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Med Sci Monit ; 22: 880-9, 2016 Mar 17.
Artigo em Inglês | MEDLINE | ID: mdl-26986029

RESUMO

BACKGROUND: We investigated the effect of grape seed proanthocyanidins (GSPs) on carbon tetrachloride (CCl4)-induced acute liver injury. MATERIAL/METHODS: Sixty SPF KM mice were randomly divided into 6 groups: the control group, CCl4-model group, bifendate group (DDB group), and low-, moderate-, and high-dose GSP groups. The following parameters were measured: serum levels of alanine aminotransferase (ALT); aspartate aminotransferase (AST); tumor necrosis factor (TNF)-α; interleukin-6 (IL-6); high-mobility group box (HMGB)-1; body weight; liver, spleen, and thymus indexes; superoxide dismutase (SOD) and glutathione peroxidase (GSH-Px) activity; HMGB1 mRNA; malondialdehyde (MDA) content; hepatocyte proliferation; and changes in liver histology. RESULTS: Compared to the CCl4-model group, decreases in liver index and increases in thymus index significantly increased SOD and GSH-Px activities and reduced MDA content, and higher hepatocyte proliferative activity was found in all GSP dose groups and the DDB group (all P<0.001). Compared with the CCl4-model group, serum TNF-α and IL-6 levels and HMGB 1 mRNA and protein expressions decreased significantly in the high GSP dose group (all P<0.05). CONCLUSIONS: Our results provide strong evidence that administration of GSPs might confer significant protection against CCl4-induced acute liver injury in mice.


Assuntos
Extrato de Sementes de Uva/farmacologia , Extrato de Sementes de Uva/uso terapêutico , Hepatopatias/tratamento farmacológico , Fígado/patologia , Proantocianidinas/farmacologia , Proantocianidinas/uso terapêutico , Substâncias Protetoras/farmacologia , Alanina Transaminase/sangue , Animais , Aspartato Aminotransferases/sangue , Tetracloreto de Carbono , Glutationa Peroxidase/metabolismo , Proteína HMGB1/genética , Proteína HMGB1/metabolismo , Hepatócitos/efeitos dos fármacos , Hepatócitos/metabolismo , Hepatócitos/patologia , Interleucina-6/sangue , Fígado/efeitos dos fármacos , Hepatopatias/sangue , Hepatopatias/enzimologia , Hepatopatias/patologia , Malondialdeído/metabolismo , Camundongos , RNA Mensageiro/genética , RNA Mensageiro/metabolismo , Baço/efeitos dos fármacos , Baço/patologia , Superóxido Dismutase/metabolismo , Timo/efeitos dos fármacos , Timo/patologia , Fator de Necrose Tumoral alfa/sangue , Aumento de Peso/efeitos dos fármacos
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