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Effects of Ginkgo biloba extract on expression of biomarkers during aflatoxin B1-induced hepatocarcinogenesis in Wistar rats

Yanrong Hao Jianjia Su Chao Ou Ji Cao Fang Yang Xiaoxian Duan Chun Yang Yuan Li

中德临床肿瘤学杂志(英文版)2012,Vol.11Issue(5):261-265,5.
中德临床肿瘤学杂志(英文版)2012,Vol.11Issue(5):261-265,5.DOI:10.1007/s10330-012-0967-z

Effects of Ginkgo biloba extract on expression of biomarkers during aflatoxin B1-induced hepatocarcinogenesis in Wistar rats

Effects of Ginkgo biloba extract on expression of biomarkers during aflatoxin B1-induced hepatocarcinogenesis in Wistar rats

Yanrong Hao 1Jianjia Su 2Chao Ou 2Ji Cao 2Fang Yang 2Xiaoxian Duan 2Chun Yang 2Yuan Li2

作者信息

  • 1. Department of Radiotherapy, Clinical Cancer Center, The People's Hospital of Guangxi Zhuang Autonomous Region, Nanning 530021, China
  • 2. Cancer Institute of Guangxi Cancer Hospital, Guangxi Medicial University, Nanning 530021, China
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摘要

Abstract

Objective: The aim of this study was to study the effect of Ginkgo biloba extract (EGb761) on metabolism of aflatoxin B1 (AFB1) in Wistar rats. Methods: Seventy one Wistar rats were assigned at random to groups A, B and C. Rats in groups A, B were injected with AFB1 (intraperitoneal, 100–200 μg/kg body weight, 1–3 times/week). Group C was normal control. Rats in group B were fed in food with EGb761, while rats in groups A, C were given normal food. Blood samples were collected and liver biopsies were performed on the 14th, 28th and 42nd week. All the rats were sacrificed on the 64th week. The incidence of hepatocarcinoma was investigated. The hepatic phase I drug-metabolizing enzyme Cytochrome-P450 (CYP450) and phase II metabolizing enzyme glutathione S-transferase (GST) were analyzed with spectrometry. Serum AFB1-lysine adduct levels were assessed with high performance liquid chromatography (HPLC). The expression of 8-hydroxydeoxy-guanosine (8-OHdG) was measured with immunohistochemistry. Results: The incidence of hepatocellular carcinoma (HCC) in group B was significantly lower than that in group A (26.92% vs 76.00%, P < 0.001). No HCC developed in group C. EGb761 showed no effects on the activities of CYP450 and GST in rat liver tissues. The level of AFB1-lysine adduct reached the peak (4356.01 pg/mg albumin) at the 14th week in group A. EGb761 significantly inhibited the formation of AFB1-lysine adduct in serum by 13.07% at the 14th week (P = 0.033), and 73.63% at the 42nd week (P = 0.002). The expression of 8-OHdG protein in rat liver tissues in group B was significantly lower than that in group A at the 28th, 42nd, and 64th week (P < 0.05). Conclu-sion: The main mechanism underlying the effect of EGb761 in blocking hepatocarcinogenesis induced by AFB1 may not be fully attributable to its influence on the activity of liver phase I and phase II metabolizing enzymes. EGb761 inhibits the produc-tion of AFB1-lysine adducts, decreases the expression of 8-OHdG protein, and finally alleviates the DNA oxidative injury, which may be one of the mechanisms for the effects of EGb761 in inhibiting or delaying AFB1-induced hepatocarcinogenesis.

关键词

liver neoplasms/experimental/Ginkgo biloba extract (EGb761)/aflatoxin B1 (AFB1)/AFB1-lysine adducts/8-hydroxydeoxyguanosine (8-OHdG)

Key words

liver neoplasms/experimental/Ginkgo biloba extract (EGb761)/aflatoxin B1 (AFB1)/AFB1-lysine adducts/8-hydroxydeoxyguanosine (8-OHdG)

引用本文复制引用

Yanrong Hao,Jianjia Su,Chao Ou,Ji Cao,Fang Yang,Xiaoxian Duan,Chun Yang,Yuan Li..Effects of Ginkgo biloba extract on expression of biomarkers during aflatoxin B1-induced hepatocarcinogenesis in Wistar rats [J].中德临床肿瘤学杂志(英文版),2012,11(5):261-265,5.

中德临床肿瘤学杂志(英文版)

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