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Rapamycin increases grip strength and attenuates age-related decline in maximal running distance in old low capacity runner rats
Rapamycin is known to extend lifespan. We conducted a randomized placebo-controlled study of enteric rapamycin-treatment to evaluate its effect on physical function in old low capacity runner (LCR) rats, a rat model selected from diverse genetic background for low intrinsic aerobic exercise capacity...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4925827/ https://www.ncbi.nlm.nih.gov/pubmed/26997106 http://dx.doi.org/10.18632/aging.100929 |
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author | Xue, Qian-Li Yang, Huanle Li, Hui-Fen Abadir, Peter M. Burks, Tyesha N. Koch, Lauren G. Britton, Steven L. Carlson, Joshua Chen, Laura Walston, Jeremy D. Leng, Sean X. |
author_facet | Xue, Qian-Li Yang, Huanle Li, Hui-Fen Abadir, Peter M. Burks, Tyesha N. Koch, Lauren G. Britton, Steven L. Carlson, Joshua Chen, Laura Walston, Jeremy D. Leng, Sean X. |
author_sort | Xue, Qian-Li |
collection | PubMed |
description | Rapamycin is known to extend lifespan. We conducted a randomized placebo-controlled study of enteric rapamycin-treatment to evaluate its effect on physical function in old low capacity runner (LCR) rats, a rat model selected from diverse genetic background for low intrinsic aerobic exercise capacity without genomic manipulation and characterized by increased complex disease risks and aging phenotypes. The study was performed in 12 male and 16 female LCR rats aged 16-22 months at baseline. The treatment group was fed with rapamycin-containing diet pellets at approximately 2.24mg/kg body weight per day and the placebo group with the same diet without rapamycin for six months. Observation was extended for additional 2 months. Physical function measurements include grip strength measured as maximum tensile force using a rat grip strength meter and maximum running distance (MRD) using rat physical treadmill test. The results showed that rapamycin improved grip strength by 13% (p=.036) and 60% (p<.001) from its baseline in female and male rats, respectively. Rapamycin attenuated MRD decline by 66% (p<.001) and 46% (p=.319) in females and males, respectively. These findings provide initial evidence for beneficial effect of rapamycin on physical functioning in an aging rat model of high disease risks with significant implication in humans. |
format | Online Article Text |
id | pubmed-4925827 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-49258272016-07-01 Rapamycin increases grip strength and attenuates age-related decline in maximal running distance in old low capacity runner rats Xue, Qian-Li Yang, Huanle Li, Hui-Fen Abadir, Peter M. Burks, Tyesha N. Koch, Lauren G. Britton, Steven L. Carlson, Joshua Chen, Laura Walston, Jeremy D. Leng, Sean X. Aging (Albany NY) Research Paper Rapamycin is known to extend lifespan. We conducted a randomized placebo-controlled study of enteric rapamycin-treatment to evaluate its effect on physical function in old low capacity runner (LCR) rats, a rat model selected from diverse genetic background for low intrinsic aerobic exercise capacity without genomic manipulation and characterized by increased complex disease risks and aging phenotypes. The study was performed in 12 male and 16 female LCR rats aged 16-22 months at baseline. The treatment group was fed with rapamycin-containing diet pellets at approximately 2.24mg/kg body weight per day and the placebo group with the same diet without rapamycin for six months. Observation was extended for additional 2 months. Physical function measurements include grip strength measured as maximum tensile force using a rat grip strength meter and maximum running distance (MRD) using rat physical treadmill test. The results showed that rapamycin improved grip strength by 13% (p=.036) and 60% (p<.001) from its baseline in female and male rats, respectively. Rapamycin attenuated MRD decline by 66% (p<.001) and 46% (p=.319) in females and males, respectively. These findings provide initial evidence for beneficial effect of rapamycin on physical functioning in an aging rat model of high disease risks with significant implication in humans. Impact Journals LLC 2016-03-19 /pmc/articles/PMC4925827/ /pubmed/26997106 http://dx.doi.org/10.18632/aging.100929 Text en Copyright: © 2016 Xue 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 Xue, Qian-Li Yang, Huanle Li, Hui-Fen Abadir, Peter M. Burks, Tyesha N. Koch, Lauren G. Britton, Steven L. Carlson, Joshua Chen, Laura Walston, Jeremy D. Leng, Sean X. Rapamycin increases grip strength and attenuates age-related decline in maximal running distance in old low capacity runner rats |
title | Rapamycin increases grip strength and attenuates age-related decline in maximal running distance in old low capacity runner rats |
title_full | Rapamycin increases grip strength and attenuates age-related decline in maximal running distance in old low capacity runner rats |
title_fullStr | Rapamycin increases grip strength and attenuates age-related decline in maximal running distance in old low capacity runner rats |
title_full_unstemmed | Rapamycin increases grip strength and attenuates age-related decline in maximal running distance in old low capacity runner rats |
title_short | Rapamycin increases grip strength and attenuates age-related decline in maximal running distance in old low capacity runner rats |
title_sort | rapamycin increases grip strength and attenuates age-related decline in maximal running distance in old low capacity runner rats |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4925827/ https://www.ncbi.nlm.nih.gov/pubmed/26997106 http://dx.doi.org/10.18632/aging.100929 |
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