Ca2+ rise within a narrow window of concentration prevents functional injury of mitochondria exposed to hypoxia/reoxygenation by increasing antioxidative defence


L. Schild, Bereich Pathologische Biochemie der Medizinischen Fakultät der Otto-von-Guericke-Universität Magdeburg, Leipziger Str. 44, 39120 Magdeburg, Germany Tel: +49 0931 6713644 Fax: +49 0931 6719176 E-mail:


Injury of liver by ischaemia crucially involves mitochondrial damage. The role of Ca2+ in mitochondrial damage is still unclear. We investigated the effect of low micromolar Ca2+ concentrations on respiration, membrane permeability, and antioxidative defence in liver mitochondria exposed to hypoxia/reoxygenation. Hypoxia/reoxygenation caused decrease in state 3 respiration and in the respiratory control ratio. Liver mitochondria were almost completely protected at about 2 µm Ca2+. Below and above 2 µm Ca2+, mitochondrial function was deteriorated, as indicated by the decrease in respiratory control ratio. Above 2 µm Ca2+, the mitochondrial membrane was permeabilized, as demonstrated by the sensitivity of state 3 respiration to NADH. Below 2 µm Ca2+, the nitric oxide synthase inhibitor nitro-l-arginine methylester had a protective effect. The activities of the manganese superoxide dismutase and glutathione peroxidase after hypoxia showed maximal values at about 2 µm Ca2+. We conclude that Ca2+ exerts a protective effect on mitochondria within a narrow concentration window, by increasing the antioxidative defence.