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Bioenergetic bypass using cell-permeable succinate, but not methylene blue, attenuates metformin-induced lactate production

BACKGROUND: Metformin is the most common pharmacological treatment for type 2 diabetes. It is considered safe but has been associated with the development of lactic acidosis under circumstances where plasma concentrations exceed therapeutic levels. Metformin-induced lactic acidosis has been linked t...

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Autores principales: Piel, Sarah, Ehinger, Johannes K., Chamkha, Imen, Frostner, Eleonor Åsander, Sjövall, Fredrik, Elmér, Eskil, Hansson, Magnus J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070446/
https://www.ncbi.nlm.nih.gov/pubmed/30069806
http://dx.doi.org/10.1186/s40635-018-0186-1
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author Piel, Sarah
Ehinger, Johannes K.
Chamkha, Imen
Frostner, Eleonor Åsander
Sjövall, Fredrik
Elmér, Eskil
Hansson, Magnus J.
author_facet Piel, Sarah
Ehinger, Johannes K.
Chamkha, Imen
Frostner, Eleonor Åsander
Sjövall, Fredrik
Elmér, Eskil
Hansson, Magnus J.
author_sort Piel, Sarah
collection PubMed
description BACKGROUND: Metformin is the most common pharmacological treatment for type 2 diabetes. It is considered safe but has been associated with the development of lactic acidosis under circumstances where plasma concentrations exceed therapeutic levels. Metformin-induced lactic acidosis has been linked to the drug’s toxic effect on mitochondrial function. Current treatment strategies aim to remove the drug and correct for the acidosis. With a mortality of 20%, complementary treatment strategies are needed. In this study, it was investigated whether targeting mitochondria with pharmacological agents that bypass metformin-induced mitochondrial dysfunction can counteract the energetic deficit linked to toxic doses of metformin. METHODS: The redox agent methylene blue and the cell-permeable succinate prodrug NV118 were evaluated by measuring mitochondrial respiration and lactate production of human platelets exposed to metformin and co-treated with either of the two pharmacological bypass agents. RESULTS: The cell-permeable succinate prodrug NV118 increased mitochondrial respiration which was linked to phosphorylation by the ATP-synthase and alleviated the increase in lactate production induced by toxic doses of metformin. The redox agent methylene blue, in contrast, failed to mitigate the metformin-induced changes in mitochondrial respiration and lactate generation. CONCLUSIONS: The cell-permeable succinate prodrug NV118 bypassed the mitochondrial dysfunction and counteracted the energy deficit associated with toxic doses of metformin. If similar effects of NV118 prove translatable to an in vivo effect, this pharmacological strategy presents as a promising complementary treatment for patients with metformin-induced lactic acidosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40635-018-0186-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-60704462018-08-20 Bioenergetic bypass using cell-permeable succinate, but not methylene blue, attenuates metformin-induced lactate production Piel, Sarah Ehinger, Johannes K. Chamkha, Imen Frostner, Eleonor Åsander Sjövall, Fredrik Elmér, Eskil Hansson, Magnus J. Intensive Care Med Exp Research BACKGROUND: Metformin is the most common pharmacological treatment for type 2 diabetes. It is considered safe but has been associated with the development of lactic acidosis under circumstances where plasma concentrations exceed therapeutic levels. Metformin-induced lactic acidosis has been linked to the drug’s toxic effect on mitochondrial function. Current treatment strategies aim to remove the drug and correct for the acidosis. With a mortality of 20%, complementary treatment strategies are needed. In this study, it was investigated whether targeting mitochondria with pharmacological agents that bypass metformin-induced mitochondrial dysfunction can counteract the energetic deficit linked to toxic doses of metformin. METHODS: The redox agent methylene blue and the cell-permeable succinate prodrug NV118 were evaluated by measuring mitochondrial respiration and lactate production of human platelets exposed to metformin and co-treated with either of the two pharmacological bypass agents. RESULTS: The cell-permeable succinate prodrug NV118 increased mitochondrial respiration which was linked to phosphorylation by the ATP-synthase and alleviated the increase in lactate production induced by toxic doses of metformin. The redox agent methylene blue, in contrast, failed to mitigate the metformin-induced changes in mitochondrial respiration and lactate generation. CONCLUSIONS: The cell-permeable succinate prodrug NV118 bypassed the mitochondrial dysfunction and counteracted the energy deficit associated with toxic doses of metformin. If similar effects of NV118 prove translatable to an in vivo effect, this pharmacological strategy presents as a promising complementary treatment for patients with metformin-induced lactic acidosis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40635-018-0186-1) contains supplementary material, which is available to authorized users. Springer International Publishing 2018-08-01 /pmc/articles/PMC6070446/ /pubmed/30069806 http://dx.doi.org/10.1186/s40635-018-0186-1 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Piel, Sarah
Ehinger, Johannes K.
Chamkha, Imen
Frostner, Eleonor Åsander
Sjövall, Fredrik
Elmér, Eskil
Hansson, Magnus J.
Bioenergetic bypass using cell-permeable succinate, but not methylene blue, attenuates metformin-induced lactate production
title Bioenergetic bypass using cell-permeable succinate, but not methylene blue, attenuates metformin-induced lactate production
title_full Bioenergetic bypass using cell-permeable succinate, but not methylene blue, attenuates metformin-induced lactate production
title_fullStr Bioenergetic bypass using cell-permeable succinate, but not methylene blue, attenuates metformin-induced lactate production
title_full_unstemmed Bioenergetic bypass using cell-permeable succinate, but not methylene blue, attenuates metformin-induced lactate production
title_short Bioenergetic bypass using cell-permeable succinate, but not methylene blue, attenuates metformin-induced lactate production
title_sort bioenergetic bypass using cell-permeable succinate, but not methylene blue, attenuates metformin-induced lactate production
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070446/
https://www.ncbi.nlm.nih.gov/pubmed/30069806
http://dx.doi.org/10.1186/s40635-018-0186-1
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