Flavonoids and Organic Acids Affect Phase II Metabolism based on the Regulation of UGT1A1 Expression and Function.

Crystal structure Nrf2 UGTs. mechanism polyphenols

Journal

Current computer-aided drug design
ISSN: 1875-6697
Titre abrégé: Curr Comput Aided Drug Des
Pays: United Arab Emirates
ID NLM: 101265750

Informations de publication

Date de publication:
17 May 2024
Historique:
received: 01 02 2024
revised: 15 04 2024
accepted: 29 04 2024
medline: 20 5 2024
pubmed: 20 5 2024
entrez: 20 5 2024
Statut: aheadofprint

Résumé

Exogenous substances modulate metabolism by regulating the expression and function of UDP-glycosyltransferases (UGTs). However, the exact mechanism in the intestine was rarely understood. Herein, we explored the effects of representative flavonoids and organic acids on the regulation of UGT1A1. MTT assays and western blot analysis were used to explore the effect of polyphenols. X-ray diffraction was used to reveal the catalytic mechanisms of UGTs. MTT assays showed that these compounds basically had no cytotoxicity, even in concentrations up to 200 μM. Then, through western blot assays, UGT1A1 expression was increased after being treated with liquiritigenin and caffeic acid. Furthermore, liquiritigenin and caffeic acid enhanced the nuclear translocation of Nrf2. Moreover, a 2.5-Å crystal structure of the complex containing UGTs C-terminal domain and organic acid was solved, and the UDPGA binding pocket could be occupied by organic acid, suggesting the enzyme activity might be impaired by organic acid. Above all, liquiritigenin and caffeic acid maintained the metabolism balance by upregulating the expression of UGT1A1 via Nrf2 activation and inhibiting the enzyme activity in Caco-2 cells.

Sections du résumé

BACKGROUND BACKGROUND
Exogenous substances modulate metabolism by regulating the expression and function of UDP-glycosyltransferases (UGTs). However, the exact mechanism in the intestine was rarely understood. Herein, we explored the effects of representative flavonoids and organic acids on the regulation of UGT1A1.
METHODS METHODS
MTT assays and western blot analysis were used to explore the effect of polyphenols. X-ray diffraction was used to reveal the catalytic mechanisms of UGTs.
RESULTS RESULTS
MTT assays showed that these compounds basically had no cytotoxicity, even in concentrations up to 200 μM. Then, through western blot assays, UGT1A1 expression was increased after being treated with liquiritigenin and caffeic acid. Furthermore, liquiritigenin and caffeic acid enhanced the nuclear translocation of Nrf2. Moreover, a 2.5-Å crystal structure of the complex containing UGTs C-terminal domain and organic acid was solved, and the UDPGA binding pocket could be occupied by organic acid, suggesting the enzyme activity might be impaired by organic acid.
CONCLUSION CONCLUSIONS
Above all, liquiritigenin and caffeic acid maintained the metabolism balance by upregulating the expression of UGT1A1 via Nrf2 activation and inhibiting the enzyme activity in Caco-2 cells.

Identifiants

pubmed: 38766819
pii: CAD-EPUB-140425
doi: 10.2174/0115734099300793240509103320
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Auteurs

Lin Zhang (L)

State Key Laboratory of Traditional Chinese Medicine Syndrome, Guangzhou University of Chinese Medicine, International Institute for Translational Chinese, Guangzhou, 510006, China.
School of Pharmacy, Jiangxi Science and Technology Normal University, Jiangxi, 330013, China.

Xuerong Zhang (X)

State Key Laboratory of Traditional Chinese Medicine Syndrome, Guangzhou University of Chinese Medicine, International Institute for Translational Chinese, Guangzhou, 510006, China.

Caiyan Wang (C)

State Key Laboratory of Traditional Chinese Medicine Syndrome, Guangzhou University of Chinese Medicine, International Institute for Translational Chinese, Guangzhou, 510006, China.

Classifications MeSH