Evidence map›Paper›PMID 26009541›Full record

ReviewThe Journal of general physiology2015

The couplonopathies: A comparative approach to a class of diseases of skeletal and cardiac muscle.

Eduardo Ríos, Lourdes Figueroa, Carlo Manno, Natalia Kraeva, Sheila Riazi

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of general physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

28 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Skeletal muscle disorders as risk factors for type 2 diabetes.Molecular and cellular endocrinology · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Elevated CaFrontiers in physiology · 2022
    Article
  7. Article
  8. Article
  9. Preserved CaDiabetologia · 2020
    Article
  10. Article
  11. CaCells · 2019
    Review
  12. Article
  13. Article
  14. Article
  15. The clinical spectrum ofNeurology · 2018
    Article
  16. Junctional membrane CaProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  17. A privileged role for neuronal NaThe Journal of general physiology · 2018
    Article
  18. Review
  19. Voltage modulates halothane-triggered CaThe Journal of general physiology · 2018
    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

5 authors at 2 institutions in 2 countries.

Eduardo RíosSection of Cellular Signaling, Department of Molecular Biophysics and Physiology, Rush University, Chicago, IL 60612 erios@rush.edu.
Lourdes FigueroaSection of Cellular Signaling, Department of Molecular Biophysics and Physiology, Rush University, Chicago, IL 60612.
Carlo MannoSection of Cellular Signaling, Department of Molecular Biophysics and Physiology, Rush University, Chicago, IL 60612.
Natalia KraevaMalignant Hyperthermia Investigation Unit, University Health Network, Toronto General Hospital, Toronto, Ontario M5G 2C4, Canada.
Sheila RiaziMalignant Hyperthermia Investigation Unit, University Health Network, Toronto General Hospital, Toronto, Ontario M5G 2C4, Canada.
Rush University · USToronto General Hospital · CA

Funding

Skeletal Muscle. Ca Release Control Inside the Sarcoplasmic Reticulum.R01AR049184 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI RIOS, EDUARDO · 2003 to 2013
$3.1M
CALCIUM MOVEMENTS IN EXCITATION-CONTRACTION COUPLING.R37AR032808 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI RIOS, EDUARDO · 1996 to 2005
$2.6M
CALCIUM MOVEMENTS IN EXCITATION-CONTRACTION COUPLINGR01AR032808 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI RIOS, EDUARDO · 1986 to 2011
$1.6M
Roles of Calsequestrin in the Control of Calcium Signals in Health and DiseaseR01GM111254 · NIGMS · RUSH UNIVERSITY MEDICAL CENTER · PI KANG, CHULHEE, RIOS, EDUARDO · 2014 to 2017
$1.4M
Dual Confocal Microscopic ScannerS10RR024707 · NCRR · RUSH UNIVERSITY MEDICAL CENTER · PI RIOS, EDUARDO · 2008 to 2008
$500k
NCRR NIH HHS S10 RR024707NIAMS NIH HHS AR032808NIAMS NIH HHS AR-049184NIAMS NIH HHS R01 AR032808NIAMS NIH HHS R01 AR049184NIAMS NIH HHS R37 AR032808NIGMS NIH HHS GM-111254NIGMS NIH HHS R01 GM111254
6 · The paper itself

Abstract

A novel category of diseases of striated muscle is proposed, the couplonopathies, as those that affect components of the couplon and thereby alter its operation. Couplons are the functional units of intracellular calcium release in excitation-contraction coupling. They comprise dihydropyridine receptors, ryanodine receptors (Ca2+ release channels), and a growing list of ancillary proteins whose alteration may lead to disease. Within a generally similar plan, the couplons of skeletal and cardiac muscle show, in a few places, marked structural divergence associated with critical differences in the mechanisms whereby they fulfill their signaling role. Most important among these are the presence of a mechanical or allosteric communication between voltage sensors and Ca2+ release channels, exclusive to the skeletal couplon, and the smaller capacity of the Ca stores in cardiac muscle, which results in greater swings of store concentration during physiological function. Consideration of these structural and functional differences affords insights into the pathogenesis of several couplonopathies. The exclusive mechanical connection of the skeletal couplon explains differences in pathogenesis between malignant hyperthermia (MH) and catecholaminergic polymorphic ventricular tachycardia (CPVT), conditions most commonly caused by mutations in homologous regions of the skeletal and cardiac Ca(2+) release channels. Based on mechanistic considerations applicable to both couplons, we identify the plasmalemma as a site of secondary modifications, typically an increase in store-operated calcium entry, that are relevant in MH pathogenesis. Similar considerations help explain the different consequences that mutations in triadin and calsequestrin have in these two tissues. As more information is gathered on the composition of cardiac and skeletal couplons, this comparative and mechanistic approach to couplonopathies should be useful to understand pathogenesis, clarify diagnosis, and propose tissue-specific drug development.

Indexed as

Excitation Contraction CouplingMyocardial ContractionAnimalsCalcium Channels, L-TypeCalsequestrinCardiomyopathiesCarrier ProteinsGenetic Predisposition to DiseaseHumansMuscle ProteinsMuscle, SkeletalMuscular DiseasesMutationMyocardiumPhenotypeRyanodine Receptor Calcium Release ChannelCalcium Channels, L-TypeCalsequestrinCarrier ProteinsMuscle ProteinsRyanodine Receptor Calcium Release Channeltriadin

Identifiers

PMID26009541
PMCPMC4442791
OpenAlexW2270786369

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.