Temperature-dependence of mitochondrial function and production of reactive oxygen species in the intertidal mud clam Mya arenaria

J Exp Biol. 2002 Jul;205(Pt 13):1831-41. doi: 10.1242/jeb.205.13.1831.

Abstract

Mitochondrial respiration, energetic coupling to phosphorylation and the production of reactive oxygen species (ROS) were studied in mitochondria isolated from the eurythermal bivalve Mya arenaria (Myoidea) from a low-shore intertidal population of the German Wadden Sea. Measurements were conducted both within the range of the habitat temperatures (5-15 degrees C) and when subjected to heat exposure at 20 degrees C and 25 degrees C. Experimental warming resulted in an increase in the rate of state 3 and state 4 respiration in isolated mitochondria. The highest respiratory coupling ratios (RCR) were found at 15 degrees C; at higher temperatures mitochondrial coupling decreased, and release of ROS doubled between 15 and 25 degrees C. ROS production was 2-3% of total oxygen consumption in state 3 (0.3-0.5 nmol ROS mg(-1) protein min(-1)) at the habitat temperature, reaching a maximum of 4.3 % of state 3 respiration and 7 % of oligomycin-induced state 4+ respiration under heat stress. Thus, state 4 respiration, previously interpreted exclusively as a measure of proton leakage, included a significant contribution from ROS formation in this animal, especially under conditions of heat stress. Oxygen radical formation was directly dependent on temperature-controlled respiration rates in states 3 and 4 and inversely related to mitochondrial coupling (RCR+) in state 4. Mitochondrial ROS formation is therefore involved in cellular heat stress in this eurythermal marine ectotherm.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Bivalvia / cytology
  • Bivalvia / metabolism*
  • Catalase / metabolism
  • Cell Respiration / physiology
  • Free Radical Scavengers / metabolism
  • Malondialdehyde / metabolism
  • Microscopy, Confocal
  • Mitochondria / metabolism*
  • Oxidation-Reduction
  • Reactive Oxygen Species / metabolism*
  • Rhodamines / metabolism
  • Superoxide Dismutase / metabolism
  • Temperature

Substances

  • Antioxidants
  • Free Radical Scavengers
  • Reactive Oxygen Species
  • Rhodamines
  • dihydrorhodamine 123
  • Malondialdehyde
  • Catalase
  • Superoxide Dismutase