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4,4'Dimethoxychalcone: a natural flavonoid that promotes health through autophagy-dependent and -independent effects
The age-induced deterioration of the organism results in detrimental and ultimately lethal pathologies. The process of aging itself involves a plethora of different mechanisms that should be subverted concurrently to delay and/or prevent age-related maladies. We have identified a natural compound, 4...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693465/ https://www.ncbi.nlm.nih.gov/pubmed/31248332 http://dx.doi.org/10.1080/15548627.2019.1632623 |
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author | Zimmermann, Andreas Kainz, Katharina Hofer, Sebastian J. Bauer, Maria A. Schroeder, Sabrina Dengjel, Jörn Pietrocola, Federico Kepp, Oliver Ruckenstuhl, Christoph Eisenberg, Tobias Sigrist, Stephan J. Madeo, Frank Carmona-Gutierrez, Didac Kroemer, Guido |
author_facet | Zimmermann, Andreas Kainz, Katharina Hofer, Sebastian J. Bauer, Maria A. Schroeder, Sabrina Dengjel, Jörn Pietrocola, Federico Kepp, Oliver Ruckenstuhl, Christoph Eisenberg, Tobias Sigrist, Stephan J. Madeo, Frank Carmona-Gutierrez, Didac Kroemer, Guido |
author_sort | Zimmermann, Andreas |
collection | PubMed |
description | The age-induced deterioration of the organism results in detrimental and ultimately lethal pathologies. The process of aging itself involves a plethora of different mechanisms that should be subverted concurrently to delay and/or prevent age-related maladies. We have identified a natural compound, 4,4ʹ-dimethoxychalcone (DMC), which promotes longevity in yeast, worms and flies, and protects mice from heart injury and liver toxicity. Interestingly, both the DMC-mediated lifespan extension and the cardioprotection depend on macroautophagy/autophagy whereas hepatoprotection does not. DMC induces autophagy by inhibiting specific GATA transcription factors (TFs), independently of the TORC1 kinase pathway. The autophagy-independent beneficial effects of DMC might involve its antioxidative properties. DMC treatment results in a phylogenetically conserved, systemic impact on the metabolome, which is most prominently characterized by changes in cellular amino acid composition. Altogether, DMC exerts multiple, geroprotective effects by igniting distinct pathways, and thus represents a potential pharmacological agent that delays aging through multipronged effects. |
format | Online Article Text |
id | pubmed-6693465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-66934652019-08-26 4,4'Dimethoxychalcone: a natural flavonoid that promotes health through autophagy-dependent and -independent effects Zimmermann, Andreas Kainz, Katharina Hofer, Sebastian J. Bauer, Maria A. Schroeder, Sabrina Dengjel, Jörn Pietrocola, Federico Kepp, Oliver Ruckenstuhl, Christoph Eisenberg, Tobias Sigrist, Stephan J. Madeo, Frank Carmona-Gutierrez, Didac Kroemer, Guido Autophagy Commentary The age-induced deterioration of the organism results in detrimental and ultimately lethal pathologies. The process of aging itself involves a plethora of different mechanisms that should be subverted concurrently to delay and/or prevent age-related maladies. We have identified a natural compound, 4,4ʹ-dimethoxychalcone (DMC), which promotes longevity in yeast, worms and flies, and protects mice from heart injury and liver toxicity. Interestingly, both the DMC-mediated lifespan extension and the cardioprotection depend on macroautophagy/autophagy whereas hepatoprotection does not. DMC induces autophagy by inhibiting specific GATA transcription factors (TFs), independently of the TORC1 kinase pathway. The autophagy-independent beneficial effects of DMC might involve its antioxidative properties. DMC treatment results in a phylogenetically conserved, systemic impact on the metabolome, which is most prominently characterized by changes in cellular amino acid composition. Altogether, DMC exerts multiple, geroprotective effects by igniting distinct pathways, and thus represents a potential pharmacological agent that delays aging through multipronged effects. Taylor & Francis 2019-06-28 /pmc/articles/PMC6693465/ /pubmed/31248332 http://dx.doi.org/10.1080/15548627.2019.1632623 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Commentary Zimmermann, Andreas Kainz, Katharina Hofer, Sebastian J. Bauer, Maria A. Schroeder, Sabrina Dengjel, Jörn Pietrocola, Federico Kepp, Oliver Ruckenstuhl, Christoph Eisenberg, Tobias Sigrist, Stephan J. Madeo, Frank Carmona-Gutierrez, Didac Kroemer, Guido 4,4'Dimethoxychalcone: a natural flavonoid that promotes health through autophagy-dependent and -independent effects |
title | 4,4'Dimethoxychalcone: a natural flavonoid that promotes health through autophagy-dependent and -independent effects |
title_full | 4,4'Dimethoxychalcone: a natural flavonoid that promotes health through autophagy-dependent and -independent effects |
title_fullStr | 4,4'Dimethoxychalcone: a natural flavonoid that promotes health through autophagy-dependent and -independent effects |
title_full_unstemmed | 4,4'Dimethoxychalcone: a natural flavonoid that promotes health through autophagy-dependent and -independent effects |
title_short | 4,4'Dimethoxychalcone: a natural flavonoid that promotes health through autophagy-dependent and -independent effects |
title_sort | 4,4'dimethoxychalcone: a natural flavonoid that promotes health through autophagy-dependent and -independent effects |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6693465/ https://www.ncbi.nlm.nih.gov/pubmed/31248332 http://dx.doi.org/10.1080/15548627.2019.1632623 |
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