Chemomodulatory effect of Ficus racemosa extract against chemically induced renal carcinogenesis and oxidative damage response in Wistar rats

被引:48
作者
Khan, N [1 ]
Sultana, S [1 ]
机构
[1] Hamdard Univ, Sect Chemoprevent & Nutr Toxicol, Dept Med Elementol & Toxicol, Fac Sci, New Delhi 110062, India
关键词
carcinogenesis; chemoprevention; ferric nitrilotriacetate; Ficus racemosa extract; oxidative stress;
D O I
10.1016/j.lfs.2004.12.041
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
Ferric nitrilotriacetate (Fe-NTA) is a well-known renal carcinogen. In this communication, we show the chemopreventive effect of Ficus racemosa extract against Fe-NTA-induced renal oxidative stress, hyper-proliferative response and renal carcinogenesis in rats. Fe-NTA (9 mg Fe/kg body weight, intraperitoneally) enhances renal lipid peroxidation, xanthine oxidase, gamma-glutamyl transpeptidase and hydrogen peroxide (H2O2) generation with reduction in renal glutathione content, antioxidant enzymes, viz., glutathione peroxidase, glutathione reductase, catalase, glucose-6-phosphate dehydrogenase and phase-II metabolising enzymes such as glutathione-S-transferase and quinone reductase. It also enhances blood urea nitrogen, serum creatinine, ornithine decarboxylase (ODC) activity and thymidine [H-3] incorporation into renal DNA. It also enhances DEN (N-diethylnitrosamine) initiated renal carcinogenesis by increasing the percentage incidence of tumors. Treatment of rats orally with F racemosa extract (200 and 400 mg/kg body weight) resulted in significant decrease in gamma-glutamyl transpeptidase, lipid peroxidation, xanthine oxidase, H2O2 generation, blood urea nitrogen, serum creatinine, renal ODC activity, DNA synthesis (P < 0.001) and incidence of tumors. Renal glutathione content (P < 0.01), glutathione metabolizing enzymes (P < 0.001) and antioxidant enzymes were also recovered to significant level (P < 0.001). Thus, our data suggests that F racemosa extract is a potent chemopreventive agent and suppresses Fe-NTA-induced renal carcinogenesis and oxidative damage response in Wistar rats. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1194 / 1210
页数:17
相关论文
共 46 条
[1]
[Anonymous], 1975, CLIN CHEM
[2]
ANTONIO A, 1988, J ETHNOPHARMACOL, V61, P215
[3]
Methodological considerations for characterizing potential antioxidant actions of bioactive components in plant foods [J].
Aruoma, OI .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2003, 523 :9-20
[4]
Athar M, 1996, BIOCHEM MOL BIOL INT, V39, P813
[5]
AWAI M, 1979, AM J PATHOL, V95, P663
[6]
Baruah K. K., 1992, Indian Journal of Animal Nutrition, V9, P107
[7]
INCREASE OF NAD(P)H-QUINONE REDUCTASE BY DIETARY ANTIOXIDANTS - POSSIBLE ROLE IN PROTECTION AGAINST CARCINOGENESIS AND TOXICITY [J].
BENSON, AM ;
HUNKELER, MJ ;
TALALAY, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (09) :5216-5220
[8]
CARLBERG I, 1975, J BIOL CHEM, V250, P5475
[9]
Claiborne A., 1985, CRC HDB METHODS OXYG, P283
[10]
Iron and its sensitive balance in the cell [J].
De Freitas, JM ;
Meneghini, R .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2001, 475 (1-2) :153-159