Evidence map›Paper›PMID 16113111›Full record

ArticleBiophysical journal2005

Variability in couplon size in rabbit ventricular myocytes.

Masashi Inoue, John H B Bridge

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Regulation of Na/Ca exchange by cytoplasmic protons modifies intracellular calcium dynamics and the cardiac response to ischemia.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. CaJournal of molecular and cellular cardiology · 2023
    Article
  3. Article
  4. Article
  5. Article
  6. Calcium alternans in cardiac myocytes: order from disorder.Journal of molecular and cellular cardiology · 2013
    Review
  7. CaV1.2 sparklets in heart and vascular smooth muscle.Journal of molecular and cellular cardiology · 2013
    Review
  8. The interaction of Ca2+ with sarcomeric proteins: role in function and dysfunction of the heart.American journal of physiology. Heart and circulatory physiology · 2012
    Review
  9. Multi-scale modeling in biology: how to bridge the gaps between scales?Progress in biophysics and molecular biology · 2011
    Review
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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

2 authors at 1 institution in 1 country.

Masashi InoueNora Eccles Harrison Cardiovascular Research and Training Institute, University of Utah, 95 South 2000 East, Salt Lake City, UT 84112-5000, USA. inoue@cvrti.utah.edu
John H B Bridge
University of Utah · US

Funding

Metabolic Regulation of Cardiac E-C CouplingR01HL070828 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GOLDHABER, JOSHUA I · 2002 to 2013
$3.8M
RELATIONSHIPS BETWEEN SPARKS AND THEIR TRIGGERS IN HEARTR01HL062690 · NHLBI · UNIVERSITY OF UTAH · PI BRIDGE, JOHN H B · 1999 to 2008
$2.5M
Calcium Signaling, Metabolism, and EC Coupling in HeartR56HL070828 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI GOLDHABER, JOSHUA I · 2008 to 2008
$385k
NHLBI NIH HHS HL 62690NHLBI NIH HHS HL 70828NHLBI NIH HHS R01 HL062690NHLBI NIH HHS R01 HL070828NHLBI NIH HHS R56 HL070828
6 · The paper itself

Abstract

Variation in couplon size is thought to be essential for graded Ca(2+) transients in cardiac myocytes. We examined this variation by investigating spark appearance in rabbit ventricular myocytes at various locations and at potentials from -20 to 0 mV. At 0 mV, sparks appeared at the beginning of the voltage step with a probability of unity. On the other hand, at -20 mV, sparks appeared later during the voltage step with a lower probability. The cumulative spark probabilities at various potentials were fitted with exponential functions of both time and voltage. Spark latency became longer as spark probability decreased at more negative potentials. At -20 mV, the cumulative spark probability and the mean spark latency were not only variable among locations but also inversely related. Under the assumption that a single opening of an L-type Ca(2+) channel triggers a spark, we suggest a simple mathematical explanation for the distribution of spark appearance. The variation in spark probability and latency with location suggests that the couplon size, and hence the number of L-type Ca(2+) channels in a couplon is variable.

Indexed as

AnimalsBiophysicsCalciumCalcium Channels, L-TypeElectrophysiologyHeart VentriclesMembrane PotentialsMicroscopy, ConfocalMicroscopy, FluorescenceModels, BiologicalMyocytes, CardiacPatch-Clamp TechniquesProtein Structure, TertiaryRabbitsTime FactorsCalciumCalcium Channels, L-Type

Identifiers

PMID16113111
PMCPMC1366807
OpenAlexW2024116142

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.