Background: Cardiovascular disorders are a major cause of morbidity and mortality in diabetic patients. Increased vascular permeability is a hallmark of diabetic vasculopathy, and the administration of natural products with antioxidant activity could restore vascular function. Objectives: In this study, the effect of chronic treatment with sesamin on vascular permeability in rats with streptozotocin ( STZ)- induced diabetes was investigated. Materials and Methods: Male diabetic rats received sesamin at a dose of either 10 or 20 mg/kg for 7 weeks, beginning 1 week after diabetes induction. Vascular permeability was estimated by measuring Evans blue dye extravasation. Oxidative stress markers, including malondialdehyde (MDA) and superoxide dismutase (SOD) activity, were also measured in aortic tissue. Results: Extravasation of Evans blue dye increased significantly in the diabetic group compared to that in the control group (p < 0.05), and treatment with sesamin significantly and dose-dependently decreased this extravasation (p < 0.05). Diabetic rats also had elevated malondialdehyde ( MDA) and reduced superoxide dismutase (SOD) activity ( p<0.005-0.001), and chronic treatment with sesamin (20 mg/kg) significantly reversed the elevated MDA content (p < 0.05) and reduced SOD activity (p < 0.05). Conclusions: Chronic treatment of diabetic rats with sesamin could dose-dependently improve aortic permeability, partly through the attenuation of oxidative stress in aortic tissue. (C) 2011 Kowsar M.P.Co.All rights reserved.Background: Cardiovascular disorders are a major cause of morbidity and mortality in diabetic patients. Increased vascular permeability is a hallmark of diabetic vasculopathy, and the administration of natural products with antioxidant activity could restore vascular function. Objectives: In this study, the effect of chronic treatment with sesamin on vascular permeability in rats with streptozotocin (STZ)- induced diabetes was investigated. Materials and Methods: Male diabetic rats received sesamin at a dose of either 10 or 20 mg/kg for 7 weeks, beginning 1 week after diabetes induction. Vascular permeability was estimated by measuring Evans blue dye extravasation. Oxidative stress markers, including malondialdehyde (MDA) and superoxide dismutase (SOD) activity, were also measured in aortic tissue. Results: Extravasation of Evans blue dye increased significantly in the diabetic group compared to that in the control group (p < 0.05), and treatment with sesamin significantly and dose-dependently decreased this extravasation (p < 0.05). Diabetic rats also had elevated malondialdehyde (MDA) and reduced superoxide dismutase (SOD) activity ( p<0.005-0.001), and chronic treatment with sesamin (20 mg/kg) significantly reversed the elevated MDA content (p < 0.05) and reduced SOD activity ( p < 0.05). Conclusions: Chronic treatment of diabetic rats with sesamin could dose-dependently improve aortic permeability, partly through the attenuation of oxidative stress in aortic tissue. (C) 2011 Kowsar M.P.Co.All rights reserved.
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Univ Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, BrazilUniv Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, Brazil
Finamor, Isabela A.
Saccol, Etiane M. H.
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Univ Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, BrazilUniv Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, Brazil
Saccol, Etiane M. H.
Gabriel, Diogo
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Univ Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, BrazilUniv Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, Brazil
Gabriel, Diogo
Ourique, Giovana M.
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Univ Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, BrazilUniv Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, Brazil
Ourique, Giovana M.
Riffel, Ana P. K.
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Univ Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, BrazilUniv Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, Brazil
Riffel, Ana P. K.
Konrad, Signora P.
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Univ Vale Rio Sinos UNISINOS, Nutr Coll, Sao Leopoldo, RS, BrazilUniv Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, Brazil
Konrad, Signora P.
Bello-Klein, Adriane
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Univ Fed Rio Grande do Sul, Dept Physiol, UFRGS, Porto Alegre, RS, BrazilUniv Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, Brazil
Bello-Klein, Adriane
Partata, Wania
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Univ Fed Rio Grande do Sul, Dept Physiol, UFRGS, Porto Alegre, RS, BrazilUniv Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, Brazil
Partata, Wania
Baldisserotto, Bernardo
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Univ Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, BrazilUniv Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, Brazil
Baldisserotto, Bernardo
Llesuy, Susana F.
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Univ Buenos Aires, Dept Analyt Chem & Phys Chem, Buenos Aires, DF, ArgentinaUniv Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, Brazil
Llesuy, Susana F.
Pavanato, Maria A.
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Univ Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, BrazilUniv Fed Santa Maria, Dept Physiol & Pharmacol, UFSM, BR-97105900 Santa Maria, RS, Brazil