Evidence map›Paper›PMID 35444559›Full record

ArticleFrontiers in physiology2022

Contractile State Dependent Sarcomere Length Variability in Isolated Guinea-Pig Cardiomyocytes.

Oleg Lookin, Anastasia Khokhlova, Tatiana Myachina, Xenia Butova, Olivier Cazorla, Pieter de Tombe

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Article in Frontiers in physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 11 citations in OpenAlex.

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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

6 authors at 3 institutions in 3 countries.

Oleg LookinInstitute of Immunology and Physiology, Ural Branch of Russian Academy of Sciences, Yekaterinburg, Russia.
Anastasia KhokhlovaInstitute of Immunology and Physiology, Ural Branch of Russian Academy of Sciences, Yekaterinburg, Russia.
Tatiana MyachinaInstitute of Immunology and Physiology, Ural Branch of Russian Academy of Sciences, Yekaterinburg, Russia.
Xenia ButovaInstitute of Immunology and Physiology, Ural Branch of Russian Academy of Sciences, Yekaterinburg, Russia.
Olivier CazorlaLaboratoire "Physiologie et Médecine Expérimentale du Coeur et des Muscles", Phymedexp, INSERM-CNRS - Montpellier University, Montpellier, France.
Pieter de TombeLaboratoire "Physiologie et Médecine Expérimentale du Coeur et des Muscles", Phymedexp, INSERM-CNRS - Montpellier University, Montpellier, France.
Institute of Immunology and Physiology · RUCentre National de la Recherche Scientifique · FRUniversité de Montpellier · FR

Funding

Sarcomeric Modifications and Progressive Cardiac MaladaptationP01HL062426 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DE TOMBE, PIETER P. · 2000 to 2020
$42.4M
NHLBI NIH HHS P01 HL062426
6 · The paper itself

Abstract

Cardiomyocytes contract keeping their sarcomere length (SL) close to optimal values for force generation. Transmural heterogeneity in SL across the ventricular wall coordinates the contractility of the whole-ventricle. SL heterogeneity (variability) exists not only at the tissue (macroscale) level, but also presents at the level of a single cardiomyocyte (microscale level). However, transmural differences in intracellular SL variability and its possible dependence on the state of contraction (e.g. end-diastole or end-systole) have not been previously reported. In the present study, we studied three aspects of sarcomere-to-sarcomere variability in intact cardiomyocytes isolated from the left ventricle of healthy guinea-pig: 1) transmural differences in SL distribution between subepi- (EPI) and subendocardial (ENDO) cardiomyocytes; 2) the dependence of intracellular variability in SL upon the state of contraction; 3) local differences in SL variability, comparing SL distributions between central and peripheral regions within the cardiomyocyte. To characterize the intracellular variability of SL, we used different normality tests for the assessment of SL distributions, as well as nonparametric coefficients to quantify the variability. We found that individual SL values in the end-systolic state of contraction followed a normal distribution to a lesser extent as compared to the end-diastolic state of contraction (∼1.3-fold and ∼1.6-fold in ENDO and EPI, respectively). The relative and absolute coefficients of sarcomere-to-sarcomere variability in end-systolic SL were significantly greater (∼1.3-fold) as compared to end-diastolic SL. This was independent of both the transmural region across the left ventricle and the intracellular region within the cardiomyocyte. We conclude that the intracellular variability in SL, which exists in normal intact guinea-pig cardiomyocytes, is affected by the contractile state of the myocyte. This phenomenon may play a role in inter-sarcomere communication in the beating heart.

Indexed as

guinea-pig cardiomyocytesintracellular variabilitynormal distributionsarcomere lengthtransmural heterogeneity

Identifiers

PMID35444559
PMCPMC9013801
OpenAlexW4225882270

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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.