Chemopreventive effect of sinapic acid on 1, 2-dimethylhydrazine-induced experimental rat colon carcinogenesis. (December 2014)

• Record Type: Journal Article
• Authors: Balaji, C; Muthukumaran, J; Nalini, N
• Is Part Of: Human & experimental toxicology. Volume 33:Number 12(2014:Dec.)
• Page Start: 1253
• Page End: 1268
• Publication Date: 2014-12
• Subjects: Sinapic acid -- colon cancer -- chemoprevention -- oxidative stress -- xenobiotics; Toxicology -- Periodicals; 615.9
• DOI: 10.1177/0960327114522501
• Languages: English
• ISSNs: 0960-3271

Abstract

Sinapic acid (SA) is a naturally occurring phenolic acid found in various herbal plants which is attributed with numerous pharmacological properties. This study was aimed to investigate the chemopreventive effect of SA on 1, 2-dimethylhydrazine (DMH)-induced rat colon carcinogenesis. Rats were treated with DMH injections (20 mg kg −1 bodyweight (b.w.) subcutaneously once a week for the first 4 consecutive weeks and SA (20, 40 and 80 mg kg −1 b.w.) post orally for 16 weeks. At the end of the 16-week experimental period, all the rats were killed, and the tissues were evaluated biochemically. Our results reveal that DMH alone treatment decreased the levels/activities of lipid peroxidation by-products such as thiobarbituric acid reactive substances, conjugated dienes and antioxidants such as superoxide dismutase, catalase, glutathione reductase, glutathione peroxidase and reduced glutathione in the intestine and colonic tissues which were reversed on supplementation with SA. Moreover, the activities of drug-metabolizing enzymes of phase I (cytochrome P450 and P4502E1) were enhanced and those of phase II (glutathione- S -transferase, DT-diaphorase and uridine diphosphate glucuronosyl transferase) were diminished in the liver and colonic mucosa of DMH alone-treated rats and were reversed on supplementation with SA. All the above changes were supported by the histopathological observations of the rat liver and colon. These findings suggest that SA at the dose of 40 mg kg −1 b.w. was the most effective dose against DMH-induced colon carcinogenesis, and thus, SA could be used as a potential chemopreventive agent.