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Calcium transport by rat brain mitochondria and oxidation of 2-oxoglutarate
Authors:Phyllis A Bernard  Ronald S Cockrell
Institution:Edward A. Doisy Department of Biochemistry St. Louis University School of Medicine, 1402 S. Grand Blvd., St. Louis, MO 63104 U.S.A.
Abstract:Contrary to previous reports brain mitochondria have a substantial capacity for net Ca2+ uptake (approx. 1.2 μeq. Ca2+ per mg protein) providing succinate is the oxidizable substrate. ATP stimulates calcium uptake (to 1.8 μeq. per mg protein), but is not required. The accumulation of Ca2+ with NAD-linked substrates is, however, significantly less. With 2-oxoglutarate, very limited Ca2+ uptake occurs before respiration is inhibited. At low concentrations (10 μM), Ca2+ stimulates the 2-oxoglutarate dehydrogenase activity of detergent solubilized mitochondria. Millimolar Ca2+] is required for inhibition. Therefore, Ca2+ inhibition of 2-oxoglutarate oxidation can explain the low maximum uptake with this substrate, but probably not by directly effecting the dehydrogenase. Hence, the oxidation of 2-oxoglutarate can be either enhanced or suppressed depending upon the net Ca2+ accumulated by brain mitochondria.
Keywords:2-Oxoglutarate dehydrogenase  Respiration  Brain mitochondria  (Rat)  FCCP  To whom correspondence should be addressed  
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