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1.
Pathol Int ; 50(1): 20-33, 2000 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-10692174

RESUMO

It is essential to analyze functions of megamitochondria (MG) to elucidate the mechanism of the formation of MG induced under various pathological conditions. The MG fraction obtained by a routine isolation procedure for normal mitochondria always consists of a mixed population of mitochondria enlarged to various degrees and also normal-sized ones. The purpose of the present study is to answer the question of whether or not data obtained from the MG fraction consisting of such a heterogeneous population of mitochondria with respect to their sizes really reflect functions of MG. In the present study mitochondria were obtained from the livers of rats treated with a 1% hydrazine diet for 8 days and those given 32% ethanol in drinking water for up to 2 months using various isolation procedures. Results obtained are summarized as follows: (i) mitochondria enlarged to various degrees and normal-sized ones are sometimes connected with each other by a narrow stalk in the hepatocyte of hydrazine-treated animals, and such connections are maintained to some extent when mitochondria are isolated; and (ii) mitochondria obtained from experimental animals by a routine isolation procedure for mitochondria ((700-7000)gR2"') and those obtained by alternative isolation procedure yielding the heavy ((500-2000)gR2"') and light ((2000-7000)gR2"') fractions show some functional similarities: decreases in the content of cytochrome a + a3; decreases in oxygen consumptions and phosphorylating abilities; decreases in monoamine oxidase and cytochrome c oxidase activities; lowered membrane potential of mitochondria; decreases in the rate of the generation of reactive oxygen species. These results may suggest that mitochondria enlarged to various degrees and normal-sized ones are functionally similar to each other and that the MG fraction obtained by a routine isolation procedure for normal mitochondria can be applied to the study of the function of MG.


Assuntos
Etanol/farmacologia , Hidrazinas/farmacologia , Fígado/efeitos dos fármacos , Mitocôndrias Hepáticas/fisiologia , Animais , Fracionamento Celular , Complexo IV da Cadeia de Transporte de Elétrons/metabolismo , Citometria de Fluxo , Fígado/citologia , Masculino , Potenciais da Membrana/efeitos dos fármacos , Mitocôndrias Hepáticas/ultraestrutura , Monoaminoxidase/metabolismo , Fosforilação Oxidativa , Consumo de Oxigênio/efeitos dos fármacos , Ratos , Ratos Wistar , Espécies Reativas de Oxigênio
2.
Arch Biochem Biophys ; 366(1): 157-67, 1999 Jun 01.
Artigo em Inglês | MEDLINE | ID: mdl-10334876

RESUMO

Effects of CoQ10 and cycloheximide (CHX) on hydrazine- and chloramphenicol (CP)-induced morphological and some functional changes of mitochondria using cultured rat hepatocytes and effects on the process of recovery from CP intoxication using mouse liver were examined. Results obtained are summarized as follows: (1) The formation of megamitochondria induced in the hepatocytes cultured for 22 h in the presence of 2 mM hydrazine or CP (300 microgram/ml) was suppressed by pretreatment of hepatocytes with CoQ10 (1 microM) or CHX (0.5 microgram/ml). This was proved by electron microscopic analysis of mitochondria. (2) Treatment of hepatocytes with hydrazine for 48 h or longer caused decreases in the membrane potential of mitochondria, which were suppressed by CoQ10. (3) Treatment of hepatocytes with hydrazine for 22 h or longer caused remarkable increases in intracellular levels of reactive oxygen species in hepatocytes, which were suppressed by CoQ10. (4) The process of recovery from the CP-induced changes of mitochondria in mouse liver was accelerated by CoQ10 and CHX.


Assuntos
Sequestradores de Radicais Livres/farmacologia , Mitocôndrias Hepáticas/efeitos dos fármacos , Ubiquinona/análogos & derivados , Animais , Apoptose/efeitos dos fármacos , Cloranfenicol/farmacologia , Coenzimas , Cicloeximida/farmacologia , Hidrazinas/farmacologia , Masculino , Potenciais da Membrana/efeitos dos fármacos , Mitocôndrias Hepáticas/patologia , Ratos , Ratos Wistar , Espécies Reativas de Oxigênio , Ubiquinona/farmacologia
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