Mitochondrial membrane fluidity, potential, and calcium transients in the myocardium from acute diabetic ratsThis paper is one of a selection of papers published in this Special Issue, entitled The Cellular and Molecular Basis of Cardiovascular Dysfunction, Dhalla 70th Birthday Tribute

• Published in: Canadian journal of physiology and pharmacology 2007-03, Vol.85 (3-4), p.372-381
• Main Authors: Waczulikova, Iveta, Habodaszova, Dana, Cagalinec, Michal, Ferko, Miroslav, Ulicna, Olga, Mateasik, Anton, Sikurova, Libusa, Ziegelhöffer, Attila
• Format: Article
• Language: English
• Subjects: calcium transient; cardiac mitochondria; cardiomyocyte; confocal microscopy; diabète induit par la streptozotocine; fluidité membranaire; fluorescence spectroscopy; membrane fluidity; microscopie confocale; mitochondries cardiaques; potentiel transmembranaire; spectroscopie de fluorescence; streptozotocin diabetes; transitoire calcique; transmembrane potential
• ISSN: 0008-4212; 1205-7541
• DOI: 10.1139/Y07-035

In this study, we report for the first time concurrent measurements of membrane potential and dynamics and respiratory chain activities in rat heart mitochondria, as well as calcium transients in the hearts of rats in an early phase of streptozotocin diabetes, not yet accompanied with diabetes-induced complications. Quantitative relationships among these variables were assessed. The mitochondria from diabetic rats exhibited decreased fluorescence anisotropy values of diphenylhexatriene. This indicates that hydrophobic core of the membranes was more fluid compared with controls (p < 0.05). We discuss the changes in fluidity as having been associated with augmented energy transduction through the diabetic membranes. Reduced ratio of JC-1 fluorescence (aggregates to monomers) in the mitochondria from diabetic hearts reflected descendent transmembrane potential. A significant negative association between membrane fluidity and potential in the diabetic group was found (p < 0.05;; r = 0.67). Further, we observed an increase in calcium transient amplitude (CTA) in the diabetic cardiomyocytes (p = 0.048). We conclude that some of the calcium-induced regulatory events that dictate fuel selection and capacity for ATP production in diabetic heart occur at the membrane level. Our findings offer new insight into acute diabetes-induced changes in cardiac mitochondria.