Increased oxidative stress and CaMKII activity contribute to electro‐mechanical defects in cardiomyocytes from a murine model of Huntington's disease

• Published in: The FEBS journal 2019-01, Vol.286 (1), p.110-123
• Main Authors: Joviano‐Santos, Julliane Vasconcelos, Santos‐Miranda, Artur, Botelho, Ana Flávia Machado, Jesus, Itamar Couto Guedes, Andrade, Jéssica Neves, Oliveira Barreto, Tatiane, Magalhães‐Gomes, Matheus Proença S., Valadão, Priscila Aparecida Costa, Cruz, Jader dos Santos, Melo, Marília Martins, Guatimosim, Silvia, Guatimosim, Cristina
• Format: Article
• Language: English
• Subjects: Abnormalities; Action potential; Animal models; Arrhythmia; Brain; Ca2+/calmodulin-dependent protein kinase II; Calcium; Calcium homeostasis; Calcium ions; Calcium signalling; Calcium-binding protein; Calmodulin; CaMKII; Cardiomyocytes; Cardiovascular diseases; Conduction; Defects; Disturbances; Genetic disorders; Glutathione; Glutathione peroxidase; Health risks; Homeostasis; Huntington's disease; Huntingtons disease; Kinases; Mechanical properties; Mice; Mitochondria; oxidative damage; Oxidative stress; Peroxidase; Prolongation; Proteins; Superoxide dismutase
• ISSN: 1742-464X; 1742-4658
• DOI: 10.1111/febs.14706

Huntington's disease (HD) is a neurodegenerative genetic disorder. Although described as a brain pathology, there is evidence suggesting that defects in other systems can contribute to disease progression. In line with this, cardiovascular defects are a major cause of death in HD. To date, relatively little is known about the peripheral abnormalities associated with the disease. Here, we applied a range of assays to evaluate cardiac electro‐mechanical properties in vivo, using a previously characterized mouse model of HD (BACHD), and in vitro, using cardiomyocytes isolated from the same mice. We observed conduction disturbances including QT interval prolongation in BACHD mice, indicative of cardiac dysfunction. Cardiomyocytes from these mice demonstrated cellular electro‐mechanical abnormalities, including a prolonged action potential, arrhythmic contractions, and relaxation disturbances. Cellular arrhythmia was accompanied by an increase in calcium waves and increased Ca2+/calmodulin‐dependent protein kinase II activity, suggesting that disruption of calcium homeostasis plays a key part. We also described structural abnormalities in the mitochondria of BACHD‐derived cardiomyocytes, indicative of oxidative stress. Consistent with this, imbalances in superoxide dismutase and glutathione peroxidase activities were detected. Our data provide an in vivo demonstration of cardiac abnormalities in HD together with new insights into the cellular mechanistic basis, providing a possible explanation for the higher cardiovascular risk in HD. Huntington's disease (HD) is a neurodegenerative disorder and the main cause of patients' death is related to cardiovascular defects. Here, we investigated cardiac dysfunction and its mechanisms in 12‐month‐old BACHD mice, which correspond to the late clinical manifestation in humans. Our data provide an in vivo demonstration together with a new evidence of the cellular mechanistic basis in cardiac HD.