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2023-08-20

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cc-by-nc-nd (c) Sánchez-Pérez, Patricia et al., 2023
Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/224701

Energy substrate metabolism, mitochondrial structure and oxidative stress after cardiac ischemia-reperfusion in mice lacking UCP3.

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https://doi.org/10.1016/j.freeradbiomed.2023.05.014

Resum

Myocardial ischemia-reperfusion (IR) injury may result in cardiomyocyte dysfunction. Mitochondria play a critical role in cardiomyocyte recovery after IR injury. The mitochondrial uncoupling protein 3 (UCP3) has been proposed to reduce mitochondrial reactive oxygen species (ROS) production and to facilitate fatty acid oxidation. As both mechanisms might be protective following IR injury, we investigated functional, mitochondrial structural, and metabolic cardiac remodeling in wild-type mice and in mice lacking UCP3 (UCP3-KO) after IR. Results showed that infarct size in isolated perfused hearts subjected to IR ex vivo was larger in adult and old UCP3-KO mice than in equivalent wild-type mice, and was accompanied by higher levels of creatine kinase in the effluent and by more pronounced mitochondrial structural changes. The greater myocardial damage in UCP3-KO hearts was confirmed in vivo after coronary artery occlusion followed by reperfusion. S1QEL, a suppressor of superoxide generation from site IQ in complex I, limited infarct size in UCP3-KO hearts, pointing to exacerbated superoxide production as a possible cause of the damage. Metabolomics analysis of isolated perfused hearts confirmed the reported accumulation of succinate, xanthine and hypoxanthine during ischemia, and a shift to anaerobic glucose utilization, which all recovered upon reoxygenation. The metabolic response to ischemia and IR was similar in UCP3-KO and wild-type hearts, being lipid and energy metabolism the most affected pathways. Fatty acid oxidation and complex I (but not complex II) activity were equally impaired after IR. Overall, our results indicate that UCP3 deficiency promotes enhanced superoxide generation and mitochondrial structural changes that increase the vulnerability of the myocardium to IR injury.

Matèries

Àcids grassos, Malalties coronàries, Metabolisme energètic

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Fatty acids, Coronary diseases, Energy metabolism

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Articles publicats en revistes (Ciències Fisiològiques)
Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

Citació

SÁNCHEZ-PÉREZ, Patricia, MATA, Ana, TORP, May-kristin, LÓPEZ BERNARDO, Elia, HEIESTAD, Christina m., ARONSEN, Jan magnus, MOLINA-IRACHETA, Antonio, JIMÉNEZ-BORREGUERO, Luis j., GARCÍA-ROVES, Pablo m. (pablo miguel), COSTA, Ana s.h., FREZZA, Christian, MURPHY, Michael p., STENSLOKKEN, Kåre-olav, CADENAS, Susana. Energy substrate metabolism, mitochondrial structure and oxidative stress after cardiac ischemia-reperfusion in mice lacking UCP3.. _Free Radical Biology and Medicine_. 2023. Vol. 205, núm. 244-261. [consulta: 8 de gener de 2026]. ISSN: 0891-5849. [Disponible a: https://hdl.handle.net/2445/224701]

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