Effect of hesperetin, a citrus flavonoid, on bacterial enzymes and carcinogen-induced aberrant crypt foci in colon cancer rats: a dose-dependent study

被引:50
作者
Aranganathan, Selvaraj [1 ]
Selvam, Jayabal Panneer [1 ]
Nalini, Namasivayam [1 ]
机构
[1] Annamalai Univ, Dept Biochem & Biotechnol, Annamalainagar 608002, Tamil Nadu, India
关键词
D O I
10.1211/jpp/60.10.0015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hesperetin, an important bioactive compound in Chinese traditional medicine, has antioxidant and anticarcinogenic properties. Hesperetin is found in abundance in orange and grape juices (200-590 mg L-1) consumed in the daily diet. We have investigated the effect of different doses of hesperetin on faecal and colonic mucosal bacterial enzymes and aberrant crypt foci (ACF) in 1,2-dimethylhydrazine (DMH)-induced colon carcinogenesis in male Wistar rats. The rats were divided into six groups and were fed a modified pellet diet for 16 weeks. Group 1 served as control and group 2 received the modified pellet diet along with hesperetin (30 mg kg(-1)). The rats in groups 3-6 rats were given a weekly subcutaneous injection of DMH (20 mg kg(-1)) for the first four weeks. Hesperetin was supplemented orally at different doses (10, 20 or 30 mg kg(-1)) for a total of 16 weeks. At the end of the experimental period all rats were killed. In DMH-treated rats, the activity of faecal and colonic mucosal bacterial enzymes, such as beta-glucuronidase, beta-galactosidase, beta-glucosidase, nitroreductase, sulfatase and mucinase, were significantly elevated, but in rats supplemented hesperetin along with DMH the activity was significantly lowered (P < 0.05). The total number of aberrant crypts was significantly increased in unsupplemented DMH-treated rats, while hesperetin supplementation to DMH-treated rats significantly reduced the total number of crypts. The results demonstrated that hesperetin supplementation at a dose of 20 mg kg(-1) played a potent role in suppressing the formation of aberrant crypt foci and reducing the activity of bacterial enzymes in colon cancer.
引用
收藏
页码:1385 / 1392
页数:8
相关论文
共 36 条
[1]   DNA damage and aberrant crypt foci as putative biomarkers to evaluate the chemopreventive effect of annatto (Bixa orellana L.) in rat colon carcinogenesis [J].
Agner, AR ;
Bazo, AP ;
Ribeiro, LR ;
Salvadori, DMF .
MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2005, 582 (1-2) :146-154
[2]   OBSERVATION AND QUANTIFICATION OF ABERRANT CRYPTS IN THE MURINE COLON TREATED WITH A COLON CARCINOGEN - PRELIMINARY FINDINGS [J].
BIRD, RP .
CANCER LETTERS, 1987, 37 (02) :147-151
[3]   ROLE OF ABERRANT CRYPT FOCI IN UNDERSTANDING THE PATHOGENESIS OF COLON-CANCER [J].
BIRD, RP .
CANCER LETTERS, 1995, 93 (01) :55-71
[4]  
Bratton AC, 1939, J BIOL CHEM, V128, P537
[5]   Antioxidant activity and phenolic compounds of 112 traditional Chinese medicinal plants associated with anticancer [J].
Cai, YZ ;
Luo, Q ;
Sun, M ;
Corke, H .
LIFE SCIENCES, 2004, 74 (17) :2157-2184
[6]   Improvement in intestinall function and health by the peel fibre derived from Citrus sinensis L cv Liucheng [J].
Chau, CF ;
Sheu, F ;
Huang, YL ;
Su, LH .
JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, 2005, 85 (07) :1211-1216
[7]   Interaction of the breast cancer resistance protein with plant polyphenols [J].
Cooray, HC ;
Janvilisri, T ;
van Veen, HW ;
Hladky, SB ;
Barrand, MA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2004, 317 (01) :269-275
[8]   Evaluation of fecal mutagenicity and colorectal cancer risk [J].
de Kok, TMCM ;
van Maanen, JMS .
MUTATION RESEARCH-REVIEWS IN MUTATION RESEARCH, 2000, 463 (01) :53-101
[9]   Dose dependent inhibitory effect of dietary caraway on 1,2-dimethylhydrazine induced colonic aberrant crypt foci and bacterial enzyme activity in rats [J].
Deeptha, Kumaraswami ;
Kamaleeswari, Muthaiyan ;
Sengottuvelan, Murugan ;
Nalini, Namasivayam .
INVESTIGATIONAL NEW DRUGS, 2006, 24 (06) :479-488
[10]   Fenugreek affects the activity of β-glucuronidase and mucinase in the colon [J].
Devasena, T ;
Menon, VP .
PHYTOTHERAPY RESEARCH, 2003, 17 (09) :1088-1091