Article

Gene expression profiling in male B6C3F1 mouse livers exposed to kava identifies--changes in drug metabolizing genes and potential mechanisms linked to kava toxicity.

Division of Systems Toxicology, National Center for Toxicological Research, FDA, Jefferson, AR 72079, USA.
Food and chemical toxicology: an international journal published for the British Industrial Biological Research Association (impact factor: 2.99). 11/2009; 48(2):686-96. DOI:10.1016/j.fct.2009.11.050 pp.686-96
Source: PubMed

ABSTRACT The association of kava products with liver-related health risks has prompted regulatory action in many countries. We used a genome-wide gene expression approach to generate global gene expression profiles from the livers of male B6C3F1 mice administered kava extract by gavage for 14 weeks, and identified the differentially expressed drug metabolizing genes in response to kava treatments. Analyses of gene functions and pathways reveal that the levels of significant numbers of genes involving drug metabolism were changed and that the pathways involving xenobiotics metabolism, Nrf2-mediated oxidative stress response, mitochondrial functions and others, were altered. Our results indicate that kava extract can significantly modulate drug metabolizing enzymes, potentially leading to herb-drug interactions and hepatotoxicity.

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Keywords

differentially
 
drug metabolizing genes
 
gavage
 
gene functions
 
genes
 
genome-wide gene expression approach
 
global gene expression profiles
 
hepatotoxicity
 
herb-drug interactions
 
kava products
 
kava treatments
 
liver-related health risks
 
male B6C3F1 mice
 
mitochondrial functions
 
Nrf2-mediated oxidative stress response
 
others
 
pathways
 
regulatory action
 
significant numbers