Reduction in hypoxia‐reoxygenation‐induced myocardial mitochondrial damage with exogenous methane. Issue 11 (4th May 2021)

• Record Type: Journal Article
• Authors: Jász, Dávid Kurszán; Szilágyi, Ágnes Lilla; Tuboly, Eszter; Baráth, Bálint; Márton, Anett Roxána; Varga, Petra; Varga, Gabriella; Érces, Dániel; Mohácsi, Árpád; Szabó, Anna; Bozó, Renáta; Gömöri, Kamilla; Görbe, Anikó; Boros, Mihály; Hartmann, Petra
• Is Part Of: Journal of cellular and molecular medicine. Volume 25:Issue 11(2021)
• Page Start: 5113
• Page End: 5123
• Publication Date: 2021-05-04
• Subjects: anoxia -- cardiomyocytes -- complex I -- methane -- mitochondrial membrane potential -- mitochondrial respiration -- reoxygenation; Cytology; Medicine; Molecular Biology; Cytologie -- Périodiques; Médecine -- Périodiques; Biologie moléculaire -- Périodiques; Cytology -- Periodicals; Medicine -- Periodicals; Molecular biology -- Periodicals; 611.01805
• DOI: 10.1111/jcmm.16498
• Languages: English
• ISSNs: 1582-1838

Abstract

Abstract: Albeit previous experiments suggest potential anti‐inflammatory effect of exogenous methane (CH4 ) in various organs, the mechanism of its bioactivity is not entirely understood. We aimed to investigate the potential mitochondrial effects and the underlying mechanisms of CH4 in rat cardiomyocytes and mitochondria under simulated ischaemia/reperfusion (sI/R) conditions. Three‐day‐old cultured cardiomyocytes were treated with 2.2% CH4 ‐artificial air mixture during 2‐hour‐long reoxygenation following 4‐hour‐long anoxia (sI/R and sI/R + CH4, n = 6‐6), with normoxic groups serving as controls (SH and SH + CH4 ; n = 6‐6). Mitochondrial functions were investigated with high‐resolution respirometry, and mitochondrial membrane injury was detected by cytochrome c release and apoptotic characteristics by using TUNEL staining. CH4 admixture had no effect on complex II (CII)‐linked respiration under normoxia but significantly decreased the complex I (CI)‐linked oxygen consumption. Nevertheless, addition of CH4 in the sI/R + CH4 group significantly reduced the respiratory activity of CII in contrast to CI and the CH4 treatment diminished mitochondrial H2 O2 production. Substrate‐induced changes to membrane potential were partially preserved by CH4, and additionally, cytochrome c release and apoptosis of cardiomyocytes were reduced in the CH4 ‐treated group. In conclusion, the addition of CH4 decreases mitochondrial ROS generation via blockade of electron transport at CI and reduces anoxia‐reoxygenation‐induced mitochondrial dysfunction and cardiomyocyte injury in vitro.