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Therapeutic effects of Tetanus neurotoxin in spinal cord injury: a case series on four dogs

STUDY DESIGN: Case series on four dogs. OBJECTIVES: To determine the alleviation of motor symptoms in spinal cord injury (SCI) by tetanus neurotoxin (TeNT). SETTING: Different Berlin veterinary clinics, Germany. METHODS: We report on the effect of intramuscular injections of low-dose TeNT into paret...

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Autores principales: Hesse, Stefan, Kutschenko, Anna, Bryl, Beatrice, Deutschland, Martin, Liebetanz, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026047/
https://www.ncbi.nlm.nih.gov/pubmed/32066656
http://dx.doi.org/10.1038/s41394-020-0258-9
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author Hesse, Stefan
Kutschenko, Anna
Bryl, Beatrice
Deutschland, Martin
Liebetanz, David
author_facet Hesse, Stefan
Kutschenko, Anna
Bryl, Beatrice
Deutschland, Martin
Liebetanz, David
author_sort Hesse, Stefan
collection PubMed
description STUDY DESIGN: Case series on four dogs. OBJECTIVES: To determine the alleviation of motor symptoms in spinal cord injury (SCI) by tetanus neurotoxin (TeNT). SETTING: Different Berlin veterinary clinics, Germany. METHODS: We report on the effect of intramuscular injections of low-dose TeNT into paretic hind limb muscles 2–157 weeks after SCI due to lumbar disc herniation in a clinical case series on four dogs. All dogs underwent unsuccessful or incomplete surgical decompression prior to TeNT treatment. TeNT was injected on a compassionate basis. Stance, gait ability and the diameter of the rectus femoris muscle were assessed as parameters. RESULTS: All four dogs improved their stance and three of these dogs improved in gait at 4 and 6 weeks after TeNT injections without evidence of side effects or spreading of TeNT effects. At the same time, the size of the rectus femoris muscle diameter increased considerably as compared with baseline (baseline: 100%; 4 weeks: 148.7% ± 10.9%; 6 weeks: 137.1% ± 7.9%). CONCLUSIONS: Facilitation of α-motor neurons by TeNT injections into paretic hind limb muscles of four dogs improved standing and/or gait abilities and partly reversed muscle atrophy after SCI. The absence of generalized or painful muscle spasms supports the safety of low-dose TeNT. Therefore, TeNT might evolve as a promising therapeutic option for muscle paresis of central origin, e.g. in individuals with SCI, stroke or multiple sclerosis.
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spelling pubmed-70260472020-03-03 Therapeutic effects of Tetanus neurotoxin in spinal cord injury: a case series on four dogs Hesse, Stefan Kutschenko, Anna Bryl, Beatrice Deutschland, Martin Liebetanz, David Spinal Cord Ser Cases Article STUDY DESIGN: Case series on four dogs. OBJECTIVES: To determine the alleviation of motor symptoms in spinal cord injury (SCI) by tetanus neurotoxin (TeNT). SETTING: Different Berlin veterinary clinics, Germany. METHODS: We report on the effect of intramuscular injections of low-dose TeNT into paretic hind limb muscles 2–157 weeks after SCI due to lumbar disc herniation in a clinical case series on four dogs. All dogs underwent unsuccessful or incomplete surgical decompression prior to TeNT treatment. TeNT was injected on a compassionate basis. Stance, gait ability and the diameter of the rectus femoris muscle were assessed as parameters. RESULTS: All four dogs improved their stance and three of these dogs improved in gait at 4 and 6 weeks after TeNT injections without evidence of side effects or spreading of TeNT effects. At the same time, the size of the rectus femoris muscle diameter increased considerably as compared with baseline (baseline: 100%; 4 weeks: 148.7% ± 10.9%; 6 weeks: 137.1% ± 7.9%). CONCLUSIONS: Facilitation of α-motor neurons by TeNT injections into paretic hind limb muscles of four dogs improved standing and/or gait abilities and partly reversed muscle atrophy after SCI. The absence of generalized or painful muscle spasms supports the safety of low-dose TeNT. Therefore, TeNT might evolve as a promising therapeutic option for muscle paresis of central origin, e.g. in individuals with SCI, stroke or multiple sclerosis. Nature Publishing Group UK 2020-02-17 /pmc/articles/PMC7026047/ /pubmed/32066656 http://dx.doi.org/10.1038/s41394-020-0258-9 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hesse, Stefan
Kutschenko, Anna
Bryl, Beatrice
Deutschland, Martin
Liebetanz, David
Therapeutic effects of Tetanus neurotoxin in spinal cord injury: a case series on four dogs
title Therapeutic effects of Tetanus neurotoxin in spinal cord injury: a case series on four dogs
title_full Therapeutic effects of Tetanus neurotoxin in spinal cord injury: a case series on four dogs
title_fullStr Therapeutic effects of Tetanus neurotoxin in spinal cord injury: a case series on four dogs
title_full_unstemmed Therapeutic effects of Tetanus neurotoxin in spinal cord injury: a case series on four dogs
title_short Therapeutic effects of Tetanus neurotoxin in spinal cord injury: a case series on four dogs
title_sort therapeutic effects of tetanus neurotoxin in spinal cord injury: a case series on four dogs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7026047/
https://www.ncbi.nlm.nih.gov/pubmed/32066656
http://dx.doi.org/10.1038/s41394-020-0258-9
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