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1.
Acta Cir Bras ; 31(3): 183-9, 2016 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-27050789

RESUMO

PURPOSE: To determine the effect of grape-seed extract against ischemia/reperfusion injury in cholestatic liver. METHODS: Eighteen Wistar albino rats were divided into three groups. In control and study groups, cholestasis was provided by bile duct ligation. Seven days later, the rats were subjected to 30 min hepatic ischemia, followed by 60 min of reperfusion. Oral administration of 50 mg/kg/day grape-seed extract was started 15 days before bile duct ligation and continued to the second operation in the study group. Serum, plasma and liver samples were taken. Laboratory analysis, tissue gluthation, malondialdehyde, myeloperoxidase levels and histopathological examination were performed. RESULTS: Significant decrease in liver gluthation level and significant increase in malondialdehyde level and myeloperoxidase activity were observed after ischemia/reperfusion in cholestatic rats. Serum and plasma levels for laboratory analysis were also significantly higher in cholestatic I/R group. Hepatic necrosis and fibrosis were detected in histopathological examination. Oral grape-seed extract administiration reversed all these parameters and histopathological findings except serum bilirubin levels. CONCLUSION: Oral grape-seed extract treatment can improve liver functions and attenuate the inflammation and oxidative stress in cholestatic ischemia/reperfusion injury.


Assuntos
Antioxidantes/farmacologia , Colestase/complicações , Extrato de Sementes de Uva/farmacologia , Traumatismo por Reperfusão/prevenção & controle , Alanina Transaminase/efeitos dos fármacos , Alanina Transaminase/metabolismo , Animais , Aspartato Aminotransferases/efeitos dos fármacos , Aspartato Aminotransferases/metabolismo , Bilirrubina/metabolismo , Colestase/metabolismo , Colestase/patologia , Modelos Animais de Doenças , Inflamação/metabolismo , Lactato Desidrogenases/efeitos dos fármacos , Lactato Desidrogenases/metabolismo , Fígado/efeitos dos fármacos , Fígado/patologia , Masculino , Estresse Oxidativo/efeitos dos fármacos , Ratos Wistar , Traumatismo por Reperfusão/metabolismo
2.
Acta cir. bras ; Acta cir. bras;31(3): 183-189, Mar. 2016. tab, graf
Artigo em Inglês | LILACS | ID: lil-777096

RESUMO

ABSTRACT PURPOSE: To determine the effect of grape-seed extract against ischemia/reperfusion injury in cholestatic liver. METHODS: Eighteen Wistar albino rats were divided into three groups. In control and study groups, cholestasis was provided by bile duct ligation. Seven days later, the rats were subjected to 30 min hepatic ischemia, followed by 60 min of reperfusion. Oral administration of 50 mg/kg/day grape-seed extract was started 15 days before bile duct ligation and continued to the second operation in the study group. Serum, plasma and liver samples were taken. Laboratory analysis, tissue gluthation, malondialdehyde, myeloperoxidase levels and histopathological examination were performed. RESULTS: Significant decrease in liver gluthation level and significant increase in malondialdehyde level and myeloperoxidase activity were observed after ischemia/reperfusion in cholestatic rats. Serum and plasma levels for laboratory analysis were also significantly higher in cholestatic I/R group. Hepatic necrosis and fibrosis were detected in histopathological examination. Oral grape-seed extract administiration reversed all these parameters and histopathological findings except serum bilirubin levels. CONCLUSION: Oral grape-seed extract treatment can improve liver functions and attenuate the inflammation and oxidative stress in cholestatic ischemia/reperfusion injury.


Assuntos
Animais , Masculino , Traumatismo por Reperfusão/prevenção & controle , Colestase/complicações , Extrato de Sementes de Uva/farmacologia , Antioxidantes/farmacologia , Aspartato Aminotransferases/efeitos dos fármacos , Aspartato Aminotransferases/metabolismo , Bilirrubina/metabolismo , Traumatismo por Reperfusão/metabolismo , Colestase/metabolismo , Colestase/patologia , Ratos Wistar , Estresse Oxidativo/efeitos dos fármacos , Lactato Desidrogenases/efeitos dos fármacos , Lactato Desidrogenases/metabolismo , Alanina Transaminase/efeitos dos fármacos , Alanina Transaminase/metabolismo , Modelos Animais de Doenças , Inflamação/metabolismo , Fígado/efeitos dos fármacos , Fígado/patologia
3.
Cell Biochem Funct ; 29(5): 384-93, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-21538411

RESUMO

The specific activities of zinc/copper (Zn/Cu)-superoxide dismutase (SOD-1) and manganese (Mn)-superoxide dismutase (SOD-2) were assayed in young passage 5 fibroblasts and in serially subcultured cells that were characterized as senescent at passages 15-35. SOD-1 and SOD-2 activities did not significantly change in senescent and young cells cultured in either routine medium [minimum essential medium 1 (MEM1)], or in Zn, Cu and Mn supplemented medium (MEM2) containing normal human plasma levels of the cations. SOD-1 and SOD-2 activities, however, underwent parallel progressive significant activity increases in senescent passage 20 and 25 cells, which peaked in value in passage 30 and 35 cells subcultured in supplemented medium (MEM3) containing triple human plasma levels of the cations. Concurrently, superoxide radical generation rates underwent progressive significant increases in senescent passage 15-25 cells, which peaked in value in passage 30 and 35 cells subcultured in MEM1 or MEM2. These rates, however, were significantly lowered in senescent cells subcultured in MEM3. We infer that it was only possible to significantly stimulate SOD-1 and SOD-2 activities in senescent MEM3 cultured cells enabling them to combat oxidative stress.


Assuntos
Senescência Celular/fisiologia , Fibroblastos/efeitos dos fármacos , Micronutrientes/farmacologia , Superóxido Dismutase/efeitos dos fármacos , Cátions/farmacologia , Proliferação de Células/efeitos dos fármacos , Células Cultivadas , Senescência Celular/efeitos dos fármacos , Cobre/farmacologia , Meios de Cultura , Relação Dose-Resposta a Droga , Fibroblastos/fisiologia , Glicogênio Fosforilase/efeitos dos fármacos , Glicogênio Fosforilase/metabolismo , Humanos , Lactato Desidrogenases/efeitos dos fármacos , Lactato Desidrogenases/metabolismo , Manganês/farmacologia , Fosfofrutoquinases/efeitos dos fármacos , Fosfofrutoquinases/metabolismo , Pele/citologia , Superóxido Dismutase/metabolismo , Superóxido Dismutase-1 , Superóxidos/metabolismo , Zinco/farmacologia
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