Evidence map›Paper›PMID 10066927›Full record

ArticleThe Journal of physiology1999

Relationship between L-type Ca2+ current and unitary sarcoplasmic reticulum Ca2+ release events in rat ventricular myocytes.

M L Collier, A P Thomas, J R Berlin

Abstract 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 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Review
  2. CaJournal of molecular and cellular cardiology · 2023
    Article
  3. Review
  4. Improper Remodeling of Organelles Deputed to CaInternational journal of molecular sciences · 2021
    Review
  5. Interplay among distinct CaThe Journal of physiology · 2017
    Article
  6. Ca2+ channel nanodomains boost local Ca2+ amplitude.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Coupled dynamics of voltage and calcium in paced cardiac cells.Physical review. E, Statistical, nonlinear, and soft matter physics · 2005
    Article
  15. Article
  16. Effects of caffeine on potassium currents in isolated rat ventricular myocytes.Pflugers Archiv : European journal of physiology · 2003
    Article
  17. Article
  18. Review
  19. Article
  20. 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

3 authors.

M L CollierDepartment of Physiology, Allegheny University of the Health Sciences, Philadelphia, PA, USA.
A P Thomas
J R Berlin

Funding

EFFECTS OF COCAINE ON CARDIAC MUSCLE CELLSR01DA006290 · NIDA · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI THOMAS, ANDREW P · 1992 to 1998
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INTRACELLULAR CALCIUM REGULATION IN CARDIAC MUSCLE CELLSR01HL043712 · NHLBI · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI BERLIN, JOSHUA R · 1995 to 1998
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SARCOLEMMAL CALCIUM TRANSPORT MECHANISMS IN HEART CELLSR29HL043712 · NHLBI · GRADUATE HOSPITAL (PHILADELPHIA) · PI BERLIN, JOSHUA R · 1990 to 1994
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NHLBI NIH HHS HL43712NIDA NIH HHS DA06290
6 · The paper itself

Abstract

1. The time courses of Ca2+ current and Ca2+ spark occurrence were determined in single rat ventricular myocytes voltage clamped with patch pipettes containing 0.1 microM fluo-3. Acquisition of line-scan images on a laser scanning confocal microscope was synchronized with measurement of Cd2+-sensitive Ca2+ currents. In most cells, individual Ca2+ sparks were observed by reducing Ca2+ current density with nifedipine (0.1-8 microM). 2. Ca2+ sparks elicited by depolarizing voltage-clamp pulses had a peak [Ca2+] amplitude of 289 +/- 3 nM with a decay half-time of 20.8 +/- 0.2 ms and a full width at half-maximum of 1.40 +/- 0.03 microm (mean +/- s. e.m., n = 345), independent of the membrane potential. 3. The time between the beginning of a depolarization and the initiation of each Ca2+ spark was calculated and data were pooled to construct waiting time histograms. Exponential functions were fitted to these histograms and to the decaying phase of the Ca2+ current. This analysis showed that the time constants describing Ca2+ current and Ca2+ spark occurrence at membrane potentials between -30 mV and +30 mV were not significantly different. At +50 mV, in the absence of nifedipine, the time constant describing Ca2+ spark occurrence was significantly larger than the time constant of the Ca2+ current. 4. A simple model is developed using Poisson statistics to relate macroscopic Ca2+ current to the opening of single L-type Ca2+ channels at the dyad junction and to the time course of Ca2+ spark occurrence. The model suggests that the time courses of macroscopic Ca2+ current and Ca2+ spark occurrence should be closely related when opening of a single L-type Ca2+ channel initiates a Ca2+ spark. By comparison with the data, the model suggests that Ca2+ sparks are initiated by the opening of a single L-type Ca2+ channel at all membrane potentials encountered during an action potential.

Indexed as

AlgorithmsAniline CompoundsAnimalsCadmiumCalciumCalcium Channel BlockersCalcium ChannelsCalcium Channels, L-TypeCalcium SignalingFluorescent DyesHeart VentriclesIn Vitro TechniquesMaleMembrane PotentialsMicroscopy, ConfocalMyocardiumAniline CompoundsCadmiumCalciumCalcium Channel BlockersCalcium ChannelsCalcium Channels, L-TypeFluo-3Fluorescent DyesNifedipineXanthenes

Identifiers

PMID10066927
PMCPMC2269204

What OpenQuestion holds

Texttitle and abstract
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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.