Mechanism of contraction rhythm homeostasis for hyperthermal sarcomeric oscillations of neonatal cardiomyocytes

Abstract The heart rhythm is maintained by oscillatory changes in [Ca2+]. However, it has been suggested that the rapid drop in blood pressure that occurs with a slow decrease in [Ca2+] preceding early diastolic filling is related to the mechanism of rapid sarcomere lengthening associated with spont...

Full description

Bibliographic Details
Main Authors: Seine A. Shintani, Takumi Washio, Hideo Higuchi
Format: Article
Language:English
Published: Nature Publishing Group 2020-11-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-020-77443-x
id doaj-75cbc6b6536c4aa6a0c62c35a9726143
record_format Article
spelling doaj-75cbc6b6536c4aa6a0c62c35a97261432020-12-08T13:18:13ZengNature Publishing GroupScientific Reports2045-23222020-11-0110111210.1038/s41598-020-77443-xMechanism of contraction rhythm homeostasis for hyperthermal sarcomeric oscillations of neonatal cardiomyocytesSeine A. Shintani0Takumi Washio1Hideo Higuchi2Department of Biomedical Sciences, College of Life and Health Sciences, Chubu UniversityUT-Heart Inc.Department of Physics, Graduate School of Science, The University of TokyoAbstract The heart rhythm is maintained by oscillatory changes in [Ca2+]. However, it has been suggested that the rapid drop in blood pressure that occurs with a slow decrease in [Ca2+] preceding early diastolic filling is related to the mechanism of rapid sarcomere lengthening associated with spontaneous tension oscillation at constant intermediate [Ca2+]. Here, we analyzed a new type of oscillation called hyperthermal sarcomeric oscillation. Sarcomeres in rat neonatal cardiomyocytes that were warmed at 38–42 °C oscillated at both slow (~ 1.4 Hz), Ca2+-dependent frequencies and fast (~ 7 Hz), Ca2+-independent frequencies. Our high-precision experimental observations revealed that the fast sarcomeric oscillation had high and low peak-to-peak amplitude at low and high [Ca2+], respectively; nevertheless, the oscillation period remained constant. Our numerical simulations suggest that the regular and fast rthythm is maintained by the unchanged cooperative binding behavior of myosin molecules during slow oscillatory changes in [Ca2+].https://doi.org/10.1038/s41598-020-77443-x
collection DOAJ
language English
format Article
sources DOAJ
author Seine A. Shintani
Takumi Washio
Hideo Higuchi
spellingShingle Seine A. Shintani
Takumi Washio
Hideo Higuchi
Mechanism of contraction rhythm homeostasis for hyperthermal sarcomeric oscillations of neonatal cardiomyocytes
Scientific Reports
author_facet Seine A. Shintani
Takumi Washio
Hideo Higuchi
author_sort Seine A. Shintani
title Mechanism of contraction rhythm homeostasis for hyperthermal sarcomeric oscillations of neonatal cardiomyocytes
title_short Mechanism of contraction rhythm homeostasis for hyperthermal sarcomeric oscillations of neonatal cardiomyocytes
title_full Mechanism of contraction rhythm homeostasis for hyperthermal sarcomeric oscillations of neonatal cardiomyocytes
title_fullStr Mechanism of contraction rhythm homeostasis for hyperthermal sarcomeric oscillations of neonatal cardiomyocytes
title_full_unstemmed Mechanism of contraction rhythm homeostasis for hyperthermal sarcomeric oscillations of neonatal cardiomyocytes
title_sort mechanism of contraction rhythm homeostasis for hyperthermal sarcomeric oscillations of neonatal cardiomyocytes
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2020-11-01
description Abstract The heart rhythm is maintained by oscillatory changes in [Ca2+]. However, it has been suggested that the rapid drop in blood pressure that occurs with a slow decrease in [Ca2+] preceding early diastolic filling is related to the mechanism of rapid sarcomere lengthening associated with spontaneous tension oscillation at constant intermediate [Ca2+]. Here, we analyzed a new type of oscillation called hyperthermal sarcomeric oscillation. Sarcomeres in rat neonatal cardiomyocytes that were warmed at 38–42 °C oscillated at both slow (~ 1.4 Hz), Ca2+-dependent frequencies and fast (~ 7 Hz), Ca2+-independent frequencies. Our high-precision experimental observations revealed that the fast sarcomeric oscillation had high and low peak-to-peak amplitude at low and high [Ca2+], respectively; nevertheless, the oscillation period remained constant. Our numerical simulations suggest that the regular and fast rthythm is maintained by the unchanged cooperative binding behavior of myosin molecules during slow oscillatory changes in [Ca2+].
url https://doi.org/10.1038/s41598-020-77443-x
work_keys_str_mv AT seineashintani mechanismofcontractionrhythmhomeostasisforhyperthermalsarcomericoscillationsofneonatalcardiomyocytes
AT takumiwashio mechanismofcontractionrhythmhomeostasisforhyperthermalsarcomericoscillationsofneonatalcardiomyocytes
AT hideohiguchi mechanismofcontractionrhythmhomeostasisforhyperthermalsarcomericoscillationsofneonatalcardiomyocytes
_version_ 1724389280465289216