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Determination of metformin bio-distribution by LC-MS/MS in mice treated with a clinically relevant paradigm
Metformin, an anti-diabetes drug, has been recently emerging as a potential “anti-aging” intervention based on its reported beneficial actions against aging in preclinical studies. Nonetheless, very few metformin studies using mice have determined metformin concentrations and many effects of metform...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289415/ https://www.ncbi.nlm.nih.gov/pubmed/32525922 http://dx.doi.org/10.1371/journal.pone.0234571 |
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author | Chaudhari, Kiran Wang, Jianmei Xu, Yong Winters, Ali Wang, Linshu Dong, Xiaowei Cheng, Eric Y. Liu, Ran Yang, Shao-Hua |
author_facet | Chaudhari, Kiran Wang, Jianmei Xu, Yong Winters, Ali Wang, Linshu Dong, Xiaowei Cheng, Eric Y. Liu, Ran Yang, Shao-Hua |
author_sort | Chaudhari, Kiran |
collection | PubMed |
description | Metformin, an anti-diabetes drug, has been recently emerging as a potential “anti-aging” intervention based on its reported beneficial actions against aging in preclinical studies. Nonetheless, very few metformin studies using mice have determined metformin concentrations and many effects of metformin have been observed in preclinical studies using doses/concentrations that were not relevant to therapeutic levels in human. We developed a liquid chromatography-tandem mass spectrometry protocol for metformin measurement in plasma, liver, brain, kidney, and muscle of mice. Young adult male and female C57BL/6 mice were voluntarily treated with metformin of 4 mg/ml in drinking water which translated to the maximum dose of 2.5 g/day in humans. A clinically relevant steady-state plasma metformin concentrations were achieved at 7 and 30 days after treatment in male and female mice. Metformin concentrations were slightly higher in muscle than in plasma, while, ~3 and 6-fold higher in the liver and kidney than in plasma, respectively. Low metformin concentration was found in the brain at ~20% of the plasma level. Furthermore, gender difference in steady-state metformin bio-distribution was observed. Our study established steady-state metformin levels in plasma, liver, muscle, kidney, and brain of normoglycemic mice treated with a clinically relevant dose, providing insight into future metformin preclinical studies for potential clinical translation. |
format | Online Article Text |
id | pubmed-7289415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-72894152020-06-15 Determination of metformin bio-distribution by LC-MS/MS in mice treated with a clinically relevant paradigm Chaudhari, Kiran Wang, Jianmei Xu, Yong Winters, Ali Wang, Linshu Dong, Xiaowei Cheng, Eric Y. Liu, Ran Yang, Shao-Hua PLoS One Research Article Metformin, an anti-diabetes drug, has been recently emerging as a potential “anti-aging” intervention based on its reported beneficial actions against aging in preclinical studies. Nonetheless, very few metformin studies using mice have determined metformin concentrations and many effects of metformin have been observed in preclinical studies using doses/concentrations that were not relevant to therapeutic levels in human. We developed a liquid chromatography-tandem mass spectrometry protocol for metformin measurement in plasma, liver, brain, kidney, and muscle of mice. Young adult male and female C57BL/6 mice were voluntarily treated with metformin of 4 mg/ml in drinking water which translated to the maximum dose of 2.5 g/day in humans. A clinically relevant steady-state plasma metformin concentrations were achieved at 7 and 30 days after treatment in male and female mice. Metformin concentrations were slightly higher in muscle than in plasma, while, ~3 and 6-fold higher in the liver and kidney than in plasma, respectively. Low metformin concentration was found in the brain at ~20% of the plasma level. Furthermore, gender difference in steady-state metformin bio-distribution was observed. Our study established steady-state metformin levels in plasma, liver, muscle, kidney, and brain of normoglycemic mice treated with a clinically relevant dose, providing insight into future metformin preclinical studies for potential clinical translation. Public Library of Science 2020-06-11 /pmc/articles/PMC7289415/ /pubmed/32525922 http://dx.doi.org/10.1371/journal.pone.0234571 Text en © 2020 Chaudhari et al 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 author and source are credited. |
spellingShingle | Research Article Chaudhari, Kiran Wang, Jianmei Xu, Yong Winters, Ali Wang, Linshu Dong, Xiaowei Cheng, Eric Y. Liu, Ran Yang, Shao-Hua Determination of metformin bio-distribution by LC-MS/MS in mice treated with a clinically relevant paradigm |
title | Determination of metformin bio-distribution by LC-MS/MS in mice treated with a clinically relevant paradigm |
title_full | Determination of metformin bio-distribution by LC-MS/MS in mice treated with a clinically relevant paradigm |
title_fullStr | Determination of metformin bio-distribution by LC-MS/MS in mice treated with a clinically relevant paradigm |
title_full_unstemmed | Determination of metformin bio-distribution by LC-MS/MS in mice treated with a clinically relevant paradigm |
title_short | Determination of metformin bio-distribution by LC-MS/MS in mice treated with a clinically relevant paradigm |
title_sort | determination of metformin bio-distribution by lc-ms/ms in mice treated with a clinically relevant paradigm |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289415/ https://www.ncbi.nlm.nih.gov/pubmed/32525922 http://dx.doi.org/10.1371/journal.pone.0234571 |
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