Protective effect of caffeic acid phenethyl ester (CAPE) administration on cisplatin-induced oxidative damage to liver in rat

被引:103
作者
Iraz, Mustafa [1 ]
Ozerol, Elif
Gulec, Mukaddes
Tasdemir, Seda
Idiz, Nuri
Fadillioglu, Ersin
Naziroglu, Mustafa
Akyol, Omer
机构
[1] Inonu Univ, Fac Med, Dept Pharmacol, TR-44280 Malatya, Turkey
[2] Inonu Univ, Fac Med, Dept Biochem & Physiol, Malatya, Turkey
[3] Ankara Univ, Fac Med, Dept Forens Toxicol, TR-06100 Ankara, Turkey
[4] Inonu Univ, Fac Med, Dept Physiol, Malatya, Turkey
[5] Rhein Westfal TH Aachen, Fac Med, Inst Physiol, D-52057 Aachen, Germany
[6] Hacettepe Univ, Fac Med, Dept Biochem, Ankara, Turkey
关键词
cisplatin; antioxidant; caffeic acid phenethyl ester; rat; liver;
D O I
10.1002/cbf.1232
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cisplatin is one of the most active cytotoxic agents in the treatment of cancer. High doses of cisplatin have also been known to produce hepatotoxicity. Several studies suggest that supplementation with an antioxidant can influence cisplatin-induced hepatotoxicity. The present study was designed to determine the effects of cisplatin on the liver oxidant/antioxidant system, and the possible protective effects of caffeic acid phenethyl ester (CAPE) on liver toxicity induced by cisplatin. Twenty-four adult female Wistar albino rats were divided into four groups of six rats each: control, cisplatin, CAPE, and cisplatin + CAPE. Cisplatin and CAPE were injected intraperitoneally. Liver tissue was removed to study the activities of catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), myeloperoxidase (MPO), xanthine oxidase (XO), adenosine deaminase (ADA), and the levels of malondialdehyde and nitric oxide (NO). The activities of SOD and GSH-Px increased in the cisplatin + CAPE and CAPE groups compared with the cisplatin group. CAT activity was higher in the cisplatin + CAPE group than the other three groups. XO activity was lower in the cisplatin group than the control group. MPO activity was also increased in the cisplatin group compared to the control and CAPE groups. It can be concluded that CAPE may prevent cisplatin-induced oxidative changes in liver by strengthening the antioxidant defence system by reducing reactive oxygen species and increasing antioxidant enzyme activities. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:357 / 361
页数:5
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