RESUMO
2,6-Dimethyl-3,5-dimethoxycarbonyl-4-(O-difluromethoxyphenyl)-1,4- dihydropyridine (ryodipine) (2 x 10(-4) M) significantly blocks the resting Sr++ uptake in sartorius and iliofibularis muscles of Rana temporaria without changes in Ca++ and Mg++ content. Dihydropyridine CGP (2.10(-4) M) increased both [Sp++] and [Ca++] (mumol/g dr. w.) by about 20 and 13%, respectively, as compared with paired control muscles, whereas [Mg++] remained unaffected. The [Sr++] changes are interpreted as specific dihydropyridine-effect on the Ca(++)-channels in the muscle membrane.
Assuntos
Cálcio/metabolismo , Di-Hidropiridinas/farmacologia , Músculos/efeitos dos fármacos , Estrôncio/metabolismo , Animais , Cálcio/análise , Técnicas In Vitro , Soluções Isotônicas , Músculos/análise , Músculos/metabolismo , Nifedipino/análogos & derivados , Nifedipino/farmacologia , Piridinas/farmacologia , Rana temporaria , Solução de Ringer , Estrôncio/análiseRESUMO
2,6-Dimethyl-3,5-dimethoxycarbonyl-4-(o-difluromethoxyphenyl)- 1,4-dihydropyridine (ryodipine) blocks Ca-channels in phasic muscle fibres from ileofibularis and semitendinosus muscle of Rana esculenta. Ryodipine and some other newly synthesized dihydropyridines (10(-7)-10(-4) M) exerted a slight, if any, effect on the steady-state of potassium chord conductance in isotonic K+-sulfate solution. The effluxes of potassium and rubidium from the sartorius muscle of Rana temporaria also remained unchanged after addition of 2 x 10(-4) M ryodipine. Thus, the nonspecific dihydropyridine effect on ion transport seems to be poorly expressed.
Assuntos
Di-Hidropiridinas/farmacologia , Músculos/efeitos dos fármacos , Animais , Transporte Biológico/efeitos dos fármacos , Bloqueadores dos Canais de Cálcio/farmacologia , Canais de Cálcio/efeitos dos fármacos , Canais de Cálcio/metabolismo , Permeabilidade da Membrana Celular/efeitos dos fármacos , Relação Dose-Resposta a Droga , Potenciais da Membrana/efeitos dos fármacos , Músculos/metabolismo , Nifedipino/análogos & derivados , Nifedipino/farmacologia , Canais de Potássio/efeitos dos fármacos , Canais de Potássio/metabolismo , Rana esculenta , Rana temporariaAssuntos
Bloqueadores dos Canais de Cálcio/uso terapêutico , Doença das Coronárias/tratamento farmacológico , Nifedipino/análogos & derivados , Doença Aguda , Animais , Aspartato Aminotransferases/sangue , Creatina Quinase/sangue , Masculino , Nifedipino/uso terapêutico , Ratos , Verapamil/uso terapêuticoRESUMO
Prophylactic injection of the natural antioxidant alpha-tocopherol and synthetic antioxidants ionol, diludin and 6-mercurascan prevented the development of lesions during acute renal ischemia and subsequent reperfusion. Ionol proved more effective on intraperitoneal injection than on intragastric route of administration. It has been demonstrated that antiischemic effect of ionol is related to its ability to exhibit the process of lipid peroxidation.
Assuntos
Antioxidantes/uso terapêutico , Isquemia/tratamento farmacológico , Rim/irrigação sanguínea , Animais , Hidroxitolueno Butilado/uso terapêutico , Dicarbetoxi-Di-Hidrocolidina/análogos & derivados , Dicarbetoxi-Di-Hidrocolidina/uso terapêutico , Fluoresceínas/uso terapêutico , Masculino , Compostos Organomercúricos/uso terapêutico , Ratos , Vitamina E/uso terapêuticoRESUMO
Effect of antioxidants on the rate of free radical peroxidation was studied in mitochondria in presence of Fe2+. For this purpose derivatives of 1,4-dihydroxypyridine, their heteroaromatic analogues, NAD-H+ and butyl hydroxytoluene (35 substances) were tested in the system by chemoluminescence. Several 1,4-dihydroxypyridine derivatives were found to be effective reagents in the system and could be compared by the activity with the recognized synthetic antioxidant butyl hydroxytoluene.