Drug Metabolism Letters

Zhiyang Zhao
Cambridge, MA


Effect of Pinocembrin Isolated from Boesenbergia pandurata on Xenobiotic-Metabolizing Enzymes in Rat Liver

Author(s): Charatda Punvittayagul, Rawiwan Wongpoomchai, Sirinya Taya and Wilart Pompimon

Affiliation: Department of Biochemistry, Faculty of Medicine, Chiang Mai University, Chiang Mai Thailand 50200.


Pinocembrin, 5, 7 – dihydroxyflavanone, is one of the flavanones found in the rhizomes of Boesenbergia pandurata. Previous study demonstrated that pinocembrin was neither toxic nor mutagenic to male rats. This study evaluated the effects of pinocembrin on phase I and II xenobiotic-metabolizing enzymes in rat liver. It was found that heme oxygenase activity significantly increased in 10 and 100 mg/kg bw of pinocembrin treated groups (p < 0.05). However, pinocembrin did not affect the activities of NADPH: cytochrome P450 reductase, NADPH: quinone reductase, UDPglucuronosyltransferase and glutathione-S-transferase. It also did not affect the expression of phase I metabolizing enzymes, including CYP1A1, CYP2B1, CYP2C11, CYP2E1, CYP3A2, and NADPH: cytochrome P450 reductase. In conclusion, short-term treatment of pinocembrin in Wistar rats increased the activity of heme oxygenase but did not affect on the activities of other phase II xenobiotic-metabolizing enzymes or the expression of cytochrome P450 enzymes.

Keywords: 5, 7, –, dihydroxyflavanone, Boesenbergia pandurata, cytochrome P450, fingerroot, pinocembrin, xenobiotic metabolizing enzymes, flavanones, heme oxygenase, cytochrome P450 reductase, quinone reductase, glucuronosyltransferase, glutathione-S-transferase, chemical carcinogens, cytochrome P450 mono-oxygenases, reactive electro-philic metabolites, carcinogenesis, detoxification, acclimatization period, bovine serum albumin (BSA), potassium phosphate buffer, hemin, biliverdin reductase, N-naphthylethylene, spectrophotometer, cytosolic protein, Western Blot Analysis, gel elec-trophoresis, horseradish peroxidase, kal-Wallis test, stress-responsive enzyme, hepatocarcinogen, narin-genin, pinobanksin, chrysin, hepatocarcinogenesis, antimutagenicity, anticarcinogenicity

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Article Details

Page: [1 - 5]
Pages: 5
DOI: 10.2174/187231211794455226