Protective effect of ferulic acid on 7, 12-dimethylbenz[a]anthracene-induced skin carcinogenesis in Swiss albino mice

被引:57
作者
Alias, Linsa Mary [1 ]
Manoharan, Shanmugam [1 ]
Vellaichamy, Lakshmanan [1 ]
Balakrishnan, Subramanian [1 ]
Ramachandran, Cinnamanoor Rajamani [2 ]
机构
[1] Annamalai Univ, Dept Biochem & Biotechnol, Fac Sci, Annamalainagar 608002, Tamil Nadu, India
[2] Annamalai Univ, Dept Oral & Maxillofacial Pathol, Rajah Muthiah Dent Coll & Hosp, Annamalainagar 608002, Tamil Nadu, India
关键词
Skin cancer; Ferulic acid; Lipid peroxidation; Antioxidants; Detoxication agents; LIPID-PEROXIDATION; ANTIOXIDANTS; ASSAY;
D O I
10.1016/j.etp.2008.09.001
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Our aim was to evaluate and compare the chemopreventive potential of topically applied and orally administered ferulic acid in 7,12-dimethylbetz[a]anthracene (DMBA)-induced skin carcinogenesis. Estimating the status of phase I and phase II detoxication agents, lipid peroxidation byproducts and antioxidants during DMBA-induced skin carcinogenesis assessed the mechanistic pathway for its chemopreventive efficacy. Skin squamous cell carcinoma was induced in the shaved back of mice, by painting with DM BA (25 mu g in 0.1 mL(-1) acetone) twice weekly for 8 weeks. We have observed 100% tumor formation in the 15th week of experimental period in mice treated with DMBA alone. Marked alterations in the status of phase I and phase II detoxication agents, lipid peroxidaton byproducts and antioxidants were observed in tumor bearing mice. Oral administration of ferulic acid completely prevented the formation of skin tumors, whereas topically applied ferulic acid did not show significant chemopreventive activity during DMBA-induced mouse skin carcinogenesis. Also, oral administration of ferulic acid reverted the status of phase I and phase II detoxication agents, lipid peroxidaton byproducts and antioxidants to near-normal range ill DMBA-treated mice. Our results thus demonstrate that orally administered ferulic acid has potent suppressing effect on cell proliferation during DMBA-induced skin carcinogenesis. This is probably due to its modulating effect on the status of lipid peroxidation, antioxidants and detoxication agents during DMBA-induced skin carcinogenesis. (c) 2008 Elsevier GmbH. All rights reserved.
引用
收藏
页码:205 / 214
页数:10
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