Evidence map›Paper›PMID 24947416›Full record

ArticleCardiovascular research2014

Direct measurements of SR free Ca reveal the mechanism underlying the transient effects of RyR potentiation under physiological conditions.

David J Greensmith, Gina L J Galli, Andrew W Trafford, David A Eisner

Open access · hybridAbstract read
In one paragraph

Article in Cardiovascular research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Modeling sarcoplasmic reticulum CaBiophysics reports · 2024
    Article
  2. Article
  3. Article
  4. Caspofungin induces the release of CaScientific reports · 2020
    Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Considerations for anFrontiers in pharmacology · 2019
    Review
  10. Ups and downs of calcium in the heart.The Journal of physiology · 2018
    Article
  11. Systolic [CaThe Journal of physiology · 2017
    Article
  12. Article
  13. Review
  14. Sarcolemmal distribution ofAmerican journal of physiology. Heart and circulatory physiology · 2017
    Article
  15. Article
  16. A technical review of optical mapping of intracellular calcium within myocardial tissue.American journal of physiology. Heart and circulatory physiology · 2016
    Review
  17. Article
  18. Article
  19. 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

4 authors at 1 institution in 1 country.

David J GreensmithUnit of Cardiac Physiology, Institute of Cardiovascular Science, Manchester Academic Health Science Centre, 3.18 Core Technology Facility, 46 Grafton Street, Manchester M13 9NT, UK.
Gina L J GalliUnit of Cardiac Physiology, Institute of Cardiovascular Science, Manchester Academic Health Science Centre, 3.18 Core Technology Facility, 46 Grafton Street, Manchester M13 9NT, UK.
Andrew W TraffordUnit of Cardiac Physiology, Institute of Cardiovascular Science, Manchester Academic Health Science Centre, 3.18 Core Technology Facility, 46 Grafton Street, Manchester M13 9NT, UK.
David A EisnerUnit of Cardiac Physiology, Institute of Cardiovascular Science, Manchester Academic Health Science Centre, 3.18 Core Technology Facility, 46 Grafton Street, Manchester M13 9NT, UK eisner@man.ac.uk.
Manchester Academic Health Science Centre · GB

Funding

British Heart Foundation FS/09/036/27823British Heart Foundation FS/10/71/28563British Heart Foundation FS/12/57/29717British Heart Foundation PG/08/078/25593British Heart Foundation PG/09/062/27872British Heart Foundation PG/10/89/28630British Heart Foundation PG/11/16/28777
6 · The paper itself

Abstract

aimsMost of the calcium that activates contraction is released from the sarcoplasmic reticulum (SR) through the ryanodine receptor (RyR). It is controversial whether activators of the RyR produce a maintained increase in the amplitude of the systolic Ca transient. We therefore aimed to examine the effects of activation of the RyR in large animals under conditions designed to be as physiological as possible while simultaneously measuring SR and cytoplasmic Ca. METHODS AND

resultsExperiments were performed on ventricular myocytes from canine and ovine hearts. Cytoplasmic Ca was measured with fluo-3 and SR Ca with mag-fura-2. Application of caffeine resulted in a brief increase in the amplitude of the systolic Ca transient accompanied by an increase of action potential duration. These effects disappeared with a rate constant of ∼3 s(-1). Similar effects were seen in cells taken from sheep in which heart failure had been induced by rapid pacing. The decrease of Ca transient amplitude was accompanied by a decrease of SR Ca content. During this phase, the maximum (end-diastolic) SR Ca content fell while the minimum systolic increased.

conclusionsThis study shows that, under conditions designed to be as physiological as possible, potentiation of RyR opening has no maintained effect on the systolic Ca transient. This result makes it unlikely that potentiation of the RyR has a maintained role in positive inotropy.

Indexed as

Aniline CompoundsAnimalsCalciumCalcium SignalingCells, CulturedDogsFura-2HeartMyocardial ContractionMyocytes, CardiacRyanodine Receptor Calcium Release ChannelSarcoplasmic ReticulumSheepXanthenes2-(2-(5-carboxy)oxazole)-5-hydroxy-6-aminobenzofuran-N,N,O-triacetic acidAniline CompoundsCalciumFluo-3Fura-2Ryanodine Receptor Calcium Release ChannelXanthenesCalciumRyanodine receptorSarcoplasmic reticulum

Identifiers

PMID24947416
PMCPMC4145011
OpenAlexW2110600542

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.