Evidence map›Paper›PMID 11351026›Full record

ArticleThe Journal of physiology2001

Voltage-dependent Ca2+ release in rat megakaryocytes requires functional IP3 receptors.

M J Mason, M P Mahaut-Smith

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

13 citing papers in PubMed, 37 citations in OpenAlex.

  1. The significance of interstitial cells in neurogastroenterology.Journal of neurogastroenterology and motility · 2014
    Article
  2. Article
  3. Article
  4. Modulation of Gq-protein-coupled inositol trisphosphate and Ca2+ signaling by the membrane potential.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2006
    Article
  5. Metabotropic Ca(2+) channel-induced Ca(2+) release and ATP-dependent facilitation of arterial myocyte contraction.Proceedings of the National Academy of Sciences of the United States of America · 2006
    Article
  6. Article
  7. Article
  8. Article
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  10. Article
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  12. Article
  13. Alkyl Mercury-Induced Toxicity: Multiple Mechanisms of Action.Reviews of environmental contamination and toxicology
    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

2 authors at 1 institution in 1 country.

M J MasonDepartment of Physiology, University of Cambridge, Cambridge CB2 3EG, UK. mjm39@cam.ac.uk
M P Mahaut-Smith
University of Cambridge · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Using simultaneous whole-cell patch-clamp and fluorescence measurements of [Ca2+]i in rat megakaryocytes we have investigated the requirement for functional inositol 1,4,5-trisphosphate (IP3) receptors in Ca2+ release induced by membrane depolarization during agonist stimulation. Voltage-dependent Ca2+ release was observed during application of the IP3-generating agonists U46619 (a thromboxane A2 analogue) and ADP. Furthermore, voltage-dependent Ca2+ release was observed in the absence of exogenous agonist following sensitization of IP3 receptors with thimerosal. Depolarization-induced Ca2+ release was not detected during depletion of intracellular Ca2+ stores by thapsigargin. Thus, depletion of stores alone is not sufficient to confer voltage dependence upon the Ca2+ release mechanism. Block of IP3 receptors by carbacyclin-stimulated elevations in cAMP, uncaging of cAMP or exposure to a high concentration of caffeine reversibly abolished Ca2+ increases stimulated by both ADP and depolarization. The cAMP-dependent block was prevented by a peptide inhibitor of protein kinase A, indicating that an alteration of adenylate cyclase activity leading to modulation of protein kinase A activity does not underlie the control of Ca2+ release by voltage. These results are consistent with the requirement for functional IP3 receptors for voltage control of Ca2+ release from intracellular stores during inositol lipid signalling. The data also indicate the involvement of a voltage sensor downstream of surface membrane receptors in the depolarization-evoked Ca2+ response.

Indexed as

15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic AcidAdenosine DiphosphateAnimalsAnti-Infective Agents, LocalCaffeineCalciumCalcium ChannelsCalcium SignalingEnzyme InhibitorsEpoprostenolInositol 1,4,5-Trisphosphate ReceptorsMaleMegakaryocytesPatch-Clamp TechniquesPhosphodiesterase InhibitorsPlatelet Aggregation Inhibitors15-Hydroxy-11 alpha,9 alpha-(epoxymethano)prosta-5,13-dienoic AcidAdenosine DiphosphateAnti-Infective Agents, LocalCaffeineCalciumCalcium ChannelscarboprostacyclinEnzyme InhibitorsEpoprostenolInositol 1,4,5-Trisphosphate ReceptorsPhosphodiesterase InhibitorsPlatelet Aggregation InhibitorsReceptors, Cytoplasmic and NuclearThapsigarginThimerosalVasoconstrictor Agents

Identifiers

PMID11351026
PMCPMC2278605
OpenAlexW2092109348

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.