Author
Listed:
- Simon Faissner
(University of Calgary
St. Josef-Hospital, Ruhr-University Bochum)
- Manoj Mishra
(University of Calgary)
- Deepak K. Kaushik
(University of Calgary)
- Jianxiong Wang
(University of Calgary)
- Yan Fan
(University of Calgary)
- Claudia Silva
(University of Calgary)
- Gail Rauw
(Department of Psychiatry, University of Alberta)
- Luanne Metz
(University of Calgary)
- Marcus Koch
(University of Calgary)
- V. Wee Yong
(University of Calgary)
Abstract
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.
Suggested Citation
Simon Faissner & Manoj Mishra & Deepak K. Kaushik & Jianxiong Wang & Yan Fan & Claudia Silva & Gail Rauw & Luanne Metz & Marcus Koch & V. Wee Yong, 2017.
"Systematic screening of generic drugs for progressive multiple sclerosis identifies clomipramine as a promising therapeutic,"
Nature Communications, Nature, vol. 8(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-02119-6
DOI: 10.1038/s41467-017-02119-6
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-02119-6. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.