Evidence map›Paper›PMID 33410862›Full record

ArticleThe Journal of general physiology2021

Thermal modulation of epicardial Ca2+ dynamics uncovers molecular mechanisms of Ca2+ alternans.

Jose Millet, Yuriana Aguilar-Sanchez, Dmytro Kornyeyev, Maedeh Bazmi, Diego Fainstein, Julio A Copello, Ariel L Escobar

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of general physiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Cardiac Applications of CRISPR/AAV-Mediated Precise Genome Editing.bioRxiv : the preprint server for biology · 2024
    Article
  3. Review
  4. Article
  5. Article
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  10. Article
  11. Role of Reduced Sarco-Endoplasmic Reticulum CaFrontiers in physiology · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 3 countries.

Jose Millet *Institute of Information and Communication Technologies, Universitat Politècnica de València and Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares, Valencia, Spain.
Yuriana Aguilar-Sanchez *Department of Physiology and Biophysics, School of Medicine, Rush University Medical Center, Chicago, IL.
Dmytro KornyeyevDepartment of Bioengineering, School of Engineering, University of California Merced, Merced, CA.
Maedeh BazmiSchool of Natural Sciences, University of California, Merced, Merced, CA.
Diego FainsteinFacultad de Ingeniería, Universidad Nacional de Entre Ríos, Entre Ríos, Argentina.
Julio A CopelloDepartment of Pharmacology, Southern Illinois University School of Medicine, Springfield, IL.
Ariel L EscobarDepartment of Bioengineering, School of Engineering, University of California Merced, Merced, CA.
University of California, Merced · USCentro de Investigación Biomédica en Red · ESRush University Medical Center · USSouthern Illinois University School of Medicine · US

Funding

Subcellular Origin of T-wave Alternans in the Beating Mouse HeartR01HL084487 · NHLBI · UNIVERSITY OF CALIFORNIA, MERCED · PI ESCOBAR, ARIEL L · 2007 to 2011
$1.9M
NHLBI NIH HHS R01 HL084487
6 · The paper itself

Abstract

Ca2+ alternans (Ca-Alts) are alternating beat-to-beat changes in the amplitude of Ca2+ transients that frequently occur during tachycardia, ischemia, or hypothermia that can lead to sudden cardiac death. Ca-Alts appear to result from a variation in the amount of Ca2+ released from the sarcoplasmic reticulum (SR) between two consecutive heartbeats. This variable Ca2+ release has been attributed to the alternation of the action potential duration, delay in the recovery from inactivation of RYR Ca2+ release channel (RYR2), or an incomplete Ca2+ refilling of the SR. In all three cases, the RYR2 mobilizes less Ca2+ from the SR in an alternating manner, thereby generating an alternating profile of the Ca2+ transients. We used a new experimental approach, fluorescence local field optical mapping (FLOM), to record at the epicardial layer of an intact heart with subcellular resolution. In conjunction with a local cold finger, a series of images were recorded within an area where the local cooling induced a temperature gradient. Ca-Alts were larger in colder regions and occurred without changes in action potential duration. Analysis of the change in the enthalpy and Q10 of several kinetic processes defining intracellular Ca2+ dynamics indicated that the effects of temperature change on the relaxation of intracellular Ca2+ transients involved both passive and active mechanisms. The steep temperature dependency of Ca-Alts during tachycardia suggests Ca-Alts are generated by insufficient SERCA-mediated Ca2+ uptake into the SR. We found that Ca-Alts are heavily dependent on intra-SR Ca2+ and can be promoted through partial pharmacologic inhibition of SERCA2a. Finally, the FLOM experimental approach has the potential to help us understand how arrhythmogenesis correlates with the spatial distribution of metabolically impaired myocytes along the myocardium.

Indexed as

CalciumMyocytes, CardiacCalcium SignalingRyanodine Receptor Calcium Release ChannelSarcoplasmic ReticulumCalciumRyanodine Receptor Calcium Release Channel

Identifiers

PMID33410862
PMCPMC7797898
OpenAlexW3120494428

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.