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Delayed Azithromycin Treatment Improves Recovery After Mouse Spinal Cord Injury

After spinal cord injury (SCI), macrophages infiltrate into the lesion and can adopt a wide spectrum of activation states. However, the pro-inflammatory, pathological macrophage activation state predominates and contributes to progressive neurodegeneration. Azithromycin (AZM), an FDA approved macrol...

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Autores principales: Kopper, Timothy J., McFarlane, Katelyn E., Bailey, William M., Orr, Michael B., Zhang, Bei, Gensel, John C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851268/
https://www.ncbi.nlm.nih.gov/pubmed/31780896
http://dx.doi.org/10.3389/fncel.2019.00490
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author Kopper, Timothy J.
McFarlane, Katelyn E.
Bailey, William M.
Orr, Michael B.
Zhang, Bei
Gensel, John C.
author_facet Kopper, Timothy J.
McFarlane, Katelyn E.
Bailey, William M.
Orr, Michael B.
Zhang, Bei
Gensel, John C.
author_sort Kopper, Timothy J.
collection PubMed
description After spinal cord injury (SCI), macrophages infiltrate into the lesion and can adopt a wide spectrum of activation states. However, the pro-inflammatory, pathological macrophage activation state predominates and contributes to progressive neurodegeneration. Azithromycin (AZM), an FDA approved macrolide antibiotic, has been demonstrated to have immunomodulatory properties in a variety of inflammatory conditions. Indeed, we previously observed that post-SCI AZM treatment reduces pro-inflammatory macrophage activation. Further, a combined pre- and post-injury treatment paradigm improved functional recovery from SCI. Therefore, for the current study, we hypothesize that post-injury AZM treatment will improve recovery from SCI. To test this hypothesis, we examined the therapeutic potential of delayed AZM treatment on locomotor, sensory, and anatomical recovery. We administered AZM beginning 30-min, 3-h, or 24-h following contusion SCI in female mice, and then daily for 7 days. AZM administration beginning 30-min and 3-h post-injury improved locomotor recovery with increased stepping function relative to vehicle controls. Further, delaying treatment for 30-min after SCI significantly reduced lesion pathology. Initiating AZM treatment 24-h post-injury was not therapeutically effective. Regardless of the timing of the initial treatment, AZM did not statistically reduce the development of neuropathic pain (mechanical allodynia) nor increase neuron survival. Collectively, these results add to a growing body of evidence supporting AZM’s translational potential as a therapeutic agent for SCI and other neuroinflammatory conditions in which patients currently have very few options.
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spelling pubmed-68512682019-11-28 Delayed Azithromycin Treatment Improves Recovery After Mouse Spinal Cord Injury Kopper, Timothy J. McFarlane, Katelyn E. Bailey, William M. Orr, Michael B. Zhang, Bei Gensel, John C. Front Cell Neurosci Cellular Neuroscience After spinal cord injury (SCI), macrophages infiltrate into the lesion and can adopt a wide spectrum of activation states. However, the pro-inflammatory, pathological macrophage activation state predominates and contributes to progressive neurodegeneration. Azithromycin (AZM), an FDA approved macrolide antibiotic, has been demonstrated to have immunomodulatory properties in a variety of inflammatory conditions. Indeed, we previously observed that post-SCI AZM treatment reduces pro-inflammatory macrophage activation. Further, a combined pre- and post-injury treatment paradigm improved functional recovery from SCI. Therefore, for the current study, we hypothesize that post-injury AZM treatment will improve recovery from SCI. To test this hypothesis, we examined the therapeutic potential of delayed AZM treatment on locomotor, sensory, and anatomical recovery. We administered AZM beginning 30-min, 3-h, or 24-h following contusion SCI in female mice, and then daily for 7 days. AZM administration beginning 30-min and 3-h post-injury improved locomotor recovery with increased stepping function relative to vehicle controls. Further, delaying treatment for 30-min after SCI significantly reduced lesion pathology. Initiating AZM treatment 24-h post-injury was not therapeutically effective. Regardless of the timing of the initial treatment, AZM did not statistically reduce the development of neuropathic pain (mechanical allodynia) nor increase neuron survival. Collectively, these results add to a growing body of evidence supporting AZM’s translational potential as a therapeutic agent for SCI and other neuroinflammatory conditions in which patients currently have very few options. Frontiers Media S.A. 2019-11-06 /pmc/articles/PMC6851268/ /pubmed/31780896 http://dx.doi.org/10.3389/fncel.2019.00490 Text en Copyright © 2019 Kopper, McFarlane, Bailey, Orr, Zhang and Gensel. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular Neuroscience
Kopper, Timothy J.
McFarlane, Katelyn E.
Bailey, William M.
Orr, Michael B.
Zhang, Bei
Gensel, John C.
Delayed Azithromycin Treatment Improves Recovery After Mouse Spinal Cord Injury
title Delayed Azithromycin Treatment Improves Recovery After Mouse Spinal Cord Injury
title_full Delayed Azithromycin Treatment Improves Recovery After Mouse Spinal Cord Injury
title_fullStr Delayed Azithromycin Treatment Improves Recovery After Mouse Spinal Cord Injury
title_full_unstemmed Delayed Azithromycin Treatment Improves Recovery After Mouse Spinal Cord Injury
title_short Delayed Azithromycin Treatment Improves Recovery After Mouse Spinal Cord Injury
title_sort delayed azithromycin treatment improves recovery after mouse spinal cord injury
topic Cellular Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6851268/
https://www.ncbi.nlm.nih.gov/pubmed/31780896
http://dx.doi.org/10.3389/fncel.2019.00490
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