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Metformin Inhibits Mitochondrial Complex I To Promote Health
The major function of mitochondria in cellular homeostasis has been the generation of ATP through oxidative phosphorylation. However, we have previously demonstrated that mitochondria can serve as signaling organelles by releasing low levels of reactive oxygen species (ROS) and TCA cycle metabolites...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Oxford University Press
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8680347/ http://dx.doi.org/10.1093/geroni/igab046.1760 |
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author | Chandel, Navdeep |
author_facet | Chandel, Navdeep |
author_sort | Chandel, Navdeep |
collection | PubMed |
description | The major function of mitochondria in cellular homeostasis has been the generation of ATP through oxidative phosphorylation. However, we have previously demonstrated that mitochondria can serve as signaling organelles by releasing low levels of reactive oxygen species (ROS) and TCA cycle metabolites that are essential for hypoxic activation of HIF, antigen activation of T cells, cellular differentiation and proliferation of cancer cells. The anti-diabetic drug metformin has been proposed to inhibit mitochondrial complex I. We will present data indicating that metformin inhibits mitochondrial complex I to exert it’s biological effects through controlling ROS, ATP, and NAD+. |
format | Online Article Text |
id | pubmed-8680347 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-86803472021-12-17 Metformin Inhibits Mitochondrial Complex I To Promote Health Chandel, Navdeep Innov Aging Abstracts The major function of mitochondria in cellular homeostasis has been the generation of ATP through oxidative phosphorylation. However, we have previously demonstrated that mitochondria can serve as signaling organelles by releasing low levels of reactive oxygen species (ROS) and TCA cycle metabolites that are essential for hypoxic activation of HIF, antigen activation of T cells, cellular differentiation and proliferation of cancer cells. The anti-diabetic drug metformin has been proposed to inhibit mitochondrial complex I. We will present data indicating that metformin inhibits mitochondrial complex I to exert it’s biological effects through controlling ROS, ATP, and NAD+. Oxford University Press 2021-12-17 /pmc/articles/PMC8680347/ http://dx.doi.org/10.1093/geroni/igab046.1760 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of The Gerontological Society of America. https://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/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Abstracts Chandel, Navdeep Metformin Inhibits Mitochondrial Complex I To Promote Health |
title | Metformin Inhibits Mitochondrial Complex I To Promote Health |
title_full | Metformin Inhibits Mitochondrial Complex I To Promote Health |
title_fullStr | Metformin Inhibits Mitochondrial Complex I To Promote Health |
title_full_unstemmed | Metformin Inhibits Mitochondrial Complex I To Promote Health |
title_short | Metformin Inhibits Mitochondrial Complex I To Promote Health |
title_sort | metformin inhibits mitochondrial complex i to promote health |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8680347/ http://dx.doi.org/10.1093/geroni/igab046.1760 |
work_keys_str_mv | AT chandelnavdeep metformininhibitsmitochondrialcomplexitopromotehealth |