AI Article Synopsis

  • Dietary polyphenols from sources like allspice, clove, and thyme show potential as cancer-preventive agents by activating enzymes linked to drug metabolism and detoxification.
  • Clove and thyme extracts, along with compounds like curcumin and resveratrol, were found to activate the PXR and related CYP3A4 promoter, although clove did not correlate as expected.
  • Thyme extract and quercetin specifically activated protective enzymes (HO-1, GI-GPx), while the effects of other polyphenols varied, suggesting they influence enzyme expression through different mechanisms that need further investigation.

Article Abstract

Based on animal models, dietary polyphenols are predicted to be promising chemopreventive agents in humans. Allspice, clove, and thyme extracts as well as defined dietary polyphenolic compounds were, therefore, tested for their ability to activate mechanisms related to phase 1 enzymes, i.e., the PXR-regulated CYP3A4 promoter, and phase 2 enzymes, i.e. the EpRE-regulated promoters of gastrointestinal glutathione peroxidase (GI-GPx) and heme oxygenase-1 (HO-1), examples of Nrf2-regulated genes. From the compounds tested, clove and thyme extracts as well as curcumin and resveratrol activated the PXR. PXR activation correlated with the activation of the CYP3A4 promoter in the case of thyme extract, curcumin, and resveratrol, but not in the case of clove extract. Allspice extract, EGCG, and quercetin did not activate PXR but enhanced CYP3A4 promoter activity. Thyme extract and quercetin activated the EpRE of HO-1. Both significantly activated the GI-GPx promoter, effects that depended on a functional EpRE. Resveratrol did not activate the isolated EpRE but enhanced the GI-GPx promoter activity, whereas clove extract even inhibited it. It is concluded that individual polyphenols as well as polyphenol-rich plant extracts may affect phase 1 and 2 enzyme expression by distinct mechanisms that must be elucidated, before potential health effects can reliably be predicted.

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Source
http://dx.doi.org/10.1016/j.freeradbiomed.2006.09.028DOI Listing

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