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1.
Biomed Khim ; 54(5): 607-13, 2008.
Artigo em Russo | MEDLINE | ID: mdl-19105403

RESUMO

In erythrocytes and blood plasma of patients with the complicated peptic ulcer and postresectional syndromes there was the increase of conjugated dienes (and in the second group the increase in antioxidant activity). Under these conditions the main change was the sharp and identical decrease in glutathione activity. In patients with uncomplicated peptic ulcer there was sharp increase in erythrocyte and plasma glutathione activity and plasma GSH. In operated but basically healthy patients plasma glutathione peroxidase remained decreased but plasma GSH sharply increased. Evidently complicated peptic ulcer is characterized by decreased functioning of the glutathione system. Activation of this system and the decrease or disappearance of manifestations of oxidative stress are associated with a favorable course of this disease, especially at uncomplicated peptic ulcer. The revealed changes significantly differ from those observed in viral hepatitis, bile excretory treat diseases and strokes.


Assuntos
Antioxidantes/análise , Eritrócitos/metabolismo , Glutationa/sangue , Estresse Oxidativo , Úlcera Péptica/sangue , Feminino , Hepatite Viral Humana/sangue , Humanos , Masculino , Úlcera Péptica/cirurgia , Acidente Vascular Cerebral/sangue
2.
Biokhimiia ; 53(2): 227-32, 1988 Feb.
Artigo em Russo | MEDLINE | ID: mdl-3163503

RESUMO

The anthracycline antibiotics rubomycin (daunorubicin) and carminomycin at concentrations which stimulate mitochondrial respiration in the absence of ADP induce the swelling of rat liver mitochondria. Under these conditions, the lipid peroxidation (LPO) inhibitor ionol slows down both the respiration and swelling of mitochondria. This suggests that stimulation of respiration and swelling under effects of the antibiotics largely depend on LPO. In the presence of the respiration inhibitor antimycin no effect of ionol is observed. Adriamycin (doxorubicin) stimulates mitochondrial respiration in a lesser degree than rubomycin and carminomycin and fails to induce mitochondrial swelling.


Assuntos
Antibióticos Antineoplásicos/farmacologia , Mitocôndrias Hepáticas/efeitos dos fármacos , Dilatação Mitocondrial/efeitos dos fármacos , Consumo de Oxigênio/efeitos dos fármacos , Animais , Hidroxitolueno Butilado/farmacologia , Carrubicina/farmacologia , Daunorrubicina/farmacologia , Doxorrubicina/farmacologia , Técnicas In Vitro , Membranas Intracelulares/efeitos dos fármacos , Membranas Intracelulares/metabolismo , Peróxidos Lipídicos/metabolismo , Potenciais da Membrana/efeitos dos fármacos , Mitocôndrias Hepáticas/metabolismo , Naftacenos/farmacologia , Permeabilidade , Ratos
3.
Biokhimiia ; 52(1): 53-7, 1987 Jan.
Artigo em Russo | MEDLINE | ID: mdl-3814654

RESUMO

A comparative study on the effects of antitumour antibiotics of the anthracycline group (rubomycin, carminomycin and adriamycin) on respiration and oxidative phosphorylation in liver mitochondria in various metabolic states has been carried out for the first time. It was shown that the antibiotics under study cause partial inhibition of mitochondrial state 3 respiration, which is eliminated by an uncoupler. Treatment of liver mitochondria with the antibiotics decreases the ADP/O and respiratory control values and stimulates state 4 respiration. The latter is partly inhibited by oligomycin. The uncoupled respiration is decelerated in the presence of the antibiotics. Under these conditions the oxidation of succinate is inhibited by lower concentrations of the antibiotics than that of NAD+-dependent substrates. It was shown that the maximal activity is exerted by the most polar agent carminomycin, while the hydrophobic rubomycin is the least active. The experimental results are discussed in terms of the toxic effect of antitumour antibiotics.


Assuntos
Carrubicina/farmacologia , Daunorrubicina/análogos & derivados , Daunorrubicina/farmacologia , Doxorrubicina/farmacologia , Mitocôndrias Hepáticas/metabolismo , Consumo de Oxigênio/efeitos dos fármacos , Difosfato de Adenosina/metabolismo , Animais , Técnicas In Vitro , Cinética , Oxigênio/metabolismo , Ratos , Desacopladores/farmacologia
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