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Can Vitamin D Suppress Endothelial Cells Apoptosis in Multiple Sclerosis Patients?

BACKGROUND: Multiple sclerosis (MS) is an autoimmune disease of central nerves system, in which neurological disabilities occur in young adults. Despite increasing number of studies on MS, some aspects of this disorder are still unclear. In the previous studies, it has been proven that there is dire...

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Autores principales: Dehghani, Leila, Meamar, Rokhsareh, Etemadifar, Masoud, Sheshde, Zahra Dehghani, Shaygannejad, Vahid, Sharifkhah, Mostafa, Tahani, Soheil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678220/
https://www.ncbi.nlm.nih.gov/pubmed/23776726
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author Dehghani, Leila
Meamar, Rokhsareh
Etemadifar, Masoud
Sheshde, Zahra Dehghani
Shaygannejad, Vahid
Sharifkhah, Mostafa
Tahani, Soheil
author_facet Dehghani, Leila
Meamar, Rokhsareh
Etemadifar, Masoud
Sheshde, Zahra Dehghani
Shaygannejad, Vahid
Sharifkhah, Mostafa
Tahani, Soheil
author_sort Dehghani, Leila
collection PubMed
description BACKGROUND: Multiple sclerosis (MS) is an autoimmune disease of central nerves system, in which neurological disabilities occur in young adults. Despite increasing number of studies on MS, some aspects of this disorder are still unclear. In the previous studies, it has been proven that there is direct relation between MS incidence and vitamin D deficiency. Thereby, strong evidence in MS pathogenesis suggests that endothelial cells (EC) could be harmed in MS. In addition, functional changes in EC and macrovascular injuries lead blood-brain barrier disruption in MS. Current study is the first investigation to elucidate positive influences of vitamin D against EC apoptosis in MS. METHODS: Human umbilical vein endothelial cells (HUVECs) were cultured and then treated with sera from patients with active MS (in relapse) and sera from healthy volunteer participants as control group (each group n=15). 3-(4,5-dimethylthiazol-2-yl)-5- (3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt (MTS) assay for cell surveillance and cell-death detection kit for evaluating apoptosis were used in this study. RESULTS: There was a significant decrease in apoptosis rate by the serum of patients, just when 1,25(OH)(2)D3 applied before treating HUVECs with sera from active MS (in relapse). Furthermore, the cells surveillance increased markedly with the presence of 1,25(OH)(2)D(3) in culture, too. CONCLUSION: Withregard to increment in EC apoptosis rate, which treated by the sera from MS patients and decrement in apoptosis rate by the presence of vitamin D in culture media, it could be proposed that vitamin D pre-treatment can be used for MS patients, due to its beneficial effects on protecting EC apoptosis.
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spelling pubmed-36782202013-06-17 Can Vitamin D Suppress Endothelial Cells Apoptosis in Multiple Sclerosis Patients? Dehghani, Leila Meamar, Rokhsareh Etemadifar, Masoud Sheshde, Zahra Dehghani Shaygannejad, Vahid Sharifkhah, Mostafa Tahani, Soheil Int J Prev Med Original Article BACKGROUND: Multiple sclerosis (MS) is an autoimmune disease of central nerves system, in which neurological disabilities occur in young adults. Despite increasing number of studies on MS, some aspects of this disorder are still unclear. In the previous studies, it has been proven that there is direct relation between MS incidence and vitamin D deficiency. Thereby, strong evidence in MS pathogenesis suggests that endothelial cells (EC) could be harmed in MS. In addition, functional changes in EC and macrovascular injuries lead blood-brain barrier disruption in MS. Current study is the first investigation to elucidate positive influences of vitamin D against EC apoptosis in MS. METHODS: Human umbilical vein endothelial cells (HUVECs) were cultured and then treated with sera from patients with active MS (in relapse) and sera from healthy volunteer participants as control group (each group n=15). 3-(4,5-dimethylthiazol-2-yl)-5- (3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt (MTS) assay for cell surveillance and cell-death detection kit for evaluating apoptosis were used in this study. RESULTS: There was a significant decrease in apoptosis rate by the serum of patients, just when 1,25(OH)(2)D3 applied before treating HUVECs with sera from active MS (in relapse). Furthermore, the cells surveillance increased markedly with the presence of 1,25(OH)(2)D(3) in culture, too. CONCLUSION: Withregard to increment in EC apoptosis rate, which treated by the sera from MS patients and decrement in apoptosis rate by the presence of vitamin D in culture media, it could be proposed that vitamin D pre-treatment can be used for MS patients, due to its beneficial effects on protecting EC apoptosis. Medknow Publications & Media Pvt Ltd 2013-05 /pmc/articles/PMC3678220/ /pubmed/23776726 Text en Copyright: © International Journal of Preventive Medicine http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Dehghani, Leila
Meamar, Rokhsareh
Etemadifar, Masoud
Sheshde, Zahra Dehghani
Shaygannejad, Vahid
Sharifkhah, Mostafa
Tahani, Soheil
Can Vitamin D Suppress Endothelial Cells Apoptosis in Multiple Sclerosis Patients?
title Can Vitamin D Suppress Endothelial Cells Apoptosis in Multiple Sclerosis Patients?
title_full Can Vitamin D Suppress Endothelial Cells Apoptosis in Multiple Sclerosis Patients?
title_fullStr Can Vitamin D Suppress Endothelial Cells Apoptosis in Multiple Sclerosis Patients?
title_full_unstemmed Can Vitamin D Suppress Endothelial Cells Apoptosis in Multiple Sclerosis Patients?
title_short Can Vitamin D Suppress Endothelial Cells Apoptosis in Multiple Sclerosis Patients?
title_sort can vitamin d suppress endothelial cells apoptosis in multiple sclerosis patients?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678220/
https://www.ncbi.nlm.nih.gov/pubmed/23776726
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