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ISX-9 potentiates CaMKIIδ-mediated BMAL1 activation to enhance circadian amplitude
Circadian dysregulation associates with numerous diseases including metabolic dysfunction, sleep disorder, depression and aging. Given that declined circadian amplitude is a trait commonly found with compromised health, interventions that design in precluding circadian amplitude from dampening will...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334596/ https://www.ncbi.nlm.nih.gov/pubmed/35902736 http://dx.doi.org/10.1038/s42003-022-03725-x |
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author | Li, Huilin Ou, Jiali Li, Yaqun Xu, Niannian Li, Qing Wu, Ping Peng, Chao Tang, Yun-Chi Chang, Hung-Chun |
author_facet | Li, Huilin Ou, Jiali Li, Yaqun Xu, Niannian Li, Qing Wu, Ping Peng, Chao Tang, Yun-Chi Chang, Hung-Chun |
author_sort | Li, Huilin |
collection | PubMed |
description | Circadian dysregulation associates with numerous diseases including metabolic dysfunction, sleep disorder, depression and aging. Given that declined circadian amplitude is a trait commonly found with compromised health, interventions that design in precluding circadian amplitude from dampening will aid to mitigate complex, circadian-related diseases. Here we identify a neurogenic small molecule ISX-9 that is able to support persistent and higher amplitude of circadian oscillations. ISX-9 improves diurnal metabolic rhythms in middle-aged mice. Moreover, the ISX-9-treated mice show better sleep homeostasis with increased delta power during the day time and higher locomotive activity in the dark period. ISX-9 augments CaMKIIδ expression and increases BMAL1 activity via eliciting CaMKIIδ-mediated phosphorylation on BMAL1 residues S513/S515/S516, accordingly composes a positive feedback effect on enhancing circadian amplitude. CaMKIIδ-targeting, and the use of ISX-9 may serve as decent choices for treating circadian-related disorders. |
format | Online Article Text |
id | pubmed-9334596 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93345962022-07-30 ISX-9 potentiates CaMKIIδ-mediated BMAL1 activation to enhance circadian amplitude Li, Huilin Ou, Jiali Li, Yaqun Xu, Niannian Li, Qing Wu, Ping Peng, Chao Tang, Yun-Chi Chang, Hung-Chun Commun Biol Article Circadian dysregulation associates with numerous diseases including metabolic dysfunction, sleep disorder, depression and aging. Given that declined circadian amplitude is a trait commonly found with compromised health, interventions that design in precluding circadian amplitude from dampening will aid to mitigate complex, circadian-related diseases. Here we identify a neurogenic small molecule ISX-9 that is able to support persistent and higher amplitude of circadian oscillations. ISX-9 improves diurnal metabolic rhythms in middle-aged mice. Moreover, the ISX-9-treated mice show better sleep homeostasis with increased delta power during the day time and higher locomotive activity in the dark period. ISX-9 augments CaMKIIδ expression and increases BMAL1 activity via eliciting CaMKIIδ-mediated phosphorylation on BMAL1 residues S513/S515/S516, accordingly composes a positive feedback effect on enhancing circadian amplitude. CaMKIIδ-targeting, and the use of ISX-9 may serve as decent choices for treating circadian-related disorders. Nature Publishing Group UK 2022-07-28 /pmc/articles/PMC9334596/ /pubmed/35902736 http://dx.doi.org/10.1038/s42003-022-03725-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Li, Huilin Ou, Jiali Li, Yaqun Xu, Niannian Li, Qing Wu, Ping Peng, Chao Tang, Yun-Chi Chang, Hung-Chun ISX-9 potentiates CaMKIIδ-mediated BMAL1 activation to enhance circadian amplitude |
title | ISX-9 potentiates CaMKIIδ-mediated BMAL1 activation to enhance circadian amplitude |
title_full | ISX-9 potentiates CaMKIIδ-mediated BMAL1 activation to enhance circadian amplitude |
title_fullStr | ISX-9 potentiates CaMKIIδ-mediated BMAL1 activation to enhance circadian amplitude |
title_full_unstemmed | ISX-9 potentiates CaMKIIδ-mediated BMAL1 activation to enhance circadian amplitude |
title_short | ISX-9 potentiates CaMKIIδ-mediated BMAL1 activation to enhance circadian amplitude |
title_sort | isx-9 potentiates camkiiδ-mediated bmal1 activation to enhance circadian amplitude |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334596/ https://www.ncbi.nlm.nih.gov/pubmed/35902736 http://dx.doi.org/10.1038/s42003-022-03725-x |
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