Two cinnamate derivatives produce similar alteration in mRNA expression and activity of antioxidant enzymes in rats

✍ Scribed by Mi-Kyung Lee; Eun-Mi Park; Song-Hae Bok; Un Ju Jung; Ji-Young Kim; Yong Bok Park; Tae-Lin Huh; Oh-Shin Kwon; Myung-Sook Choi

• Publisher: John Wiley and Sons
• Year: 2003
• Tongue: English
• Weight: 123 KB
• Volume: 17
• Category: Article
• ISSN: 1095-6670
• DOI: 10.1002/jbt.10087

✦ Synopsis

Abstract

Cinnamate is a widespread secondary metabolite of phenolic compound synthesized by plants for defensive purposes. The current study was designed to investigate the effect of two structurally related cinnamate derivatives, 4‐hydroxycinnamate and 3‐(4‐hydroxyphenyl)propionic acid (HPP), on the mRNA expression and activity of antioxidant enzymes in high‐cholesterol‐fed rats. Male rats were fed a 1 g/100 g high‐cholesterol diet with supplements of either 4‐hydroxycinnamate or HPP (0.135 mmol/100 g diet) for 6 weeks. The plasma paraoxonase activity was found to be higher in the cinnamate‐derivative‐supplemented groups than in the control group. The erythrocyte superoxide dismutase (SOD) and catalase (CAT) activities, plus glutathione (GSH) level, were all significantly higher in the 4‐hydroxycinnamate‐ and HPP‐supplemented groups than in the control group. However, both 4‐hydroxycinnamate and HPP supplementation significantly lowered the hepatic activities and mRNA expression of CAT and glutathione peroxidase (GSH‐Px) compared to the control group. The hepatic mRNA expression and activity of SOD did not differ between the groups. The hepatic thiobarbituric acid reactive substances (TBARS) level was significantly lowered by the 4‐hydroxycinnamate and HPP supplementation. Accordingly, these results indicate that supplementation by 4‐hydroxycinnamate and HPP would seem to enhance the antioxidative defense of erythrocyte. Both HPP and 4‐hydroxycinnamate would appear to be beneficial in improving the function of antioxidative enzymes on a molecular level in high‐cholesterol‐fed rats. © 2003 Wiley Periodicals, Inc. J Biochem Mol Toxicol 17:255–262, 2003; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/jbt.10087