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Traumatic Brain Injury, Sleep, and Melatonin—Intrinsic Changes with Therapeutic Potential
Traumatic brain injury (TBI) is one of the most prevalent causes of morbidity in the United States and is associated with numerous chronic sequelae long after the point of injury. One of the most common long-term complaints in patients with TBI is sleep dysfunction. It is reported that alterations i...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10123665/ https://www.ncbi.nlm.nih.gov/pubmed/37092428 http://dx.doi.org/10.3390/clockssleep5020016 |
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author | Bell, Allen Hewins, Bryson Bishop, Courtney Fortin, Amanda Wang, Jonathan Creamer, Jennifer L. Collen, Jacob Werner, J. Kent |
author_facet | Bell, Allen Hewins, Bryson Bishop, Courtney Fortin, Amanda Wang, Jonathan Creamer, Jennifer L. Collen, Jacob Werner, J. Kent |
author_sort | Bell, Allen |
collection | PubMed |
description | Traumatic brain injury (TBI) is one of the most prevalent causes of morbidity in the United States and is associated with numerous chronic sequelae long after the point of injury. One of the most common long-term complaints in patients with TBI is sleep dysfunction. It is reported that alterations in melatonin follow TBI and may be linked with various sleep and circadian disorders directly (via cellular signaling) or indirectly (via free radicals and inflammatory signaling). Work over the past two decades has contributed to our understanding of the role of melatonin as a sleep regulator and neuroprotective anti-inflammatory agent. Although there is increasing interest in the treatment of insomnia following TBI, a lack of standardization and rigor in melatonin research has left behind a trail of non-generalizable data and ambiguous treatment recommendations. This narrative review describes the underlying biochemical properties of melatonin as they are relevant to TBI. We also discuss potential benefits and a path forward regarding the therapeutic management of TBI with melatonin treatment, including its role as a neuroprotectant, a somnogen, and a modulator of the circadian rhythm. |
format | Online Article Text |
id | pubmed-10123665 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101236652023-04-25 Traumatic Brain Injury, Sleep, and Melatonin—Intrinsic Changes with Therapeutic Potential Bell, Allen Hewins, Bryson Bishop, Courtney Fortin, Amanda Wang, Jonathan Creamer, Jennifer L. Collen, Jacob Werner, J. Kent Clocks Sleep Review Traumatic brain injury (TBI) is one of the most prevalent causes of morbidity in the United States and is associated with numerous chronic sequelae long after the point of injury. One of the most common long-term complaints in patients with TBI is sleep dysfunction. It is reported that alterations in melatonin follow TBI and may be linked with various sleep and circadian disorders directly (via cellular signaling) or indirectly (via free radicals and inflammatory signaling). Work over the past two decades has contributed to our understanding of the role of melatonin as a sleep regulator and neuroprotective anti-inflammatory agent. Although there is increasing interest in the treatment of insomnia following TBI, a lack of standardization and rigor in melatonin research has left behind a trail of non-generalizable data and ambiguous treatment recommendations. This narrative review describes the underlying biochemical properties of melatonin as they are relevant to TBI. We also discuss potential benefits and a path forward regarding the therapeutic management of TBI with melatonin treatment, including its role as a neuroprotectant, a somnogen, and a modulator of the circadian rhythm. MDPI 2023-04-06 /pmc/articles/PMC10123665/ /pubmed/37092428 http://dx.doi.org/10.3390/clockssleep5020016 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Bell, Allen Hewins, Bryson Bishop, Courtney Fortin, Amanda Wang, Jonathan Creamer, Jennifer L. Collen, Jacob Werner, J. Kent Traumatic Brain Injury, Sleep, and Melatonin—Intrinsic Changes with Therapeutic Potential |
title | Traumatic Brain Injury, Sleep, and Melatonin—Intrinsic Changes with Therapeutic Potential |
title_full | Traumatic Brain Injury, Sleep, and Melatonin—Intrinsic Changes with Therapeutic Potential |
title_fullStr | Traumatic Brain Injury, Sleep, and Melatonin—Intrinsic Changes with Therapeutic Potential |
title_full_unstemmed | Traumatic Brain Injury, Sleep, and Melatonin—Intrinsic Changes with Therapeutic Potential |
title_short | Traumatic Brain Injury, Sleep, and Melatonin—Intrinsic Changes with Therapeutic Potential |
title_sort | traumatic brain injury, sleep, and melatonin—intrinsic changes with therapeutic potential |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10123665/ https://www.ncbi.nlm.nih.gov/pubmed/37092428 http://dx.doi.org/10.3390/clockssleep5020016 |
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