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If started early in life, metformin treatment increases life span and postpones tumors in female SHR mice
Hyperglycemia and hyperinsulinemia accelerate both aging and cancer. Antidiabetic biguanides such as metformin decrease glucose, insulin and IGF-1 level. Metformin increases lifespan and prevents cancer in mice, although its effects vary, depending on mice strain and gender. Here we showed that chro...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3082009/ https://www.ncbi.nlm.nih.gov/pubmed/21386129 |
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author | Anisimov, Vladimir N. Berstein, Lev M. Popovich, Irina G. Zabezhinski, Mark A. Egormin, Peter A. Piskunova, Tatiana S. Semenchenko, Anna V. Tyndyk, Margarita L. Yurova, Maria N. Kovalenko, Irina G. Poroshina, Tatiana E. |
author_facet | Anisimov, Vladimir N. Berstein, Lev M. Popovich, Irina G. Zabezhinski, Mark A. Egormin, Peter A. Piskunova, Tatiana S. Semenchenko, Anna V. Tyndyk, Margarita L. Yurova, Maria N. Kovalenko, Irina G. Poroshina, Tatiana E. |
author_sort | Anisimov, Vladimir N. |
collection | PubMed |
description | Hyperglycemia and hyperinsulinemia accelerate both aging and cancer. Antidiabetic biguanides such as metformin decrease glucose, insulin and IGF-1 level. Metformin increases lifespan and prevents cancer in mice, although its effects vary, depending on mice strain and gender. Here we showed that chronic treatment of female outbred SHR mice with metformin started at the age of 3, 9 or 15 months decreased body temperature and postponed age-related switch-off of estrous function. Surprisingly, metformin did not affect levels of serum cholesterol, triglycerides, glucose and insulin. Treatment with metformin started at the age of 3 months increased mean life span by 14% and maximum life span by 1 month. The treatment started at the age of 9 months insignificantly increased mean life span by only 6%, whereas the treatment started at the age of 15 months failed to increase life span. The mean life span of tumor-free mice was increased by 21% in ‘the youngest group’, by 7% in ‘middle-aged group’ and in contrast was reduced by 13% in ‘the oldest group’. When started at the age of 3 and 9 months, metformin delayed the first tumor detection by 22% and 25%, correspondingly. Thus, in female SHR mice, metformin increased life span and postponed tumors when started at the young and middle but not at the old age. In contrast, metformin improves reproductive function when started at any age. |
format | Text |
id | pubmed-3082009 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-30820092011-04-28 If started early in life, metformin treatment increases life span and postpones tumors in female SHR mice Anisimov, Vladimir N. Berstein, Lev M. Popovich, Irina G. Zabezhinski, Mark A. Egormin, Peter A. Piskunova, Tatiana S. Semenchenko, Anna V. Tyndyk, Margarita L. Yurova, Maria N. Kovalenko, Irina G. Poroshina, Tatiana E. Aging (Albany NY) Research Paper Hyperglycemia and hyperinsulinemia accelerate both aging and cancer. Antidiabetic biguanides such as metformin decrease glucose, insulin and IGF-1 level. Metformin increases lifespan and prevents cancer in mice, although its effects vary, depending on mice strain and gender. Here we showed that chronic treatment of female outbred SHR mice with metformin started at the age of 3, 9 or 15 months decreased body temperature and postponed age-related switch-off of estrous function. Surprisingly, metformin did not affect levels of serum cholesterol, triglycerides, glucose and insulin. Treatment with metformin started at the age of 3 months increased mean life span by 14% and maximum life span by 1 month. The treatment started at the age of 9 months insignificantly increased mean life span by only 6%, whereas the treatment started at the age of 15 months failed to increase life span. The mean life span of tumor-free mice was increased by 21% in ‘the youngest group’, by 7% in ‘middle-aged group’ and in contrast was reduced by 13% in ‘the oldest group’. When started at the age of 3 and 9 months, metformin delayed the first tumor detection by 22% and 25%, correspondingly. Thus, in female SHR mice, metformin increased life span and postponed tumors when started at the young and middle but not at the old age. In contrast, metformin improves reproductive function when started at any age. Impact Journals LLC 2011-02-21 /pmc/articles/PMC3082009/ /pubmed/21386129 Text en Copyright: © 2011 Anisimov et al. http://creativecommons.org/licenses/by/2.5/ 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 the original author and source are credited |
spellingShingle | Research Paper Anisimov, Vladimir N. Berstein, Lev M. Popovich, Irina G. Zabezhinski, Mark A. Egormin, Peter A. Piskunova, Tatiana S. Semenchenko, Anna V. Tyndyk, Margarita L. Yurova, Maria N. Kovalenko, Irina G. Poroshina, Tatiana E. If started early in life, metformin treatment increases life span and postpones tumors in female SHR mice |
title | If started early in life, metformin treatment increases life span and postpones tumors in female SHR mice |
title_full | If started early in life, metformin treatment increases life span and postpones tumors in female SHR mice |
title_fullStr | If started early in life, metformin treatment increases life span and postpones tumors in female SHR mice |
title_full_unstemmed | If started early in life, metformin treatment increases life span and postpones tumors in female SHR mice |
title_short | If started early in life, metformin treatment increases life span and postpones tumors in female SHR mice |
title_sort | if started early in life, metformin treatment increases life span and postpones tumors in female shr mice |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3082009/ https://www.ncbi.nlm.nih.gov/pubmed/21386129 |
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