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Hypothermia treatment preserves mitochondrial integrity and viability of cardiomyocytes after ischaemic reperfusion injury
Journal
Injury
Journal Volume
46
Journal Issue
2
Pages
233-239
Date Issued
2015
Author(s)
Chiang C.-Y.
Pen R.-H.
Hsu C.-Y.
Abstract
Background: Haemorrhagic shock after traumatic injury carries a high mortality. Therapeutic hypothermia has been widely used in critical illness to improve the outcome in haemorrhagic shock by activation of cardiac pro-survival signalling pathways. However, the role played by the mitochondria in the cardioprotective effects of therapeutic hypothermia remains unclear. We investigated the effects of therapeutic hypothermia on mitochondrial function and integrity after haemorrhagic shock using an in vitro ischaemia-reperfusion model. Methods: H9c2 cardiomyocytes received a simulated ischaemic reperfusion injury under normothermic (37 °C) and hypothermic (31 °C) conditions. The cardiomyocytes were treated with hypoxic condition for 18 h in serum-free, glucose-free culture medium at pH 6.9 and then shifted to re-oxygenation status for 6 h in serum-containing cell culture medium at pH 7.4. Cellular survival, mitochondrial integrity, energy metabolism and calcium homeostasis were studied. Results: Hypothermia treatment lessened cell death (15.0 ± 12.7 vs. 31.9 ± 11.8%, P = 0.025) and preserved mitochondrial number (81.3 ± 17.4 vs. 45.2 ± 6.6, P = 0.03) against simulated ischaemic reperfusion injury. Hypothermia treatment ameliorated calcium overload in the intracellular (1.5 ± 0.2 vs. 9.5 ± 2.8, P < 0.001) and intra-mitochondrial (1.0 ± 0.3 vs. 1.6 ± 0.3, P = 0.014) compartments against the injury. Mitochondrial integrity was more preserved by hypothermia treatment (50.1 ± 26.6 vs. 14.8 ± 13.0%, P < 0.01) after the injury. Mitochondrial ATP concentrations were maintained with hypothermia treatment after injury (16.7 ± 9.5 vs. 6.1 ± 5.1 μM, P < 0.01). Conclusions: Hypothermia treatment at 31 °C can ameliorate cardiomyocyte damage caused by simulated ischaemic reperfusion injuries. Mitochondrial calcium homeostasis, energy metabolism, and membrane integrity are preserved and play critical roles during therapeutic hypothermia treatment. ? 2014 Elsevier Ltd. All rights reserved.
SDGs
Other Subjects
caspase 9; calcium; animal cell; apoptosis; Article; calcium cell level; calcium homeostasis; cell damage; cell death; cell hypoxia; cell survival; cell viability; controlled study; energy metabolism; enzyme activation; flow cytometry; heart mitochondrion; heart muscle cell; hemorrhagic shock; in vitro study; induced hypothermia; mitochondrial membrane potential; mitochondrion swelling; nonhuman; oxidative phosphorylation; pH; priority journal; rat; reperfusion injury; animal; cell culture; heart infarction prevention; heart muscle; heart muscle cell; human; induced hypothermia; metabolism; oxidative stress; pathology; procedures; reperfusion injury; signal transduction; warming; Animals; Calcium; Cell Survival; Cells, Cultured; Humans; Hypothermia, Induced; In Vitro Techniques; Ischemic Preconditioning, Myocardial; Myocardium; Myocytes, Cardiac; Oxidative Stress; Rats; Reperfusion Injury; Rewarming; Shock, Hemorrhagic; Signal Transduction
Publisher
Elsevier Ltd
Type
journal article