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Clock-Enhancing Small Molecules and Potential Applications in Chronic Diseases and Aging
Normal physiological functions require a robust biological timer called the circadian clock. When clocks are dysregulated, misaligned, or dampened, pathological consequences ensue, leading to chronic diseases and accelerated aging. An emerging research area is the development of clock-targeting comp...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350099/ https://www.ncbi.nlm.nih.gov/pubmed/28360884 http://dx.doi.org/10.3389/fneur.2017.00100 |
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author | Gloston, Gabrielle F. Yoo, Seung-Hee Chen, Zheng (Jake) |
author_facet | Gloston, Gabrielle F. Yoo, Seung-Hee Chen, Zheng (Jake) |
author_sort | Gloston, Gabrielle F. |
collection | PubMed |
description | Normal physiological functions require a robust biological timer called the circadian clock. When clocks are dysregulated, misaligned, or dampened, pathological consequences ensue, leading to chronic diseases and accelerated aging. An emerging research area is the development of clock-targeting compounds that may serve as drug candidates to correct dysregulated rhythms and hence mitigate disease symptoms and age-related decline. In this review, we first present a concise view of the circadian oscillator, physiological networks, and regulatory mechanisms of circadian amplitude. Given a close association of circadian amplitude dampening and disease progression, clock-enhancing small molecules (CEMs) are of particular interest as candidate chronotherapeutics. A recent proof-of-principle study illustrated that the natural polymethoxylated flavonoid nobiletin directly targets the circadian oscillator and elicits robust metabolic improvements in mice. We describe mood disorders and aging as potential therapeutic targets of CEMs. Future studies of CEMs will shed important insight into the regulation and disease relevance of circadian clocks. |
format | Online Article Text |
id | pubmed-5350099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53500992017-03-30 Clock-Enhancing Small Molecules and Potential Applications in Chronic Diseases and Aging Gloston, Gabrielle F. Yoo, Seung-Hee Chen, Zheng (Jake) Front Neurol Neuroscience Normal physiological functions require a robust biological timer called the circadian clock. When clocks are dysregulated, misaligned, or dampened, pathological consequences ensue, leading to chronic diseases and accelerated aging. An emerging research area is the development of clock-targeting compounds that may serve as drug candidates to correct dysregulated rhythms and hence mitigate disease symptoms and age-related decline. In this review, we first present a concise view of the circadian oscillator, physiological networks, and regulatory mechanisms of circadian amplitude. Given a close association of circadian amplitude dampening and disease progression, clock-enhancing small molecules (CEMs) are of particular interest as candidate chronotherapeutics. A recent proof-of-principle study illustrated that the natural polymethoxylated flavonoid nobiletin directly targets the circadian oscillator and elicits robust metabolic improvements in mice. We describe mood disorders and aging as potential therapeutic targets of CEMs. Future studies of CEMs will shed important insight into the regulation and disease relevance of circadian clocks. Frontiers Media S.A. 2017-03-15 /pmc/articles/PMC5350099/ /pubmed/28360884 http://dx.doi.org/10.3389/fneur.2017.00100 Text en Copyright © 2017 Gloston, Yoo and Chen. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Gloston, Gabrielle F. Yoo, Seung-Hee Chen, Zheng (Jake) Clock-Enhancing Small Molecules and Potential Applications in Chronic Diseases and Aging |
title | Clock-Enhancing Small Molecules and Potential Applications in Chronic Diseases and Aging |
title_full | Clock-Enhancing Small Molecules and Potential Applications in Chronic Diseases and Aging |
title_fullStr | Clock-Enhancing Small Molecules and Potential Applications in Chronic Diseases and Aging |
title_full_unstemmed | Clock-Enhancing Small Molecules and Potential Applications in Chronic Diseases and Aging |
title_short | Clock-Enhancing Small Molecules and Potential Applications in Chronic Diseases and Aging |
title_sort | clock-enhancing small molecules and potential applications in chronic diseases and aging |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5350099/ https://www.ncbi.nlm.nih.gov/pubmed/28360884 http://dx.doi.org/10.3389/fneur.2017.00100 |
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