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Effect of Local Administration of Verapamil Combined with Chitosan Based Hybrid Nanofiber Conduit on Transected Sciatic Nerve in Rat

OBJECTIVE: To assess the effect of locally administered verapamil on transected peripheral nerve regeneration and functional recovery. METHODS: Sixty male healthy white Wistar rats were divided into four experimental groups (n=15), randomly: In transected group (TC), left sciatic nerve was transecte...

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Autores principales: Alizadeh- Mohajer, Mahan, Raisi, Abbas, Farjanikish, Ghasem, Mohammadi, Rahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shiraz University of Medical Sciences 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6360005/
https://www.ncbi.nlm.nih.gov/pubmed/30719463
http://dx.doi.org/10.29252/beat-070104
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author Alizadeh- Mohajer, Mahan
Raisi, Abbas
Farjanikish, Ghasem
Mohammadi, Rahim
author_facet Alizadeh- Mohajer, Mahan
Raisi, Abbas
Farjanikish, Ghasem
Mohammadi, Rahim
author_sort Alizadeh- Mohajer, Mahan
collection PubMed
description OBJECTIVE: To assess the effect of locally administered verapamil on transected peripheral nerve regeneration and functional recovery. METHODS: Sixty male healthy white Wistar rats were divided into four experimental groups (n=15), randomly: In transected group (TC), left sciatic nerve was transected and stumps were fixed in the adjacent muscle. In treatment group defect was bridged using chitosan tube (CHIT/Verapamil) filled with 10 µL verapamil (100ng/mL). In chitosan conduit group (CHIT), the tube was filled with phosphate-buffered saline alone. In sham-operated group (SHAM), sciatic nerve was exposed and manipulated. The repair trend was examined based on behavioral and performance tests as well as the variations of the gastrocnemius muscle, morphometric indices, and immunohistochemical indices. RESULTS: Sciatic nerve functional study, muscle mass and morphometric indices confirmed faster recovery of regenerated axons in CHIT/Verapamil than CHIT group (P = 0.001). When loaded in a chitosan tube verapamil accelerated and improved functional recovery and morphometric indices of sciatic nerve. Immunohistochemical analysis revealed the S-100 protein was vastly present in the transverse nerve sections and the myelin sheath. In the treatment group (chit/verapamil), the immunohistochemical susceptibility of the axons being repaired and the axons in the myelin sheath to S-100 protein was higher than the other groups. CONCLUSION: The present study demonstrated that a single local application of verapamil could accelerate functional recovery after transection of sciatic nerve.
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spelling pubmed-63600052019-02-04 Effect of Local Administration of Verapamil Combined with Chitosan Based Hybrid Nanofiber Conduit on Transected Sciatic Nerve in Rat Alizadeh- Mohajer, Mahan Raisi, Abbas Farjanikish, Ghasem Mohammadi, Rahim Bull Emerg Trauma Original Article OBJECTIVE: To assess the effect of locally administered verapamil on transected peripheral nerve regeneration and functional recovery. METHODS: Sixty male healthy white Wistar rats were divided into four experimental groups (n=15), randomly: In transected group (TC), left sciatic nerve was transected and stumps were fixed in the adjacent muscle. In treatment group defect was bridged using chitosan tube (CHIT/Verapamil) filled with 10 µL verapamil (100ng/mL). In chitosan conduit group (CHIT), the tube was filled with phosphate-buffered saline alone. In sham-operated group (SHAM), sciatic nerve was exposed and manipulated. The repair trend was examined based on behavioral and performance tests as well as the variations of the gastrocnemius muscle, morphometric indices, and immunohistochemical indices. RESULTS: Sciatic nerve functional study, muscle mass and morphometric indices confirmed faster recovery of regenerated axons in CHIT/Verapamil than CHIT group (P = 0.001). When loaded in a chitosan tube verapamil accelerated and improved functional recovery and morphometric indices of sciatic nerve. Immunohistochemical analysis revealed the S-100 protein was vastly present in the transverse nerve sections and the myelin sheath. In the treatment group (chit/verapamil), the immunohistochemical susceptibility of the axons being repaired and the axons in the myelin sheath to S-100 protein was higher than the other groups. CONCLUSION: The present study demonstrated that a single local application of verapamil could accelerate functional recovery after transection of sciatic nerve. Shiraz University of Medical Sciences 2019-01 /pmc/articles/PMC6360005/ /pubmed/30719463 http://dx.doi.org/10.29252/beat-070104 Text en © 2019 Trauma Research Center, Shiraz University of Medical Sciences Bulletin of Emergency And Trauma articles are published under a Creative Commons license. (http://creativecommons.org/licenses/) Mandated authors will be offered CC-BY; all other authors will choose between CC-BY, CC-BY-NC and CC-BY-NC-ND.
spellingShingle Original Article
Alizadeh- Mohajer, Mahan
Raisi, Abbas
Farjanikish, Ghasem
Mohammadi, Rahim
Effect of Local Administration of Verapamil Combined with Chitosan Based Hybrid Nanofiber Conduit on Transected Sciatic Nerve in Rat
title Effect of Local Administration of Verapamil Combined with Chitosan Based Hybrid Nanofiber Conduit on Transected Sciatic Nerve in Rat
title_full Effect of Local Administration of Verapamil Combined with Chitosan Based Hybrid Nanofiber Conduit on Transected Sciatic Nerve in Rat
title_fullStr Effect of Local Administration of Verapamil Combined with Chitosan Based Hybrid Nanofiber Conduit on Transected Sciatic Nerve in Rat
title_full_unstemmed Effect of Local Administration of Verapamil Combined with Chitosan Based Hybrid Nanofiber Conduit on Transected Sciatic Nerve in Rat
title_short Effect of Local Administration of Verapamil Combined with Chitosan Based Hybrid Nanofiber Conduit on Transected Sciatic Nerve in Rat
title_sort effect of local administration of verapamil combined with chitosan based hybrid nanofiber conduit on transected sciatic nerve in rat
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6360005/
https://www.ncbi.nlm.nih.gov/pubmed/30719463
http://dx.doi.org/10.29252/beat-070104
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