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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...

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Autores principales: Faissner, Simon, Mishra, Manoj, Kaushik, Deepak K., Wang, Jianxiong, Fan, Yan, Silva, Claudia, Rauw, Gail, Metz, Luanne, Koch, Marcus, Yong, V. Wee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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.
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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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