Abstract
Introduction: In ventricular myocytes, spontaneous release of calcium (Ca2+) from the sarcoplasmic reticulum via ryanodine receptors (“Ca2+ sparks”) is acutely increased by stretch, due to a stretch-induced increase of reactive oxygen species (ROS). In acute regional ischemia there is stretch of ischemic tissue, along with an increase in Ca2+ spark rate and ROS production, each of which has been implicated in arrhythmogenesis. Yet, whether there is an impact of ischemia on the stretch-induced increase in Ca2+ sparks and ROS has not been investigated. We hypothesized that ischemia would enhance the increase of Ca2+ sparks and ROS that occurs with stretch. Methods: Isolated ventricular myocytes from mice (male, C57BL/6J) were loaded with fluorescent dye to detect Ca2+ sparks (4.6 μM Fluo-4, 10 min) or ROS (1 μM DCF, 20 min), exposed to normal Tyrode (NT) or simulated ischemia (SI) solution (hyperkalemia [15 mM potassium], acidosis [6.5 pH], and metabolic inhibition [1 mM sodium cyanide, 20 mM 2-deoxyglucose]), and subjected to sustained stretch by the carbon fiber technique (~10% increase in sarcomere length, 15 s). Ca2+ spark rate and rate of ROS production were measured by confocal microscopy. Results: Baseline Ca2+ spark rate was greater in SI (2.54 ± 0.11 sparks·s−1·100 μm−2; n = 103 cells, N = 10 mice) than NT (0.29 ± 0.05 sparks·s−1·100 μm−2; n = 33 cells, N = 9 mice; p < 0.0001). Stretch resulted in an acute increase in Ca2+ spark rate in both SI (3.03 ± 0.13 sparks·s−1·100 μm−2; p < 0.0001) and NT (0.49 ± 0.07 sparks·s−1·100 μm−2; p < 0.0001), with the increase in SI being greater than NT (+0.49 ± 0.04 vs. +0.20 ± 0.04 sparks·s−1·100 μm−2; p < 0.0001). Baseline rate of ROS production was also greater in SI (1.01 ± 0.01 normalized slope; n = 11, N = 8 mice) than NT (0.98 ± 0.01 normalized slope; n = 12, N = 4 mice; p < 0.05), but there was an acute increase with stretch only in SI (+12.5 ± 2.6%; p < 0.001). Conclusion: Ischemia enhances the stretch-induced increase of Ca2+ sparks in ventricular myocytes, with an associated enhancement of stretch-induced ROS production. This effect may be important for premature excitation and/or in the development of an arrhythmogenic substrate in acute regional ischemia.
Original language | English |
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Article number | 289 |
Journal | Frontiers in Physiology |
Volume | 11 |
DOIs | |
Publication status | Published - Apr 16 2020 |
Bibliographical note
Funding Information:This work was supported through a Mitacs—Japan Society for the Promotion of Science (JSPS) Internship funded by a Mitacs Globalink Research Award and a JSPS International Research Fellowship (IT11003 to BC), by the JSPS (KAKENHI 17K01359 and 15K21745 to GI), by the Canadian Institutes of Health Research (MOP 342562 to TAQ), and by the Natural Sciences and Engineering Research Council of Canada (RGPIN-2016-04879 to TAQ). TAQ was a National New Investigator of the Heart and Stroke Foundation of Canada.
Funding Information:
Funding. This work was supported through a Mitacs—Japan Society for the Promotion of Science (JSPS) Internship funded by a Mitacs Globalink Research Award and a JSPS International Research Fellowship (IT11003 to BC), by the JSPS (KAKENHI 17K01359 and 15K21745 to GI), by the Canadian Institutes of Health Research (MOP 342562 to TAQ), and by the Natural Sciences and Engineering Research Council of Canada (RGPIN-2016-04879 to TAQ). TAQ was a National New Investigator of the Heart and Stroke Foundation of Canada.
Publisher Copyright:
© Copyright © 2020 Cameron, Kai, Kaihara, Iribe and Quinn.
ASJC Scopus Subject Areas
- Physiology
- Physiology (medical)
PubMed: MeSH publication types
- Journal Article