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An exercise “sweet spot” reverses cognitive deficits of aging by growth-hormone-induced neurogenesis
Hippocampal function is critical for spatial and contextual learning, and its decline with age contributes to cognitive impairment. Exercise can improve hippocampal function, however, the amount of exercise and mechanisms mediating improvement remain largely unknown. Here, we show exercise reverses...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567379/ https://www.ncbi.nlm.nih.gov/pubmed/34761193 http://dx.doi.org/10.1016/j.isci.2021.103275 |
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author | Blackmore, Daniel G. Steyn, Frederik J. Carlisle, Alison O’Keeffe, Imogen Vien, King-Year Zhou, Xiaoqing Leiter, Odette Jhaveri, Dhanisha Vukovic, Jana Waters, Michael J. Bartlett, Perry F. |
author_facet | Blackmore, Daniel G. Steyn, Frederik J. Carlisle, Alison O’Keeffe, Imogen Vien, King-Year Zhou, Xiaoqing Leiter, Odette Jhaveri, Dhanisha Vukovic, Jana Waters, Michael J. Bartlett, Perry F. |
author_sort | Blackmore, Daniel G. |
collection | PubMed |
description | Hippocampal function is critical for spatial and contextual learning, and its decline with age contributes to cognitive impairment. Exercise can improve hippocampal function, however, the amount of exercise and mechanisms mediating improvement remain largely unknown. Here, we show exercise reverses learning deficits in aged (24 months) female mice but only when it occurs for a specific duration, with longer or shorter periods proving ineffective. A spike in the levels of growth hormone (GH) and a corresponding increase in neurogenesis during this sweet spot mediate this effect because blocking GH receptor with a competitive antagonist or depleting newborn neurons abrogates the exercise-induced cognitive improvement. Moreover, raising GH levels with GH-releasing hormone agonist improved cognition in nonrunners. We show that GH stimulates neural precursors directly, indicating the link between raised GH and neurogenesis is the basis for the substantially improved learning in aged animals. |
format | Online Article Text |
id | pubmed-8567379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-85673792021-11-09 An exercise “sweet spot” reverses cognitive deficits of aging by growth-hormone-induced neurogenesis Blackmore, Daniel G. Steyn, Frederik J. Carlisle, Alison O’Keeffe, Imogen Vien, King-Year Zhou, Xiaoqing Leiter, Odette Jhaveri, Dhanisha Vukovic, Jana Waters, Michael J. Bartlett, Perry F. iScience Article Hippocampal function is critical for spatial and contextual learning, and its decline with age contributes to cognitive impairment. Exercise can improve hippocampal function, however, the amount of exercise and mechanisms mediating improvement remain largely unknown. Here, we show exercise reverses learning deficits in aged (24 months) female mice but only when it occurs for a specific duration, with longer or shorter periods proving ineffective. A spike in the levels of growth hormone (GH) and a corresponding increase in neurogenesis during this sweet spot mediate this effect because blocking GH receptor with a competitive antagonist or depleting newborn neurons abrogates the exercise-induced cognitive improvement. Moreover, raising GH levels with GH-releasing hormone agonist improved cognition in nonrunners. We show that GH stimulates neural precursors directly, indicating the link between raised GH and neurogenesis is the basis for the substantially improved learning in aged animals. Elsevier 2021-10-14 /pmc/articles/PMC8567379/ /pubmed/34761193 http://dx.doi.org/10.1016/j.isci.2021.103275 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Blackmore, Daniel G. Steyn, Frederik J. Carlisle, Alison O’Keeffe, Imogen Vien, King-Year Zhou, Xiaoqing Leiter, Odette Jhaveri, Dhanisha Vukovic, Jana Waters, Michael J. Bartlett, Perry F. An exercise “sweet spot” reverses cognitive deficits of aging by growth-hormone-induced neurogenesis |
title | An exercise “sweet spot” reverses cognitive deficits of aging by growth-hormone-induced neurogenesis |
title_full | An exercise “sweet spot” reverses cognitive deficits of aging by growth-hormone-induced neurogenesis |
title_fullStr | An exercise “sweet spot” reverses cognitive deficits of aging by growth-hormone-induced neurogenesis |
title_full_unstemmed | An exercise “sweet spot” reverses cognitive deficits of aging by growth-hormone-induced neurogenesis |
title_short | An exercise “sweet spot” reverses cognitive deficits of aging by growth-hormone-induced neurogenesis |
title_sort | exercise “sweet spot” reverses cognitive deficits of aging by growth-hormone-induced neurogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8567379/ https://www.ncbi.nlm.nih.gov/pubmed/34761193 http://dx.doi.org/10.1016/j.isci.2021.103275 |
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