1Suat Çakına, 2Latife Ceyda İrkin, 3Şamil Öztürk
1Çanakkale Onsekiz Mart University, Health Service Vocational College, Çanakkale-Turkey
2Çanakkale Onsekiz Mart University, Canakkale Faculty of Applied Sciences, Department of Fisheries Technology, Çanakkale-Turkey
3Çanakkale Onsekiz Mart University, Health Service Vocational College, Çanakkale-Turkey
DOI : https://doi.org/10.47191/ijmra/v7-i01-23Google Scholar Download Pdf
ABSTRACT:
Doxorubicin (DOX) is a chemotherapeutic agent and is widely used in cancer treatment. There are some studies suggesting oxidative stress-induced toxic changes in the liver due to DOX administration. The aim of this study was to reveal the oxidative damage of DOX in liver tissue at molecular level and to evaluate the protective effect of N-acetylcysteine (NAC) against DOX oxidative damage. Twenty four rats weighing 150-200 g were randomly divided into four equal groups; group I : control, group 2: received a single dose of DOX, group 3: received NAC for 28 days and group 4: received a single dose of DOX, followed by NAC for 28 days. At the end of the experiment, heart tissues were taken from all animals. Malondialdehyde (MDA), Total Antioxidant Capacity (TAC), Total Oxidant Capacity (TOC) levels were determined in these samples by spectrophotometric methods. It was determined that TOC level increased, TAC levels decreased in the group given DOX compared to the control group. In addition, TAC levels increased in the DOX+NAC group (p0.05). It was concluded that DOX administration increased oxidative stress and NAC administration could prevent it. NAC caused modulatory effects on oxidative stress and antioxidant redox system in DOX-induced heart toxicity in the rat.
KEYWORDS:Doxorubicin, N-Acetylcysteine, Heart, Oxidative stress.
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