Bivalent metal ions modulate Cd2+ effects on isolated rat liver mitochondria

• Published in: Journal of bioenergetics and biomembranes Vol. 33; no. 4; p. 303
• Main Authors: Belyaeva, E A, Glazunov, V V, Nikitina, E R, Korotkov, S M
• Format: Journal Article
• Language: English
• Published: United States Springer Nature B.V 01.08.2001
• Subjects: Animals; Cadmium; Cadmium - pharmacology; Cations, Divalent - pharmacology; Cell Respiration - drug effects; Cesium Radioisotopes - pharmacokinetics; Drug Interactions; Intracellular Membranes - drug effects; Male; Metal ions; Metals, Heavy - pharmacology; Mitochondria; Mitochondria, Liver - drug effects; Mitochondrial DNA; Oxygen consumption; Permeability; Permeability - drug effects; Rats; Respiration; Ruthenium; Ruthenium Red - pharmacology; Uncoupling Agents - pharmacology
• ISSN: 0145-479X; 1573-6881
• DOI: 10.1023/A:1010607307099

We have studied Cd2+-induced effects on mitochondrial respiration and swelling in various media as a function of the [Cd2+] in the presence or absence of different bivalent metal ions or ruthenium red (RR). It was confirmed by monitoring oxygen consumption by isolated rat liver mitochondria that, beginning from 5 microM, Cd2+ decreased both ADP and uncoupler-stimulated respiration and increased their basal respiration when succinate was used as respiratory substrate. At concentrations higher than 5 microM, Cd2+ stimulated ion permeability of the inner mitochondrial membrane, which was monitored in this study by swelling of both nonenergized mitochondria in 125 mM KNO3 or NH4NO3 medium and succinate-energized mitochondria incubated in a medium containing 25 mM K-acetate and 100 mM sucrose. We have found substantial changes in the above-mentioned Cd2+ effects on mitochondria treated in sequence with 100 microM of Ca2+, Sr2+, Mn2+ or Ba2+(Me2+) and 7.5 microM RR, as well as the alterations in Cd2+ action on the uptake of 137Cs+ by succinate-energized mitochondria in the presence or absence of valinomycin in acetate medium (50 mM Tris-acetate and 140 mM sucrose) with or without Ca2+ or RR. The evidence obtained indicate that Ca2+ exhibits a synergestic action on all Cd2+ effects examined, whereas Sr2+ and Mn2+, conversely, are antagonistic. In the presence of RR, the Cd2+ effects on respiration [stimulation of State 4 respiration and inhibition of 2,4-dinitrophenol (DNP)-uncoupled respiration] still exist, but are observed at concentrations of cadmium more than one order higher; the inhibition of State 3 respiration by Cd2+ conversely, takes place under even lower cadmium concentrations than those determined without RR in the medium. In addition, RR added simultaneously with cadmium in the incubation medium prevents any swelling in the nitrate media, but induces an increment both in Cd2+-stimulated swelling and 137Cs+ (analog of K+) uptake in the acetate media. For the first time, we have shown that Cd2+-induced swelling in all media under study is susceptible to cyclosporin A (CSA), a high-potency inhibitor of the mitochondrial permeability transition (PT) pore. The observations are interpreted in terms of a dual effect of cadmium on respiratory chain activity and permeability transition.