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Anti-inflammatory effects of dietary vitamin D(3) in patients with multiple sclerosis

OBJECTIVE: To assess the effects of dietary vitamin D(3) on proinflammatory (interleukin-17A [IL-17A] and IL-6) and anti-inflammatory (IL-10) cytokines. METHODS: Our study was conducted on 75 participants who were divided into 3 groups: multiple sclerosis participants (MSPs, n = 25), first-degree re...

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Autores principales: Hashemi, Reza, Morshedi, Mohammad, Asghari Jafarabadi, Mohammad, Altafi, Davar, Saeed Hosseini-Asl, Seyed, Rafie-Arefhosseini, Seyed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244020/
https://www.ncbi.nlm.nih.gov/pubmed/30533524
http://dx.doi.org/10.1212/NXG.0000000000000278
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author Hashemi, Reza
Morshedi, Mohammad
Asghari Jafarabadi, Mohammad
Altafi, Davar
Saeed Hosseini-Asl, Seyed
Rafie-Arefhosseini, Seyed
author_facet Hashemi, Reza
Morshedi, Mohammad
Asghari Jafarabadi, Mohammad
Altafi, Davar
Saeed Hosseini-Asl, Seyed
Rafie-Arefhosseini, Seyed
author_sort Hashemi, Reza
collection PubMed
description OBJECTIVE: To assess the effects of dietary vitamin D(3) on proinflammatory (interleukin-17A [IL-17A] and IL-6) and anti-inflammatory (IL-10) cytokines. METHODS: Our study was conducted on 75 participants who were divided into 3 groups: multiple sclerosis participants (MSPs, n = 25), first-degree relative participants (FDRPs, n = 25), and healthy participants (HPs, n = 25). All groups received 50,000 IU vitamin D(3)/wk for 8 weeks. Serum 25-(OH) vitamin D(3) levels and messenger RNA (mRNA) expression levels of ILs were determined using electrochemiluminescence assay and real-time PCR, respectively. RESULTS: Vitamin D(3) affected the levels of IL-17A, IL-10, and IL-6 among the 3 groups (p < 0.001 for all). Levels of IL-17A (MSPs: fold change [FC] = 5.9, p = 0.014; FDRPs: FC = 5.2, p = 0.006; HPs: FC = 4.2, p = 0.012) and IL-6 (MSPs: FC = 5.6, p = 0.003; FDRPs: FC = 5.5, p = 0.002; HPs: FC = 5.1, p < 0.001) were downregulated after vitamin D(3) treatment. In addition, levels of IL-10 (MSPs: FC = 6.2, p = 0.005; FDRPs: FC = 4.6, p < 0.001; HPs: FC = 5.2, p < 0.001) were upregulated after 8 weeks. CONCLUSIONS: Although supplementation with vitamin D(3) reduced the mRNA expression levels of IL-17A and IL-6, it increased the mRNA expression level of IL-10 in all groups. However, these effects were more considerable in the MSP group than in the other groups. Of interest, in a deficiency state of serum vitamin D3, IL-17A expression had a positive feedback effect on the expression of IL-6. Conversely, in the sufficient state, IL-10 expression had a negative feedback effect on the expression of IL-17A and IL-6.
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spelling pubmed-62440202018-12-07 Anti-inflammatory effects of dietary vitamin D(3) in patients with multiple sclerosis Hashemi, Reza Morshedi, Mohammad Asghari Jafarabadi, Mohammad Altafi, Davar Saeed Hosseini-Asl, Seyed Rafie-Arefhosseini, Seyed Neurol Genet Article OBJECTIVE: To assess the effects of dietary vitamin D(3) on proinflammatory (interleukin-17A [IL-17A] and IL-6) and anti-inflammatory (IL-10) cytokines. METHODS: Our study was conducted on 75 participants who were divided into 3 groups: multiple sclerosis participants (MSPs, n = 25), first-degree relative participants (FDRPs, n = 25), and healthy participants (HPs, n = 25). All groups received 50,000 IU vitamin D(3)/wk for 8 weeks. Serum 25-(OH) vitamin D(3) levels and messenger RNA (mRNA) expression levels of ILs were determined using electrochemiluminescence assay and real-time PCR, respectively. RESULTS: Vitamin D(3) affected the levels of IL-17A, IL-10, and IL-6 among the 3 groups (p < 0.001 for all). Levels of IL-17A (MSPs: fold change [FC] = 5.9, p = 0.014; FDRPs: FC = 5.2, p = 0.006; HPs: FC = 4.2, p = 0.012) and IL-6 (MSPs: FC = 5.6, p = 0.003; FDRPs: FC = 5.5, p = 0.002; HPs: FC = 5.1, p < 0.001) were downregulated after vitamin D(3) treatment. In addition, levels of IL-10 (MSPs: FC = 6.2, p = 0.005; FDRPs: FC = 4.6, p < 0.001; HPs: FC = 5.2, p < 0.001) were upregulated after 8 weeks. CONCLUSIONS: Although supplementation with vitamin D(3) reduced the mRNA expression levels of IL-17A and IL-6, it increased the mRNA expression level of IL-10 in all groups. However, these effects were more considerable in the MSP group than in the other groups. Of interest, in a deficiency state of serum vitamin D3, IL-17A expression had a positive feedback effect on the expression of IL-6. Conversely, in the sufficient state, IL-10 expression had a negative feedback effect on the expression of IL-17A and IL-6. Wolters Kluwer 2018-11-14 /pmc/articles/PMC6244020/ /pubmed/30533524 http://dx.doi.org/10.1212/NXG.0000000000000278 Text en Copyright © 2018 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Article
Hashemi, Reza
Morshedi, Mohammad
Asghari Jafarabadi, Mohammad
Altafi, Davar
Saeed Hosseini-Asl, Seyed
Rafie-Arefhosseini, Seyed
Anti-inflammatory effects of dietary vitamin D(3) in patients with multiple sclerosis
title Anti-inflammatory effects of dietary vitamin D(3) in patients with multiple sclerosis
title_full Anti-inflammatory effects of dietary vitamin D(3) in patients with multiple sclerosis
title_fullStr Anti-inflammatory effects of dietary vitamin D(3) in patients with multiple sclerosis
title_full_unstemmed Anti-inflammatory effects of dietary vitamin D(3) in patients with multiple sclerosis
title_short Anti-inflammatory effects of dietary vitamin D(3) in patients with multiple sclerosis
title_sort anti-inflammatory effects of dietary vitamin d(3) in patients with multiple sclerosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6244020/
https://www.ncbi.nlm.nih.gov/pubmed/30533524
http://dx.doi.org/10.1212/NXG.0000000000000278
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