Evidence map›Paper›PMID 2477526›Full record

ArticleThe Journal of physiology1989

Kinetic properties of the GABAA receptor main conductance state of mouse spinal cord neurones in culture.

R L Macdonald, C J Rogers, R E Twyman

Abstract read
In one paragraph

Article in The Journal of physiology, 1989. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
–field-weighted citation impact
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

84 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Allosteric modulation of α1β3γ2 GABABiophysical journal · 2023
    Article
  5. Shisa7-Dependent Regulation of GABAThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  6. Electrophysiology of ionotropic GABA receptors.Cellular and molecular life sciences : CMLS · 2021
    Review
  7. Article
  8. Feature Article: Selective modulation of tonically active GABAExperimental biology and medicine (Maywood, N.J.) · 2018
    Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Flufenamic acid as an ion channel modulator.Pharmacology & therapeutics · 2013
    Review
  14. GABA-independent GABAA receptor openings maintain tonic currents.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  15. Article
  16. Article
  17. Influence of GABAAR monoliganded states on GABAergic responses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  18. Article
  19. Article
  20. Article

24 more citing papers are in PubMed but not listed here.

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

3 authors.

R L MacdonaldDepartment of Neurology, University of Michigan Medical Center, Ann Arbor 48104.
C J Rogers
R E Twyman

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

1. The kinetic properties of the main conductance state of gamma-aminobutyric acidA (GABA) receptor channels from somata of mouse spinal cord neurones in cell culture were investigated using patch clamp techniques. 2. Whole-cell GABA receptor currents increased in a concentration-dependent manner from 0.5 to 5 microM. 3. Single-channel currents were recorded with a main conductance state of 27.2 pS and a less frequent conductance state of 15.9 pS. The main conductance state opened singly and in bursts of several openings. 4. Mean open times of GABA receptor main conductance currents were increased and open-time frequency histograms were shifted to longer times as GABA concentration was increased from 0.5 to 5 microM. Three exponential functions were required to fit the histograms at all GABA concentrations, suggesting that the channel opened into at least three open states (O1, O2 and O3). The three functions had the same time constants (1.0 +/- 0.2, 3.7 +/- 0.4 and 11.3 +/- 0.5 ms; mean +/- S.D.) at each concentration. The increase in long open times with concentration was due to a shift in relative frequency of occurrence of openings from the shortest (O1) to the two longest (O2 and O3) open states. 5. Closed-time distributions of closures between main conductance state openings were fitted with multiple exponential functions, suggesting that the channel had several closed states. The two shortest time constants (0.24 +/- 0.03 and 2.0 +/- 0.3 ms) were concentration independent (0.5 to 5 microM). Three longer time constants decreased as concentration increased. 6. Bursts were defined as groups of openings surrounded by closures greater than a critical closed time (tc = 5 ms). Mean burst durations were increased and burst duration frequency histograms were shifted to longer times as GABA concentration was increased from 0.5 to 5 microM. Burst-duration frequency histograms were best fitted with three exponential functions. The time constants were concentration independent and were 1.0 +/- 0.2, 5.5 +/- 0.2 and 29.8 +/- 1.6 ms. The increase in burst duration with concentration was due to a relative shift from short duration bursts to longer duration bursts. 7. The shortest burst time constant was similar to the shortest open time constant suggesting that there was a population of single openings of short duration. The two longest burst time constants were longer than the two longest open time constants, suggesting that the bursts from the two longest burst components were composed of two or more openings.(ABSTRACT TRUNCATED AT 400 WORDS)

Indexed as

AnimalsCells, CulturedDose-Response Relationship, Druggamma-Aminobutyric AcidIon ChannelsKineticsMembrane PotentialsMiceReceptors, GABA-ASpinal Cordgamma-Aminobutyric AcidIon ChannelsReceptors, GABA-A

Identifiers

PMID2477526
PMCPMC1190491

What OpenQuestion holds

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Read underepoch 390

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.