Failed, Interrupted, or Inconclusive Trials on Neuroprotective and Neuroregenerative Treatment Strategies in Multiple Sclerosis: Update 2015-2020.
Journal
Drugs
ISSN: 1179-1950
Titre abrégé: Drugs
Pays: New Zealand
ID NLM: 7600076
Informations de publication
Date de publication:
Jun 2021
Jun 2021
Historique:
accepted:
15
04
2021
pubmed:
5
6
2021
medline:
20
11
2021
entrez:
4
6
2021
Statut:
ppublish
Résumé
In the recent past, a plethora of drugs have been approved for the treatment of multiple sclerosis (MS). These therapeutics are mainly confined to immunomodulatory or immunosuppressive strategies but do not sufficiently address remyelination and neuroprotection. However, several neuroregenerative agents have shown potential in pre-clinical research and entered Phase I to III clinical trials. Although none of these compounds have yet proceeded to approval, understanding the causes of failure can broaden our knowledge about neuroprotection and neuroregeneration in MS. Moreover, most of the investigated approaches are characterised by consistent mechanisms of action and proved convincing efficacy in animal studies. Therefore, learning from their failure will help us to enforce the translation of findings acquired in pre-clinical studies into clinical application. Here, we summarise trials on MS treatment published since 2015 that have either failed or were interrupted due to a lack of efficacy, adverse events, or for other reasons. We further outline the rationale underlying these drugs and analyse the background of failure to gather new insights into MS pathophysiology and optimise future study designs. For conciseness, this review focuses on agents promoting remyelination and medications with primarily neuroprotective properties or unconventional approaches. Failed clinical trials that pursue immunomodulation are presented in a separate article.
Identifiants
pubmed: 34086251
doi: 10.1007/s40265-021-01526-w
pii: 10.1007/s40265-021-01526-w
pmc: PMC8217012
doi:
Substances chimiques
Neuroprotective Agents
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
1031-1063Références
Tintore M, Vidal-Jordana A, Sastre-Garriga J. Treatment of multiple sclerosis—success from bench to bedside. Nat Rev Neurol. 2019;15(1):53–8. https://doi.org/10.1038/s41582-018-0082-z .
doi: 10.1038/s41582-018-0082-z
pubmed: 30315270
Miller DH, Leary SM. Primary-progressive multiple sclerosis. Lancet Neurol. 2007;6(10):903–12. https://doi.org/10.1016/S1474-4422(07)70243-0 .
doi: 10.1016/S1474-4422(07)70243-0
pubmed: 17884680
Mahad DH, Trapp BD, Lassmann H. Pathological mechanisms in progressive multiple sclerosis. Lancet Neurol. 2015;14(2):183–93. https://doi.org/10.1016/S1474-4422(14)70256-X .
doi: 10.1016/S1474-4422(14)70256-X
pubmed: 25772897
Faissner S, Plemel JR, Gold R, Yong VW. Progressive multiple sclerosis: from pathophysiology to therapeutic strategies. Nat Rev Drug Discov. 2019;18(12):905–22. https://doi.org/10.1038/s41573-019-0035-2 .
doi: 10.1038/s41573-019-0035-2
pubmed: 31399729
Vaughn CB, Jakimovski D, Kavak KS, Ramanathan M, Benedict RHB, Zivadinov R, et al. Epidemiology and treatment of multiple sclerosis in elderly populations. Nat Rev Neurol. 2019;15(6):329–42. https://doi.org/10.1038/s41582-019-0183-3 .
doi: 10.1038/s41582-019-0183-3
pubmed: 31000816
Stangel M, Kuhlmann T, Matthews PM, Kilpatrick TJ. Achievements and obstacles of remyelinating therapies in multiple sclerosis. Nat Rev Neurol. 2017;13(12):742–54. https://doi.org/10.1038/nrneurol.2017.139 .
doi: 10.1038/nrneurol.2017.139
pubmed: 29146953
Yong H, Chartier G, Quandt J. Modulating inflammation and neuroprotection in multiple sclerosis. J Neurosci Res. 2018;96(6):927–50. https://doi.org/10.1002/jnr.24090 .
doi: 10.1002/jnr.24090
pubmed: 28580582
Correale J, Gaitan MI, Ysrraelit MC, Fiol MP. Progressive multiple sclerosis: from pathogenic mechanisms to treatment. Brain. 2017;140(3):527–46. https://doi.org/10.1093/brain/aww258 .
doi: 10.1093/brain/aww258
pubmed: 27794524
Rolfes L, Pawlitzki M, Pfeuffer S, Huntemann N, Wiendl H, Ruck T, et al. Failed, interrupted, or inconclusive trials on immunomodulatory treatment strategies in multiple sclerosis: update 2015–2020. BioDrugs. 2020. https://doi.org/10.1007/s40259-020-00435-w .
doi: 10.1007/s40259-020-00435-w
pubmed: 32785877
pmcid: 7519896
Frischer JM, Bramow S, Dal-Bianco A, Lucchinetti CF, Rauschka H, Schmidbauer M, et al. The relation between inflammation and neurodegeneration in multiple sclerosis brains. Brain. 2009;132(Pt 5):1175–89. https://doi.org/10.1093/brain/awp070 .
doi: 10.1093/brain/awp070
pubmed: 19339255
pmcid: 2677799
Zacco A, Togo J, Spence K, Ellis A, Lloyd D, Furlong S, et al. 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors protect cortical neurons from excitotoxicity. J Neurosci. 2003;23(35):11104–11.
doi: 10.1523/JNEUROSCI.23-35-11104.2003
Wu H, Lu D, Jiang H, Xiong Y, Qu C, Li B, et al. Simvastatin-mediated upregulation of VEGF and BDNF, activation of the PI3K/Akt pathway, and increase of neurogenesis are associated with therapeutic improvement after traumatic brain injury. J Neurotrauma. 2008;25(2):130–9. https://doi.org/10.1089/neu.2007.0369 .
doi: 10.1089/neu.2007.0369
pubmed: 18260796
van der Most PJ, Dolga AM, Nijholt IM, Luiten PG, Eisel UL. Statins: mechanisms of neuroprotection. Prog Neurobiol. 2009;88(1):64–75. https://doi.org/10.1016/j.pneurobio.2009.02.002 .
doi: 10.1016/j.pneurobio.2009.02.002
pubmed: 19428962
Peng X, Jin J, Giri S, Montes M, Sujkowski D, Tang Y, et al. Immunomodulatory effects of 3-hydroxy-3-methylglutaryl coenzyme-A reductase inhibitors, potential therapy for relapsing remitting multiple sclerosis. J Neuroimmunol. 2006;178(1–2):130–9. https://doi.org/10.1016/j.jneuroim.2006.06.005 .
doi: 10.1016/j.jneuroim.2006.06.005
pubmed: 16870268
Greenwood J, Walters CE, Pryce G, Kanuga N, Beraud E, Baker D, et al. Lovastatin inhibits brain endothelial cell Rho-mediated lymphocyte migration and attenuates experimental autoimmune encephalomyelitis. FASEB J. 2003;17(8):905–7. https://doi.org/10.1096/fj.02-1014fje .
doi: 10.1096/fj.02-1014fje
pubmed: 12626426
Youssef S, Stuve O, Patarroyo JC, Ruiz PJ, Radosevich JL, Hur EM, et al. The HMG-CoA reductase inhibitor, atorvastatin, promotes a Th2 bias and reverses paralysis in central nervous system autoimmune disease. Nature. 2002;420(6911):78–84. https://doi.org/10.1038/nature01158 .
doi: 10.1038/nature01158
pubmed: 12422218
Vollmer T, Key L, Durkalski V, Tyor W, Corboy J, Markovic-Plese S, et al. Oral simvastatin treatment in relapsing-remitting multiple sclerosis. Lancet. 2004;363(9421):1607–8. https://doi.org/10.1016/S0140-6736(04)16205-3 .
doi: 10.1016/S0140-6736(04)16205-3
pubmed: 15145635
Sena A, Pedrosa R, Graca MM. Therapeutic potential of lovastatin in multiple sclerosis. J Neurol. 2003;250(6):754–5. https://doi.org/10.1007/s00415-003-1070-8 .
doi: 10.1007/s00415-003-1070-8
pubmed: 12862032
Paul F, Waiczies S, Wuerfel J, Bellmann-Strobl J, Dorr J, Waiczies H, et al. Oral high-dose atorvastatin treatment in relapsing-remitting multiple sclerosis. PLoS ONE. 2008;3(4):e1928. https://doi.org/10.1371/journal.pone.0001928 .
doi: 10.1371/journal.pone.0001928
pubmed: 18398457
pmcid: 2276246
Lanzillo R, Orefice G, Quarantelli M, Rinaldi C, Prinster A, Ventrella G, et al. Atorvastatin combined to interferon to verify the efficacy (ACTIVE) in relapsing-remitting active multiple sclerosis patients: a longitudinal controlled trial of combination therapy. Mult Scler. 2010;16(4):450–4. https://doi.org/10.1177/1352458509358909 .
doi: 10.1177/1352458509358909
pubmed: 20150398
Togha M, Karvigh SA, Nabavi M, Moghadam NB, Harirchian MH, Sahraian MA, et al. Simvastatin treatment in patients with relapsing-remitting multiple sclerosis receiving interferon beta 1a: a double-blind randomized controlled trial. Mult Scler. 2010;16(7):848–54. https://doi.org/10.1177/1352458510369147 .
doi: 10.1177/1352458510369147
pubmed: 20488825
Lanzillo R, Quarantelli M, Pozzilli C, Trojano M, Amato MP, Marrosu MG, et al. No evidence for an effect on brain atrophy rate of atorvastatin add-on to interferon beta1b therapy in relapsing-remitting multiple sclerosis (the ARIANNA study). Mult Scler. 2016;22(9):1163–73. https://doi.org/10.1177/1352458515611222 .
doi: 10.1177/1352458515611222
pubmed: 26466947
Kurtzke JF. Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS). Neurology. 1983;33(11):1444–52. https://doi.org/10.1212/wnl.33.11.1444 .
doi: 10.1212/wnl.33.11.1444
pubmed: 6685237
Amato MP, Portaccio E, Goretti B, Zipoli V, Ricchiuti L, De Caro MF, et al. The Rao’s Brief Repeatable Battery and Stroop Test: normative values with age, education and gender corrections in an Italian population. Mult Scler. 2006;12(6):787–93. https://doi.org/10.1177/1352458506070933 .
doi: 10.1177/1352458506070933
pubmed: 17263008
Rudick RA, Pace A, Rani MR, Hyde R, Panzara M, Appachi S, et al. Effect of statins on clinical and molecular responses to intramuscular interferon beta-1a. Neurology. 2009;72(23):1989–93. https://doi.org/10.1212/WNL.0b013e3181a92b96 .
doi: 10.1212/WNL.0b013e3181a92b96
pubmed: 19506220
pmcid: 2837592
Paz Soldan MM, Pittock SJ, Weigand SD, Yawn BP, Rodriguez M. Statin therapy and multiple sclerosis disability in a population-based cohort. Mult Scler. 2012;18(3):358–63. https://doi.org/10.1177/1352458511421920 .
doi: 10.1177/1352458511421920
pubmed: 21908483
Ghasami K, Faraji F, Fazeli M, Ghazavi A, Mosayebi G. Interferon beta-1a and atorvastatin in the treatment of multiple sclerosis. Iran J Immunol. 2016;13(1):16–26 (Doi: IJIv13i1A3).
pubmed: 27026043
Kamm CP, El-Koussy M, Humpert S, Findling O, von Bredow F, Burren Y, et al. Atorvastatin added to interferon beta for relapsing multiple sclerosis: a randomized controlled trial. J Neurol. 2012;259(11):2401–13. https://doi.org/10.1007/s00415-012-6513-7 .
doi: 10.1007/s00415-012-6513-7
pubmed: 22569835
pmcid: 3484273
Sorensen PS, Lycke J, Eralinna JP, Edland A, Wu X, Frederiksen JL, et al. Simvastatin as add-on therapy to interferon beta-1a for relapsing-remitting multiple sclerosis (SIMCOMBIN study): a placebo-controlled randomised phase 4 trial. Lancet Neurol. 2011;10(8):691–701. https://doi.org/10.1016/S1474-4422(11)70144-2 .
doi: 10.1016/S1474-4422(11)70144-2
pubmed: 21742556
Pihl-Jensen G, Tsakiri A, Frederiksen JL. Statin treatment in multiple sclerosis: a systematic review and meta-analysis. CNS Drugs. 2015;29(4):277–91. https://doi.org/10.1007/s40263-015-0239-x .
doi: 10.1007/s40263-015-0239-x
pubmed: 25795002
Wang J, Xiao Y, Luo M, Luo H. Statins for multiple sclerosis. Cochrane Database Syst Rev. 2011;12:CD008386. https://doi.org/10.1002/14651858.CD008386.pub3 .
doi: 10.1002/14651858.CD008386.pub3
Salvatore E, Morra VB, Orefice G. Combining beta interferon and atorvastatin may increase disease activity in multiple sclerosis. Neurology. 2009;73(13):1078. https://doi.org/10.1212/WNL.0b013e3181ab6e08 (author reply-9).
doi: 10.1212/WNL.0b013e3181ab6e08
pubmed: 19786703
Birnbaum G, Cree B, Altafullah I, Zinser M, Reder AT. Combining beta interferon and atorvastatin may increase disease activity in multiple sclerosis. Neurology. 2008;71(18):1390–5. https://doi.org/10.1212/01.wnl.0000319698.40024.1c .
doi: 10.1212/01.wnl.0000319698.40024.1c
pubmed: 18525027
Montero MT, Hernandez O, Suarez Y, Matilla J, Ferruelo AJ, Martinez-Botas J, et al. Hydroxymethylglutaryl-coenzyme A reductase inhibition stimulates caspase-1 activity and Th1-cytokine release in peripheral blood mononuclear cells. Atherosclerosis. 2000;153(2):303–13. https://doi.org/10.1016/s0021-9150(00)00417-2 .
doi: 10.1016/s0021-9150(00)00417-2
pubmed: 11164419
Miron VE, Rajasekharan S, Jarjour AA, Zamvil SS, Kennedy TE, Antel JP. Simvastatin regulates oligodendroglial process dynamics and survival. Glia. 2007;55(2):130–43. https://doi.org/10.1002/glia.20441 .
doi: 10.1002/glia.20441
pubmed: 17078030
Dhawan N, Reder A. Statins block interferon signaling in human immune cells: potential loss of the therapeutic effect of IFN-beta in multiple sclerosis. Neurology. 2007;68:A364.
Kieseier BC, Archelos JJ, Hartung HP. Different effects of simvastatin and interferon beta on the proteolytic activity of matrix metalloproteinases. Arch Neurol. 2004;61(6):929–32. https://doi.org/10.1001/archneur.61.6.929 .
doi: 10.1001/archneur.61.6.929
pubmed: 15210533
Kieseier BC. The mechanism of action of interferon-beta in relapsing multiple sclerosis. CNS Drugs. 2011;25(6):491–502. https://doi.org/10.2165/11591110-000000000-00000 .
doi: 10.2165/11591110-000000000-00000
pubmed: 21649449
Chataway J, Schuerer N, Alsanousi A, Chan D, MacManus D, Hunter K, et al. Effect of high-dose simvastatin on brain atrophy and disability in secondary progressive multiple sclerosis (MS-STAT): a randomised, placebo-controlled, phase 2 trial. Lancet. 2014;383(9936):2213–21. https://doi.org/10.1016/S0140-6736(13)62242-4 .
doi: 10.1016/S0140-6736(13)62242-4
pubmed: 24655729
Multiple Sclerosis-Simvastatin Trial 2 (MS-STAT2). In: ClinicalTrials.gov Identifier: NCT03387670. Start: 2018. Accessed 3 Jun 2020.
Lanzillo R, Moccia M, Russo CV, Carotenuto A, Nozzolillo A, Petruzzo M, et al. Therapeutic lag in reducing disability progression in relapsing-remitting multiple sclerosis: 8-year follow-up of two randomized add-on trials with atorvastatin. Mult Scler Relat Disord. 2019;28:193–6. https://doi.org/10.1016/j.msard.2018.12.042 .
doi: 10.1016/j.msard.2018.12.042
pubmed: 30623857
Cakici N, Fakkel TM, van Neck JW, Verhagen AP, Coert JH. Systematic review of treatments for diabetic peripheral neuropathy. Diabet Med. 2016;33(11):1466–76. https://doi.org/10.1111/dme.13083 .
doi: 10.1111/dme.13083
pubmed: 26822889
Rochette L, Ghibu S, Richard C, Zeller M, Cottin Y, Vergely C. Direct and indirect antioxidant properties of alpha-lipoic acid and therapeutic potential. Mol Nutr Food Res. 2013;57(1):114–25. https://doi.org/10.1002/mnfr.201200608 .
doi: 10.1002/mnfr.201200608
pubmed: 23293044
Seifar F, Khalili M, Khaledyan H, Amiri Moghadam S, Izadi A, Azimi A, et al. alpha-Lipoic acid, functional fatty acid, as a novel therapeutic alternative for central nervous system diseases: a review. Nutr Neurosci. 2019;22(5):306–16. https://doi.org/10.1080/1028415X.2017.1386755 .
doi: 10.1080/1028415X.2017.1386755
pubmed: 29185388
Ou P, Tritschler HJ, Wolff SP. Thioctic (lipoic) acid: a therapeutic metal-chelating antioxidant? Biochem Pharmacol. 1995;50(1):123–6. https://doi.org/10.1016/0006-2952(95)00116-h .
doi: 10.1016/0006-2952(95)00116-h
pubmed: 7605337
Schreibelt G, Musters RJ, Reijerkerk A, de Groot LR, van der Pol SM, Hendrikx EM, et al. Lipoic acid affects cellular migration into the central nervous system and stabilizes blood-brain barrier integrity. J Immunol. 2006;177(4):2630–7. https://doi.org/10.4049/jimmunol.177.4.2630 .
doi: 10.4049/jimmunol.177.4.2630
pubmed: 16888025
Chaudhary P, Marracci GH, Bourdette DN. Lipoic acid inhibits expression of ICAM-1 and VCAM-1 by CNS endothelial cells and T cell migration into the spinal cord in experimental autoimmune encephalomyelitis. J Neuroimmunol. 2006;175(1–2):87–96. https://doi.org/10.1016/j.jneuroim.2006.03.007 .
doi: 10.1016/j.jneuroim.2006.03.007
pubmed: 16644024
Wang KC, Tsai CP, Lee CL, Chen SY, Lin GJ, Yen MH, et al. alpha-Lipoic acid enhances endogenous peroxisome-proliferator-activated receptor-gamma to ameliorate experimental autoimmune encephalomyelitis in mice. Clin Sci (Lond). 2013;125(7):329–40. https://doi.org/10.1042/CS20120560 .
doi: 10.1042/CS20120560
pubmed: 23550596
Schillace RV, Pisenti N, Pattamanuch N, Galligan S, Marracci GH, Bourdette DN, et al. Lipoic acid stimulates cAMP production in T lymphocytes and NK cells. Biochem Biophys Res Commun. 2007;354(1):259–64. https://doi.org/10.1016/j.bbrc.2006.12.195 .
doi: 10.1016/j.bbrc.2006.12.195
pubmed: 17210133
pmcid: 4278348
Salinthone S, Yadav V, Schillace RV, Bourdette DN, Carr DW. Lipoic acid attenuates inflammation via cAMP and protein kinase A signaling. PLoS ONE. 2010. https://doi.org/10.1371/journal.pone.0013058 .
doi: 10.1371/journal.pone.0013058
pubmed: 20927401
pmcid: 2946928
Fiedler SE, Yadav V, Kerns AR, Tsang C, Markwardt S, Kim E, et al. Lipoic acid stimulates cAMP production in healthy control and secondary progressive MS subjects. Mol Neurobiol. 2018;55(7):6037–49. https://doi.org/10.1007/s12035-017-0813-y .
doi: 10.1007/s12035-017-0813-y
pubmed: 29143287
Yadav V, Marracci G, Lovera J, Woodward W, Bogardus K, Marquardt W, et al. Lipoic acid in multiple sclerosis: a pilot study. Mult Scler. 2005;11(2):159–65. https://doi.org/10.1191/1352458505ms1143oa .
doi: 10.1191/1352458505ms1143oa
pubmed: 15794388
Falardeau J, Fryman A, Wanchu R, Marracci GH, Mass M, Wooliscroft L, et al. Oral lipoic acid as a treatment for acute optic neuritis: a blinded, placebo controlled randomized trial. Mult Scler J Exp Transl Clin. 2019;5(2):2055217319850193. https://doi.org/10.1177/2055217319850193 .
doi: 10.1177/2055217319850193
pubmed: 31205740
pmcid: 6537072
Chaudhary P, Marracci G, Yu X, Galipeau D, Morris B, Bourdette D. Lipoic acid decreases inflammation and confers neuroprotection in experimental autoimmune optic neuritis. J Neuroimmunol. 2011;233(1–2):90–6. https://doi.org/10.1016/j.jneuroim.2010.12.002 .
doi: 10.1016/j.jneuroim.2010.12.002
pubmed: 21215462
pmcid: 4987082
Dietrich M, Helling N, Hilla A, Heskamp A, Issberner A, Hildebrandt T, et al. Early alpha-lipoic acid therapy protects from degeneration of the inner retinal layers and vision loss in an experimental autoimmune encephalomyelitis-optic neuritis model. J Neuroinflamm. 2018;15(1):71. https://doi.org/10.1186/s12974-018-1111-y .
doi: 10.1186/s12974-018-1111-y
Yadav V, Marracci GH, Munar MY, Cherala G, Stuber LE, Alvarez L, et al. Pharmacokinetic study of lipoic acid in multiple sclerosis: comparing mice and human pharmacokinetic parameters. Mult Scler. 2010;16(4):387–97. https://doi.org/10.1177/1352458509359722 .
doi: 10.1177/1352458509359722
pubmed: 20150394
pmcid: 3489916
Bittner F, Murchison C, Koop D, Bourdette D, Spain R. Lipoic acid pharmacokinetics at baseline and 1 year in secondary progressive MS. Neurol Neuroimmunol Neuroinflamm. 2017;4(5):e380. https://doi.org/10.1212/NXI.0000000000000380 .
doi: 10.1212/NXI.0000000000000380
pubmed: 28680918
pmcid: 5489386
Spain R, Powers K, Murchison C, Heriza E, Winges K, Yadav V, et al. Lipoic acid in secondary progressive MS: A randomized controlled pilot trial. Neurol Neuroimmunol Neuroinflamm. 2017;4(5):e374. https://doi.org/10.1212/NXI.0000000000000374 .
doi: 10.1212/NXI.0000000000000374
pubmed: 28680916
pmcid: 5489387
Lipoic Acid for Progressive Multiple Sclerosis (MS) (LAPMS). In: ClinicalTrials.gov Identifier: NCT03161028. Start: 2018. Accessed 3 Jun 2020.
Dorr J, Wernecke KD, Wurfel J, Bellmann-Strobl J, Siffrin V, Sattler MB, et al. Disease modification in multiple sclerosis by flupirtine-results of a randomized placebo controlled phase II trial. Front Neurol. 2018;9:842. https://doi.org/10.3389/fneur.2018.00842 .
doi: 10.3389/fneur.2018.00842
pubmed: 30356868
pmcid: 6190842
Schwarz M, Nolden-Koch M, Purr J, Pergande G, Block F. Antiparkinsonian effect of flupirtine in monoamine-depleted rats. J Neural Transm (Vienna). 1996;103(5):581–90. https://doi.org/10.1007/BF01273155 .
doi: 10.1007/BF01273155
pubmed: 8811503
Muller WE, Romero FJ, Perovic S, Pergande G, Pialoglou P. Protection of flupirtine on beta-amyloid-induced apoptosis in neuronal cells in vitro: prevention of amyloid-induced glutathione depletion. J Neurochem. 1997;68(6):2371–7. https://doi.org/10.1046/j.1471-4159.1997.68062371.x .
doi: 10.1046/j.1471-4159.1997.68062371.x
pubmed: 9166730
Otto M, Cepek L, Ratzka P, Doehlinger S, Boekhoff I, Wiltfang J, et al. Efficacy of flupirtine on cognitive function in patients with CJD: A double-blind study. Neurology. 2004;62(5):714–8. https://doi.org/10.1212/01.wnl.0000113764.35026.ef .
doi: 10.1212/01.wnl.0000113764.35026.ef
pubmed: 15007119
Klinger F, Geier P, Dorostkar MM, Chandaka GK, Yousuf A, Salzer I, et al. Concomitant facilitation of GABAA receptors and KV7 channels by the non-opioid analgesic flupirtine. Br J Pharmacol. 2012;166(5):1631–42. https://doi.org/10.1111/j.1476-5381.2011.01821.x .
doi: 10.1111/j.1476-5381.2011.01821.x
pubmed: 22188423
pmcid: 3419907
Jakob R, Krieglstein J. Influence of flupirtine on a G-protein coupled inwardly rectifying potassium current in hippocampal neurones. Br J Pharmacol. 1997;122(7):1333–8. https://doi.org/10.1038/sj.bjp.0701519 .
doi: 10.1038/sj.bjp.0701519
pubmed: 9421279
pmcid: 1565078
Kornhuber J, Bleich S, Wiltfang J, Maler M, Parsons CG. Flupirtine shows functional NMDA receptor antagonism by enhancing Mg2+ block via activation of voltage independent potassium channels. Rapid communication. J Neural Transm (Vienna). 1999;106(9–10):857–67. https://doi.org/10.1007/s007020050206 .
doi: 10.1007/s007020050206
Sattler MB, Williams SK, Neusch C, Otto M, Pehlke JR, Bahr M, et al. Flupirtine as neuroprotective add-on therapy in autoimmune optic neuritis. Am J Pathol. 2008;173(5):1496–507. https://doi.org/10.2353/ajpath.2008.080491 .
doi: 10.2353/ajpath.2008.080491
pubmed: 18832577
pmcid: 2570139
Puls F, Agne C, Klein F, Koch M, Rifai K, Manns MP, et al. Pathology of flupirtine-induced liver injury: a histological and clinical study of six cases. Virchows Arch. 2011;458(6):709–16. https://doi.org/10.1007/s00428-011-1087-9 .
doi: 10.1007/s00428-011-1087-9
pubmed: 21590308
Nicoletti P, Werk AN, Sawle A, Shen Y, Urban TJ, Coulthard SA, et al. HLA-DRB1*16: 01-DQB1*05: 02 is a novel genetic risk factor for flupirtine-induced liver injury. Pharmacogenet Genomics. 2016;26(5):218–24. https://doi.org/10.1097/FPC.0000000000000209 .
doi: 10.1097/FPC.0000000000000209
pubmed: 26959717
Konishi K, Fukami T, Ogiso T, Nakajima M. In vitro approach to elucidate the relevance of carboxylesterase 2 and N-acetyltransferase 2 to flupirtine-induced liver injury. Biochem Pharmacol. 2018;155:242–51. https://doi.org/10.1016/j.bcp.2018.07.019 .
doi: 10.1016/j.bcp.2018.07.019
pubmed: 30028988
Munoz Garcia D, Midaglia L, Martinez Vilela J, Marin Sanchez M, Lopez Gonzalez FJ, Arias Gomez M, et al. Associated Inosine to interferon: results of a clinical trial in multiple sclerosis. Acta Neurol Scand. 2015;131(6):405–10. https://doi.org/10.1111/ane.12333 .
doi: 10.1111/ane.12333
pubmed: 25313094
von Geldern G, Mowry EM. The influence of nutritional factors on the prognosis of multiple sclerosis. Nat Rev Neurol. 2012;8(12):678–89. https://doi.org/10.1038/nrneurol.2012.194 .
doi: 10.1038/nrneurol.2012.194
Spitsin S, Koprowski H. Role of uric acid in multiple sclerosis. Curr Top Microbiol Immunol. 2008;318:325–42. https://doi.org/10.1007/978-3-540-73677-6_13 .
doi: 10.1007/978-3-540-73677-6_13
pubmed: 18219824
Touil T, Deloire-Grassin MS, Vital C, Petry KG, Brochet B. In vivo damage of CNS myelin and axons induced by peroxynitrite. NeuroReport. 2001;12(16):3637–44. https://doi.org/10.1097/00001756-200111160-00052 .
doi: 10.1097/00001756-200111160-00052
pubmed: 11733726
Scott GS, Hooper DC. The role of uric acid in protection against peroxynitrite-mediated pathology. Med Hypotheses. 2001;56(1):95–100. https://doi.org/10.1054/mehy.2000.1118 .
doi: 10.1054/mehy.2000.1118
pubmed: 11133262
Cross AH, Manning PT, Keeling RM, Schmidt RE, Misko TP. Peroxynitrite formation within the central nervous system in active multiple sclerosis. J Neuroimmunol. 1998;88(1–2):45–56. https://doi.org/10.1016/s0165-5728(98)00078-2 .
doi: 10.1016/s0165-5728(98)00078-2
pubmed: 9688323
Hooper DC, Spitsin S, Kean RB, Champion JM, Dickson GM, Chaudhry I, et al. Uric acid, a natural scavenger of peroxynitrite, in experimental allergic encephalomyelitis and multiple sclerosis. Proc Natl Acad Sci USA. 1998;95(2):675–80. https://doi.org/10.1073/pnas.95.2.675 .
doi: 10.1073/pnas.95.2.675
pubmed: 9435251
pmcid: 18479
Junqueira SC, Dos Santos CI, Lieberknecht V, Cunha MP, Calixto JB, Rodrigues ALS, et al. Inosine, an endogenous purine nucleoside, suppresses immune responses and protects mice from experimental autoimmune encephalomyelitis: a role for A2A adenosine receptor. Mol Neurobiol. 2017;54(5):3271–85. https://doi.org/10.1007/s12035-016-9893-3 .
doi: 10.1007/s12035-016-9893-3
pubmed: 27130268
Liu B, Shen Y, Xiao K, Tang Y, Cen L, Wei J. Serum uric acid levels in patients with multiple sclerosis: a meta-analysis. Neurol Res. 2012;34(2):163–71. https://doi.org/10.1179/1743132811Y.0000000074 .
doi: 10.1179/1743132811Y.0000000074
pubmed: 22333889
Spitsin S, Hooper DC, Mikheeva T, Koprowski H. Uric acid levels in patients with multiple sclerosis: analysis in mono- and dizygotic twins. Mult Scler. 2001;7(3):165–6. https://doi.org/10.1177/135245850100700305 .
doi: 10.1177/135245850100700305
pubmed: 11475439
Gonsette RE, Sindic C, D’Hooghe MB, De Deyn PP, Medaer R, Michotte A, et al. Boosting endogenous neuroprotection in multiple sclerosis: the ASsociation of Inosine and Interferon beta in relapsing- remitting Multiple Sclerosis (ASIIMS) trial. Mult Scler. 2010;16(4):455–62. https://doi.org/10.1177/1352458509360547 .
doi: 10.1177/1352458509360547
pubmed: 20200198
Guerrero AL, Martin-Polo J, Laherran E, Gutierrez F, Iglesias F, Tejero MA, et al. Variation of serum uric acid levels in multiple sclerosis during relapses and immunomodulatory treatment. Eur J Neurol. 2008;15(4):394–7. https://doi.org/10.1111/j.1468-1331.2008.02087.x .
doi: 10.1111/j.1468-1331.2008.02087.x
pubmed: 18312403
Kean RB, Spitsin SV, Mikheeva T, Scott GS, Hooper DC. The peroxynitrite scavenger uric acid prevents inflammatory cell invasion into the central nervous system in experimental allergic encephalomyelitis through maintenance of blood-central nervous system barrier integrity. J Immunol. 2000;165(11):6511–8. https://doi.org/10.4049/jimmunol.165.11.6511 .
doi: 10.4049/jimmunol.165.11.6511
pubmed: 11086092
Kleber ME, Delgado G, Grammer TB, Silbernagel G, Huang J, Kramer BK, et al. Uric acid and cardiovascular events: a mendelian randomization study. J Am Soc Nephrol. 2015;26(11):2831–8. https://doi.org/10.1681/ASN.2014070660 .
doi: 10.1681/ASN.2014070660
pubmed: 25788527
pmcid: 4625666
Low RK, Stoller ML. Uric acid-related nephrolithiasis. Urol Clin North Am. 1997;24(1):135–48. https://doi.org/10.1016/s0094-0143(05)70359-1 .
doi: 10.1016/s0094-0143(05)70359-1
pubmed: 9048857
Franklin RJ, Ffrench-Constant C. Remyelination in the CNS: from biology to therapy. Nat Rev Neurosci. 2008;9(11):839–55. https://doi.org/10.1038/nrn2480 .
doi: 10.1038/nrn2480
pubmed: 18931697
Patrikios P, Stadelmann C, Kutzelnigg A, Rauschka H, Schmidbauer M, Laursen H, et al. Remyelination is extensive in a subset of multiple sclerosis patients. Brain. 2006;129(Pt 12):3165–72. https://doi.org/10.1093/brain/awl217 .
doi: 10.1093/brain/awl217
pubmed: 16921173
Mi S, Miller RH, Lee X, Scott ML, Shulag-Morskaya S, Shao Z, et al. LINGO-1 negatively regulates myelination by oligodendrocytes. Nat Neurosci. 2005;8(6):745–51. https://doi.org/10.1038/nn1460 .
doi: 10.1038/nn1460
pubmed: 15895088
Ruggieri S, Tortorella C, Gasperini C. Anti lingo 1 (opicinumab) a new monoclonal antibody tested in relapsing remitting multiple sclerosis. Expert Rev Neurother. 2017;17(11):1081–9. https://doi.org/10.1080/14737175.2017.1378098 .
doi: 10.1080/14737175.2017.1378098
pubmed: 28885860
Mi S, Miller RH, Tang W, Lee X, Hu B, Wu W, et al. Promotion of central nervous system remyelination by induced differentiation of oligodendrocyte precursor cells. Ann Neurol. 2009;65(3):304–15. https://doi.org/10.1002/ana.21581 .
doi: 10.1002/ana.21581
pubmed: 19334062
Gresle MM, Liu Y, Kilpatrick TJ, Kemper D, Wu QZ, Hu B, et al. Blocking LINGO-1 in vivo reduces degeneration and enhances regeneration of the optic nerve. Mult Scler J Exp Transl Clin. 2016;2:2055217316641704. https://doi.org/10.1177/2055217316641704 .
doi: 10.1177/2055217316641704
pubmed: 28607723
pmcid: 5433342
Mi S, Hu B, Hahm K, Luo Y, Kam Hui ES, Yuan Q, et al. LINGO-1 antagonist promotes spinal cord remyelination and axonal integrity in MOG-induced experimental autoimmune encephalomyelitis. Nat Med. 2007;13(10):1228–33. https://doi.org/10.1038/nm1664 .
doi: 10.1038/nm1664
pubmed: 17906634
Hanf KJM, Arndt JW, Liu Y, Gong BJ, Rushe M, Sopko R, et al. Functional activity of anti-LINGO-1 antibody opicinumab requires target engagement at a secondary binding site. MAbs. 2020;12(1):1713648. https://doi.org/10.1080/19420862.2020.1713648 .
doi: 10.1080/19420862.2020.1713648
pubmed: 31928294
pmcid: 6973334
Tran JQ, Rana J, Barkhof F, Melamed I, Gevorkyan H, Wattjes MP, et al. Randomized phase I trials of the safety/tolerability of anti-LINGO-1 monoclonal antibody BIIB033. Neurol Neuroimmunol Neuroinflamm. 2014;1(2):e18. https://doi.org/10.1212/NXI.0000000000000018 .
doi: 10.1212/NXI.0000000000000018
pubmed: 25340070
pmcid: 4202679
Cadavid D, Balcer L, Galetta S, Aktas O, Ziemssen T, Vanopdenbosch L, et al. Safety and efficacy of opicinumab in acute optic neuritis (RENEW): a randomised, placebo-controlled, phase 2 trial. Lancet Neurol. 2017;16(3):189–99. https://doi.org/10.1016/S1474-4422(16)30377-5 .
doi: 10.1016/S1474-4422(16)30377-5
pubmed: 28229892
Klistorner A, Chai Y, Leocani L, Albrecht P, Aktas O, Butzkueven H, et al. Assessment of opicinumab in acute optic neuritis using multifocal visual evoked potential. CNS Drugs. 2018;32(12):1159–71. https://doi.org/10.1007/s40263-018-0575-8 .
doi: 10.1007/s40263-018-0575-8
pubmed: 30267385
pmcid: 6280853
Aktas O, Ziemssen F, Ziemssen T, Comi G, Butzkueven H, Izquierdo G, et al. RENEWED: long-term electrophysiological and clinical outcomes in participants previously enrolled in the opicinumab phase 2 study RENEW (1599). Neurology. 2020;94(15 Supplement):1599.
Cadavid D, Mellion M, Hupperts R, Edwards KR, Calabresi PA, Drulovic J, et al. Safety and efficacy of opicinumab in patients with relapsing multiple sclerosis (SYNERGY): a randomised, placebo-controlled, phase 2 trial. Lancet Neurol. 2019;18(9):845–56. https://doi.org/10.1016/S1474-4422(19)30137-1 .
doi: 10.1016/S1474-4422(19)30137-1
pubmed: 31285147
Schwid SR, Goodman AD, McDermott MP, Bever CF, Cook SD. Quantitative functional measures in MS: what is a reliable change? Neurology. 2002;58(8):1294–6. https://doi.org/10.1212/wnl.58.8.1294 .
doi: 10.1212/wnl.58.8.1294
pubmed: 11971105
Feys P, Lamers I, Francis G, Benedict R, Phillips G, LaRocca N, et al. The Nine-Hole Peg Test as a manual dexterity performance measure for multiple sclerosis. Mult Scler. 2017;23(5):711–20. https://doi.org/10.1177/1352458517690824 .
doi: 10.1177/1352458517690824
pubmed: 28206826
pmcid: 5405844
Gronwall DM. Paced auditory serial-addition task: a measure of recovery from concussion. Percept Mot Skills. 1977;44(2):367–73. https://doi.org/10.2466/pms.1977.44.2.367 .
doi: 10.2466/pms.1977.44.2.367
pubmed: 866038
Zhu B, Calabresi P, Giovannoni G, Kapoor R, Naismith R, Hartung H-P, et al. Phase 2 AFFINITY trial evaluates opicinumab in a targeted population of patients with relapsing multiple sclerosis: rationale, design and baseline characteristics (P32–072). Neurology. 2019;92(15 Supplement):P3.2-072.
Efficacy and Safety of BIIB033 (Opicinumab) as an Add-on Therapy to Disease-Modifying Therapies (DMTs) in Relapsing Multiple Sclerosis (MS) (AFFINITY). In: ClinicalTrials.gov Identifier: NCT03222973. Start: 2017. Accessed 3 Jun 2020.
MacCannell D, Nestorov I. Model-based identification of flat dosing regimen for opicinumab AFFINITY trial. ECTRIMS Online Library. 2019:P642.
Biogen. Biogen reports Q3 2020 Results. 2020.
Cadavid D, Balcer L, Galetta S, Aktas O, Ziemssen T, Vanopdenbosch LJ, et al. Predictors of response to opicinumab in acute optic neuritis. Ann Clin Transl Neurol. 2018;5(10):1154–62. https://doi.org/10.1002/acn3.620 .
doi: 10.1002/acn3.620
pubmed: 30349850
pmcid: 6186935
Neumann B, Segel M, Chalut KJ, Franklin RJ. Remyelination and ageing: reversing the ravages of time. Mult Scler. 2019;25(14):1835–41. https://doi.org/10.1177/1352458519884006 .
doi: 10.1177/1352458519884006
pubmed: 31687878
pmcid: 7682531
Woodruff RH, Fruttiger M, Richardson WD, Franklin RJ. Platelet-derived growth factor regulates oligodendrocyte progenitor numbers in adult CNS and their response following CNS demyelination. Mol Cell Neurosci. 2004;25(2):252–62. https://doi.org/10.1016/j.mcn.2003.10.014 .
doi: 10.1016/j.mcn.2003.10.014
pubmed: 15019942
Sheikh S, Calabresi P, Giovannoni G, Kapoor R, Arnold DL, Chai Y, et al. Predictors of an opicinumab treatment effect and identification of an efficacy subpopulation: a post hoc analysis of the SYNERGY Study (P3.408). Neurology. 2018;90(15 Supplement):P3.408.
Cerina M, Narayanan V, Gobel K, Bittner S, Ruck T, Meuth P, et al. The quality of cortical network function recovery depends on localization and degree of axonal demyelination. Brain Behav Immun. 2017;59:103–17. https://doi.org/10.1016/j.bbi.2016.08.014 .
doi: 10.1016/j.bbi.2016.08.014
pubmed: 27569659
Larochelle C, Uphaus T, Prat A, Zipp F. Secondary progression in multiple sclerosis: neuronal exhaustion or distinct pathology? Trends Neurosci. 2016;39(5):325–39. https://doi.org/10.1016/j.tins.2016.02.001 .
doi: 10.1016/j.tins.2016.02.001
pubmed: 26987259
Correa MF, Dos Santos Fernandes JP. QSAR modeling of histamine H3R antagonists/inverse agonists as future drugs for neurodegenerative diseases. Curr Neuropharmacol. 2018;16(6):749–57. https://doi.org/10.2174/1570159X15666170818100644 .
doi: 10.2174/1570159X15666170818100644
pubmed: 28820054
pmcid: 6080103
Gemkow MJ, Davenport AJ, Harich S, Ellenbroek BA, Cesura A, Hallett D. The histamine H3 receptor as a therapeutic drug target for CNS disorders. Drug Discov Today. 2009;14(9–10):509–15. https://doi.org/10.1016/j.drudis.2009.02.011 .
doi: 10.1016/j.drudis.2009.02.011
pubmed: 19429511
Sadek B, Saad A, Sadeq A, Jalal F, Stark H. Histamine H3 receptor as a potential target for cognitive symptoms in neuropsychiatric diseases. Behav Brain Res. 2016;312:415–30. https://doi.org/10.1016/j.bbr.2016.06.051 .
doi: 10.1016/j.bbr.2016.06.051
pubmed: 27363923
Chen Y, Zhen W, Guo T, Zhao Y, Liu A, Rubio JP, et al. Histamine Receptor 3 negatively regulates oligodendrocyte differentiation and remyelination. PLoS ONE. 2017;12(12):e0189380. https://doi.org/10.1371/journal.pone.0189380 .
doi: 10.1371/journal.pone.0189380
pubmed: 29253893
pmcid: 5734789
Merkestein M, Gispen WH, Adan RAH. Melanocortins: brain effects. In: Squire LR, editor. Encyclopedia of neuroscience. Oxford: Academic Press; 2009. p. 713–9.
doi: 10.1016/B978-008045046-9.01448-0
Jarskog LF, Lowy MT, Grove RA, Keefe RS, Horrigan JP, Ball MP, et al. A Phase II study of a histamine H(3) receptor antagonist GSK239512 for cognitive impairment in stable schizophrenia subjects on antipsychotic therapy. Schizophr Res. 2015;164(1–3):136–42. https://doi.org/10.1016/j.schres.2015.01.041 .
doi: 10.1016/j.schres.2015.01.041
pubmed: 25728831
Grove RA, Harrington CM, Mahler A, Beresford I, Maruff P, Lowy MT, et al. A randomized, double-blind, placebo-controlled, 16-week study of the H3 receptor antagonist, GSK239512 as a monotherapy in subjects with mild-to-moderate Alzheimer’s disease. Curr Alzheimer Res. 2014;11(1):47–58. https://doi.org/10.2174/1567205010666131212110148 .
doi: 10.2174/1567205010666131212110148
pubmed: 24359500
Nathan PJ, Boardley R, Scott N, Berges A, Maruff P, Sivananthan T, et al. The safety, tolerability, pharmacokinetics and cognitive effects of GSK239512, a selective histamine H(3) receptor antagonist in patients with mild to moderate Alzheimer’s disease: a preliminary investigation. Curr Alzheimer Res. 2013;10(3):240–51. https://doi.org/10.2174/1567205011310030003 .
doi: 10.2174/1567205011310030003
pubmed: 23521503
Schwartzbach CJ, Grove RA, Brown R, Tompson D, Then Bergh F, Arnold DL. Lesion remyelinating activity of GSK239512 versus placebo in patients with relapsing-remitting multiple sclerosis: a randomised, single-blind, phase II study. J Neurol. 2017;264(2):304–15. https://doi.org/10.1007/s00415-016-8341-7 .
doi: 10.1007/s00415-016-8341-7
pubmed: 27888416
Ashworth S, Berges A, Rabiner EA, Wilson AA, Comley RA, Lai RY, et al. Unexpectedly high affinity of a novel histamine H(3) receptor antagonist, GSK239512, in vivo in human brain, determined using PET. Br J Pharmacol. 2014;171(5):1241–9. https://doi.org/10.1111/bph.12505 .
doi: 10.1111/bph.12505
pubmed: 24670146
pmcid: 3952801
Maruff P, Thomas E, Cysique L, Brew B, Collie A, Snyder P, et al. Validity of the CogState brief battery: relationship to standardized tests and sensitivity to cognitive impairment in mild traumatic brain injury, schizophrenia, and AIDS dementia complex. Arch Clin Neuropsychol. 2009;24(2):165–78. https://doi.org/10.1093/arclin/acp010 .
doi: 10.1093/arclin/acp010
pubmed: 19395350
Teuscher C, Subramanian M, Noubade R, Gao JF, Offner H, Zachary JF, et al. Central histamine H3 receptor signaling negatively regulates susceptibility to autoimmune inflammatory disease of the CNS. Proc Natl Acad Sci USA. 2007;104(24):10146–51. https://doi.org/10.1073/pnas.0702291104 .
doi: 10.1073/pnas.0702291104
pubmed: 17548817
pmcid: 1891222
Beghdadi W, Porcherie A, Schneider BS, Morisset S, Dubayle D, Peronet R, et al. Histamine H(3) receptor-mediated signaling protects mice from cerebral malaria. PLoS ONE. 2009;4(6):e6004. https://doi.org/10.1371/journal.pone.0006004 .
doi: 10.1371/journal.pone.0006004
pubmed: 19547708
pmcid: 2696087
Sharma HS, Vannemreddy P, Patnaik R, Patnaik S, Mohanty S. Histamine receptors influence blood-spinal cord barrier permeability, edema formation, and spinal cord blood flow following trauma to the rat spinal cord. Acta Neurochir Suppl. 2006;96:316–21. https://doi.org/10.1007/3-211-30714-1_67 .
doi: 10.1007/3-211-30714-1_67
pubmed: 16671478
Shi Y, Li Z, Chen R, Zhang J, Hu X, He C, et al. Immethridine, histamine H3-receptor (H3R) agonist, alleviated experimental autoimmune encephalomyelitis via inhibiting the function of dendritic cells. Oncotarget. 2017;8(43):75038–49. https://doi.org/10.18632/oncotarget.20500 .
doi: 10.18632/oncotarget.20500
pubmed: 29088843
pmcid: 5650398
Saligrama N, Noubade R, Case LK, del Rio R, Teuscher C. Combinatorial roles for histamine H1–H2 and H3–H4 receptors in autoimmune inflammatory disease of the central nervous system. Eur J Immunol. 2012;42(6):1536–46. https://doi.org/10.1002/eji.201141859 .
doi: 10.1002/eji.201141859
pubmed: 22678907
pmcid: 3508704
Iida T, Yoshikawa T, Matsuzawa T, Naganuma F, Nakamura T, Miura Y, et al. Histamine H3 receptor in primary mouse microglia inhibits chemotaxis, phagocytosis, and cytokine secretion. Glia. 2015;63(7):1213–25. https://doi.org/10.1002/glia.22812 .
doi: 10.1002/glia.22812
pubmed: 25754956
Xu J, Zhang X, Qian Q, Wang Y, Dong H, Li N, et al. Histamine upregulates the expression of histamine receptors and increases the neuroprotective effect of astrocytes. J Neuroinflamm. 2018;15(1):41. https://doi.org/10.1186/s12974-018-1068-x .
doi: 10.1186/s12974-018-1068-x
Bittner S, Ruck T, Fernandez-Orth J, Meuth SG. TREK-king the blood-brain-barrier. J Neuroimmune Pharmacol. 2014;9(3):293–301. https://doi.org/10.1007/s11481-014-9530-8 .
doi: 10.1007/s11481-014-9530-8
pubmed: 24557892
Bittner S, Ruck T, Schuhmann MK, Herrmann AM, Moha ou Maati H, Bobak N, et al. Endothelial TWIK-related potassium channel-1 (TREK1) regulates immune-cell trafficking into the CNS. Nat Med. 2013;19(9):1161–5. https://doi.org/10.1038/nm.3303 .
doi: 10.1038/nm.3303
pubmed: 23933981
Yamada K, Inagaki N. Neuroprotection by KATP channels. J Mol Cell Cardiol. 2005;38(6):945–9. https://doi.org/10.1016/j.yjmcc.2004.11.020 .
doi: 10.1016/j.yjmcc.2004.11.020
pubmed: 15910879
Garlid KD, Paucek P, Yarov-Yarovoy V, Sun X, Schindler PA. The mitochondrial KATP channel as a receptor for potassium channel openers. J Biol Chem. 1996;271(15):8796–9. https://doi.org/10.1074/jbc.271.15.8796 .
doi: 10.1074/jbc.271.15.8796
pubmed: 8621517
Shimizu K, Lacza Z, Rajapakse N, Horiguchi T, Snipes J, Busija DW. MitoK(ATP) opener, diazoxide, reduces neuronal damage after middle cerebral artery occlusion in the rat. Am J Physiol Heart Circ Physiol. 2002;283(3):H1005–11. https://doi.org/10.1152/ajpheart.00054.2002 .
doi: 10.1152/ajpheart.00054.2002
pubmed: 12181130
Yang Y, Liu X, Long Y, Wang F, Ding JH, Liu SY, et al. Activation of mitochondrial ATP-sensitive potassium channels improves rotenone-related motor and neurochemical alterations in rats. Int J Neuropsychopharmacol. 2006;9(1):51–61. https://doi.org/10.1017/S1461145705005547 .
doi: 10.1017/S1461145705005547
pubmed: 15927086
Liu D, Pitta M, Lee JH, Ray B, Lahiri DK, Furukawa K, et al. The KATP channel activator diazoxide ameliorates amyloid-beta and tau pathologies and improves memory in the 3xTgAD mouse model of Alzheimer’s disease. J Alzheimers Dis. 2010;22(2):443–57. https://doi.org/10.3233/JAD-2010-101017 .
doi: 10.3233/JAD-2010-101017
pubmed: 20847430
pmcid: 2988870
Virgili N, Mancera P, Wappenhans B, Sorrosal G, Biber K, Pugliese M, et al. K(ATP) channel opener diazoxide prevents neurodegeneration: a new mechanism of action via antioxidative pathway activation. PLoS ONE. 2013;8(9):e75189. https://doi.org/10.1371/journal.pone.0075189 .
doi: 10.1371/journal.pone.0075189
pubmed: 24040400
pmcid: 3770693
Zhou F, Yao HH, Wu JY, Ding JH, Sun T, Hu G. Opening of microglial K(ATP) channels inhibits rotenone-induced neuroinflammation. J Cell Mol Med. 2008;12(5A):1559–70. https://doi.org/10.1111/j.1582-4934.2007.00144.x .
doi: 10.1111/j.1582-4934.2007.00144.x
pubmed: 19012619
Rodriguez MJ, Martinez-Moreno M, Ortega FJ, Mahy N. Targeting microglial K(ATP) channels to treat neurodegenerative diseases: a mitochondrial issue. Oxid Med Cell Longev. 2013;2013:194546. https://doi.org/10.1155/2013/194546 .
doi: 10.1155/2013/194546
pubmed: 23844272
pmcid: 3697773
Virgili N, Espinosa-Parrilla JF, Mancera P, Pasten-Zamorano A, Gimeno-Bayon J, Rodriguez MJ, et al. Oral administration of the KATP channel opener diazoxide ameliorates disease progression in a murine model of multiple sclerosis. J Neuroinflammation. 2011;8:149. https://doi.org/10.1186/1742-2094-8-149 .
doi: 10.1186/1742-2094-8-149
pubmed: 22047130
pmcid: 3215935
Virgili N, Mancera P, Chanvillard C, Wegner A, Wappenhans B, Rodriguez MJ, et al. Diazoxide attenuates autoimmune encephalomyelitis and modulates lymphocyte proliferation and dendritic cell functionality. J Neuroimmune Pharmacol. 2014;9(4):558–68. https://doi.org/10.1007/s11481-014-9551-3 .
doi: 10.1007/s11481-014-9551-3
pubmed: 24939091
Villoslada P, Rovira A, Montalban X, Arroyo R, Paul F, Meca-Lallana V, et al. Effects of diazoxide in multiple sclerosis: a randomized, double-blind phase 2 clinical trial. Neurol Neuroimmunol Neuroinflamm. 2015;2(5):e147. https://doi.org/10.1212/NXI.0000000000000147 .
doi: 10.1212/NXI.0000000000000147
pubmed: 26405686
pmcid: 4567455
Schafer G, Wegener C, Portenhauser R, Bojanovski D. Diazoxide, an inhibitor of succinate oxidation. Biochem Pharmacol. 1969;18(10):2678–81.
pubmed: 4327387
Nishino H, Shimano Y, Kumazaki M, Sakurai T. Chronically administered 3-nitropropionic acid induces striatal lesions attributed to dysfunction of the blood-brain barrier. Neurosci Lett. 1995;186(2–3):161–4. https://doi.org/10.1016/0304-3940(95)11311-j .
doi: 10.1016/0304-3940(95)11311-j
pubmed: 7777187
Fogal B, McClaskey C, Yan S, Yan H, Rivkees SA. Diazoxide promotes oligodendrocyte precursor cell proliferation and myelination. PLoS ONE. 2010;5(5):e10906. https://doi.org/10.1371/journal.pone.0010906 .
doi: 10.1371/journal.pone.0010906
pubmed: 20531945
pmcid: 2878350
Zhu Y, Wendler CC, Shi O, Rivkees SA. Diazoxide promotes oligodendrocyte differentiation in neonatal brain in normoxia and chronic sublethal hypoxia. Brain Res. 2014;1586:64–72. https://doi.org/10.1016/j.brainres.2014.08.046 .
doi: 10.1016/j.brainres.2014.08.046
pubmed: 25157906
pmcid: 4217210
Ehling P, Bittner S, Budde T, Wiendl H, Meuth SG. Ion channels in autoimmune neurodegeneration. FEBS Lett. 2011;585(23):3836–42. https://doi.org/10.1016/j.febslet.2011.03.065 .
doi: 10.1016/j.febslet.2011.03.065
pubmed: 21501610
Goodman AD, Brown TR, Schapiro RT, Klingler M, Cohen R, Blight AR. A pooled analysis of two phase 3 clinical trials of dalfampridine in patients with multiple sclerosis. Int J MS Care. 2014;16(3):153–60. https://doi.org/10.7224/1537-2073.2013-023 .
doi: 10.7224/1537-2073.2013-023
pubmed: 25337058
pmcid: 4204376
Dietrich M, Koska V, Hecker C, Gottle P, Hilla AM, Heskamp A, et al. Protective effects of 4-aminopyridine in experimental optic neuritis and multiple sclerosis. Brain. 2020;143(4):1127–42. https://doi.org/10.1093/brain/awaa062 .
doi: 10.1093/brain/awaa062
pubmed: 32293668
Gobel K, Wedell JH, Herrmann AM, Wachsmuth L, Pankratz S, Bittner S, et al. 4-Aminopyridine ameliorates mobility but not disease course in an animal model of multiple sclerosis. Exp Neurol. 2013;248:62–71. https://doi.org/10.1016/j.expneurol.2013.05.016 .
doi: 10.1016/j.expneurol.2013.05.016
pubmed: 23748135
Moriguchi K, Miyamoto K, Fukumoto Y, Kusunoki S. 4-Aminopyridine ameliorates relapsing remitting experimental autoimmune encephalomyelitis in SJL/J mice. J Neuroimmunol. 2018;323:131–5. https://doi.org/10.1016/j.jneuroim.2018.08.007 .
doi: 10.1016/j.jneuroim.2018.08.007
pubmed: 30139717
Cutter GR, Baier ML, Rudick RA, Cookfair DL, Fischer JS, Petkau J, et al. Development of a multiple sclerosis functional composite as a clinical trial outcome measure. Brain. 1999;122(Pt 5):871–82. https://doi.org/10.1093/brain/122.5.871 .
doi: 10.1093/brain/122.5.871
pubmed: 10355672
Ruck T, Bittner S, Simon OJ, Gobel K, Wiendl H, Schilling M, et al. Long-term effects of dalfampridine in patients with multiple sclerosis. J Neurol Sci. 2014;337(1–2):18–24. https://doi.org/10.1016/j.jns.2013.11.011 .
doi: 10.1016/j.jns.2013.11.011
pubmed: 24290498
Goodman AD, Cohen JA, Cross A, Vollmer T, Rizzo M, Cohen R, et al. Fampridine-SR in multiple sclerosis: a randomized, double-blind, placebo-controlled, dose-ranging study. Mult Scler. 2007;13(3):357–68. https://doi.org/10.1177/1352458506069538 .
doi: 10.1177/1352458506069538
pubmed: 17439905
Goodman AD, Brown TR, Cohen JA, Krupp LB, Schapiro R, Schwid SR, et al. Dose comparison trial of sustained-release fampridine in multiple sclerosis. Neurology. 2008;71(15):1134–41. https://doi.org/10.1212/01.wnl.0000326213.89576.0e .
doi: 10.1212/01.wnl.0000326213.89576.0e
pubmed: 18672472
Yrjanheikki J, Keinanen R, Pellikka M, Hokfelt T, Koistinaho J. Tetracyclines inhibit microglial activation and are neuroprotective in global brain ischemia. Proc Natl Acad Sci USA. 1998;95(26):15769–74. https://doi.org/10.1073/pnas.95.26.15769 .
doi: 10.1073/pnas.95.26.15769
pubmed: 9861045
pmcid: 28119
Kim HS, Suh YH. Minocycline and neurodegenerative diseases. Behav Brain Res. 2009;196(2):168–79. https://doi.org/10.1016/j.bbr.2008.09.040 .
doi: 10.1016/j.bbr.2008.09.040
pubmed: 18977395
Brundula V, Rewcastle NB, Metz LM, Bernard CC, Yong VW. Targeting leukocyte MMPs and transmigration: minocycline as a potential therapy for multiple sclerosis. Brain. 2002;125(Pt 6):1297–308. https://doi.org/10.1093/brain/awf133 .
doi: 10.1093/brain/awf133
pubmed: 12023318
Giuliani F, Fu SA, Metz LM, Yong VW. Effective combination of minocycline and interferon-beta in a model of multiple sclerosis. J Neuroimmunol. 2005;165(1–2):83–91. https://doi.org/10.1016/j.jneuroim.2005.04.020 .
doi: 10.1016/j.jneuroim.2005.04.020
pubmed: 15958276
Giuliani F, Metz LM, Wilson T, Fan Y, Bar-Or A, Yong VW. Additive effect of the combination of glatiramer acetate and minocycline in a model of MS. J Neuroimmunol. 2005;158(1–2):213–21. https://doi.org/10.1016/j.jneuroim.2004.09.006 .
doi: 10.1016/j.jneuroim.2004.09.006
pubmed: 15589056
Giuliani F, Hader W, Yong VW. Minocycline attenuates T cell and microglia activity to impair cytokine production in T cell-microglia interaction. J Leukoc Biol. 2005;78(1):135–43. https://doi.org/10.1189/jlb.0804477 .
doi: 10.1189/jlb.0804477
pubmed: 15817702
Hou Y, Ryu CH, Park KY, Kim SM, Jeong CH, Jeun SS. Effective combination of human bone marrow mesenchymal stem cells and minocycline in experimental autoimmune encephalomyelitis mice. Stem Cell Res Ther. 2013;4(4):77. https://doi.org/10.1186/scrt228 .
doi: 10.1186/scrt228
pubmed: 23826999
pmcid: 3854709
Niimi N, Kohyama K, Matsumoto Y. Minocycline suppresses experimental autoimmune encephalomyelitis by increasing tissue inhibitors of metalloproteinases. Neuropathology. 2013;33(6):612–20. https://doi.org/10.1111/neup.12039 .
doi: 10.1111/neup.12039
pubmed: 23581743
Tikka TM, Koistinaho JE. Minocycline provides neuroprotection against N-methyl-D-aspartate neurotoxicity by inhibiting microglia. J Immunol. 2001;166(12):7527–33. https://doi.org/10.4049/jimmunol.166.12.7527 .
doi: 10.4049/jimmunol.166.12.7527
pubmed: 11390507
Faissner S, Mahjoub Y, Mishra M, Haupeltshofer S, Hahn JN, Gold R, et al. Unexpected additive effects of minocycline and hydroxychloroquine in models of multiple sclerosis: Prospective combination treatment for progressive disease? Mult Scler. 2018;24(12):1543–56. https://doi.org/10.1177/1352458517728811 .
doi: 10.1177/1352458517728811
pubmed: 28857721
Metz LM, Li DKB, Traboulsee AL, Duquette P, Eliasziw M, Cerchiaro G, et al. Trial of minocycline in a clinically isolated syndrome of multiple sclerosis. N Engl J Med. 2017;376(22):2122–33. https://doi.org/10.1056/NEJMoa1608889 .
doi: 10.1056/NEJMoa1608889
pubmed: 28564557
Zhang Y, Metz LM, Yong VW, Bell RB, Yeung M, Patry DG, et al. Pilot study of minocycline in relapsing-remitting multiple sclerosis. Can J Neurol Sci. 2008;35(2):185–91. https://doi.org/10.1017/s0317167100008611 .
doi: 10.1017/s0317167100008611
pubmed: 18574932
Metz LM, Li D, Traboulsee A, Myles ML, Duquette P, Godin J, et al. Glatiramer acetate in combination with minocycline in patients with relapsing–remitting multiple sclerosis: results of a Canadian, multicenter, double-blind, placebo-controlled trial. Mult Scler. 2009;15(10):1183–94. https://doi.org/10.1177/1352458509106779 .
doi: 10.1177/1352458509106779
pubmed: 19776092
Sorensen PS, Sellebjerg F, Lycke J, Farkkila M, Creange A, Lund CG, et al. Minocycline added to subcutaneous interferon beta-1a in multiple sclerosis: randomized RECYCLINE study. Eur J Neurol. 2016;23(5):861–70. https://doi.org/10.1111/ene.12953 .
doi: 10.1111/ene.12953
pubmed: 26848561
Baer AS, Syed YA, Kang SU, Mitteregger D, Vig R, Ffrench-Constant C, et al. Myelin-mediated inhibition of oligodendrocyte precursor differentiation can be overcome by pharmacological modulation of Fyn-RhoA and protein kinase C signalling. Brain. 2009;132(Pt 2):465–81. https://doi.org/10.1093/brain/awn334 .
doi: 10.1093/brain/awn334
pubmed: 19208690
pmcid: 2640211
Miron VE. Microglia-driven regulation of oligodendrocyte lineage cells, myelination, and remyelination. J Leukoc Biol. 2017;101(5):1103–8. https://doi.org/10.1189/jlb.3RI1116-494R .
doi: 10.1189/jlb.3RI1116-494R
pubmed: 28250011
Li J, Zhang L, Chu Y, Namaka M, Deng B, Kong J, et al. Astrocytes in oligodendrocyte lineage development and white matter pathology. Front Cell Neurosci. 2016;10:119. https://doi.org/10.3389/fncel.2016.00119 .
doi: 10.3389/fncel.2016.00119
pubmed: 27242432
pmcid: 4861901
Larsen PH, Wells JE, Stallcup WB, Opdenakker G, Yong VW. Matrix metalloproteinase-9 facilitates remyelination in part by processing the inhibitory NG2 proteoglycan. J Neurosci. 2003;23(35):11127–35.
doi: 10.1523/JNEUROSCI.23-35-11127.2003
Kozovska ME, Hong J, Zang YC, Li S, Rivera VM, Killian JM, et al. Interferon beta induces T-helper 2 immune deviation in MS. Neurology. 1999;53(8):1692–7. https://doi.org/10.1212/wnl.53.8.1692 .
doi: 10.1212/wnl.53.8.1692
pubmed: 10563614
Waldmann R, Champigny G, Bassilana F, Heurteaux C, Lazdunski M. A proton-gated cation channel involved in acid-sensing. Nature. 1997;386(6621):173–7. https://doi.org/10.1038/386173a0 .
doi: 10.1038/386173a0
pubmed: 9062189
Arias RL, Sung ML, Vasylyev D, Zhang MY, Albinson K, Kubek K, et al. Amiloride is neuroprotective in an MPTP model of Parkinson’s disease. Neurobiol Dis. 2008;31(3):334–41. https://doi.org/10.1016/j.nbd.2008.05.008 .
doi: 10.1016/j.nbd.2008.05.008
pubmed: 18606547
Xiong ZG, Zhu XM, Chu XP, Minami M, Hey J, Wei WL, et al. Neuroprotection in ischemia: blocking calcium-permeable acid-sensing ion channels. Cell. 2004;118(6):687–98. https://doi.org/10.1016/j.cell.2004.08.026 .
doi: 10.1016/j.cell.2004.08.026
pubmed: 15369669
Wong HK, Bauer PO, Kurosawa M, Goswami A, Washizu C, Machida Y, et al. Blocking acid-sensing ion channel 1 alleviates Huntington’s disease pathology via an ubiquitin-proteasome system-dependent mechanism. Hum Mol Genet. 2008;17(20):3223–35. https://doi.org/10.1093/hmg/ddn218 .
doi: 10.1093/hmg/ddn218
pubmed: 18658163
Vergo S, Craner MJ, Etzensperger R, Attfield K, Friese MA, Newcombe J, et al. Acid-sensing ion channel 1 is involved in both axonal injury and demyelination in multiple sclerosis and its animal model. Brain. 2011;134(Pt 2):571–84. https://doi.org/10.1093/brain/awq337 .
doi: 10.1093/brain/awq337
pubmed: 21233144
Friese MA, Craner MJ, Etzensperger R, Vergo S, Wemmie JA, Welsh MJ, et al. Acid-sensing ion channel-1 contributes to axonal degeneration in autoimmune inflammation of the central nervous system. Nat Med. 2007;13(12):1483–9. https://doi.org/10.1038/nm1668 .
doi: 10.1038/nm1668
pubmed: 17994101
Bernardinelli L, Murgia SB, Bitti PP, Foco L, Ferrai R, Musu L, et al. Association between the ACCN1 gene and multiple sclerosis in Central East Sardinia. PLoS ONE. 2007;2(5):e480. https://doi.org/10.1371/journal.pone.0000480 .
doi: 10.1371/journal.pone.0000480
pubmed: 17534430
pmcid: 1868958
Arun T, Tomassini V, Sbardella E, de Ruiter MB, Matthews L, Leite MI, et al. Targeting ASIC1 in primary progressive multiple sclerosis: evidence of neuroprotection with amiloride. Brain. 2013;136(Pt 1):106–15. https://doi.org/10.1093/brain/aws325 .
doi: 10.1093/brain/aws325
pubmed: 23365093
McKee JB, Cottriall CL, Elston J, Epps S, Evangelou N, Gerry S, et al. Amiloride does not protect retinal nerve fibre layer thickness in optic neuritis in a phase 2 randomised controlled trial. Mult Scler. 2019;25(2):246–55. https://doi.org/10.1177/1352458517742979 .
doi: 10.1177/1352458517742979
pubmed: 29172994
Chataway J, De Angelis F, Connick P, Parker RA, Plantone D, Doshi A, et al. Efficacy of three neuroprotective drugs in secondary progressive multiple sclerosis (MS-SMART): a phase 2b, multiarm, double-blind, randomised placebo-controlled trial. Lancet Neurol. 2020;19(3):214–25. https://doi.org/10.1016/S1474-4422(19)30485-5 .
doi: 10.1016/S1474-4422(19)30485-5
pubmed: 31981516
pmcid: 7029307
Pasternak B, Svanstrom H, Nielsen NM, Melbye M, Hviid A. Use of amiloride and multiple sclerosis: registry-based cohort studies. Pharmacoepidemiol Drug Saf. 2012;21(8):890–5. https://doi.org/10.1002/pds.3269 .
doi: 10.1002/pds.3269
pubmed: 22555991
Toosy AT, Mason DF, Miller DH. Optic neuritis. Lancet Neurol. 2014;13(1):83–99. https://doi.org/10.1016/S1474-4422(13)70259-X .
doi: 10.1016/S1474-4422(13)70259-X
pubmed: 24331795
Beck RW, Cleary PA, Anderson MM Jr, Keltner JL, Shults WT, Kaufman DI, et al. A randomized, controlled trial of corticosteroids in the treatment of acute optic neuritis. The Optic Neuritis Study Group. N Engl J Med. 1992;326(9):581–8. https://doi.org/10.1056/NEJM199202273260901 .
doi: 10.1056/NEJM199202273260901
pubmed: 1734247
Bitsch A, Bruhn H, Vougioukas V, Stringaris A, Lassmann H, Frahm J, et al. Inflammatory CNS demyelination: histopathologic correlation with in vivo quantitative proton MR spectroscopy. AJNR Am J Neuroradiol. 1999;20(9):1619–27.
pubmed: 10543631
pmcid: 7056180
pH-weighted MRI in Multiple Sclerosis: A Surrogate Marker of Tissue Metabolic Stress. In: ClinicalTrials.gov Identifier: NCT03028675. Start: 2017. Accessed 3 Jun 2020.
Wong DT, Perry KW, Bymaster FP. Case history: the discovery of fluoxetine hydrochloride (Prozac). Nat Rev Drug Discov. 2005;4(9):764–74. https://doi.org/10.1038/nrd1821 .
doi: 10.1038/nrd1821
pubmed: 16121130
Flax JW, Gray J, Herbert J. Effect of fluoxetine on patients with multiple sclerosis. Am J Psychiatry. 1991;148(11):1603. https://doi.org/10.1176/ajp.148.11.1603a .
doi: 10.1176/ajp.148.11.1603a
pubmed: 1928482
Yuan XQ, Qiu G, Liu XJ, Liu S, Wu Y, Wang X, et al. Fluoxetine promotes remission in acute experimental autoimmune encephalomyelitis in rats. NeuroImmunoModulation. 2012;19(4):201–8. https://doi.org/10.1159/000334095 .
doi: 10.1159/000334095
pubmed: 22441536
Bhat R, Mahapatra S, Axtell RC, Steinman L. Amelioration of ongoing experimental autoimmune encephalomyelitis with fluoxetine. J Neuroimmunol. 2017;313:77–81. https://doi.org/10.1016/j.jneuroim.2017.10.012 .
doi: 10.1016/j.jneuroim.2017.10.012
pubmed: 29153612
Mostert JP, Sijens PE, Oudkerk M, De Keyser J. Fluoxetine increases cerebral white matter NAA/Cr ratio in patients with multiple sclerosis. Neurosci Lett. 2006;402(1–2):22–4. https://doi.org/10.1016/j.neulet.2006.03.042 .
doi: 10.1016/j.neulet.2006.03.042
pubmed: 16644118
Kong EK, Peng L, Chen Y, Yu AC, Hertz L. Up-regulation of 5-HT2B receptor density and receptor-mediated glycogenolysis in mouse astrocytes by long-term fluoxetine administration. Neurochem Res. 2002;27(1–2):113–20. https://doi.org/10.1023/a:1014862808126 .
doi: 10.1023/a:1014862808126
pubmed: 11930908
Allaman I, Fiumelli H, Magistretti PJ, Martin JL. Fluoxetine regulates the expression of neurotrophic/growth factors and glucose metabolism in astrocytes. Psychopharmacology. 2011;216(1):75–84. https://doi.org/10.1007/s00213-011-2190-y .
doi: 10.1007/s00213-011-2190-y
pubmed: 21301813
Deak F, Lasztoczi B, Pacher P, Petheo GL, Valeria K, Spat A. Inhibition of voltage-gated calcium channels by fluoxetine in rat hippocampal pyramidal cells. Neuropharmacology. 2000;39(6):1029–36. https://doi.org/10.1016/s0028-3908(99)00206-3 .
doi: 10.1016/s0028-3908(99)00206-3
pubmed: 10727713
Pancrazio JJ, Kamatchi GL, Roscoe AK, Lynch C 3rd. Inhibition of neuronal Na+ channels by antidepressant drugs. J Pharmacol Exp Ther. 1998;284(1):208–14.
pubmed: 9435180
Lee JY, Kim HS, Choi HY, Oh TH, Yune TY. Fluoxetine inhibits matrix metalloprotease activation and prevents disruption of blood-spinal cord barrier after spinal cord injury. Brain. 2012;135(Pt 8):2375–89. https://doi.org/10.1093/brain/aws171 .
doi: 10.1093/brain/aws171
pubmed: 22798270
Lee JY, Lee HE, Kang SR, Choi HY, Ryu JH, Yune TY. Fluoxetine inhibits transient global ischemia-induced hippocampal neuronal death and memory impairment by preventing blood-brain barrier disruption. Neuropharmacology. 2014;79:161–71. https://doi.org/10.1016/j.neuropharm.2013.11.011 .
doi: 10.1016/j.neuropharm.2013.11.011
pubmed: 24316161
Branco-de-Almeida LS, Kajiya M, Cardoso CR, Silva MJ, Ohta K, Rosalen PL, et al. Selective serotonin reuptake inhibitors attenuate the antigen presentation from dendritic cells to effector T lymphocytes. FEMS Immunol Med Microbiol. 2011;62(3):283–94. https://doi.org/10.1111/j.1574-695X.2011.00816.x .
doi: 10.1111/j.1574-695X.2011.00816.x
pubmed: 21569123
pmcid: 3147168
Diamond M, Kelly JP, Connor TJ. Antidepressants suppress production of the Th1 cytokine interferon-gamma, independent of monoamine transporter blockade. Eur Neuropsychopharmacol. 2006;16(7):481–90. https://doi.org/10.1016/j.euroneuro.2005.11.011 .
doi: 10.1016/j.euroneuro.2005.11.011
pubmed: 16388933
Cambron M, Mostert J, D’Hooghe M, Nagels G, Willekens B, Debruyne J, et al. Fluoxetine in progressive multiple sclerosis: the FLUOX-PMS trial. Mult Scler. 2019;25(13):1728–35. https://doi.org/10.1177/1352458519843051 .
doi: 10.1177/1352458519843051
pubmed: 31218911
Mostert J, Heersema T, Mahajan M, Van Der Grond J, Van Buchem MA, De Keyser J. The effect of fluoxetine on progression in progressive multiple sclerosis: a double-blind, randomized, placebo-controlled trial. ISRN Neurol. 2013;2013:370943. https://doi.org/10.1155/2013/370943 .
doi: 10.1155/2013/370943
pubmed: 23984093
pmcid: 3747490
Kenis G, Maes M. Effects of antidepressants on the production of cytokines. Int J Neuropsychopharmacol. 2002;5(4):401–12. https://doi.org/10.1017/S1461145702003164 .
doi: 10.1017/S1461145702003164
pubmed: 12466038
Mitsonis CI, Zervas IM, Potagas CM, Mitropoulos PA, Dimopoulos NP, Sfagos CA, et al. Effects of escitalopram on stress-related relapses in women with multiple sclerosis: an open-label, randomized, controlled, one-year follow-up study. Eur Neuropsychopharmacol. 2010;20(2):123–31. https://doi.org/10.1016/j.euroneuro.2009.10.004 .
doi: 10.1016/j.euroneuro.2009.10.004
pubmed: 19931427
Mostert JP, Admiraal-Behloul F, Hoogduin JM, Luyendijk J, Heersema DJ, van Buchem MA, et al. Effects of fluoxetine on disease activity in relapsing multiple sclerosis: a double-blind, placebo-controlled, exploratory study. J Neurol Neurosurg Psychiatry. 2008;79(9):1027–31. https://doi.org/10.1136/jnnp.2007.139345 .
doi: 10.1136/jnnp.2007.139345
pubmed: 18450787
Macrez R, Stys PK, Vivien D, Lipton SA, Docagne F. Mechanisms of glutamate toxicity in multiple sclerosis: biomarker and therapeutic opportunities. Lancet Neurol. 2016;15(10):1089–102. https://doi.org/10.1016/S1474-4422(16)30165-X .
doi: 10.1016/S1474-4422(16)30165-X
pubmed: 27571160
Pitt D, Werner P, Raine CS. Glutamate excitotoxicity in a model of multiple sclerosis. Nat Med. 2000;6(1):67–70. https://doi.org/10.1038/71555 .
doi: 10.1038/71555
pubmed: 10613826
Gilgun-Sherki Y, Panet H, Melamed E, Offen D. Riluzole suppresses experimental autoimmune encephalomyelitis: implications for the treatment of multiple sclerosis. Brain Res. 2003;989(2):196–204. https://doi.org/10.1016/s0006-8993(03)03343-2 .
doi: 10.1016/s0006-8993(03)03343-2
pubmed: 14556941
Bellingham MC. A review of the neural mechanisms of action and clinical efficiency of riluzole in treating amyotrophic lateral sclerosis: what have we learned in the last decade? CNS Neurosci Ther. 2011;17(1):4–31. https://doi.org/10.1111/j.1755-5949.2009.00116.x .
doi: 10.1111/j.1755-5949.2009.00116.x
pubmed: 20236142
pmcid: 6493865
Killestein J, Kalkers NF, Polman CH. Glutamate inhibition in MS: the neuroprotective properties of riluzole. J Neurol Sci. 2005;233(1–2):113–5. https://doi.org/10.1016/j.jns.2005.03.011 .
doi: 10.1016/j.jns.2005.03.011
pubmed: 15949499
Waubant E, Maghzi AH, Revirajan N, Spain R, Julian L, Mowry EM, et al. A randomized controlled phase II trial of riluzole in early multiple sclerosis. Ann Clin Transl Neurol. 2014;1(5):340–7. https://doi.org/10.1002/acn3.60 .
doi: 10.1002/acn3.60
pubmed: 25356404
pmcid: 4184685
Lovera JF, Frohman E, Brown TR, Bandari D, Nguyen L, Yadav V, et al. Memantine for cognitive impairment in multiple sclerosis: a randomized placebo-controlled trial. Mult Scler. 2010;16(6):715–23. https://doi.org/10.1177/1352458510367662 .
doi: 10.1177/1352458510367662
pubmed: 20483885
Jaber S, Polster BM. Idebenone and neuroprotection: antioxidant, pro-oxidant, or electron carrier? J Bioenerg Biomembr. 2015;47(1–2):111–8. https://doi.org/10.1007/s10863-014-9571-y .
doi: 10.1007/s10863-014-9571-y
pubmed: 25262284
Suno M, Nagaoka A. Inhibition of lipid peroxidation by a novel compound, idebenone (CV-2619). Jpn J Pharmacol. 1984;35(2):196–8. https://doi.org/10.1254/jjp.35.196 .
doi: 10.1254/jjp.35.196
pubmed: 6748380
Shirani A, Okuda DT, Stuve O. Therapeutic advances and future prospects in progressive forms of multiple sclerosis. Neurotherapeutics. 2016;13(1):58–69. https://doi.org/10.1007/s13311-015-0409-z .
doi: 10.1007/s13311-015-0409-z
pubmed: 26729332
pmcid: 4720678
Mordente A, Martorana GE, Minotti G, Giardina B. Antioxidant properties of 2,3-dimethoxy-5-methyl-6-(10-hydroxydecyl)-1,4-benzoquinone (idebenone). Chem Res Toxicol. 1998;11(1):54–63. https://doi.org/10.1021/tx970136j .
doi: 10.1021/tx970136j
pubmed: 9477226
Erb M, Hoffmann-Enger B, Deppe H, Soeberdt M, Haefeli RH, Rummey C, et al. Features of idebenone and related short-chain quinones that rescue ATP levels under conditions of impaired mitochondrial complex I. PLoS ONE. 2012;7(4):e36153. https://doi.org/10.1371/journal.pone.0036153 .
doi: 10.1371/journal.pone.0036153
pubmed: 22558363
pmcid: 3338594
Haefeli RH, Erb M, Gemperli AC, Robay D, Courdier Fruh I, Anklin C, et al. NQO1-dependent redox cycling of idebenone: effects on cellular redox potential and energy levels. PLoS ONE. 2011;6(3):e17963. https://doi.org/10.1371/journal.pone.0017963 .
doi: 10.1371/journal.pone.0017963
pubmed: 21483849
pmcid: 3069029
Yan A, Liu Z, Song L, Wang X, Zhang Y, Wu N, et al. Idebenone alleviates neuroinflammation and modulates microglial polarization in LPS-stimulated BV2 cells and MPTP-induced Parkinson’s disease mice. Front Cell Neurosci. 2018;12:529. https://doi.org/10.3389/fncel.2018.00529 .
doi: 10.3389/fncel.2018.00529
pubmed: 30687016
Kosa P, Wu T, Phillips J, Leinonen M, Masvekar R, Komori M, et al. Idebenone does not inhibit disability progression in primary progressive MS. Mult Scler Relat Disord. 2020;45:102434. https://doi.org/10.1016/j.msard.2020.102434 .
doi: 10.1016/j.msard.2020.102434
pubmed: 32784117
Weideman AM, Barbour C, Tapia-Maltos MA, Tran T, Jackson K, Kosa P, et al. New multiple sclerosis disease severity scale predicts future accumulation of disability. Front Neurol. 2017;8:598. https://doi.org/10.3389/fneur.2017.00598 .
doi: 10.3389/fneur.2017.00598
pubmed: 29176958
pmcid: 5686060
Idebenone for Primary Progressive Multiple Sclerosis. In: ClinicalTrials.gov Identifier: NCT01854359. Start: 2013. Accessed 3 Jun 2020.
Fiebiger SM, Bros H, Grobosch T, Janssen A, Chanvillard C, Paul F, et al. The antioxidant idebenone fails to prevent or attenuate chronic experimental autoimmune encephalomyelitis in the mouse. J Neuroimmunol. 2013;262(1–2):66–71. https://doi.org/10.1016/j.jneuroim.2013.07.002 .
doi: 10.1016/j.jneuroim.2013.07.002
pubmed: 23871488
King MS, Sharpley MS, Hirst J. Reduction of hydrophilic ubiquinones by the flavin in mitochondrial NADH:ubiquinone oxidoreductase (Complex I) and production of reactive oxygen species. Biochemistry. 2009;48(9):2053–62. https://doi.org/10.1021/bi802282h .
doi: 10.1021/bi802282h
pubmed: 19220002
Esposti MD, Ngo A, Ghelli A, Benelli B, Carelli V, McLennan H, et al. The interaction of Q analogs, particularly hydroxydecyl benzoquinone (idebenone), with the respiratory complexes of heart mitochondria. Arch Biochem Biophys. 1996;330(2):395–400. https://doi.org/10.1006/abbi.1996.0267 .
doi: 10.1006/abbi.1996.0267
pubmed: 8660670
Stringer JL, Gaikwad A, Gonzales BN, Long DJ Jr, Marks LM, Jaiswal AK. Presence and induction of the enzyme NAD(P)H: quinone oxidoreductase 1 in the central nervous system. J Comp Neurol. 2004;471(3):289–97. https://doi.org/10.1002/cne.20048 .
doi: 10.1002/cne.20048
pubmed: 14991562
Jaber SM, Ge SX, Milstein JL, VanRyzin JW, Waddell J, Polster BM. Idebenone has distinct effects on mitochondrial respiration in cortical astrocytes as compared to cortical neurons due to differential NQO1 activity. J Neurosci. 2020. https://doi.org/10.1523/JNEUROSCI.1632-17.2020 .
doi: 10.1523/JNEUROSCI.1632-17.2020
pubmed: 32350039
pmcid: 7275857
Sugawa M, Sakurai Y, Ishikawa-Ieda Y, Suzuki H, Asou H. Effects of erythropoietin on glial cell development; oligodendrocyte maturation and astrocyte proliferation. Neurosci Res. 2002;44(4):391–403. https://doi.org/10.1016/s0168-0102(02)00161-x .
doi: 10.1016/s0168-0102(02)00161-x
pubmed: 12445627
Bernaudin M, Bellail A, Marti HH, Yvon A, Vivien D, Duchatelle I, et al. Neurons and astrocytes express EPO mRNA: oxygen-sensing mechanisms that involve the redox-state of the brain. Glia. 2000;30(3):271–8.
doi: 10.1002/(SICI)1098-1136(200005)30:3<271::AID-GLIA6>3.0.CO;2-H
Hasselblatt M, Ehrenreich H, Siren AL. The brain erythropoietin system and its potential for therapeutic exploitation in brain disease. J Neurosurg Anesthesiol. 2006;18(2):132–8. https://doi.org/10.1097/00008506-200604000-00007 .
doi: 10.1097/00008506-200604000-00007
pubmed: 16628067
Brines M, Cerami A. Emerging biological roles for erythropoietin in the nervous system. Nat Rev Neurosci. 2005;6(6):484–94. https://doi.org/10.1038/nrn1687 .
doi: 10.1038/nrn1687
pubmed: 15928718
Kang SY, Kang JH, Choi JC, Lee JS, Lee CS, Shin T. Expression of erythropoietin in the spinal cord of lewis rats with experimental autoimmune encephalomyelitis. J Clin Neurol. 2009;5(1):39–45. https://doi.org/10.3988/jcn.2009.5.1.39 .
doi: 10.3988/jcn.2009.5.1.39
pubmed: 19513333
pmcid: 2686895
Savino C, Pedotti R, Baggi F, Ubiali F, Gallo B, Nava S, et al. Delayed administration of erythropoietin and its non-erythropoietic derivatives ameliorates chronic murine autoimmune encephalomyelitis. J Neuroimmunol. 2006;172(1–2):27–37. https://doi.org/10.1016/j.jneuroim.2005.10.016 .
doi: 10.1016/j.jneuroim.2005.10.016
pubmed: 16337691
Yuan R, Maeda Y, Li W, Lu W, Cook S, Dowling P. Erythropoietin: a potent inducer of peripheral immuno/inflammatory modulation in autoimmune EAE. PLoS ONE. 2008;3(4):e1924. https://doi.org/10.1371/journal.pone.0001924 .
doi: 10.1371/journal.pone.0001924
pubmed: 18382691
pmcid: 2271128
Diem R, Sattler MB, Merkler D, Demmer I, Maier K, Stadelmann C, et al. Combined therapy with methylprednisolone and erythropoietin in a model of multiple sclerosis. Brain. 2005;128(Pt 2):375–85. https://doi.org/10.1093/brain/awh365 .
doi: 10.1093/brain/awh365
pubmed: 15601662
Cho YK, Kim G, Park S, Sim JH, Won YJ, Hwang CH, et al. Erythropoietin promotes oligodendrogenesis and myelin repair following lysolecithin-induced injury in spinal cord slice culture. Biochem Biophys Res Commun. 2012;417(2):753–9. https://doi.org/10.1016/j.bbrc.2011.12.029 .
doi: 10.1016/j.bbrc.2011.12.029
pubmed: 22197819
Mirzaie J, Raoofi A, Jamalpoor Z, Nezhadi A, Golmohammadi R. Protective impacts of erythropoietin on myelinization of oligodendrocytes and schwann cells in CNS and PNS following cuprizone-induced multiple sclerosis- histology, molecular, and functional studies. J Chem Neuroanat. 2020;104:101750. https://doi.org/10.1016/j.jchemneu.2020.101750 .
doi: 10.1016/j.jchemneu.2020.101750
pubmed: 31954768
Zhang J, Li Y, Cui Y, Chen J, Lu M, Elias SB, et al. Erythropoietin treatment improves neurological functional recovery in EAE mice. Brain Res. 2005;1034(1–2):34–9. https://doi.org/10.1016/j.brainres.2004.11.036 .
doi: 10.1016/j.brainres.2004.11.036
pubmed: 15713257
Campana WM, Myers RR. Erythropoietin and erythropoietin receptors in the peripheral nervous system: changes after nerve injury. FASEB J. 2001;15(10):1804–6. https://doi.org/10.1096/fj.00-0857fje .
doi: 10.1096/fj.00-0857fje
pubmed: 11481236
Chattopadhyay A, Choudhury TD, Bandyopadhyay D, Datta AG. Protective effect of erythropoietin on the oxidative damage of erythrocyte membrane by hydroxyl radical. Biochem Pharmacol. 2000;59(4):419–25. https://doi.org/10.1016/s0006-2952(99)00277-4 .
doi: 10.1016/s0006-2952(99)00277-4
pubmed: 10644050
Siren AL, Fratelli M, Brines M, Goemans C, Casagrande S, Lewczuk P, et al. Erythropoietin prevents neuronal apoptosis after cerebral ischemia and metabolic stress. Proc Natl Acad Sci USA. 2001;98(7):4044–9. https://doi.org/10.1073/pnas.051606598 .
doi: 10.1073/pnas.051606598
pubmed: 11259643
pmcid: 31176
Ehrenreich H, Fischer B, Norra C, Schellenberger F, Stender N, Stiefel M, et al. Exploring recombinant human erythropoietin in chronic progressive multiple sclerosis. Brain. 2007;130(Pt 10):2577–88. https://doi.org/10.1093/brain/awm203 .
doi: 10.1093/brain/awm203
pubmed: 17728357
Creange A, Lefaucheur JP, Balleyguier MO, Galacteros F. Iron depletion induced by bloodletting and followed by rhEPO administration as a therapeutic strategy in progressive multiple sclerosis: a pilot, open-label study with neurophysiological measurements. Neurophysiol Clin. 2013;43(5–6):303–12. https://doi.org/10.1016/j.neucli.2013.09.004 .
doi: 10.1016/j.neucli.2013.09.004
pubmed: 24314757
Schreiber K, Magyari M, Sellebjerg F, Iversen P, Garde E, Madsen CG, et al. High-dose erythropoietin in patients with progressive multiple sclerosis: a randomized, placebo-controlled, phase 2 trial. Mult Scler. 2017;23(5):675–85. https://doi.org/10.1177/1352458516661048 .
doi: 10.1177/1352458516661048
pubmed: 27481206
Freeman JA, Hobart JC, Langdon DW, Thompson AJ. Clinical appropriateness: a key factor in outcome measure selection: the 36 item short form health survey in multiple sclerosis. J Neurol Neurosurg Psychiatry. 2000;68(2):150–6. https://doi.org/10.1136/jnnp.68.2.150 .
doi: 10.1136/jnnp.68.2.150
pubmed: 10644779
pmcid: 1736771
Najmi Varzaneh F, Najmi Varzaneh F, Azimi AR, Rezaei N, Sahraian MA. Efficacy of combination therapy with erythropoietin and methylprednisolone in clinical recovery of severe relapse in multiple sclerosis. Acta Neurol Belg. 2014;114(4):273–8. https://doi.org/10.1007/s13760-014-0286-y .
doi: 10.1007/s13760-014-0286-y
pubmed: 24604685
Suhs KW, Hein K, Sattler MB, Gorlitz A, Ciupka C, Scholz K, et al. A randomized, double-blind, phase 2 study of erythropoietin in optic neuritis. Ann Neurol. 2012;72(2):199–210. https://doi.org/10.1002/ana.23573 .
doi: 10.1002/ana.23573
pubmed: 22926853
Diem R, Molnar F, Beisse F, Gross N, Druschler K, Heinrich SP, et al. Treatment of optic neuritis with erythropoietin (TONE): a randomised, double-blind, placebo-controlled trial-study protocol. BMJ Open. 2016;6(3):e010956. https://doi.org/10.1136/bmjopen-2015-010956 .
doi: 10.1136/bmjopen-2015-010956
pubmed: 26932144
pmcid: 4785322
Pollock C, Johnson DW, Horl WH, Rossert J, Casadevall N, Schellekens H, et al. Pure red cell aplasia induced by erythropoiesis-stimulating agents. Clin J Am Soc Nephrol. 2008;3(1):193–9. https://doi.org/10.2215/CJN.02440607 .
doi: 10.2215/CJN.02440607
pubmed: 18178785
Yasuda Y, Fujita Y, Matsuo T, Koinuma S, Hara S, Tazaki A, et al. Erythropoietin regulates tumour growth of human malignancies. Carcinogenesis. 2003;24(6):1021–9. https://doi.org/10.1093/carcin/bgg060 .
doi: 10.1093/carcin/bgg060
pubmed: 12807756
Henke M, Laszig R, Rube C, Schafer U, Haase KD, Schilcher B, et al. Erythropoietin to treat head and neck cancer patients with anaemia undergoing radiotherapy: randomised, double-blind, placebo-controlled trial. Lancet. 2003;362(9392):1255–60. https://doi.org/10.1016/S0140-6736(03)14567-9 .
doi: 10.1016/S0140-6736(03)14567-9
pubmed: 14575968
Pajonk F, Weil A, Sommer A, Suwinski R, Henke M. The erythropoietin-receptor pathway modulates survival of cancer cells. Oncogene. 2004;23(55):8987–91. https://doi.org/10.1038/sj.onc.1208140 .
doi: 10.1038/sj.onc.1208140
pubmed: 15480420
Brines M, Grasso G, Fiordaliso F, Sfacteria A, Ghezzi P, Fratelli M, et al. Erythropoietin mediates tissue protection through an erythropoietin and common beta-subunit heteroreceptor. Proc Natl Acad Sci USA. 2004;101(41):14907–12. https://doi.org/10.1073/pnas.0406491101 .
doi: 10.1073/pnas.0406491101
pubmed: 15456912
pmcid: 522054
Yuan R, Wang B, Lu W, Maeda Y, Dowling P. A Distinct Region in erythropoietin that induces immuno/inflammatory modulation and tissue protection. Neurotherapeutics. 2015;12(4):850–61. https://doi.org/10.1007/s13311-015-0379-1 .
doi: 10.1007/s13311-015-0379-1
pubmed: 26271954
pmcid: 4604189
Magnetic Resonance Imaging Study of JM-4 in Multiple Sclerosis/Clinically Patients. In: ClinicalTrials.gov Identifier: NCT03887065. Start: 2019. Accessed 3 Jun 2020.
Paul PSL, Debruyne D, Bernard D, Mock DM, Defer GL. Pharmacokinetics and pharmacodynamics of MD1003 (high-dose biotin) in the treatment of progressive multiple sclerosis. Expert Opin Drug Metab Toxicol. 2016;12(3):327–44. https://doi.org/10.1517/17425255.2016.1136288 .
doi: 10.1517/17425255.2016.1136288
Mock DM. Biotin: from nutrition to therapeutics. J Nutr. 2017;147(8):1487–92. https://doi.org/10.3945/jn.116.238956 .
doi: 10.3945/jn.116.238956
pubmed: 28701385
pmcid: 5525106
Anagnostouli M, Livaniou E, Nyalala JO, Evangelatos G, Zournas C, Ithakissios DS, et al. Cerebrospinal fluid levels of biotin in various neurological disorders. Acta Neurol Scand. 1999;99(6):387–92. https://doi.org/10.1111/j.1600-0404.1999.tb07369.x .
doi: 10.1111/j.1600-0404.1999.tb07369.x
pubmed: 10577274
Wolf B, Grier RE, Allen RJ, Goodman SI, Kien CL. Biotinidase deficiency: the enzymatic defect in late-onset multiple carboxylase deficiency. Clin Chim Acta. 1983;131(3):273–81. https://doi.org/10.1016/0009-8981(83)90096-7 .
doi: 10.1016/0009-8981(83)90096-7
pubmed: 6883721
Wolf B. Biotinidase deficiency should be considered in individuals thought to have multiple sclerosis and related disorders. Mult Scler Relat Disord. 2019;28:26–30. https://doi.org/10.1016/j.msard.2018.11.030 .
doi: 10.1016/j.msard.2018.11.030
pubmed: 30551056
Tong L. Structure and function of biotin-dependent carboxylases. Cell Mol Life Sci. 2013;70(5):863–91. https://doi.org/10.1007/s00018-012-1096-0 .
doi: 10.1007/s00018-012-1096-0
pubmed: 22869039
Sedel F, Bernard D, Mock DM, Tourbah A. Targeting demyelination and virtual hypoxia with high-dose biotin as a treatment for progressive multiple sclerosis. Neuropharmacology. 2016;110(Pt B):644–53. https://doi.org/10.1016/j.neuropharm.2015.08.028 .
doi: 10.1016/j.neuropharm.2015.08.028
pubmed: 26327679
Rasband MN, Macklin WB. Chapter 10—myelin structure and biochemistry. In: Brady ST, Siegel GJ, Albers RW, Price DL, editors. Basic neurochemistry. 8th ed. New York: Academic Press; 2012. p. 180–99.
doi: 10.1016/B978-0-12-374947-5.00010-9
Sedel F, Papeix C, Bellanger A, Touitou V, Lebrun-Frenay C, Galanaud D, et al. High doses of biotin in chronic progressive multiple sclerosis: a pilot study. Mult Scler Relat Disord. 2015;4(2):159–69. https://doi.org/10.1016/j.msard.2015.01.005 .
doi: 10.1016/j.msard.2015.01.005
pubmed: 25787192
Tourbah A, Lebrun-Frenay C, Edan G, Clanet M, Papeix C, Vukusic S, et al. MD1003 (high-dose biotin) for the treatment of progressive multiple sclerosis: a randomised, double-blind, placebo-controlled study. Mult Scler. 2016;22(13):1719–31. https://doi.org/10.1177/1352458516667568 .
doi: 10.1177/1352458516667568
pubmed: 27589059
pmcid: 5098693
Cree BAC, Cutter G, Wolinsky JS, Freedman MS, Comi G, Giovannoni G, et al. Safety and efficacy of MD1003 (high-dose biotin) in patients with progressive multiple sclerosis (SPI2): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet Neurol. 2020;19(12):988–97. https://doi.org/10.1016/S1474-4422(20)30347-1 .
doi: 10.1016/S1474-4422(20)30347-1
pubmed: 33222767
Birnbaum G, Stulc J. High dose biotin as treatment for progressive multiple sclerosis. Mult Scler Relat Disord. 2017;18:141–3. https://doi.org/10.1016/j.msard.2017.09.030 .
doi: 10.1016/j.msard.2017.09.030
pubmed: 29141796
Couloume L, Barbin L, Leray E, Wiertlewski S, Le Page E, Kerbrat A, et al. High-dose biotin in progressive multiple sclerosis: a prospective study of 178 patients in routine clinical practice. Mult Scler. 2019. https://doi.org/10.1177/1352458519894713 .
doi: 10.1177/1352458519894713
pubmed: 31845825
Buonvicino D, Ranieri G, Pratesi S, Guasti D, Chiarugi A. Neuroimmunological characterization of a mouse model of primary progressive experimental autoimmune encephalomyelitis and effects of immunosuppressive or neuroprotective strategies on disease evolution. Exp Neurol. 2019;322:113065. https://doi.org/10.1016/j.expneurol.2019.113065 .
doi: 10.1016/j.expneurol.2019.113065
pubmed: 31536728
Tourbah A, Gout O, Vighetto A, Deburghgraeve V, Pelletier J, Papeix C, et al. MD1003 (High-Dose Pharmaceutical-Grade Biotin) for the treatment of chronic visual loss related to optic neuritis in multiple sclerosis: a randomized, double-blind, Placebo-Controlled Study. CNS Drugs. 2018;32(7):661–72. https://doi.org/10.1007/s40263-018-0528-2 .
doi: 10.1007/s40263-018-0528-2
pubmed: 29808469
pmcid: 6061426
Lebrun C, Cohen M, Mondot L, Ayrignac X, Labauge P. A case report of solitary sclerosis: this is really multiple sclerosis. Neurol Ther. 2017;6(2):259–63. https://doi.org/10.1007/s40120-017-0082-8 .
doi: 10.1007/s40120-017-0082-8
pubmed: 28840523
pmcid: 5700904
Demas A, Cochin JP, Hardy C, Vaschalde Y, Bourre B, Labauge P. Tardive reactivation of progressive multiple sclerosis during treatment with biotin. Neurol Ther. 2020;9(1):181–5. https://doi.org/10.1007/s40120-019-00175-2 .
doi: 10.1007/s40120-019-00175-2
pubmed: 31858407
Granella F, Curti E, Tsantes E, Siena E. Breakthrough disease under high-dose biotin treatment in progressive multiple sclerosis. ECTRIMS Online Libr. 2017;200405:P750.
Branger P, Parienti JJ, Derache N, Kassis N, Assouad R, Maillart E, et al. Relapses during high-dose biotin treatment in progressive multiple sclerosis: a case-crossover and propensity score-adjusted prospective cohort. Neurotherapeutics. 2020. https://doi.org/10.1007/s13311-020-00880-z .
doi: 10.1007/s13311-020-00880-z
pubmed: 32557122
Pignolet B, Ciron J, Bucciarelli F, Scandella L, Biotti D, Lerebours F, et al. Immunomodulation associated with clinical and MRI worsening in patients with progressive MS treated with MD1003 (high dose pharmaceutical grade biotin). ECTRIMS Online Libr. 2018;228721:P878.
Moisset X, Mathais S, Pereira B, Taithe F, Ciron J, Labauge P, et al. Incidence of relapses in patients with purified high dose biotin-treated progressive multiple sclerosis (IPBio-SeP study): a second intermediate analysis of a French, multicenter study. ECTRIMS Online Library. 2019;279034:P674.
Young W. Review of lithium effects on brain and blood. Cell Transplant. 2009;18(9):951–75. https://doi.org/10.3727/096368909X471251 .
doi: 10.3727/096368909X471251
pubmed: 19523343
De Sarno P, Axtell RC, Raman C, Roth KA, Alessi DR, Jope RS. Lithium prevents and ameliorates experimental autoimmune encephalomyelitis. J Immunol. 2008;181(1):338–45. https://doi.org/10.4049/jimmunol.181.1.338 .
doi: 10.4049/jimmunol.181.1.338
pubmed: 18566399
Ahn M, Kim J, Park C, Cho J, Jee Y, Jung K, et al. Potential involvement of glycogen synthase kinase (GSK)-3beta in a rat model of multiple sclerosis: evidenced by lithium treatment. Anat Cell Biol. 2017;50(1):48–59. https://doi.org/10.5115/acb.2017.50.1.48 .
doi: 10.5115/acb.2017.50.1.48
pubmed: 28417055
pmcid: 5386926
Rowse AL, Naves R, Cashman KS, McGuire DJ, Mbana T, Raman C, et al. Lithium controls central nervous system autoimmunity through modulation of IFN-gamma signaling. PLoS ONE. 2012;7(12):e52658. https://doi.org/10.1371/journal.pone.0052658 .
doi: 10.1371/journal.pone.0052658
pubmed: 23285134
pmcid: 3532311
Beurel E, Yeh WI, Michalek SM, Harrington LE, Jope RS. Glycogen synthase kinase-3 is an early determinant in the differentiation of pathogenic Th17 cells. J Immunol. 2011;186(3):1391–8. https://doi.org/10.4049/jimmunol.1003511 .
doi: 10.4049/jimmunol.1003511
pubmed: 21191064
Li W, Li R, Zhao S, Jiang C, Liu Z, Tang X. Lithium posttreatment alleviates blood-brain barrier injury after intracerebral hemorrhage in rats. Neuroscience. 2018;383:129–37. https://doi.org/10.1016/j.neuroscience.2018.05.001 .
doi: 10.1016/j.neuroscience.2018.05.001
pubmed: 29775701
Karimi A, Bahrampour K, Momeni Moghaddam MA, Asadikaram G, Ebrahimi G, Torkzadeh-Mahani M, et al. Evaluation of lithium serum level in multiple sclerosis patients: a neuroprotective element. Mult Scler Relat Disord. 2017;17:244–8. https://doi.org/10.1016/j.msard.2017.08.019 .
doi: 10.1016/j.msard.2017.08.019
pubmed: 29055468
Booth DR, Arthur AT, Teutsch SM, Bye C, Rubio J, Armati PJ, et al. Gene expression and genotyping studies implicate the interleukin 7 receptor in the pathogenesis of primary progressive multiple sclerosis. J Mol Med (Berl). 2005;83(10):822–30. https://doi.org/10.1007/s00109-005-0684-y .
doi: 10.1007/s00109-005-0684-y
pubmed: 16075257
Rinker JR 2nd, Meador WR, King P. Randomized feasibility trial to assess tolerance and clinical effects of lithium in progressive multiple sclerosis. Heliyon. 2020;6(7):e04528. https://doi.org/10.1016/j.heliyon.2020.e04528 .
doi: 10.1016/j.heliyon.2020.e04528
pubmed: 32760832
pmcid: 7393418
Vickrey BG, Hays RD, Harooni R, Myers LW, Ellison GW. A health-related quality of life measure for multiple sclerosis. Qual Life Res. 1995;4(3):187–206. https://doi.org/10.1007/BF02260859 .
doi: 10.1007/BF02260859
pubmed: 7613530
Fancy SP, Baranzini SE, Zhao C, Yuk DI, Irvine KA, Kaing S, et al. Dysregulation of the Wnt pathway inhibits timely myelination and remyelination in the mammalian CNS. Genes Dev. 2009;23(13):1571–85. https://doi.org/10.1101/gad.1806309 .
doi: 10.1101/gad.1806309
pubmed: 19515974
pmcid: 2704469
Ouyang S, Zeng Q, Tang N, Guo H, Tang R, Yin W, et al. Akt-1 and Akt-2 differentially regulate the development of experimental autoimmune encephalomyelitis by controlling proliferation of thymus-derived regulatory T cells. J Immunol. 2019;202(5):1441–52. https://doi.org/10.4049/jimmunol.1701204 .
doi: 10.4049/jimmunol.1701204
pubmed: 30692211
Rinker JR 2nd, Cossey TC, Cutter GR, Culpepper WJ. A retrospective review of lithium usage in veterans with multiple sclerosis. Mult Scler Relat Disord. 2013;2(4):327–33. https://doi.org/10.1016/j.msard.2013.03.004 .
doi: 10.1016/j.msard.2013.03.004
pubmed: 25877842
Wiendl H, Hohlfeld R. Therapeutic approaches in multiple sclerosis: lessons from failed and interrupted treatment trials. BioDrugs. 2002;16(3):183–200. https://doi.org/10.2165/00063030-200216030-00003 .
doi: 10.2165/00063030-200216030-00003
pubmed: 12102646
Meuth SG, Bittner S, Ulzheimer JC, Kleinschnitz C, Kieseier BC, Wiendl H. Therapeutic approaches to multiple sclerosis: an update on failed, interrupted, or inconclusive trials of neuroprotective and alternative treatment strategies. BioDrugs. 2010;24(5):317–30. https://doi.org/10.2165/11537190-000000000-00000 .
doi: 10.2165/11537190-000000000-00000
pubmed: 20795753
Ulzheimer JC, Meuth SG, Bittner S, Kleinschnitz C, Kieseier BC, Wiendl H. Therapeutic approaches to multiple sclerosis: an update on failed, interrupted, or inconclusive trials of immunomodulatory treatment strategies. BioDrugs. 2010;24(4):249–74. https://doi.org/10.2165/11537160-000000000-00000 .
doi: 10.2165/11537160-000000000-00000
pubmed: 20623991
Pfeuffer S, Ruck T, Kleinschnitz C, Wiendl H, Meuth SG. Failed, interrupted and inconclusive trials on relapsing multiple sclerosis treatment: update 2010–2015. Expert Rev Neurother. 2016;16(6):689–700. https://doi.org/10.1080/14737175.2016.1176531 .
doi: 10.1080/14737175.2016.1176531
pubmed: 27058174
Wooliscroft L, Silbermann E, Cameron M, Bourdette D. Approaches to remyelination therapies in multiple sclerosis. Curr Treat Options Neurol. 2019;21(7):34. https://doi.org/10.1007/s11940-019-0574-1 .
doi: 10.1007/s11940-019-0574-1
pubmed: 31250211
Jensen SK, Michaels NJ, Ilyntskyy S, Keough MB, Kovalchuk O, Yong VW. Multimodal enhancement of remyelination by exercise with a pivotal role for oligodendroglial PGC1alpha. Cell Rep. 2018;24(12):3167–79. https://doi.org/10.1016/j.celrep.2018.08.060 .
doi: 10.1016/j.celrep.2018.08.060
pubmed: 30232000
Yednock TA, Cannon C, Fritz LC, Sanchez-Madrid F, Steinman L, Karin N. Prevention of experimental autoimmune encephalomyelitis by antibodies against alpha 4 beta 1 integrin. Nature. 1992;356(6364):63–6. https://doi.org/10.1038/356063a0 .
doi: 10.1038/356063a0
pubmed: 1538783
Polman CH, O’Connor PW, Havrdova E, Hutchinson M, Kappos L, Miller DH, et al. A randomized, placebo-controlled trial of natalizumab for relapsing multiple sclerosis. N Engl J Med. 2006;354(9):899–910. https://doi.org/10.1056/NEJMoa044397 .
doi: 10.1056/NEJMoa044397
pubmed: 16510744
Hall SM. The effect of injections of lysophosphatidyl choline into white matter of the adult mouse spinal cord. J Cell Sci. 1972;10(2):535–46.
doi: 10.1242/jcs.10.2.535
Plemel JR, Liu WQ, Yong VW. Remyelination therapies: a new direction and challenge in multiple sclerosis. Nat Rev Drug Discov. 2017;16(9):617–34. https://doi.org/10.1038/nrd.2017.115 .
doi: 10.1038/nrd.2017.115
pubmed: 28685761
Basso AS, Frenkel D, Quintana FJ, Costa-Pinto FA, Petrovic-Stojkovic S, Puckett L, et al. Reversal of axonal loss and disability in a mouse model of progressive multiple sclerosis. J Clin Invest. 2008;118(4):1532–43. https://doi.org/10.1172/JCI33464 .
doi: 10.1172/JCI33464
pubmed: 18340379
pmcid: 2267014
Constantinescu CS, Farooqi N, O’Brien K, Gran B. Experimental autoimmune encephalomyelitis (EAE) as a model for multiple sclerosis (MS). Br J Pharmacol. 2011;164(4):1079–106. https://doi.org/10.1111/j.1476-5381.2011.01302.x .
doi: 10.1111/j.1476-5381.2011.01302.x
pubmed: 21371012
pmcid: 3229753
Llovera G, Liesz A. The next step in translational research: lessons learned from the first preclinical randomized controlled trial. J Neurochem. 2016;139(Suppl 2):271–9. https://doi.org/10.1111/jnc.13516 .
doi: 10.1111/jnc.13516
pubmed: 26968835
Schmierer K, Scaravilli F, Altmann DR, Barker GJ, Miller DH. Magnetization transfer ratio and myelin in postmortem multiple sclerosis brain. Ann Neurol. 2004;56(3):407–15. https://doi.org/10.1002/ana.20202 .
doi: 10.1002/ana.20202
pubmed: 15349868
Cerina M, Muthuraman M, Gallus M, Koirala N, Dik A, Wachsmuth L, et al. Myelination- and immune-mediated MR-based brain network correlates. J Neuroinflamm. 2020;17(1):186. https://doi.org/10.1186/s12974-020-01827-z .
doi: 10.1186/s12974-020-01827-z
Bodini B, Veronese M, Garcia-Lorenzo D, Battaglini M, Poirion E, Chardain A, et al. Dynamic imaging of individual remyelination profiles in multiple sclerosis. Ann Neurol. 2016;79(5):726–38. https://doi.org/10.1002/ana.24620 .
doi: 10.1002/ana.24620
pubmed: 26891452
pmcid: 5006855
Gingele S, Stangel M. Emerging myelin repair agents in preclinical and early clinical development for the treatment of multiple sclerosis. Expert Opin Investig Drugs. 2020. https://doi.org/10.1080/13543784.2020.1762567 .
doi: 10.1080/13543784.2020.1762567
pubmed: 32348161
Klistorner A, Fraser C, Garrick R, Graham S, Arvind H. Correlation between full-field and multifocal VEPs in optic neuritis. Doc Ophthalmol. 2008;116(1):19–27. https://doi.org/10.1007/s10633-007-9072-y .
doi: 10.1007/s10633-007-9072-y
pubmed: 17680288
Varhaug KN, Torkildsen O, Myhr KM, Vedeler CA. Neurofilament light chain as a biomarker in multiple sclerosis. Front Neurol. 2019;10:338. https://doi.org/10.3389/fneur.2019.00338 .
doi: 10.3389/fneur.2019.00338
pubmed: 31024432
pmcid: 6460359
Thebault S, Abdoli M, Fereshtehnejad SM, Tessier D, Tabard-Cossa V, Freedman MS. Serum neurofilament light chain predicts long term clinical outcomes in multiple sclerosis. Sci Rep. 2020;10(1):10381. https://doi.org/10.1038/s41598-020-67504-6 .
doi: 10.1038/s41598-020-67504-6
pubmed: 32587320
pmcid: 7316736
Bittner S, Steffen F, Uphaus T, Muthuraman M, Fleischer V, Salmen A, et al. Clinical implications of serum neurofilament in newly diagnosed MS patients: a longitudinal multicentre cohort study. EBioMedicine. 2020;56:102807. https://doi.org/10.1016/j.ebiom.2020.102807 .
doi: 10.1016/j.ebiom.2020.102807
pubmed: 32460167
pmcid: 7251380