Dietary flavonols and O-glycosides

Senem Kamiloglu, Merve Tomas, Esra Capanoglu*

*Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

Abstract

Flavonols are the most widespread subgroup of the flavonoids. Quercetin, kaempferol, myricetin, and isorhamnetin are the major dietary flavonol aglycones, which most commonly occur as O-glycosides in dietary sources including fruits, vegetables, tea, and wine. The role of flavonols and O-glycosides in human nutrition has gained increased interest due to their associated health beneficial effects for a number of chronic diseases, including cardiovascular diseases, diabetes, and cancer. However, the potential bioactivity of flavonols and O-glycosides will depend on their bioavailability. Following digestion, flavonol glycosides are cleaved to their aglycones, which may be metabolized in the enterocytes and further in the liver, forming glucuronidated, sulfated, and/or methylated metabolites, or they may be passively permeate the intestinal epithelial barrier. Flavonols that reach the colon may be degraded by the colonic microbiota to different metabolites, which may also contribute to the observed biological effects. In this chapter, the recent findings on the bioavailability, metabolism, bioactivity, and benefits of dietary flavonols and O-glycosides are highlighted. In addition, the recent information on food applications, safety issues, marketed products, and patents are also presented.

Original languageEnglish
Title of host publicationHandbook of Dietary Phytochemicals
PublisherSpringer Nature
Pages57-96
Number of pages40
ISBN (Electronic)9789811541483
ISBN (Print)9789811541476
DOIs
Publication statusPublished - 9 Aug 2021

Bibliographical note

Publisher Copyright:
© Springer Nature Singapore Pte Ltd. 2021. All rights reserved.

Keywords

  • Bioavailability
  • Cancer
  • Cardiovascular diseases
  • Diabetes
  • Isorhamnetin
  • Kaempferol
  • Metabolism
  • Myricetin
  • Quercetin
  • Toxicity

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