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Sulforaphane rewires central metabolism to support antioxidant response and achieve glucose homeostasis.
Bernuzzi, Federico; Maertens, Andre; Saha, Shikha; Troncoso-Rey, Perla; Ludwig, Tobias; Hiller, Karsten; Mithen, Richard F; Korcsmaros, Tamas; Traka, Maria H.
Afiliação
  • Bernuzzi F; Quadram Institute Bioscience, Norwich Research Park, Norwich, United Kingdom.
  • Maertens A; Braunschweig Integrated Centre of System Biology, Technical University of Braunschweig, Braunschweig, Germany.
  • Saha S; Quadram Institute Bioscience, Norwich Research Park, Norwich, United Kingdom.
  • Troncoso-Rey P; Quadram Institute Bioscience, Norwich Research Park, Norwich, United Kingdom.
  • Ludwig T; Braunschweig Integrated Centre of System Biology, Technical University of Braunschweig, Braunschweig, Germany.
  • Hiller K; Braunschweig Integrated Centre of System Biology, Technical University of Braunschweig, Braunschweig, Germany.
  • Mithen RF; The Liggins Institute-The University of Auckland, New Zealand.
  • Korcsmaros T; Quadram Institute Bioscience, Norwich Research Park, Norwich, United Kingdom; Imperial College London, London, United Kingdom; Earlham Institute, Norwich Research Park, Norwich, United Kingdom.
  • Traka MH; Quadram Institute Bioscience, Norwich Research Park, Norwich, United Kingdom. Electronic address: maria.traka@quadram.ac.uk.
Redox Biol ; 67: 102878, 2023 11.
Article em En | MEDLINE | ID: mdl-37703668
ABSTRACT
Cruciferous-rich diets, particularly broccoli, have been associated with reduced risk of developing cancers of various sites, cardiovascular disease and type-2 diabetes. Sulforaphane (SF), a sulfur-containing broccoli-derived metabolite, has been identified as the major bioactive compound mediating these health benefits. Sulforaphane is a potent dietary activator of the transcription factor Nuclear factor erythroid-like 2 (NRF2), the master regulator of antioxidant cell capacity responsible for inducing cytoprotective genes, but its role in glucose homeostasis remains unclear. In this study, we set to test the hypothesis that SF regulates glucose metabolism and ameliorates glucose overload and its resulting oxidative stress by inducing NRF2 in human hepatoma HepG2 cells. HepG2 cells were exposed to varying glucose concentrations basal (5.5 mM) and high glucose (25 mM), in the presence of physiological concentrations of SF (10 µM). SF upregulated the expression of glutathione (GSH) biosynthetic genes and significantly increased levels of reduced GSH. Labelled glucose and glutamine experiments to measure metabolic fluxes identified that SF increased intracellular utilisation of glycine and glutamate by redirecting the latter away from the TCA cycle and increased the import of cysteine from the media, likely to support glutathione synthesis. Furthermore, SF altered pathways generating NADPH, the necessary cofactor for oxidoreductase reactions, namely pentose phosphate pathway and 1C-metabolism, leading to the redirection of glucose away from glycolysis and towards PPP and of methionine towards methylation substrates. Finally, transcriptomic and targeted metabolomics LC-MS analysis of NRF2-KD HepG2 cells generated using CRISPR-Cas9 genome editing revealed that the above metabolic effects are mediated through NRF2. These results suggest that the antioxidant properties of cruciferous diets are intricately connected to their metabolic benefits.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator 2 Relacionado a NF-E2 / Antioxidantes Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator 2 Relacionado a NF-E2 / Antioxidantes Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article