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1.
Fundam Clin Pharmacol ; 21(5): 547-53, 2007 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-17868208

RESUMO

Pathogenesis of nephrotoxicity of the synthetic anticancer drug cisplatin (CP) involves generation of reactive oxygen species and free radicals in the kidney cortex, and cysteine prodrug l-2-oxothiazolidine-4-carboxylic acid (OTC) has been confirmed to have a strong antioxidant action. Therefore, in the present work, we aimed at testing the possible protective or palliative effect of OTC on CP nephrotoxicity in rats. OTC was given at an oral dose of 150 mg/kg/day for 7 days. On day 7, some of these rats were given a single intraperitoneal injection of CP (or vehicle) at a dose of 6 mg/kg. Rats were killed, blood and urine samples were collected, and the kidneys were removed 6 days after CP treatment. Nephrotoxicity was evaluated histopathologically by light microscopy, and biochemically by measuring the concentrations of creatinine and urea in serum, reduced glutathione (GSH) concentration and superoxide dismutase (SOD) activity in renal cortex, and by urinalyses. CP significantly increased the concentrations of urea and creatinine (P < 0.05) by about 128% and 170% respectively. CP treatment reduced cortical GSH concentration by about 34% (P < 0.05), and the activity of SOD by about 28% (P < 0.05). CP treatment significantly increased urine volume and N-acetyl-beta-D-glucosaminidase (NAG) activity, and significantly decreased osmolality and protein concentrations. OTC significantly mitigated all these effects. Sections from saline- and OTC-treated rats showed apparently normal proximal tubules. However, kidneys of CP-treated rats had a moderate degree of necrosis. This appeared to be lessened when CP was given simultaneously with OTC. The concentration of CP in the cortical tissues was not significantly altered by OTC treatment. The results suggested that OTC had ameliorated the histopathological and biochemical indices of nephrotoxicity in rats. Pending further pharmacological and toxicological studies, OTC may potentially be useful as a nephroprotective agent.


Assuntos
Antineoplásicos/toxicidade , Antioxidantes/farmacologia , Cisplatino/toxicidade , Nefropatias/tratamento farmacológico , Ácido Pirrolidonocarboxílico/farmacologia , Tiazolidinas/farmacologia , Acetilglucosaminidase/metabolismo , Administração Oral , Animais , Creatinina/sangue , Glutationa/efeitos dos fármacos , Glutationa/metabolismo , Córtex Renal/efeitos dos fármacos , Córtex Renal/fisiopatologia , Nefropatias/induzido quimicamente , Masculino , Concentração Osmolar , Pró-Fármacos , Distribuição Aleatória , Ratos , Ratos Wistar , Superóxido Dismutase/efeitos dos fármacos , Superóxido Dismutase/metabolismo , Ureia/sangue
2.
Rev Elev Med Vet Pays Trop ; 43(3): 313-6, 1990.
Artigo em Inglês | MEDLINE | ID: mdl-1966396

RESUMO

This study intends to clarify the role of apparently healthy cattle as a reservoir of bluetongue (BT) virus to sheep in the Sudan. It confirms earlier work and establishes that cattle can harbour bluetongue virus to which sheep are susceptible in the country. Experimental transmission of BT virus between the two species suggests that the best indicator to determine viraemia in apparently healthy cattle is to inoculate susceptible sheep with suspected cattle virus. The condition of the viraemia and the virus survival in the field are discussed.


Assuntos
Bluetongue/transmissão , Bovinos/microbiologia , Reservatórios de Doenças/veterinária , Animais , Suscetibilidade a Doenças , Ovinos , Sudão
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