Protective role of antioxidant vitamin E and catechin on idarubicin-induced cardiotoxicity in rats

Idarubicin is an anthracycline antibiotic extensively used in acute leukemia. In the present study we investigated whether vitamin E and catechin can reduce the toxic effects of idarubicin. Vitamin E (200 IU kg-1 week-1), catechin (200 mg kg-1 week-1), idarubicin (5 mg kg-1 week-1), idarubicin + vit...

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Main Authors: Kalender S., Kalender Y., Ates A., Yel M., Olcay E., Candan S.
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2002-01-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2002001100017
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spelling doaj-36460a3e54e543a0a06feb96cb4f217d2020-11-24T23:13:28ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research0100-879X0034-73102002-01-01351113791387Protective role of antioxidant vitamin E and catechin on idarubicin-induced cardiotoxicity in ratsKalender S.Kalender Y.Ates A.Yel M.Olcay E.Candan S.Idarubicin is an anthracycline antibiotic extensively used in acute leukemia. In the present study we investigated whether vitamin E and catechin can reduce the toxic effects of idarubicin. Vitamin E (200 IU kg-1 week-1), catechin (200 mg kg-1 week-1), idarubicin (5 mg kg-1 week-1), idarubicin + vitamin E (200 IU kg-1 week-1), and idarubicin + catechin (200 mg kg-1 week-1) combinations were given to male Sprague-Dawley rats weighing 210 to 230 g (N = 6/group). Idarubicin-treated animals exhibited a decrease in body and heart weight, a decrease in myocardial contractility, and changes in ECG parameters (P<0.01). Catechin + idarubicin- and vitamin E + idarubicin-treated groups exhibited similar alterations, but changes were attenuated in comparison to those in cardiac muscle of idarubicin-treated rats (P<0.05). Superoxide dismutase and catalase activity was reduced in the idarubicin-treated group (P<0.05). Glutathione peroxidase levels were decreased in the idarubicin-treated group (P<0.05) and reached maximum concentrations in the catechin- and catechin + idarubicin-treated groups compared to control (P<0.01). Malondialdehyde activity was decreased in the catechin + idarubicin-treated groups compared to control and increased in the other groups, reaching maximum concentrations in the vitamin E-treated group (P<0.01). In electron microscopy studies, swelling of the mitochondria and dilatation of the sarcoplasmic reticulum of myocytes were observed in the idarubicin-treated groups. In groups that were given idarubicin + vitamin E and idarubicin + catechin, the only morphological change was a weak dilatation of the sarcoplasmic reticulum. We conclude that catechin and vitamin E significantly reduce idarubicin-induced cardiotoxicity in rats.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2002001100017IdarubicinCatechinVitamin ECardiotoxicityUltrastructure
collection DOAJ
language English
format Article
sources DOAJ
author Kalender S.
Kalender Y.
Ates A.
Yel M.
Olcay E.
Candan S.
spellingShingle Kalender S.
Kalender Y.
Ates A.
Yel M.
Olcay E.
Candan S.
Protective role of antioxidant vitamin E and catechin on idarubicin-induced cardiotoxicity in rats
Brazilian Journal of Medical and Biological Research
Idarubicin
Catechin
Vitamin E
Cardiotoxicity
Ultrastructure
author_facet Kalender S.
Kalender Y.
Ates A.
Yel M.
Olcay E.
Candan S.
author_sort Kalender S.
title Protective role of antioxidant vitamin E and catechin on idarubicin-induced cardiotoxicity in rats
title_short Protective role of antioxidant vitamin E and catechin on idarubicin-induced cardiotoxicity in rats
title_full Protective role of antioxidant vitamin E and catechin on idarubicin-induced cardiotoxicity in rats
title_fullStr Protective role of antioxidant vitamin E and catechin on idarubicin-induced cardiotoxicity in rats
title_full_unstemmed Protective role of antioxidant vitamin E and catechin on idarubicin-induced cardiotoxicity in rats
title_sort protective role of antioxidant vitamin e and catechin on idarubicin-induced cardiotoxicity in rats
publisher Associação Brasileira de Divulgação Científica
series Brazilian Journal of Medical and Biological Research
issn 0100-879X
0034-7310
publishDate 2002-01-01
description Idarubicin is an anthracycline antibiotic extensively used in acute leukemia. In the present study we investigated whether vitamin E and catechin can reduce the toxic effects of idarubicin. Vitamin E (200 IU kg-1 week-1), catechin (200 mg kg-1 week-1), idarubicin (5 mg kg-1 week-1), idarubicin + vitamin E (200 IU kg-1 week-1), and idarubicin + catechin (200 mg kg-1 week-1) combinations were given to male Sprague-Dawley rats weighing 210 to 230 g (N = 6/group). Idarubicin-treated animals exhibited a decrease in body and heart weight, a decrease in myocardial contractility, and changes in ECG parameters (P<0.01). Catechin + idarubicin- and vitamin E + idarubicin-treated groups exhibited similar alterations, but changes were attenuated in comparison to those in cardiac muscle of idarubicin-treated rats (P<0.05). Superoxide dismutase and catalase activity was reduced in the idarubicin-treated group (P<0.05). Glutathione peroxidase levels were decreased in the idarubicin-treated group (P<0.05) and reached maximum concentrations in the catechin- and catechin + idarubicin-treated groups compared to control (P<0.01). Malondialdehyde activity was decreased in the catechin + idarubicin-treated groups compared to control and increased in the other groups, reaching maximum concentrations in the vitamin E-treated group (P<0.01). In electron microscopy studies, swelling of the mitochondria and dilatation of the sarcoplasmic reticulum of myocytes were observed in the idarubicin-treated groups. In groups that were given idarubicin + vitamin E and idarubicin + catechin, the only morphological change was a weak dilatation of the sarcoplasmic reticulum. We conclude that catechin and vitamin E significantly reduce idarubicin-induced cardiotoxicity in rats.
topic Idarubicin
Catechin
Vitamin E
Cardiotoxicity
Ultrastructure
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2002001100017
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