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Sulforaphane rewires central metabolism to support antioxidant response and achieve glucose homeostasis

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...

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Autores principales: Bernuzzi, Federico, Maertens, Andre, Saha, Shikha, Troncoso-Rey, Perla, Ludwig, Tobias, Hiller, Karsten, Mithen, Richard F., Korcsmaros, Tamas, Traka, Maria H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502441/
https://www.ncbi.nlm.nih.gov/pubmed/37703668
http://dx.doi.org/10.1016/j.redox.2023.102878
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author Bernuzzi, Federico
Maertens, Andre
Saha, Shikha
Troncoso-Rey, Perla
Ludwig, Tobias
Hiller, Karsten
Mithen, Richard F.
Korcsmaros, Tamas
Traka, Maria H.
author_facet Bernuzzi, Federico
Maertens, Andre
Saha, Shikha
Troncoso-Rey, Perla
Ludwig, Tobias
Hiller, Karsten
Mithen, Richard F.
Korcsmaros, Tamas
Traka, Maria H.
author_sort Bernuzzi, Federico
collection PubMed
description 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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spelling pubmed-105024412023-09-16 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. Redox Biol Research Paper 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. Elsevier 2023-09-07 /pmc/articles/PMC10502441/ /pubmed/37703668 http://dx.doi.org/10.1016/j.redox.2023.102878 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Paper
Bernuzzi, Federico
Maertens, Andre
Saha, Shikha
Troncoso-Rey, Perla
Ludwig, Tobias
Hiller, Karsten
Mithen, Richard F.
Korcsmaros, Tamas
Traka, Maria H.
Sulforaphane rewires central metabolism to support antioxidant response and achieve glucose homeostasis
title Sulforaphane rewires central metabolism to support antioxidant response and achieve glucose homeostasis
title_full Sulforaphane rewires central metabolism to support antioxidant response and achieve glucose homeostasis
title_fullStr Sulforaphane rewires central metabolism to support antioxidant response and achieve glucose homeostasis
title_full_unstemmed Sulforaphane rewires central metabolism to support antioxidant response and achieve glucose homeostasis
title_short Sulforaphane rewires central metabolism to support antioxidant response and achieve glucose homeostasis
title_sort sulforaphane rewires central metabolism to support antioxidant response and achieve glucose homeostasis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10502441/
https://www.ncbi.nlm.nih.gov/pubmed/37703668
http://dx.doi.org/10.1016/j.redox.2023.102878
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