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Food Chem Toxicol. 2013 Dec;62:707-21. doi: 10.1016/j.fct.2013.09.025. Epub 2013 Sep 27.

Metabolomics evaluation of the effects of green tea extract on acetaminophen-induced hepatotoxicity in mice.

Author information

  • 1Division of Systems Biology, National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR 72079, USA.

Abstract

Green tea has been purported to have beneficial health effects including protective effects against oxidative stress. Acetaminophen (APAP) is a widely used analgesic drug that can cause acute liver injury in overdose situations. These studies explored the effects of green tea extract (GTE) on APAP-induced hepatotoxicity in liver tissue extracts using ultra performance liquid chromatography/quadrupole time-of-flight mass spectrometry and nuclear magnetic resonance spectroscopy. Mice were orally administered GTE, APAP or GTE and APAP under three scenarios. APAP alone caused a high degree of hepatocyte necrosis associated with increases in serum transaminases and alterations in multiple metabolic pathways. The time of GTE oral administration relative to APAP either protected against or potentiated the APAP-induced hepatotoxicity. Dose dependent decreases in histopathology scores and serum transaminases were noted when GTE was administered prior to APAP; whereas, the opposite occurred when GTE was administered after APAP. Similarly, metabolites altered by APAP alone were less changed when GTE was given prior to APAP. Significantly altered pathways included fatty acid metabolism, glycerophospholipid metabolism, glutathione metabolism, and energy pathways. These studies demonstrate the complex interaction between GTE and APAP and the need to employ novel analytical strategies to understand the effects of dietary supplements on pharmaceutical compounds.

Published by Elsevier Ltd.

KEYWORDS:

3-HB; 3-Hydroxybutyrate; ALP; ALT; APAP; AST; ATP; Acetaminophen; CHOL; CTRL; CYP450; GGT; GLU; GSH; GTE; Green tea extract; Hepatotoxicity; LC/MS; LysoPC; Metabolic profiling; Metabolomics; N-acetyl-p-benzoquinone imine; NAD(+); NAPQI; NMR; PC; PCA; PLS-DA; QC; QTOF-NEG; QTOF-POS; ROS; TBILI; TRI; ULN; UPLC/MS; UPLC/QTof-MS; acetaminophen; adenosine-5′-triphosphate; alanine aminotransferase; alkaline phosphatase; aspartate aminotransferase; cholesterol; control; cytochrome P450; glucose; glutathione; green tea extract; liquid chromatography/mass spectrometry; lysophosphatidylcholine; nicotinamide adenine dinucleotide; nuclear magnetic resonance; partial least squares-discriminant analysis; phosphatidylcholine; principal component analysis; quadrupole time-of-flight negative mode; quadrupole time-of-flight positive mode; quality control; reactive oxygen species; total bilirubin; triglycerides; ultra performance liquid chromatography mass spectrometry; ultra performance liquid chromatography/quadrupole time-of-flight mass spectrometry; upper limit of normal; γ-glutamyl transferase

PMID:
24080264
[PubMed - in process]
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