INHIBITION OF RAT-BRAIN MITOCHONDRIAL CALCIUM-TRANSPORT BY CHLORDECONE

被引:31
作者
END, DW
CARCHMAN, RA
AMEEN, R
DEWEY, WL
机构
[1] Department of Pharmacology, Medical College of Virginia, Richmond
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
D O I
10.1016/0041-008X(79)90021-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Assessment of 45Ca2+ transport in rat brain mitochondria following in vitro and in vivo exposures to the neurotoxic insecticide chlordecone revealed a locus for chlordecone's mitochondrial impairment in the coupling reactions of oxidative phosphorylation. Mitochondrial 45Ca2+ transport supported by either 2 mm succinate (free energy supplied via electron transport) or 800 μm ATP (free energy supplied via the Mg2+ ATPase reaction) was inhibited by low concentrations of chlordecone (10-8-10-5 m). Administration of a tremorigenic dose (40 mg/kg, po) of chlordecone to rats similarly inhibited both succinate- and ATP-supported 45Ca2+ uptake in brain mitochondria in vitro. Studies on the subcellular distribution of [14C]chlordecone in rat brain following in vivo administrations were compared to those on the mitochondrial uptake of [14C]chlordecone in vitro. Administration of the 40-mg/kg tremorigenic dose of chlordecone produced mitochondrial chlordecone concentrations which were comparable to the tissue concentrations achieved by exposing mitochondria to a 2 × 10-6 m concentration of chlordecone in vitro. These data lend further support for mitochondrial inhibition as a mechanism for chlordecone toxicity. © 1979.
引用
收藏
页码:189 / 196
页数:8
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