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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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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. |
format | Online Article Text |
id | pubmed-10502441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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