mitotempo has been researched along with Cardiomyopathies* in 2 studies
2 other study(ies) available for mitotempo and Cardiomyopathies
Article | Year |
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Magnesium Deficiency Causes a Reversible, Metabolic, Diastolic Cardiomyopathy.
Background Dietary Mg intake is associated with a decreased risk of developing heart failure, whereas low circulating Mg level is associated with increased cardiovascular mortality. We investigated whether Mg deficiency alone could cause cardiomyopathy. Methods and Results C57BL/6J mice were fed with a low Mg (low-Mg, 15-30 mg/kg Mg) or a normal Mg (nl-Mg, 600 mg/kg Mg) diet for 6 weeks. To test reversibility, half of the low-Mg mice were fed then with nl-Mg diet for another 6 weeks. Low-Mg diet significantly decreased mouse serum Mg (0.38±0.03 versus 1.14±0.03 mmol/L for nl-Mg; Topics: Adenosine Triphosphate; Animals; Antioxidants; Calcium Signaling; Cardiomyopathies; Carrier Proteins; Diastole; Disease Models, Animal; Magnesium Deficiency; Mice, Inbred C57BL; Mitochondria, Heart; Myocardial Contraction; Myocytes, Cardiac; Organophosphorus Compounds; Piperidines; Reactive Oxygen Species; Ventricular Function, Left | 2021 |
Mitochondrial dysfunction causing cardiac sodium channel downregulation in cardiomyopathy.
Cardiomyopathy is associated with cardiac Na(+) channel downregulation that may contribute to arrhythmias. Previously, we have shown that elevated intracellular NADH causes a decrease in cardiac Na(+) current (I(Na)) signaled by an increase in mitochondrial reactive oxygen species (ROS). In this study, we tested whether the NADH-mitochondria ROS pathway was involved in the reduction of I(Na) in a nonischemic cardiomyopathic model and correlated the findings with myopathic human hearts. Nonischemic cardiomyopathy was induced in C57BL/6 mice by hypertension after unilateral nephrectomy, deoxycorticosterone acetate (DOCA) pellet implantation, and salt water substitution. Sham operated mice were used as controls. After six weeks, heart tissue and ventricular myocytes isolated from mice were utilized for whole cell patch clamp recording, NADH/NAD(+) level measurements, and mitochondrial ROS monitoring with confocal microscopy. Human explanted hearts were studied using optical mapping. Compared to the sham mice, the arterial blood pressure was higher, the left ventricular volume was significantly enlarged (104.7±3.9 vs. 87.9±6.1 μL, P<0.05), and the ejection fraction was reduced (37.1±1.8% vs. 49.4±3.7%, P<0.05) in DOCA mice. Both the whole cell and cytosolic NADH level were increased (279±70% and 123±2% of sham, respectively, P<0.01), I(Na) was decreased (60±10% of sham, P<0.01), and mitochondrial ROS overproduction was observed (2.9±0.3-fold of sham, P<0.01) in heart tissue and myocytes of myopathic mice vs. sham. Treatment of myocytes with NAD(+) (500 μM), mitoTEMPO (10 μM), chelerythrine (50 μM), or forskolin (5 μM) restored I(Na) back to the level of sham. Injection of NAD(+) (100mg/kg) or mitoTEMPO (0.7 mg/kg) twice (at 24h and 1h before myocyte isolation) to animals also restored I(Na). All treatments simultaneously reduced mitochondrial ROS levels to that of controls. CD38 was found to transduce the extracellular NAD(+) signal. Correlating with the mouse model, failing human hearts showed a reduction in conduction velocity that improved with NAD(+). Nonischemic cardiomyopathy was associated with elevated NADH level, PKC activation, mitochondrial ROS overproduction, and a concomitant decrease in I(Na). Reducing mitochondrial ROS by application of NAD(+), mitoTEMPO, PKC inhibitors, or PKA activators, restored I(Na). NAD(+) improved conduction velocity in human myopathic hearts. Topics: Action Potentials; ADP-ribosyl Cyclase 1; Animals; Benzophenanthridines; Cardiomyopathies; Colforsin; Down-Regulation; Heart Conduction System; Humans; In Vitro Techniques; Membrane Glycoproteins; Membrane Potentials; Mice; Mice, Inbred C57BL; Mitochondria, Heart; Myocytes, Cardiac; NAD; NAV1.5 Voltage-Gated Sodium Channel; Organophosphorus Compounds; Oxidative Stress; Patch-Clamp Techniques; Piperidines; Reactive Oxygen Species | 2013 |