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Effects of imeglimin on mitochondrial function, AMPK activity, and gene expression in hepatocytes

Imeglimin is a recently launched antidiabetic drug structurally related to metformin. To provide insight into the pharmacological properties of imeglimin, we investigated its effects on hepatocytes and compared them with those of metformin. The effects of imeglimin on mitochondrial function in HepG2...

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Autores principales: Hozumi, Kaori, Sugawara, Kenji, Ishihara, Takaya, Ishihara, Naotada, Ogawa, Wataru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9839736/
https://www.ncbi.nlm.nih.gov/pubmed/36639407
http://dx.doi.org/10.1038/s41598-023-27689-y
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author Hozumi, Kaori
Sugawara, Kenji
Ishihara, Takaya
Ishihara, Naotada
Ogawa, Wataru
author_facet Hozumi, Kaori
Sugawara, Kenji
Ishihara, Takaya
Ishihara, Naotada
Ogawa, Wataru
author_sort Hozumi, Kaori
collection PubMed
description Imeglimin is a recently launched antidiabetic drug structurally related to metformin. To provide insight into the pharmacological properties of imeglimin, we investigated its effects on hepatocytes and compared them with those of metformin. The effects of imeglimin on mitochondrial function in HepG2 cells or mouse primary hepatocytes were examined with an extracellular flux analyzer and on gene expression in HepG2 cells by comprehensive RNA-sequencing analysis. The effects of the drug on AMPK activity in HepG2 cells, mouse primary hepatocytes, and mouse liver were also examined. Treatment of HepG2 cells or mouse primary hepatocytes with imeglimin reduced the oxygen consumption rate coupled to ATP production. Imeglimin activated AMPK in these cells whereas the potency was smaller than metformin. Bolus administration of imeglimin in mice also activated AMPK in the liver. Whereas the effects of imeglimin and metformin on gene expression in HepG2 cells were similar overall, the expression of genes encoding proteins of mitochondrial respiratory complex III and complex I was upregulated by imeglimin but not by metformin. Our results suggest that imeglimin and metformin exert similar pharmacological effects on mitochondrial respiration, AMPK activity, and gene expression in cultured hepatocytes, whereas the two drugs differ in their effects on the expression of certain genes related to mitochondrial function.
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spelling pubmed-98397362023-01-15 Effects of imeglimin on mitochondrial function, AMPK activity, and gene expression in hepatocytes Hozumi, Kaori Sugawara, Kenji Ishihara, Takaya Ishihara, Naotada Ogawa, Wataru Sci Rep Article Imeglimin is a recently launched antidiabetic drug structurally related to metformin. To provide insight into the pharmacological properties of imeglimin, we investigated its effects on hepatocytes and compared them with those of metformin. The effects of imeglimin on mitochondrial function in HepG2 cells or mouse primary hepatocytes were examined with an extracellular flux analyzer and on gene expression in HepG2 cells by comprehensive RNA-sequencing analysis. The effects of the drug on AMPK activity in HepG2 cells, mouse primary hepatocytes, and mouse liver were also examined. Treatment of HepG2 cells or mouse primary hepatocytes with imeglimin reduced the oxygen consumption rate coupled to ATP production. Imeglimin activated AMPK in these cells whereas the potency was smaller than metformin. Bolus administration of imeglimin in mice also activated AMPK in the liver. Whereas the effects of imeglimin and metformin on gene expression in HepG2 cells were similar overall, the expression of genes encoding proteins of mitochondrial respiratory complex III and complex I was upregulated by imeglimin but not by metformin. Our results suggest that imeglimin and metformin exert similar pharmacological effects on mitochondrial respiration, AMPK activity, and gene expression in cultured hepatocytes, whereas the two drugs differ in their effects on the expression of certain genes related to mitochondrial function. Nature Publishing Group UK 2023-01-13 /pmc/articles/PMC9839736/ /pubmed/36639407 http://dx.doi.org/10.1038/s41598-023-27689-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hozumi, Kaori
Sugawara, Kenji
Ishihara, Takaya
Ishihara, Naotada
Ogawa, Wataru
Effects of imeglimin on mitochondrial function, AMPK activity, and gene expression in hepatocytes
title Effects of imeglimin on mitochondrial function, AMPK activity, and gene expression in hepatocytes
title_full Effects of imeglimin on mitochondrial function, AMPK activity, and gene expression in hepatocytes
title_fullStr Effects of imeglimin on mitochondrial function, AMPK activity, and gene expression in hepatocytes
title_full_unstemmed Effects of imeglimin on mitochondrial function, AMPK activity, and gene expression in hepatocytes
title_short Effects of imeglimin on mitochondrial function, AMPK activity, and gene expression in hepatocytes
title_sort effects of imeglimin on mitochondrial function, ampk activity, and gene expression in hepatocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9839736/
https://www.ncbi.nlm.nih.gov/pubmed/36639407
http://dx.doi.org/10.1038/s41598-023-27689-y
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