanomolar and micromolar concentrations, with maximum potentiation comparable to that of saturating benzodiazepine effects. ANNINE-6 and ANNINE-6plus had no detectable effect on GABA(A) receptor function. Even dyes with no activity on GABA(A) receptors at baseline induced photodynamic enhancement of GABA(A) receptors. The basal effects of dyes were sufficient to prolong IPSCs and to dampen network activity in multielectrode array recordings. Therefore, the dual effects of voltage-sensitive dyes on GABAergic inhibition require caution in dye use for studies of excitability and network activity.

Indexed as

AnimalsCells, CulturedDose-Response Relationship, DrugFemaleFluorescent DyesGABA AgentsGABA AgonistsGABA AntagonistsHippocampusInhibitory Postsynaptic PotentialsMicroscopy, ConfocalMicroscopy, FluorescenceNeural InhibitionNeuronsOocytesPatch-Clamp TechniquesFluorescent DyesGABA AgentsGABA AgonistsGABA AntagonistsReceptors, GABA-A

Identifiers

PMID20181584
PMCPMC2840391
OpenAlexW2112736669

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.