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Journal of Medicinal Plants. 2005; 4 (Supp. 1): 42-45
em Persa | IMEMR | ID: emr-72120

RESUMO

Cisplatin is an important anticancer drug, can be used in the treatment of several kinds of tumor. But its severe adverse effect i.e. kidney toxicity limited its uses. The present study undertaken to find out the protective effect of methanolic extract of Silybum marianum seeds [MES] and standard silymarin against cisplatin-induced renal toxicity. 48 male 10-8 week old wistar rats randomly divided into 6 group. They caged in same environmental condition. First group kept as control received saline, and second group received cisplantin [3 mg/kg] by single intraperitoneal injection. 3rd and 4th groups received silymarin and MES 2 hour before cisplatin administration. 5th and 6th group received silymarin and MES 2 hour after cisplatin administration. Over five days, cisplatin treated rats showed kidney tubular necrosis and elevation in blood urea nitrogen [BUN] and serum creatinine [Scr] Pretreatment of animals with silymarin [50 mg/kg] and MES [600 mg/kg] 2h before cisplatin administration reduced BUN and Scr as well as prevent the kidney tubular damage significantly. Rats treated with silymarin and MES 2h after cisplatin administration had BUN lower but mild to moderate kidney tubular necrosis was observed. These results suggested that silymarin as well as MES may protect kidney against cisplatin-induced renal toxicity and might serve as a novel combination agent with cisplatin to limit renal injury if clinical study proved its efficacy


Assuntos
Masculino , Animais de Laboratório , Silybum marianum , Cisplatino/efeitos adversos , Nefropatias/etiologia , Efeitos Colaterais e Reações Adversas Relacionados a Medicamentos , Cisplatino/administração & dosagem , Necrose Tubular Aguda/etiologia , Nitrogênio da Ureia Sanguínea , Creatinina/sangue , Ratos
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