Comparing Electron Leak in Vertebrate Muscle Mitochondria.

Integr Comp Biol

Department of Biological Sciences, University of Manitoba, 50 Sifton Road, Winnipeg, Manitoba, Canada R3T2N2.

Published: September 2018

AI Article Synopsis

  • Mitochondria produce reactive oxygen species (ROS) during ATP generation, impacting cell signaling and survival.
  • Recent research highlights how temperature affects ROS production in mitochondria, indicating that current experimental methods may not account for species-specific thermal variability.
  • The study suggests using an "oxidant ratio" (comparing electron leak to antioxidant capacity) for more accurate comparisons of mitochondrial ROS metabolism among different species.

Article Abstract

Mitochondrial electron transfer for oxidative ATP regeneration is linked to reactive oxygen species (ROS) production in aerobic eukaryotic cells. Because they can contribute to signaling as well as oxidative damage in cells, these ROS have profound impact for the physiology and survival of the organism. Although mitochondria have been recognized as a potential source for ROS for about 50 years, the mechanistic understanding on molecular sites and processes has advanced recently. Most experimental approaches neglect thermal variability among species although temperature impacts mitochondrial processes significantly. Here we delineate the importance of temperature by comparing muscle mitochondrial ROS formation across species. Measuring the thermal sensitivity of respiration, electron leak rate (ROS formation), and the antioxidant capacity (measured as H2O2 consumption) in intact mitochondria of representative ectothermic and endothermic vertebrate species, our results suggest that using a common assay temperature is inappropriate for comparisons of organisms with differing body temperatures. Moreover, we propose that measuring electron leak relative to the mitochondrial antioxidant capacity (the oxidant ratio) may be superior to normalizing relative to respiration rates or mitochondrial protein for comparisons of mitochondrial metabolism of ROS across species of varying mitochondrial respiratory capacities.

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Source
http://dx.doi.org/10.1093/icb/icy095DOI Listing

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