Efficacy of Ciprofloxacin/Celecoxib combination in zebrafish models of amyotrophic lateral sclerosis
Author
Goldshtein, HagitMuhire, Alexandre
Petel Legare, Virginie
Pushett, Avital
Rotkopf, Ron
Shefner, Jeremy M.
Peterson, Randall T.
Armstrong, Gary A. B.
Russek-Blum, Niva
Affiliation
Univ Arizona, Barrow Neurol InstIssue Date
2020-09
Metadata
Show full item recordPublisher
WILEYCitation
Goldshtein, H., Muhire, A., Petel Legare, V., Pushett, A., Rotkopf, R., Shefner, J. M., ... & Russek‐Blum, N. (2020). Efficacy of Ciprofloxacin/Celecoxib combination in zebrafish models of amyotrophic lateral sclerosis. Annals of clinical and translational neurology, 7(10), 1883-1897.Rights
© 2020 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Objective: To evaluate the efficacy of a fixed-dose combination of two approved drugs, Ciprofloxacin and Celecoxib, as a potential therapeutic treatment for amyotrophic lateral sclerosis (ALS). Methods: Toxicity and efficacy of Ciprofloxacin and Celecoxib were tested, each alone and in distinct ratio combinations in SOD1 G93R transgenic zebrafish model for ALS. Quantification of swimming measures following stimuli, measurements of axonal projections from the spinal cord, neuromuscular junction structure and morphometric analysis of microglia cells were performed in the combination- treatedvsnontreated mutant larvae. Additionally, quantifications of touch-evoked locomotor escape response were conducted in treatedvsnontreated zebrafish expressing theTARDBPG348C ALS variant. Results: When administered individually, Ciprofloxacin had a mild effect and Celecoxib had no therapeutic effect. However, combined Ciprofloxacin and Celecoxib (Cipro/Celecox) treatment caused a significant increase of similar to 84% in the distance the SOD1 G93R transgenic larvae swam. Additionally, Cipro/Celecox elicited recovery of impaired motor neurons morphology and abnormal neuromuscular junction structure and preserved the ramified morphology of microglia cells in the SOD1 mutants. Furthermore, larvae expressing the TDP-43 mutation displayed evoked touch responses that were significantly longer in swim distance (110% increase) and significantly higher in maximal swim velocity (similar to 44% increase) when treated with Cipro/Celecox combination. Interpretation: Cipro/Celecox combination improved locomotor and cellular deficits of ALS zebrafish models. These results identify this novel combination as effective, and may prove promising for the treatment of ALS.Note
Open access journalISSN
2328-9503PubMed ID
32915525Version
Final published versionae974a485f413a2113503eed53cd6c53
10.1002/acn3.51174
Scopus Count
Collections
Except where otherwise noted, this item's license is described as © 2020 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association. This is an open access article under the terms of the Creative Commons Attribution License.
Related articles
- A genetic model of amyotrophic lateral sclerosis in zebrafish displays phenotypic hallmarks of motoneuron disease.
- Authors: Ramesh T, Lyon AN, Pineda RH, Wang C, Janssen PM, Canan BD, Burghes AH, Beattie CE
- Issue date: 2010 Sep-Oct
- Early interneuron dysfunction in ALS: insights from a mutant sod1 zebrafish model.
- Authors: McGown A, McDearmid JR, Panagiotaki N, Tong H, Al Mashhadi S, Redhead N, Lyon AN, Beattie CE, Shaw PJ, Ramesh TM
- Issue date: 2013 Feb
- The Novel Small Molecule TRVA242 Stabilizes Neuromuscular Junction Defects in Multiple Animal Models of Amyotrophic Lateral Sclerosis.
- Authors: Bose P, Tremblay E, Maios C, Narasimhan V, Armstrong GAB, Liao M, Parker JA, Robitaille R, Wen XY, Barden C, Drapeau P
- Issue date: 2019 Oct
- Neuromuscular effects of G93A-SOD1 expression in zebrafish.
- Authors: Sakowski SA, Lunn JS, Busta AS, Oh SS, Zamora-Berridi G, Palmer M, Rosenberg AA, Philip SG, Dowling JJ, Feldman EL
- Issue date: 2012 Aug 31
- INaP selective inhibition reverts precocious inter- and motorneurons hyperexcitability in the Sod1-G93R zebrafish ALS model.
- Authors: Benedetti L, Ghilardi A, Rottoli E, De Maglie M, Prosperi L, Perego C, Baruscotti M, Bucchi A, Del Giacco L, Francolini M
- Issue date: 2016 Apr 15

