Evidence map›Paper›PMID 10432342›Full record

ArticleThe Journal of physiology1999

Rat supraoptic magnocellular neurones show distinct large conductance, Ca2+-activated K+ channel subtypes in cell bodies versus nerve endings.

A M Dopico, H Widmer, G Wang, J R Lemos, S N Treistman

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 1999. 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
1.5field-weighted citation impact, top 18% 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, 97 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Large conductance voltage-and calcium-activated KFrontiers in pharmacology · 2024
    Review
  5. Article
  6. Review
  7. Article
  8. Phosphatidylinositol 4,5-bisphosphate (PIPThe Journal of physiology · 2017
    Article
  9. Article
  10. Article
  11. Modulation of BK Channels by Ethanol.International review of neurobiology · 2016
    Review
  12. BK Channels in the Central Nervous System.International review of neurobiology · 2016
    Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  19. Article
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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

5 authors at 1 institution in 1 country.

A M DopicoDepartment of Pharmacology and Molecular Toxicology and Interdepartmental Program in Neuroscience, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655, USA.
H Widmer
G Wang
J R Lemos
S N Treistman
University of Massachusetts Chan Medical School · US

Funding

DEPOLARIZATION/SECRETION COUPLING IN NERVE TERMINALSR01NS029470 · NINDS · WORCESTER FOUNDATION FOR BIOMEDICAL RES · PI LEMOS, JOSE R · 1991 to 2012
$4.3M
ALCOHOL ACTION ON NERVE TERMINALS IN SELECTED STRAINSR01AA008003 · NIAAA · WORCESTER FOUNDATION FOR BIOMEDICAL RES · PI TREISTMAN, STEVEN N · 1989 to 2009
$3.5M
NIAAA NIH HHS AA 08003NIAAA NIH HHS R01 AA008003NINDS NIH HHS NS 29470NINDS NIH HHS R01 NS029470
6 · The paper itself

Abstract

1. Large conductance, Ca2+-activated K+ (BK) channels were identified in freshly dissociated rat supraoptic neurones using patch clamp techniques. 2. The single channel conductance of cell body BK channels, recorded from inside-out patches in symmetric 145 mM K+, was 246.1 pS, compared with 213 pS in nerve ending BK channels (P<0.01). 3. At low open probability (Po), the reciprocal of the slope in the ln(NPo)-voltage relationship (N, number of available channels in the patch) for cell body and nerve ending channels were similar: 11 vs. 14 mV per e-fold change in NPo, respectively. 4. At 40 mV, the [Ca2+]i producing half-maximal activation was 273 nM, as opposed to >1.53 microM for the neurohypophysial channel, indicating the higher Ca2+ sensitivity of the cell body isochannel. 5. Cell body BK channels showed fast kinetics (open time constant, 8.5 ms; fast closed time constant, 1.6 and slow closed time constant, 12.7 ms), identifying them as 'type I' isochannels, as opposed to the slow gating (type II) of neurohypophysial BK channels. 6. Cell body BK activity was reduced by 10 nM charybdotoxin (NPo, 37% of control), or 10 nM iberiotoxin (NPo, 5% of control), whereas neurohypophysial BK channels are insensitive to charybdotoxin at concentrations as high as 360 nM. 7. Whilst blockade of nerve ending BK channels markedly slowed the repolarization of evoked single spikes, blockade of cell body channels was without effect on repolarization of evoked single spikes. 8. Ethanol reversibly increased neurohypophysial BK channel activity (EC50, 22 mM; maximal effect, 100 mM). In contrast, ethanol (up to 100 mM) failed to increase cell body BK channel activity. 9. In conclusion, we have characterized BK channels in supraoptic neuronal cell bodies, and demonstrated that they display different electrophysiological and pharmacological properties from their counterparts in the nerve endings.

Indexed as

BenzylisoquinolinesPotassium Channels, Calcium-ActivatedAlkaloidsAnimalsCalciumCalcium Channel BlockersEvoked PotentialsIon Channel GatingLarge-Conductance Calcium-Activated Potassium ChannelsMaleNerve EndingsNeuronsPatch-Clamp TechniquesPotassium ChannelsRatsReaction TimeAlkaloidsBenzylisoquinolinesCalciumCalcium Channel BlockersLarge-Conductance Calcium-Activated Potassium ChannelsPotassium ChannelsPotassium Channels, Calcium-Activatedtetrandrine

Identifiers

PMID10432342
PMCPMC2269476
OpenAlexW1968775375

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.