the redox imbalance and the reduction of contractile protein content in rat hearts administered with l-thyroxine and doxorubicin氧化还原平衡和减少老鼠的心脏收缩蛋白质含量的管理与甲状腺素和阿霉素.pdfVIP
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the redox imbalance and the reduction of contractile protein content in rat hearts administered with l-thyroxine and doxorubicin氧化还原平衡和减少老鼠的心脏收缩蛋白质含量的管理与甲状腺素和阿霉素
Hindawi Publishing Corporation
Oxidative Medicine and Cellular Longevity
Volume 2012, Article ID 681367, 9 pages
doi:10.1155/2012/681367
Research Article
The Redox Imbalance and the Reduction of
Contractile Protein Content in Rat Hearts Administered with
L-Thyroxine and Doxorubicin
Agnieszka Korga,1 Jaroslaw Dudka,1 Franciszek Burdan,2 Justyna Sliwinska,3
Slawomir Mandziuk,4 and Katarzyna Dawidek-Pietryka5
1 Medical Biology Unit, Medical University of Lublin, 20-950 Lublin, Poland
2 Human Anatomy Department, Medical University of Lublin, 20-950 Lublin, Poland
3 Clinical Pathomorphology Department, Medical University of Lublin, 20-950 Lublin, Poland
4 Oncological Pneumology and Alergology Department, Medical University of Lublin, 20-950 Lublin, Poland
5 Lloyds Pharmacy, 333 Meadowhead, Sheffi eld S8 9TU, UK
Correspondence should be addressed to Agnieszka Korga, a.korg@interia.pl
Received 7 August 2011; Revised 15 October 2011; Accepted 15 November 2011
Academic Editor: Neelam Khaper
Copyright © 2012 Agnieszka Korga et al. This is an open access article distributed under the Creative Commons Attribution
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly
cited.
Oxidative stress and disorders in calcium balance play a crucial role in the doxorubicin-induced cardiotoxicity. Moreover, many
cardiotoxic targets of doxorubicin are regulated by iodothyronine hormones. The aim of the study was to evaluate effects of
tetraiodothyronine (0.2, 2 mg/L) on oxidative stress in the cardiac muscle as well as contractility and cardiomyocyte damage
markers in rats receiving doxorubicin (1.5 mg/kg) once a week for ten weeks. Doxorubicin was administered alone (DOX)
or
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