Inhibitory effects of rooibos (Aspalathus linearis) against reactive carbonyl species and advanced glycation end product formation in a glucose-bovine serum albumin model and cookies

Yen Tung Chen, You Yu Lin, Min Hsiung Pan, Chi Tang Ho, Wei Lun Hung

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)

Abstract

In thermally processed foods, several heat-induced toxicants are potentially formed due to the Maillard reaction, such as α-dicarbonyls and advanced glycation end products (AGEs). In the present work, we found that the methylglyoxal (MGO)-trapping and antiglycative activities of the herbal tea samples correlated strongly with their total phenolic and flavonoid contents. Among the tested herbal tea samples, rooibos exhibited the strongest MGO-trapping and antiglycative activities against AGEs formation. Aspalathin, orientin and isoorientin were further identified as the major bioactive compounds of rooibos that scavenged MGO to form the corresponding mono-MGO adducts. Moreover, the contents of dicarbonyls and AGEs in the cookie were remarkably reduced by fortification with rooibos. Altogether, our current findings suggested that rooibos might serve as a functional ingredient to reduce intake of dietary reactive carbonyl species (RCS) and AGEs from thermally processed foods, especially bakery products.

Original languageEnglish
Article number100515
JournalFood Chemistry: X
Volume16
DOIs
Publication statusPublished - Dec 2022

Keywords

  • Advanced glycation end products
  • Aspalathin (PubChem CID: 11282394)
  • Cookies
  • Herbal tea
  • Isoorientin (PubChem CID: 114776)
  • Isovitexin (PubChem CID: 162350)
  • Methylglyoxal
  • Methylglyoxal (PubChem CID: 880)
  • Nε-(carboxymethyl)lysine (PubChem CID: 123800)
  • Orientin (PubChem CID: 5281675)
  • Reactive carbonyl species
  • Vitexin (PubChem CID: 5280441)

ASJC Scopus subject areas

  • Analytical Chemistry
  • Food Science

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