RESUMO
Embriões de pacu Piaractus mesopotamicus foram submetidos a sete tratamentos, com o objetivo de se testar a toxicidade de 2 crioprotetores: glicerol e dimetilsulfóxido (DMSO), e suas associações à sacarose, a temperatura ambiente de 28°C. Nenhum embrião sobreviveu aos tratamentos contendo glicerol. O DMSO foi o crioprotetor que apresentou menor toxicidade aos embriões de pacu.
Fish embryos Piaractus mesopotamicus were submetted to seven treatments to test. the toxicity of two cryoprotectants: glicerol and dimethilfoxidy (DMSO), and its associations with sucrose, at 28°C. There were no survival in treatments containing glicerol. DMSO was the cryoprotectant hat show little toxicity to the embryos.
Assuntos
Animais , Dimetil Sulfóxido/toxicidade , Técnicas Reprodutivas/veterinária , Crioprotetores/toxicidade , Embrião não Mamífero , Peixes/embriologia , Glicerol/toxicidadeRESUMO
The present work was designed to evaluate the effects of some antioxidants; vitamin E, vitamin C, deferoxamine and the ACE inhibitors [captopril and enalapril] on renal functions and peroxidative changes in glycerol-induced ARF in the rat. Drugs were given before and after induction of ARF by im injection of hypertonic glycerol solution. Serum and urinary urea, creatinine concentrations, urinary/serum urea and creatinine ratios, creatinine clearance, serum malondialdehyde as well as renal reduced glutathione concentrations were estimated. All the above mentioned drugs showed a significant renoprotective effect by improving the marked deterioration of the estimated kidney function tests in the uremic rats
Assuntos
Animais de Laboratório , Injúria Renal Aguda/veterinária , Antioxidantes/farmacologia , Inibidores da Enzima Conversora de Angiotensina/farmacologia , Testes de Função Renal , Peroxidases/efeitos dos fármacos , Glicerol/toxicidade , Rim/efeitos dos fármacos , Antioxidantes/farmacologiaRESUMO
1. Several mechanisms have been suggested for the renal damage induced by intramuscular injection of glycerol. 2. We investigated the role of beta recetor desensitization by propranolol, and blocking calcium channels by verapamil in providing protection to the renal tissue from glycerol-induced acute renal failure. 3. Propranolol but not verapamil provided a significant protection reflected by lowering blood urea and serum creatinine and attenuating histopathological changes. 4. We conclude that acute renal failure induced by glycerol may be partly mediated by stimulation of renal beta receptor