Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
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
_version_ 1784594219014291456
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
work_keys_str_mv AT blackmoredanielg anexercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT steynfrederikj anexercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT carlislealison anexercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT okeeffeimogen anexercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT vienkingyear anexercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT zhouxiaoqing anexercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT leiterodette anexercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT jhaveridhanisha anexercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT vukovicjana anexercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT watersmichaelj anexercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT bartlettperryf anexercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT blackmoredanielg exercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT steynfrederikj exercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT carlislealison exercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT okeeffeimogen exercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT vienkingyear exercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT zhouxiaoqing exercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT leiterodette exercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT jhaveridhanisha exercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT vukovicjana exercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT watersmichaelj exercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis
AT bartlettperryf exercisesweetspotreversescognitivedeficitsofagingbygrowthhormoneinducedneurogenesis