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Dynamic muscle paralytic effects of a novel botulinum toxin A free of neurotoxin‐associated proteins

Structurally, botulinum toxin type A (BTX‐A) is composed of neurotoxin and nontoxic complexing proteins (CPs), and the neurotoxin has the function of blocking acetylcholine release from the neuromuscular junction and therefore paralyzing muscles. Nowadays, a novel botulinum toxin A free of CPs (chin...

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Autores principales: Liu, Wu‐chao, Su, Jun‐hui, Feng, Ya, Xiang, Xue‐rui, Pan, Li‐zhen, Liu, Ying, Ma, Lin, Nie, Zhi‐yu, Zhang, Xue‐ping, Jin, Ling‐jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051373/
https://www.ncbi.nlm.nih.gov/pubmed/35484714
http://dx.doi.org/10.1002/prp2.955
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author Liu, Wu‐chao
Su, Jun‐hui
Feng, Ya
Xiang, Xue‐rui
Pan, Li‐zhen
Liu, Ying
Ma, Lin
Nie, Zhi‐yu
Zhang, Xue‐ping
Jin, Ling‐jing
author_facet Liu, Wu‐chao
Su, Jun‐hui
Feng, Ya
Xiang, Xue‐rui
Pan, Li‐zhen
Liu, Ying
Ma, Lin
Nie, Zhi‐yu
Zhang, Xue‐ping
Jin, Ling‐jing
author_sort Liu, Wu‐chao
collection PubMed
description Structurally, botulinum toxin type A (BTX‐A) is composed of neurotoxin and nontoxic complexing proteins (CPs), and the neurotoxin has the function of blocking acetylcholine release from the neuromuscular junction and therefore paralyzing muscles. Nowadays, a novel botulinum toxin A free of CPs (chinbotulinumtoxin A, A/Chin) is produced, and the present study comprehensively evaluated the dynamic paralytic effect of A/Chin on the gastrocnemius muscle of rats. Different doses (0.01, 0.1, 0.5, 1, 2, and 4 U) of A/Chin and other BTX‐As with and without CPs were administered to the gastrocnemius muscles of rats and muscle strength was measured and compared at different postinjection timepoints (from day 0 to 84). With the dose increased, time‐to‐peak paralytic effect of other BTX‐As varied from day 3 to day 14, while A/Chin groups showed rapid and steady time to peak on day 3. At the lowest dose of 0.01 U, A/Chin showed significantly better peak paralytic effect than the others on day 3. When the dose increased to 0.5 U and more, A/Chin group also showed significant paralytic effect when the paralytic effect of other BTX‐As was worn off. Moreover, the paralytic effect of A/Chin was confirmed as muscle atrophy while hematoxylin–eosin staining was performed. In conclusion, compared with other BTX‐As, A/Chin showed rapid and steady time‐to‐peak paralytic effect and long‐term paralytic efficacy at the same dose level. And it might lay a solid foundation for further wide application of A/Chin in both clinical and cosmetic areas.
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spelling pubmed-90513732022-05-02 Dynamic muscle paralytic effects of a novel botulinum toxin A free of neurotoxin‐associated proteins Liu, Wu‐chao Su, Jun‐hui Feng, Ya Xiang, Xue‐rui Pan, Li‐zhen Liu, Ying Ma, Lin Nie, Zhi‐yu Zhang, Xue‐ping Jin, Ling‐jing Pharmacol Res Perspect Original Articles Structurally, botulinum toxin type A (BTX‐A) is composed of neurotoxin and nontoxic complexing proteins (CPs), and the neurotoxin has the function of blocking acetylcholine release from the neuromuscular junction and therefore paralyzing muscles. Nowadays, a novel botulinum toxin A free of CPs (chinbotulinumtoxin A, A/Chin) is produced, and the present study comprehensively evaluated the dynamic paralytic effect of A/Chin on the gastrocnemius muscle of rats. Different doses (0.01, 0.1, 0.5, 1, 2, and 4 U) of A/Chin and other BTX‐As with and without CPs were administered to the gastrocnemius muscles of rats and muscle strength was measured and compared at different postinjection timepoints (from day 0 to 84). With the dose increased, time‐to‐peak paralytic effect of other BTX‐As varied from day 3 to day 14, while A/Chin groups showed rapid and steady time to peak on day 3. At the lowest dose of 0.01 U, A/Chin showed significantly better peak paralytic effect than the others on day 3. When the dose increased to 0.5 U and more, A/Chin group also showed significant paralytic effect when the paralytic effect of other BTX‐As was worn off. Moreover, the paralytic effect of A/Chin was confirmed as muscle atrophy while hematoxylin–eosin staining was performed. In conclusion, compared with other BTX‐As, A/Chin showed rapid and steady time‐to‐peak paralytic effect and long‐term paralytic efficacy at the same dose level. And it might lay a solid foundation for further wide application of A/Chin in both clinical and cosmetic areas. John Wiley and Sons Inc. 2022-04-28 /pmc/articles/PMC9051373/ /pubmed/35484714 http://dx.doi.org/10.1002/prp2.955 Text en © 2022 The Authors. Pharmacology Research & Perspectives published by John Wiley & Sons Ltd, British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Liu, Wu‐chao
Su, Jun‐hui
Feng, Ya
Xiang, Xue‐rui
Pan, Li‐zhen
Liu, Ying
Ma, Lin
Nie, Zhi‐yu
Zhang, Xue‐ping
Jin, Ling‐jing
Dynamic muscle paralytic effects of a novel botulinum toxin A free of neurotoxin‐associated proteins
title Dynamic muscle paralytic effects of a novel botulinum toxin A free of neurotoxin‐associated proteins
title_full Dynamic muscle paralytic effects of a novel botulinum toxin A free of neurotoxin‐associated proteins
title_fullStr Dynamic muscle paralytic effects of a novel botulinum toxin A free of neurotoxin‐associated proteins
title_full_unstemmed Dynamic muscle paralytic effects of a novel botulinum toxin A free of neurotoxin‐associated proteins
title_short Dynamic muscle paralytic effects of a novel botulinum toxin A free of neurotoxin‐associated proteins
title_sort dynamic muscle paralytic effects of a novel botulinum toxin a free of neurotoxin‐associated proteins
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9051373/
https://www.ncbi.nlm.nih.gov/pubmed/35484714
http://dx.doi.org/10.1002/prp2.955
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