This study was undertaken to investigate whether administration of melatonin protects PVB-Induced oxidative and metabolic toxicity in the liver of Wistar rats. Adult male Wistar rats were intraperitoneally injected with either melatonin or PVB (cisplatin, vinblastine, and bleomycin) alone or combination for a period of 9 weeks. A significant increase in lipid peroxidation levels and decrease in catalase and superoxide dismutase activity levels were observed in the liver mitochondria of rats treated with PVB indicating increased oxidative stress. PVB treatment significantly decreased the succinate dehydrogenase activity with a significant increase in lactate dehydrogenase, glucose-6-phosphate dehydrogenase, aspartate aminotransaminase, alanine aminotransaminase, and glutamate dehydrogenase activities indicating deranged hepatic metabolism. Melatonin administration, on the other hand was found to significantly improve PVB-Induced biochemical changes, bringing them closer to the controls. The results from the study provide evidence that treatment with PVB affects hepatic metabolism in rats by inducing oxidative stress followed by decreasing mitochondrial oxidation and also point towards the clinical potential of melatonin as an adjuvant therapy to conventional chemotherapeutic regimens. J. Exp. Zool. 323A: 301-308, 2015. (c) 2015 Wiley Periodicals, Inc.
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Fed Univ Rio Grande Sul UFRGS, Fac Biol Sci, Dept Physiol, Porto Alegre, RS, Brazil
Hosp Clin Porto Alegre HCPA, Expt Res Ctr, Expt Lab Pulmonol & Inflammat Sci, Porto Alegre, RS, BrazilFed Univ Rio Grande Sul UFRGS, Fac Biol Sci, Dept Physiol, Porto Alegre, RS, Brazil
Martins, Gabriela S.
Rosa, Carlos Gustavo S.
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Lutheran Univ Brazil ULBRA, Cellular & Mol Biol Program, Canoas, RS, BrazilFed Univ Rio Grande Sul UFRGS, Fac Biol Sci, Dept Physiol, Porto Alegre, RS, Brazil
Rosa, Carlos Gustavo S.
Schemitt, Elizangela G.
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Hosp Clin Porto Alegre HCPA, Expt Res Ctr, Expt Lab Pulmonol & Inflammat Sci, Porto Alegre, RS, BrazilFed Univ Rio Grande Sul UFRGS, Fac Biol Sci, Dept Physiol, Porto Alegre, RS, Brazil
Schemitt, Elizangela G.
Colares, Josieli R.
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Hosp Clin Porto Alegre HCPA, Expt Res Ctr, Expt Lab Pulmonol & Inflammat Sci, Porto Alegre, RS, BrazilFed Univ Rio Grande Sul UFRGS, Fac Biol Sci, Dept Physiol, Porto Alegre, RS, Brazil
Colares, Josieli R.
Fonseca, Sandielly R. B.
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Hosp Clin Porto Alegre HCPA, Expt Res Ctr, Expt Lab Pulmonol & Inflammat Sci, Porto Alegre, RS, BrazilFed Univ Rio Grande Sul UFRGS, Fac Biol Sci, Dept Physiol, Porto Alegre, RS, Brazil
Fonseca, Sandielly R. B.
Brasil, Marilda S.
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Fed Univ Rio Grande Sul UFRGS, Fac Biol Sci, Dept Physiol, Porto Alegre, RS, Brazil
Hosp Clin Porto Alegre HCPA, Expt Res Ctr, Expt Lab Pulmonol & Inflammat Sci, Porto Alegre, RS, BrazilFed Univ Rio Grande Sul UFRGS, Fac Biol Sci, Dept Physiol, Porto Alegre, RS, Brazil
Brasil, Marilda S.
Engeroff, Millena
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Hosp Clin Porto Alegre HCPA, Expt Res Ctr, Expt Lab Pulmonol & Inflammat Sci, Porto Alegre, RS, BrazilFed Univ Rio Grande Sul UFRGS, Fac Biol Sci, Dept Physiol, Porto Alegre, RS, Brazil
Engeroff, Millena
Marroni, Norma P.
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Fed Univ Rio Grande Sul UFRGS, Fac Biol Sci, Dept Physiol, Porto Alegre, RS, Brazil
Hosp Clin Porto Alegre HCPA, Expt Res Ctr, Expt Lab Pulmonol & Inflammat Sci, Porto Alegre, RS, BrazilFed Univ Rio Grande Sul UFRGS, Fac Biol Sci, Dept Physiol, Porto Alegre, RS, Brazil