Evidence map›Paper›PMID 1722514›Full record

ArticleThe Journal of membrane biology1991

Anion channels from rat brain synaptosomal membranes incorporated into planar bilayers.

K Nomura, M Sokabe

Abstract read
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In one paragraph

Article in The Journal of membrane biology, 1991. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
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

2 authors.

K NomuraDepartment of Pediatrics, Nagoya University School of Medicine, Japan.
M Sokabe

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Synaptic membranes from rat brain were incorporated into planar lipid bilayers, and the characteristics of two types of anion-selective channels (type I and type II) were investigated. In asymmetric BaCl2 buffers (cis, 100 mM/trans, 25 mM), single channel conductances at -40 mV were 70 pS (type I) and 120 pS (type II). Permeability ratios (PNa:PBa:PCl) calculated from the Goldman-Hodgkin-Katz current equation for type I and type II channels were 0.23:0.04:1 and 0.05:0.03:1, respectively. Both channels exhibited characteristic voltage-dependent bursting activities. Open probability for type I channels had a maximum of approximately 0.7 at about 0 mV and decreased to zero at greater transmembrane potentials of either polarity. Type II channels were relatively voltage independent at negative voltages and were inactivated at highly positive voltages. Type I channels showed spontaneous irreversible inactivation often preceded by sudden transition to subconducting states. DIDS blocked type I channels only from the cis side, while it blocked type II channels from either side.

Indexed as

Barium CompoundsChlorides4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid4-Acetamido-4'-isothiocyanatostilbene-2,2'-disulfonic AcidAnimalsBariumCell MembraneCell Membrane PermeabilityElectric ConductivityElectric StimulationFemaleIon ChannelsLipid BilayersRatsRats, Inbred StrainsSodium Chloride4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid4-Acetamido-4'-isothiocyanatostilbene-2,2'-disulfonic AcidBariumbarium chlorideBarium CompoundsChloridesIon ChannelsLipid BilayersSodium Chloride

Identifiers

PMID1722514

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.