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顺铂对大鼠产生毒性作用后肝脏腺苷脱氨酶、黄嘌呤氧化酶、过氧化氢酶、超氧化物歧化酶的活性以及丙二醛和一氧化氮的水平:咖啡酸苯乙酯的保护作用

The activities of liver adenosine deaminase, xanthine oxidase, catalase, superoxide dismutase enzymes and the levels of malondialdehyde and nitric oxide after cisplatin toxicity in rats: protective effect of caffeic acid phenethyl ester.

作者信息

Yilmaz H Ramazan, Sogut Sadik, Ozyurt Birsen, Ozugurlu Fikret, Sahin Semsettin, Isik Bunyamin, Uz Ebru, Ozyurt Huseyin

机构信息

Department of Medical Biology and Genetics, Faculty of Medicine, Suleyman Demirel University, Isparta, Turkey.

出版信息

Toxicol Ind Health. 2005 May;21(3-4):67-73. doi: 10.1191/0748233705th216oa.

Abstract

The aim of this experimental study was to investigate the effects of caffeic acid phenethyl ester (CAPE), an antioxidant agent, on cisplatin-induced hepatotoxicity through adenosine deaminase (AD), xanthine oxidase (XO), catalase (CAT), superoxide dismutase (SOD) activities and malondialdehyde (MDA) and nitric oxide (NO) levels in liver tissue of rats. Wistar albino rats were divided into three groups: control group (n = 6), cisplatin group (n = 9) and CAPE + cisplatin group (n = 8). All the chemicals used were applied intraperitoneally. Spectrophotometric methods were used to determine the activities of the above-mentioned enzymes in the liver tissue. NO level and XO activity were found to be increased in the cisplatin group compared to the control group. NO level was found to be decreased in the cisplatin + CAPE group in comparison with the cisplatin group. There was no significant change in the activity of XO between the cisplatin and cisplatin + CAPE groups. The activity of SOD was lower in the cisplatin group than both the control and cisplatin + CAPE groups. There was no significant change in the activity of CAT between the control and cisplatin groups. CAT activity was increased in the cisplatin + CAPE group compared to the cisplatin group. The AD activity and MDA level remained unchanged in all groups. The results obtained suggested that CAPE significantly attenuated the hepatotoxicity as an indirect target of cisplatin in an animal model of cisplatin-induced nephrotoxicity.

摘要

本实验研究的目的是通过测定大鼠肝组织中腺苷脱氨酶(AD)、黄嘌呤氧化酶(XO)、过氧化氢酶(CAT)、超氧化物歧化酶(SOD)的活性以及丙二醛(MDA)和一氧化氮(NO)的水平,来研究抗氧化剂咖啡酸苯乙酯(CAPE)对顺铂诱导的肝毒性的影响。将Wistar白化大鼠分为三组:对照组(n = 6)、顺铂组(n = 9)和CAPE +顺铂组(n = 8)。所有使用的化学物质均通过腹腔注射给药。采用分光光度法测定肝组织中上述酶的活性。结果发现,与对照组相比,顺铂组的NO水平和XO活性升高。与顺铂组相比,顺铂+ CAPE组的NO水平降低。顺铂组和顺铂+ CAPE组之间XO活性没有显著变化。顺铂组的SOD活性低于对照组和顺铂+ CAPE组。对照组和顺铂组之间CAT活性没有显著变化。与顺铂组相比,顺铂+ CAPE组的CAT活性增加。所有组的AD活性和MDA水平均保持不变。所得结果表明,在顺铂诱导的肾毒性动物模型中,CAPE作为顺铂的间接靶点可显著减轻肝毒性。

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