A Combination of Polymethoxyflavones from Citrus sinensis and Prenylflavonoids from Humulus lupulus Counteracts IL-1β-Induced Differentiated Caco-2 Cells Dysfunction via a Modulation of NF-κB/Nrf2 Activation
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Published:2023-08-16
Issue:8
Volume:12
Page:1621
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ISSN:2076-3921
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Container-title:Antioxidants
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language:en
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Short-container-title:Antioxidants
Author:
Restivo Ignazio1ORCID, Basilicata Manuela Giovanna2, Giardina Ilenia Concetta1ORCID, Massaro Alessandro1, Pepe Giacomo2, Salviati Emanuela2ORCID, Pecoraro Camilla3ORCID, Carbone Daniela3ORCID, Cascioferro Stella3ORCID, Parrino Barbara3ORCID, Diana Patrizia3ORCID, Ostacolo Carmine2ORCID, Campiglia Pietro2ORCID, Attanzio Alessandro1ORCID, D’Anneo Antonella1ORCID, Pojero Fanny1ORCID, Allegra Mario1ORCID, Tesoriere Luisa1ORCID
Affiliation:
1. Department of Biological, Chemical and Pharmaceutical Sciences and Technologies, University of Palermo, Via Archirafi 28, 90123 Palermo, Italy 2. Department of Pharmacy, University of Salerno, 84084 Fisciano, Italy 3. Department of Biological, Chemical and Pharmaceutical Sciences and Technologies, University of Palermo, Via Archirafi 32, 90123 Palermo, Italy
Abstract
We here investigated the anti-inflammatory activity of a polymethoxylated flavone-containing fraction (PMFF) from Citrus sinensis and of a prenylflavonoid-containing one (PFF) from Humulus lupulus, either alone or in combination (MIX). To this end, an in vitro model of inflammatory bowel disease (IBD), consisting of differentiated, interleukin (IL)-1β-stimulated Caco-2 cells, was employed. We demonstrated that non-cytotoxic concentrations of either PMFF or PFF or MIX reduced nitric oxide (NO) production while PFF and MIX, but not PMFF, also inhibited prostaglandin E2 release. Coherently, MIX suppressed both inducible NO synthase and cyclooxygenase-2 over-expression besides NF-κB activation. Moreover, MIX increased nuclear factor erythroid 2–related factor 2 (Nrf2) activation, heme oxygenase-1 expression, restoring GSH and reactive oxygen and nitrogen species (RONs) levels. Remarkably, these effects with MIX were stronger than those produced by PMFF or PFF alone. Noteworthy, nobiletin (NOB) and xanthohumol (XTM), two of the most represented phytochemicals in PMFF and PFF, respectively, synergistically inhibited RONs production. Overall, our results demonstrate that MIX enhances the anti-inflammatory and anti-oxidative effects of the individual fractions in a model of IBD, via a mechanism involving modulation of NF-κB and Nrf2 signalling. Synergistic interactions between NOB and XTM emerge as a relevant aspect underlying this evidence.
Funder
Italian Ministry of Education, University and Research, European Union
Subject
Cell Biology,Clinical Biochemistry,Molecular Biology,Biochemistry,Physiology
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