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Melatonin Acts as Antioxidant and Improves Sleep in MS Patients
The relationship between the prevalence of multiple sclerosis (MS) and sunlight’s ultraviolet radiation was proved. Oxidative stress plays a role in the pathogenic traits of MS. Melatonin possesses antioxidative properties and regulates circadian rhythms. Sleep disturbances in MS patients are common...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122810/ https://www.ncbi.nlm.nih.gov/pubmed/24974099 http://dx.doi.org/10.1007/s11064-014-1347-6 |
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author | Adamczyk-Sowa, Monika Pierzchala, Krystyna Sowa, Pawel Mucha, Sebastian Sadowska-Bartosz, Izabela Adamczyk, Jowita Hartel, Marcin |
author_facet | Adamczyk-Sowa, Monika Pierzchala, Krystyna Sowa, Pawel Mucha, Sebastian Sadowska-Bartosz, Izabela Adamczyk, Jowita Hartel, Marcin |
author_sort | Adamczyk-Sowa, Monika |
collection | PubMed |
description | The relationship between the prevalence of multiple sclerosis (MS) and sunlight’s ultraviolet radiation was proved. Oxidative stress plays a role in the pathogenic traits of MS. Melatonin possesses antioxidative properties and regulates circadian rhythms. Sleep disturbances in MS patients are common and contribute to daytime fatigue. The aim of study was to evaluate 5 mg daily melatonin supplementation over 90 days on serum total oxidant status (TOS), total antioxidant capacity (TAC) and its influence on sleep quality and depression level of MS patients. A case–control prospective study was performed on 102 MS patients and 20 controls matched for age and sex. The Kurtzke’s Expanded Disability Status Scale, magnetic resonance imaging examinations, Athens Insomnia Scale (AIS), Beck Depression Inventory questionnaires were completed. Serum TOS and TAC levels were measured. We observed higher serum levels of TOS in all MS groups, while after melatonin treatment the TOS levels significantly decreased. The TAC level was significantly lower only in mitoxantrone-treated group and it increased after melatonin supplementation. A strong positive correlation between T1Gd(+) number lesions and TAC level in interferon-beta-1A group was observed. AIS group mean score above 6 defining insomnia were observed in interferon-beta-1B-group, glatiramer acetate-group and mitoxantrone-group: 6.62 ± 2.88, 8.45 ± 2.07, 11.1 ± 3.25, respectively. After melatonin treatment the AIS mean scores decrease in glatiramer acetate-group and mitoxantrone-group achieving 5.25 ± 1.14 and 7.08 ± 2.39, respectively (p < 0.05). Finding from our study suggest that melatonin can act as an antioxidant and improves reduced sleep quality in MS patients. |
format | Online Article Text |
id | pubmed-4122810 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-41228102014-08-08 Melatonin Acts as Antioxidant and Improves Sleep in MS Patients Adamczyk-Sowa, Monika Pierzchala, Krystyna Sowa, Pawel Mucha, Sebastian Sadowska-Bartosz, Izabela Adamczyk, Jowita Hartel, Marcin Neurochem Res Original Paper The relationship between the prevalence of multiple sclerosis (MS) and sunlight’s ultraviolet radiation was proved. Oxidative stress plays a role in the pathogenic traits of MS. Melatonin possesses antioxidative properties and regulates circadian rhythms. Sleep disturbances in MS patients are common and contribute to daytime fatigue. The aim of study was to evaluate 5 mg daily melatonin supplementation over 90 days on serum total oxidant status (TOS), total antioxidant capacity (TAC) and its influence on sleep quality and depression level of MS patients. A case–control prospective study was performed on 102 MS patients and 20 controls matched for age and sex. The Kurtzke’s Expanded Disability Status Scale, magnetic resonance imaging examinations, Athens Insomnia Scale (AIS), Beck Depression Inventory questionnaires were completed. Serum TOS and TAC levels were measured. We observed higher serum levels of TOS in all MS groups, while after melatonin treatment the TOS levels significantly decreased. The TAC level was significantly lower only in mitoxantrone-treated group and it increased after melatonin supplementation. A strong positive correlation between T1Gd(+) number lesions and TAC level in interferon-beta-1A group was observed. AIS group mean score above 6 defining insomnia were observed in interferon-beta-1B-group, glatiramer acetate-group and mitoxantrone-group: 6.62 ± 2.88, 8.45 ± 2.07, 11.1 ± 3.25, respectively. After melatonin treatment the AIS mean scores decrease in glatiramer acetate-group and mitoxantrone-group achieving 5.25 ± 1.14 and 7.08 ± 2.39, respectively (p < 0.05). Finding from our study suggest that melatonin can act as an antioxidant and improves reduced sleep quality in MS patients. Springer US 2014-06-30 2014 /pmc/articles/PMC4122810/ /pubmed/24974099 http://dx.doi.org/10.1007/s11064-014-1347-6 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Original Paper Adamczyk-Sowa, Monika Pierzchala, Krystyna Sowa, Pawel Mucha, Sebastian Sadowska-Bartosz, Izabela Adamczyk, Jowita Hartel, Marcin Melatonin Acts as Antioxidant and Improves Sleep in MS Patients |
title | Melatonin Acts as Antioxidant and Improves Sleep in MS Patients |
title_full | Melatonin Acts as Antioxidant and Improves Sleep in MS Patients |
title_fullStr | Melatonin Acts as Antioxidant and Improves Sleep in MS Patients |
title_full_unstemmed | Melatonin Acts as Antioxidant and Improves Sleep in MS Patients |
title_short | Melatonin Acts as Antioxidant and Improves Sleep in MS Patients |
title_sort | melatonin acts as antioxidant and improves sleep in ms patients |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4122810/ https://www.ncbi.nlm.nih.gov/pubmed/24974099 http://dx.doi.org/10.1007/s11064-014-1347-6 |
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