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The effect of a pharmaceutical ghrelin agonist on lifespan in C57BL/6J male mice: A controlled experiment
Interventions for animal lifespan extension like caloric restriction (CR) have identified physiologic and biochemical pathways related to hunger and energy‐sensing status as possible contributors, but mechanisms have not been fully elucidated. Prior studies using ghrelin agonists show greater food i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086516/ https://www.ncbi.nlm.nih.gov/pubmed/36734122 http://dx.doi.org/10.1111/acel.13787 |
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author | Kaiser, Kathryn A. Kadish, Inga van Groen, Thomas Smith, Daniel L. Dickinson, Stephanie Henschel, Beate Parker, Erik S. Brown, Andrew W. Allison, David B. |
author_facet | Kaiser, Kathryn A. Kadish, Inga van Groen, Thomas Smith, Daniel L. Dickinson, Stephanie Henschel, Beate Parker, Erik S. Brown, Andrew W. Allison, David B. |
author_sort | Kaiser, Kathryn A. |
collection | PubMed |
description | Interventions for animal lifespan extension like caloric restriction (CR) have identified physiologic and biochemical pathways related to hunger and energy‐sensing status as possible contributors, but mechanisms have not been fully elucidated. Prior studies using ghrelin agonists show greater food intake but no effect on lifespan in rodent models. This experiment in male C57BL/6J mice tested the influence of ghrelin agonism for perceived hunger, in the absence of CR, on longevity. Mice aged 4 weeks were allowed to acclimate for 2 weeks prior to being assigned (N = 60/group). Prior to lights off daily (12:12 cycle), animals were fed a ghrelin agonist pill (LY444711; Eli Lilly) or a placebo control (Ctrl) until death. Treatment (GhrAg) animals were pair‐fed daily based on the group mean food intake consumed by Ctrl (ad libitum feeding) the prior week. Results indicate an increased lifespan effect (log‐rank p = 0.0032) for GhrAg versus placebo Ctrl, which weighed significantly more than GhrAg (adjusted for baseline weight). Further studies are needed to determine the full scope of effects of this ghrelin agonist, either directly via increased ghrelin receptor signaling or indirectly via other hypothalamic, systemic, or tissue‐specific mechanisms. |
format | Online Article Text |
id | pubmed-10086516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-100865162023-04-12 The effect of a pharmaceutical ghrelin agonist on lifespan in C57BL/6J male mice: A controlled experiment Kaiser, Kathryn A. Kadish, Inga van Groen, Thomas Smith, Daniel L. Dickinson, Stephanie Henschel, Beate Parker, Erik S. Brown, Andrew W. Allison, David B. Aging Cell Short Communication Interventions for animal lifespan extension like caloric restriction (CR) have identified physiologic and biochemical pathways related to hunger and energy‐sensing status as possible contributors, but mechanisms have not been fully elucidated. Prior studies using ghrelin agonists show greater food intake but no effect on lifespan in rodent models. This experiment in male C57BL/6J mice tested the influence of ghrelin agonism for perceived hunger, in the absence of CR, on longevity. Mice aged 4 weeks were allowed to acclimate for 2 weeks prior to being assigned (N = 60/group). Prior to lights off daily (12:12 cycle), animals were fed a ghrelin agonist pill (LY444711; Eli Lilly) or a placebo control (Ctrl) until death. Treatment (GhrAg) animals were pair‐fed daily based on the group mean food intake consumed by Ctrl (ad libitum feeding) the prior week. Results indicate an increased lifespan effect (log‐rank p = 0.0032) for GhrAg versus placebo Ctrl, which weighed significantly more than GhrAg (adjusted for baseline weight). Further studies are needed to determine the full scope of effects of this ghrelin agonist, either directly via increased ghrelin receptor signaling or indirectly via other hypothalamic, systemic, or tissue‐specific mechanisms. John Wiley and Sons Inc. 2023-02-03 /pmc/articles/PMC10086516/ /pubmed/36734122 http://dx.doi.org/10.1111/acel.13787 Text en © 2023 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Kaiser, Kathryn A. Kadish, Inga van Groen, Thomas Smith, Daniel L. Dickinson, Stephanie Henschel, Beate Parker, Erik S. Brown, Andrew W. Allison, David B. The effect of a pharmaceutical ghrelin agonist on lifespan in C57BL/6J male mice: A controlled experiment |
title | The effect of a pharmaceutical ghrelin agonist on lifespan in C57BL/6J male mice: A controlled experiment |
title_full | The effect of a pharmaceutical ghrelin agonist on lifespan in C57BL/6J male mice: A controlled experiment |
title_fullStr | The effect of a pharmaceutical ghrelin agonist on lifespan in C57BL/6J male mice: A controlled experiment |
title_full_unstemmed | The effect of a pharmaceutical ghrelin agonist on lifespan in C57BL/6J male mice: A controlled experiment |
title_short | The effect of a pharmaceutical ghrelin agonist on lifespan in C57BL/6J male mice: A controlled experiment |
title_sort | effect of a pharmaceutical ghrelin agonist on lifespan in c57bl/6j male mice: a controlled experiment |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10086516/ https://www.ncbi.nlm.nih.gov/pubmed/36734122 http://dx.doi.org/10.1111/acel.13787 |
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