Toxicological evaluation of chronic exposure to the organochalcogen 3-methyl-1-phenyl-2-(phenylseleno)oct-2-en-1-one in male rats |
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Authors: | Amanda Mello,Maria Carla Medeiros,Denise dos Santos Lacerda,Rodrigo B. de Andrade,Tanise Gemelli,Robson Brum Guerra,Clovis Milton Duval Wannmacher,Rosane Gomez,Clá udia Funchal |
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Affiliation: | 1. Centro Universitário Metodista do IPA, Porto Alegre – RS, Brazil;2. Departamento de Bioquímica, Universidade Federal do Rio Grande do Sul, Porto Alegre – RS, Brazil;3. Instituto Federal de Educação, Ciência e Tecnologia do Rio Grande do Sul, Sertão – RS, Brazil;4. Departamento de Farmacologia, Universidade Federal do Rio Grande do Sul, Porto Alegre – RS, Brazil |
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Abstract: | The aim of this study was to evaluate the effect of chronic treatment with the organochalcogen 3-methyl-1-phenyl-2-(phenylseleno)oct-2-en-1-one on some behavioral and biochemical parameters in the brain, liver, kidney and serum of 90-day-old male Wistar rats. The animals received the organoselenium at doses of 125, 250 or 500 μg/kg body weight intraperitoneally once daily for 30 days. Results showed that chronic treatment with this compound induced behavioral changes in animals, such as increasing of rearing at dose of 250 μg/kg and increasing of ambulation in all concentrations tested. On the other hand, we did not observe any alterations in the body weight gain of the animals. Moreover, the activity of the enzyme creatine kinase (CK) decreased in the cerebral cortex, cerebellum and kidney and increased in the liver after the chronic treatment with the organoselenium compound at dose of 500 μg/kg. The compound also increased aspartate aminotransferase (AST) and urea levels in serum of rats at 500 μg/kg. Glucose, cholesterol, triglycerides, creatinine, alanine aminotransferase (ALT) and lactate dehydrogenase (LDH) levels were not changed by the treatment. Our results thus show that chronic administration of 3-methyl-1-phenyl-2-(phenylseleno)oct-2-en-1-one is able to significantly change the activity of CK in Wistar rats, resulting in a change in cellular energy homeostasis in these tissues, liver damage and behavioral changes in the animals studied. |
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Keywords: | Se, selenium CK, creatine kinase BB-CK, cytosolic brain type CK Mi-CK, mitochondrial CK SH, thiol ALT, alanine aminotransferase AST, aspartate aminotransferase LDH, lactate dehydrogenase |
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