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Alpha-ketoglutarate extends Drosophila lifespan by inhibiting mTOR and activating AMPK
Alpha-ketoglutarate (AKG) is a key metabolite of the tricarboxylic acid (TCA) cycle, an essential process influencing the mitochondrial oxidative respiration rate. Recent studies have shown that dietary AKG reduces mTOR pathway activation by inhibiting ATP synthase, thereby extending the lifespan of...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629006/ https://www.ncbi.nlm.nih.gov/pubmed/31242135 http://dx.doi.org/10.18632/aging.102045 |
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author | Su, Yuan Wang, Tao Wu, Nan Li, Diyan Fan, Xiaolan Xu, Zhongxian Mishra, Shailendra Kumar Yang, Mingyao |
author_facet | Su, Yuan Wang, Tao Wu, Nan Li, Diyan Fan, Xiaolan Xu, Zhongxian Mishra, Shailendra Kumar Yang, Mingyao |
author_sort | Su, Yuan |
collection | PubMed |
description | Alpha-ketoglutarate (AKG) is a key metabolite of the tricarboxylic acid (TCA) cycle, an essential process influencing the mitochondrial oxidative respiration rate. Recent studies have shown that dietary AKG reduces mTOR pathway activation by inhibiting ATP synthase, thereby extending the lifespan of nematodes. Although AKG also extends lifespan in fruit flies, the antiaging mechanisms of AKG in these organisms remain unclear. In the present study, we explored changes in gene expression associated with the extension of Drosophila lifespan mediated by dietary AKG. Supplementation of the flies’ diets with 5 μM AKG extended their lifespan but reduced their reproductive performance. Dietary AKG also enhanced vertical climbing ability, but did not protect against oxidative stress or increase tolerance to starvation. AKG-reared flies were resistant to heat stress and demonstrated higher expression of heat shock protein genes (Hsp22 and Hsp70) than control flies. In addition, AKG significantly upregulated mRNA expression of cry, FoxO, HNF4, p300, Sirt1 and AMPKα, and downregulated expression of HDAC4, PI3K, TORC, PGC, and SREBP. The metabolic effects of AKG supplementation included a reduction in the ATP/ADP ratio and increased autophagy. Collectively, these observations indicate that AKG extends Drosophila lifespan by activating AMPK signaling and inhibiting the mTOR pathway. |
format | Online Article Text |
id | pubmed-6629006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
spelling | pubmed-66290062019-07-18 Alpha-ketoglutarate extends Drosophila lifespan by inhibiting mTOR and activating AMPK Su, Yuan Wang, Tao Wu, Nan Li, Diyan Fan, Xiaolan Xu, Zhongxian Mishra, Shailendra Kumar Yang, Mingyao Aging (Albany NY) Research Paper Alpha-ketoglutarate (AKG) is a key metabolite of the tricarboxylic acid (TCA) cycle, an essential process influencing the mitochondrial oxidative respiration rate. Recent studies have shown that dietary AKG reduces mTOR pathway activation by inhibiting ATP synthase, thereby extending the lifespan of nematodes. Although AKG also extends lifespan in fruit flies, the antiaging mechanisms of AKG in these organisms remain unclear. In the present study, we explored changes in gene expression associated with the extension of Drosophila lifespan mediated by dietary AKG. Supplementation of the flies’ diets with 5 μM AKG extended their lifespan but reduced their reproductive performance. Dietary AKG also enhanced vertical climbing ability, but did not protect against oxidative stress or increase tolerance to starvation. AKG-reared flies were resistant to heat stress and demonstrated higher expression of heat shock protein genes (Hsp22 and Hsp70) than control flies. In addition, AKG significantly upregulated mRNA expression of cry, FoxO, HNF4, p300, Sirt1 and AMPKα, and downregulated expression of HDAC4, PI3K, TORC, PGC, and SREBP. The metabolic effects of AKG supplementation included a reduction in the ATP/ADP ratio and increased autophagy. Collectively, these observations indicate that AKG extends Drosophila lifespan by activating AMPK signaling and inhibiting the mTOR pathway. Impact Journals 2019-06-26 /pmc/articles/PMC6629006/ /pubmed/31242135 http://dx.doi.org/10.18632/aging.102045 Text en Copyright © 2019 Su et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC BY) 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Su, Yuan Wang, Tao Wu, Nan Li, Diyan Fan, Xiaolan Xu, Zhongxian Mishra, Shailendra Kumar Yang, Mingyao Alpha-ketoglutarate extends Drosophila lifespan by inhibiting mTOR and activating AMPK |
title | Alpha-ketoglutarate extends Drosophila lifespan by inhibiting mTOR and activating AMPK |
title_full | Alpha-ketoglutarate extends Drosophila lifespan by inhibiting mTOR and activating AMPK |
title_fullStr | Alpha-ketoglutarate extends Drosophila lifespan by inhibiting mTOR and activating AMPK |
title_full_unstemmed | Alpha-ketoglutarate extends Drosophila lifespan by inhibiting mTOR and activating AMPK |
title_short | Alpha-ketoglutarate extends Drosophila lifespan by inhibiting mTOR and activating AMPK |
title_sort | alpha-ketoglutarate extends drosophila lifespan by inhibiting mtor and activating ampk |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629006/ https://www.ncbi.nlm.nih.gov/pubmed/31242135 http://dx.doi.org/10.18632/aging.102045 |
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