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Effect of Zofenopril on regeneration of sciatic nerve crush injury in a rat model

BACKGROUND: Zofenopril is an antioxidant agent which has been shown to have beneficial effects in hypertension and heart failure. The aim of this study was to test the effects of Zofenopril on nerve regeneration and scarring in a rat model of peripheral nerve crush injury. METHODS: Twenty-one adult...

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Autores principales: Kalender, Ali Murat, Dogan, Ali, Bakan, Vedat, Yildiz, Huseyin, Gokalp, Mehmet Ata, Kalender, Mahmut
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2700796/
https://www.ncbi.nlm.nih.gov/pubmed/19508704
http://dx.doi.org/10.1186/1749-7221-4-6
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author Kalender, Ali Murat
Dogan, Ali
Bakan, Vedat
Yildiz, Huseyin
Gokalp, Mehmet Ata
Kalender, Mahmut
author_facet Kalender, Ali Murat
Dogan, Ali
Bakan, Vedat
Yildiz, Huseyin
Gokalp, Mehmet Ata
Kalender, Mahmut
author_sort Kalender, Ali Murat
collection PubMed
description BACKGROUND: Zofenopril is an antioxidant agent which has been shown to have beneficial effects in hypertension and heart failure. The aim of this study was to test the effects of Zofenopril on nerve regeneration and scarring in a rat model of peripheral nerve crush injury. METHODS: Twenty-one adult Sprague-Dawley rats underwent a surgical procedure involving right sciatic nerve crush injury. 15 mg/kg Zofenopril was administered orally to seven rats in group Z for seven days. Seven rats in group S received saline orally for seven days. Seven rats in the control group C received no drug after crush injury. Fourteenth and 42nd days after injury, functional and electromyography assessments of nerves were performed. Functional recovery was analyzed using a walking track assessment, and quantified using the sciatic functional index (SFI). After these evaluations, all rats were sacrificed and microscopic evaluations were performed. RESULTS: The Sciatic functional Index (SFI) in group Z on 14(th )day is different significantly from group S and group C (p = 0.037). But on 42(nd )day there was no difference between groups (p = 0.278). The statistical analyses of electromyelographic (EMG) studies showed that the latency in group Z is significantly different from group S (p = 0.006) and group C (p = 0.045). But on 42(nd )day there was no difference between groups like SFI (p = 0.147). The amplitude was evaluated better in group Z than others (p < 0.05). In microscopic evaluation, we observed the highest number of nerve regeneration in the group Z and the lowest in the group C. But it was not significant statistically. CONCLUSION: Our results demonstrate that Zofenopril promotes the regeneration of peripheral nerve injuries in rat models.
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spelling pubmed-27007962009-06-24 Effect of Zofenopril on regeneration of sciatic nerve crush injury in a rat model Kalender, Ali Murat Dogan, Ali Bakan, Vedat Yildiz, Huseyin Gokalp, Mehmet Ata Kalender, Mahmut J Brachial Plex Peripher Nerve Inj Research Article BACKGROUND: Zofenopril is an antioxidant agent which has been shown to have beneficial effects in hypertension and heart failure. The aim of this study was to test the effects of Zofenopril on nerve regeneration and scarring in a rat model of peripheral nerve crush injury. METHODS: Twenty-one adult Sprague-Dawley rats underwent a surgical procedure involving right sciatic nerve crush injury. 15 mg/kg Zofenopril was administered orally to seven rats in group Z for seven days. Seven rats in group S received saline orally for seven days. Seven rats in the control group C received no drug after crush injury. Fourteenth and 42nd days after injury, functional and electromyography assessments of nerves were performed. Functional recovery was analyzed using a walking track assessment, and quantified using the sciatic functional index (SFI). After these evaluations, all rats were sacrificed and microscopic evaluations were performed. RESULTS: The Sciatic functional Index (SFI) in group Z on 14(th )day is different significantly from group S and group C (p = 0.037). But on 42(nd )day there was no difference between groups (p = 0.278). The statistical analyses of electromyelographic (EMG) studies showed that the latency in group Z is significantly different from group S (p = 0.006) and group C (p = 0.045). But on 42(nd )day there was no difference between groups like SFI (p = 0.147). The amplitude was evaluated better in group Z than others (p < 0.05). In microscopic evaluation, we observed the highest number of nerve regeneration in the group Z and the lowest in the group C. But it was not significant statistically. CONCLUSION: Our results demonstrate that Zofenopril promotes the regeneration of peripheral nerve injuries in rat models. BioMed Central 2009-06-09 /pmc/articles/PMC2700796/ /pubmed/19508704 http://dx.doi.org/10.1186/1749-7221-4-6 Text en Copyright © 2009 Kalender et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kalender, Ali Murat
Dogan, Ali
Bakan, Vedat
Yildiz, Huseyin
Gokalp, Mehmet Ata
Kalender, Mahmut
Effect of Zofenopril on regeneration of sciatic nerve crush injury in a rat model
title Effect of Zofenopril on regeneration of sciatic nerve crush injury in a rat model
title_full Effect of Zofenopril on regeneration of sciatic nerve crush injury in a rat model
title_fullStr Effect of Zofenopril on regeneration of sciatic nerve crush injury in a rat model
title_full_unstemmed Effect of Zofenopril on regeneration of sciatic nerve crush injury in a rat model
title_short Effect of Zofenopril on regeneration of sciatic nerve crush injury in a rat model
title_sort effect of zofenopril on regeneration of sciatic nerve crush injury in a rat model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2700796/
https://www.ncbi.nlm.nih.gov/pubmed/19508704
http://dx.doi.org/10.1186/1749-7221-4-6
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