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Systematic screening of generic drugs for progressive multiple sclerosis identifies clomipramine as a promising therapeutic
The treatment of progressive multiple sclerosis (MS) is unsatisfactory. One reason is that the drivers of disease, which include iron-mediated neurotoxicity, lymphocyte activity, and oxidative stress, are not simultaneously targeted. Here we present a systematic screen to identify generic, orally av...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736601/ https://www.ncbi.nlm.nih.gov/pubmed/29259169 http://dx.doi.org/10.1038/s41467-017-02119-6 |
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author | Faissner, Simon Mishra, Manoj Kaushik, Deepak K. Wang, Jianxiong Fan, Yan Silva, Claudia Rauw, Gail Metz, Luanne Koch, Marcus Yong, V. Wee |
author_facet | Faissner, Simon Mishra, Manoj Kaushik, Deepak K. Wang, Jianxiong Fan, Yan Silva, Claudia Rauw, Gail Metz, Luanne Koch, Marcus Yong, V. Wee |
author_sort | Faissner, Simon |
collection | PubMed |
description | The treatment of progressive multiple sclerosis (MS) is unsatisfactory. One reason is that the drivers of disease, which include iron-mediated neurotoxicity, lymphocyte activity, and oxidative stress, are not simultaneously targeted. Here we present a systematic screen to identify generic, orally available medications that target features of progressive MS. Of 249 medications that cross the blood–brain barrier, 35 prevent iron-mediated neurotoxicity in culture. Of these, several antipsychotics and antidepressants strongly reduce T-cell proliferation and oxidative stress. We focus on the antidepressant clomipramine and found that it additionally inhibits B-lymphocyte activity. In mice with experimental autoimmune encephalomyelitis, a model of MS, clomipramine ameliorates clinical signs of acute and chronic phases. Histologically, clomipramine reduces inflammation and microglial activation, and preserves axonal integrity. In summary, we present a systematic approach to identify generic medications for progressive multiple sclerosis with the potential to advance rapidly into clinical trials, and we highlight clomipramine for further development. |
format | Online Article Text |
id | pubmed-5736601 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57366012017-12-21 Systematic screening of generic drugs for progressive multiple sclerosis identifies clomipramine as a promising therapeutic Faissner, Simon Mishra, Manoj Kaushik, Deepak K. Wang, Jianxiong Fan, Yan Silva, Claudia Rauw, Gail Metz, Luanne Koch, Marcus Yong, V. Wee Nat Commun Article The treatment of progressive multiple sclerosis (MS) is unsatisfactory. One reason is that the drivers of disease, which include iron-mediated neurotoxicity, lymphocyte activity, and oxidative stress, are not simultaneously targeted. Here we present a systematic screen to identify generic, orally available medications that target features of progressive MS. Of 249 medications that cross the blood–brain barrier, 35 prevent iron-mediated neurotoxicity in culture. Of these, several antipsychotics and antidepressants strongly reduce T-cell proliferation and oxidative stress. We focus on the antidepressant clomipramine and found that it additionally inhibits B-lymphocyte activity. In mice with experimental autoimmune encephalomyelitis, a model of MS, clomipramine ameliorates clinical signs of acute and chronic phases. Histologically, clomipramine reduces inflammation and microglial activation, and preserves axonal integrity. In summary, we present a systematic approach to identify generic medications for progressive multiple sclerosis with the potential to advance rapidly into clinical trials, and we highlight clomipramine for further development. Nature Publishing Group UK 2017-12-19 /pmc/articles/PMC5736601/ /pubmed/29259169 http://dx.doi.org/10.1038/s41467-017-02119-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Faissner, Simon Mishra, Manoj Kaushik, Deepak K. Wang, Jianxiong Fan, Yan Silva, Claudia Rauw, Gail Metz, Luanne Koch, Marcus Yong, V. Wee Systematic screening of generic drugs for progressive multiple sclerosis identifies clomipramine as a promising therapeutic |
title | Systematic screening of generic drugs for progressive multiple sclerosis identifies clomipramine as a promising therapeutic |
title_full | Systematic screening of generic drugs for progressive multiple sclerosis identifies clomipramine as a promising therapeutic |
title_fullStr | Systematic screening of generic drugs for progressive multiple sclerosis identifies clomipramine as a promising therapeutic |
title_full_unstemmed | Systematic screening of generic drugs for progressive multiple sclerosis identifies clomipramine as a promising therapeutic |
title_short | Systematic screening of generic drugs for progressive multiple sclerosis identifies clomipramine as a promising therapeutic |
title_sort | systematic screening of generic drugs for progressive multiple sclerosis identifies clomipramine as a promising therapeutic |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5736601/ https://www.ncbi.nlm.nih.gov/pubmed/29259169 http://dx.doi.org/10.1038/s41467-017-02119-6 |
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