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Nimodipine Promotes Functional Recovery After Spinal Cord Injury in Rats

Spinal cord injury (SCI) is a devastating condition that results in severe motor, sensory, and autonomic dysfunction. The L-/T-type calcium channel blocker nimodipine (NMD) exerts a protective effect on neuronal injury; however, the protective effects of long-term administration of NMD in subjects w...

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Autores principales: Guo, Fangliang, Zheng, Xiaolong, He, Ziyu, Zhang, Ruoying, Zhang, Song, Wang, Minghuan, Chen, Hong, Wang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8477750/
https://www.ncbi.nlm.nih.gov/pubmed/34594224
http://dx.doi.org/10.3389/fphar.2021.733420
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author Guo, Fangliang
Zheng, Xiaolong
He, Ziyu
Zhang, Ruoying
Zhang, Song
Wang, Minghuan
Chen, Hong
Wang, Wei
author_facet Guo, Fangliang
Zheng, Xiaolong
He, Ziyu
Zhang, Ruoying
Zhang, Song
Wang, Minghuan
Chen, Hong
Wang, Wei
author_sort Guo, Fangliang
collection PubMed
description Spinal cord injury (SCI) is a devastating condition that results in severe motor, sensory, and autonomic dysfunction. The L-/T-type calcium channel blocker nimodipine (NMD) exerts a protective effect on neuronal injury; however, the protective effects of long-term administration of NMD in subjects with SCI remain unknown. Thus, the aim of this study was to evaluate the role of long-term treatment with NMD on a clinically relevant SCI model. Female rats with SCI induced by 25 mm contusion were subcutaneously injected with vehicle or 10 mg/kg NMD daily for six consecutive weeks. We monitored the motor score, hind limb grip strength, pain-related behaviors, and bladder function in this study to assess the efficacy of NMD in rats with SCI. Rats treated with NMD showed improvements in locomotion, pain-related behaviors, and spasticity-like symptoms, but not in open-field spontaneous activity, hind limb grip strength or bladder function. SCI lesion areas and perilesional neuronal numbers, gliosis and calcitonin gene-related peptide (CGRP(+)) fiber sprouting in the lumbar spinal cord and the expression of K(+)–Cl(−) cotransporter 2 (KCC2) on lumbar motor neurons were also observed to further explore the possible protective mechanisms of NMD. NMD-treated rats showed greater tissue preservation with reduced lesion areas and increased perilesional neuronal sparing. NMD-treated rats also showed improvements in gliosis, CGRP(+) fiber sprouting in the lumbar spinal cord, and KCC2 expression in lumbar motor neurons. Together, these results indicate that long-term treatment with NMD improves functional recovery after SCI, which may provide a potential therapeutic strategy for the treatment of SCI.
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spelling pubmed-84777502021-09-29 Nimodipine Promotes Functional Recovery After Spinal Cord Injury in Rats Guo, Fangliang Zheng, Xiaolong He, Ziyu Zhang, Ruoying Zhang, Song Wang, Minghuan Chen, Hong Wang, Wei Front Pharmacol Pharmacology Spinal cord injury (SCI) is a devastating condition that results in severe motor, sensory, and autonomic dysfunction. The L-/T-type calcium channel blocker nimodipine (NMD) exerts a protective effect on neuronal injury; however, the protective effects of long-term administration of NMD in subjects with SCI remain unknown. Thus, the aim of this study was to evaluate the role of long-term treatment with NMD on a clinically relevant SCI model. Female rats with SCI induced by 25 mm contusion were subcutaneously injected with vehicle or 10 mg/kg NMD daily for six consecutive weeks. We monitored the motor score, hind limb grip strength, pain-related behaviors, and bladder function in this study to assess the efficacy of NMD in rats with SCI. Rats treated with NMD showed improvements in locomotion, pain-related behaviors, and spasticity-like symptoms, but not in open-field spontaneous activity, hind limb grip strength or bladder function. SCI lesion areas and perilesional neuronal numbers, gliosis and calcitonin gene-related peptide (CGRP(+)) fiber sprouting in the lumbar spinal cord and the expression of K(+)–Cl(−) cotransporter 2 (KCC2) on lumbar motor neurons were also observed to further explore the possible protective mechanisms of NMD. NMD-treated rats showed greater tissue preservation with reduced lesion areas and increased perilesional neuronal sparing. NMD-treated rats also showed improvements in gliosis, CGRP(+) fiber sprouting in the lumbar spinal cord, and KCC2 expression in lumbar motor neurons. Together, these results indicate that long-term treatment with NMD improves functional recovery after SCI, which may provide a potential therapeutic strategy for the treatment of SCI. Frontiers Media S.A. 2021-09-13 /pmc/articles/PMC8477750/ /pubmed/34594224 http://dx.doi.org/10.3389/fphar.2021.733420 Text en Copyright © 2021 Guo, Zheng, He, Zhang, Zhang, Wang, Chen and Wang. https://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 Pharmacology
Guo, Fangliang
Zheng, Xiaolong
He, Ziyu
Zhang, Ruoying
Zhang, Song
Wang, Minghuan
Chen, Hong
Wang, Wei
Nimodipine Promotes Functional Recovery After Spinal Cord Injury in Rats
title Nimodipine Promotes Functional Recovery After Spinal Cord Injury in Rats
title_full Nimodipine Promotes Functional Recovery After Spinal Cord Injury in Rats
title_fullStr Nimodipine Promotes Functional Recovery After Spinal Cord Injury in Rats
title_full_unstemmed Nimodipine Promotes Functional Recovery After Spinal Cord Injury in Rats
title_short Nimodipine Promotes Functional Recovery After Spinal Cord Injury in Rats
title_sort nimodipine promotes functional recovery after spinal cord injury in rats
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8477750/
https://www.ncbi.nlm.nih.gov/pubmed/34594224
http://dx.doi.org/10.3389/fphar.2021.733420
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