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Metformin Impairs Spatial Memory and Visual Acuity in Old Male Mice
Metformin is an oral anti-diabetic used as first-line therapy for type 2 diabetes. Because benefits of metformin extend beyond diabetes to other age-related pathology, and because its effect on gene expression profiles resembles that of caloric restriction, metformin has a potential as an anti-aging...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JKL International LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287385/ https://www.ncbi.nlm.nih.gov/pubmed/28203479 http://dx.doi.org/10.14336/AD.2016.1010 |
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author | Thangthaeng, Nopporn Rutledge, Margaret Wong, Jessica M. Vann, Philip H. Forster, Michael J. Sumien, Nathalie |
author_facet | Thangthaeng, Nopporn Rutledge, Margaret Wong, Jessica M. Vann, Philip H. Forster, Michael J. Sumien, Nathalie |
author_sort | Thangthaeng, Nopporn |
collection | PubMed |
description | Metformin is an oral anti-diabetic used as first-line therapy for type 2 diabetes. Because benefits of metformin extend beyond diabetes to other age-related pathology, and because its effect on gene expression profiles resembles that of caloric restriction, metformin has a potential as an anti-aging intervention and may soon be assessed as an intervention to extend healthspan. However, beneficial actions of metformin in the central nervous system have not been clearly established. The current study examined the effect of chronic oral metformin treatment on motor and cognitive function when initiated in young, middle-aged, or old male mice. C57BL/6 mice aged 4, 11, or 22 months were randomly assigned to either a metformin group (2 mg/ml in drinking water) or a control group. The mice were monitored weekly for body weight, as well as food and water intake and a battery of behavioral tests for motor, cognitive and visual function was initiated after the first month of treatment. Liver, hippocampus and cortex were collected at the end of the study to assess redox homeostasis. Overall, metformin supplementation in male mice failed to affect blood glucose, body weights and redox homeostasis at any age. It also had no beneficial effect on age-related declines in psychomotor, cognitive or sensory functions. However, metformin treatment had a deleterious effect on spatial memory and visual acuity, and reduced SOD activity in brain regions. These data confirm that metformin treatment may be associated with deleterious effect resulting from the action of metformin on the central nervous system. |
format | Online Article Text |
id | pubmed-5287385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | JKL International LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-52873852017-02-15 Metformin Impairs Spatial Memory and Visual Acuity in Old Male Mice Thangthaeng, Nopporn Rutledge, Margaret Wong, Jessica M. Vann, Philip H. Forster, Michael J. Sumien, Nathalie Aging Dis Original Article Metformin is an oral anti-diabetic used as first-line therapy for type 2 diabetes. Because benefits of metformin extend beyond diabetes to other age-related pathology, and because its effect on gene expression profiles resembles that of caloric restriction, metformin has a potential as an anti-aging intervention and may soon be assessed as an intervention to extend healthspan. However, beneficial actions of metformin in the central nervous system have not been clearly established. The current study examined the effect of chronic oral metformin treatment on motor and cognitive function when initiated in young, middle-aged, or old male mice. C57BL/6 mice aged 4, 11, or 22 months were randomly assigned to either a metformin group (2 mg/ml in drinking water) or a control group. The mice were monitored weekly for body weight, as well as food and water intake and a battery of behavioral tests for motor, cognitive and visual function was initiated after the first month of treatment. Liver, hippocampus and cortex were collected at the end of the study to assess redox homeostasis. Overall, metformin supplementation in male mice failed to affect blood glucose, body weights and redox homeostasis at any age. It also had no beneficial effect on age-related declines in psychomotor, cognitive or sensory functions. However, metformin treatment had a deleterious effect on spatial memory and visual acuity, and reduced SOD activity in brain regions. These data confirm that metformin treatment may be associated with deleterious effect resulting from the action of metformin on the central nervous system. JKL International LLC 2017-02-01 /pmc/articles/PMC5287385/ /pubmed/28203479 http://dx.doi.org/10.14336/AD.2016.1010 Text en Copyright: © 2017 Thangthaeng, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. http://creativecommons.org/licenses/by/2.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Original Article Thangthaeng, Nopporn Rutledge, Margaret Wong, Jessica M. Vann, Philip H. Forster, Michael J. Sumien, Nathalie Metformin Impairs Spatial Memory and Visual Acuity in Old Male Mice |
title | Metformin Impairs Spatial Memory and Visual Acuity in Old Male Mice |
title_full | Metformin Impairs Spatial Memory and Visual Acuity in Old Male Mice |
title_fullStr | Metformin Impairs Spatial Memory and Visual Acuity in Old Male Mice |
title_full_unstemmed | Metformin Impairs Spatial Memory and Visual Acuity in Old Male Mice |
title_short | Metformin Impairs Spatial Memory and Visual Acuity in Old Male Mice |
title_sort | metformin impairs spatial memory and visual acuity in old male mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5287385/ https://www.ncbi.nlm.nih.gov/pubmed/28203479 http://dx.doi.org/10.14336/AD.2016.1010 |
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