ToxSci Advance Access published online on February 27, 2007
Toxicological Sciences, doi:10.1093/toxsci/kfm035
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Effects of Kava Alkaloid, Pipermethystine, and Kavalactones on Oxidative Stress and Cytochrome P450 in F-344 Rats
1 Laboratory of Metabolic Disorders and Alternative Medicine 2 Department of Molecular Biosciences and Bioengineering 3 Department of Tropical Plant and Soil Sciences, College of Tropical Agriculture and Human Resources, University of Hawaii at Manoa, Honolulu, Hawaii, 96822 4 Biostatistics and Data Management Facility, Asia-Pacific Institute of Tropical Medicine and Infectious Diseases, John A. Burns School of Medicine, Honolulu, HI 96813
* Corresponding Author: Pratibha V. Nerurkar, Ph.D., Laboratory of Metabolic Disorders and Alternative Medicine, Department of Molecular Biosciences and Bioengineering, College of Tropical Agriculture and Human Resources, 1955 East-West Road, Agriculture Science Building, Room 218, Honolulu, HI 96822, Phone: (808) 956-9195, Fax: (808) 956-3542, E-mail: pratibha{at}hawaii.edu.
limsteve{at}hawaii.edu, dragull{at}hawaii.edu, tangcs{at}hawaii.edu, hcbitt{at}hawaii.edu, efird{at}pbrc.hawaii.edu, pratibha{at}hawaii.edu
Received January 22, 2007; revision received January 22, 2007; accepted February 19, 2007
| Abstract |
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Kava containing products remain popular in the United States and continue to be sold in health food stores and ethnic markets regardless of the fact that it was banned in Western countries such as Germany, France, Switzerland, Australia, and Canada, following reports of alleged hepatotoxicity. It is therefore critical to establish efficacy and verify adverse effects and/or herb-drug interactions for kava-kava (Piper methysticum). We have previously demonstrated that kava alkaloid, pipermethystine (PM), abundant in leaves and stem peelings, induces mitochondrial toxicity in human hepatoma cells, HepG2, as compared with the bioactive components, kavalactones (KL), abundant in the rhizome. The current study compared short-term toxic effects of PM in F-344 rats to acetone-water extracts of kava rhizome (KRE). Treatment of F-344 rats with PM (10 mg/kg) and KRE (100 mg/kg) for two weeks failed to elicit any significant changes in liver function tests or cause severe hepatic toxicity as measured by lipid peroxidation and apoptosis markers such as malonaldehyde (MDA), Bax and Bcl2, respectively. However, PM-treated rats demonstrated a significant increase in hepatic glutathione (GSH), cytosolic superoxide dismutase (Cu/Zn SOD), tumor necrosis factor
(TNF-
) mRNA expression and cytochrome (CYP) P450 2E1, and 1A2, suggesting adaptation to oxidative stress and possible drug-drug interactions.
Key Words: kava; pipermethystine; kavalactones; oxidative stress; cytochrome P450.
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