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Influence of galantamine on peripheral nerve degeneration after experimental compression injury of the rat sciatic nerve
BACKGROUND: Galantamine is well-known for its neuroprotective effects and is currently used in the treatment of individuals with Alzheimer’s disease. In this study, we induced experimental sciatic nerve injury (SCI) in rats to test the beneficial effects of galantamine. METHODS: Thirty male Wistar a...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Kare Publishing
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493531/ https://www.ncbi.nlm.nih.gov/pubmed/35485563 http://dx.doi.org/10.14744/tjtes.2020.56573 |
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author | Alagöz, Fatih Sahinoglu, Mert Billur, Deniz Aydın, Sevim Akdağ, Rifat Karakoyun, Durmuş Oğuz Daglioglu, Ergun |
author_facet | Alagöz, Fatih Sahinoglu, Mert Billur, Deniz Aydın, Sevim Akdağ, Rifat Karakoyun, Durmuş Oğuz Daglioglu, Ergun |
author_sort | Alagöz, Fatih |
collection | PubMed |
description | BACKGROUND: Galantamine is well-known for its neuroprotective effects and is currently used in the treatment of individuals with Alzheimer’s disease. In this study, we induced experimental sciatic nerve injury (SCI) in rats to test the beneficial effects of galantamine. METHODS: Thirty male Wistar albino rats were divided into three groups, as follows: sham, SCI + saline, and SCI + galantamine. After the administration of an intraperitoneal ketamine and xylazine mixture, which was used for anesthesia, SCI was induced by surgical clip compression at the midthigh region of the rats. After surgery, a single daily intraperitoneal dose of galantamine was administered for 7 days, and nerve tissue sections were obtained 1 week after injury. Histopathology studies were performed to assess neural thickness and apoptotic cell counts, and light microscopic morphological examination was used to determine a potential beneficial effect of galantamine on peripheral nerve degeneration. RESULTS: We observed a markedly increased microvasculature, increased nerve fiber thickness, and a statistically significant increase in apoptotic cell counts distal to the level of injury in the saline group compared with the sham group. However, the increases in nerve fiber thickness and apoptotic cell counts were less in the galantamine group compared with the saline group. CONCLUSION: In our experimental model, pharmacological intervention with galantamine demonstrated a protective effect on degeneration after peripheral nerve injury. |
format | Online Article Text |
id | pubmed-10493531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Kare Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-104935312023-09-12 Influence of galantamine on peripheral nerve degeneration after experimental compression injury of the rat sciatic nerve Alagöz, Fatih Sahinoglu, Mert Billur, Deniz Aydın, Sevim Akdağ, Rifat Karakoyun, Durmuş Oğuz Daglioglu, Ergun Ulus Travma Acil Cerrahi Derg Experimental Study BACKGROUND: Galantamine is well-known for its neuroprotective effects and is currently used in the treatment of individuals with Alzheimer’s disease. In this study, we induced experimental sciatic nerve injury (SCI) in rats to test the beneficial effects of galantamine. METHODS: Thirty male Wistar albino rats were divided into three groups, as follows: sham, SCI + saline, and SCI + galantamine. After the administration of an intraperitoneal ketamine and xylazine mixture, which was used for anesthesia, SCI was induced by surgical clip compression at the midthigh region of the rats. After surgery, a single daily intraperitoneal dose of galantamine was administered for 7 days, and nerve tissue sections were obtained 1 week after injury. Histopathology studies were performed to assess neural thickness and apoptotic cell counts, and light microscopic morphological examination was used to determine a potential beneficial effect of galantamine on peripheral nerve degeneration. RESULTS: We observed a markedly increased microvasculature, increased nerve fiber thickness, and a statistically significant increase in apoptotic cell counts distal to the level of injury in the saline group compared with the sham group. However, the increases in nerve fiber thickness and apoptotic cell counts were less in the galantamine group compared with the saline group. CONCLUSION: In our experimental model, pharmacological intervention with galantamine demonstrated a protective effect on degeneration after peripheral nerve injury. Kare Publishing 2022-03-01 /pmc/articles/PMC10493531/ /pubmed/35485563 http://dx.doi.org/10.14744/tjtes.2020.56573 Text en Copyright © 2022 Turkish Journal of Trauma and Emergency Surgery https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License |
spellingShingle | Experimental Study Alagöz, Fatih Sahinoglu, Mert Billur, Deniz Aydın, Sevim Akdağ, Rifat Karakoyun, Durmuş Oğuz Daglioglu, Ergun Influence of galantamine on peripheral nerve degeneration after experimental compression injury of the rat sciatic nerve |
title | Influence of galantamine on peripheral nerve degeneration after experimental compression injury of the rat sciatic nerve |
title_full | Influence of galantamine on peripheral nerve degeneration after experimental compression injury of the rat sciatic nerve |
title_fullStr | Influence of galantamine on peripheral nerve degeneration after experimental compression injury of the rat sciatic nerve |
title_full_unstemmed | Influence of galantamine on peripheral nerve degeneration after experimental compression injury of the rat sciatic nerve |
title_short | Influence of galantamine on peripheral nerve degeneration after experimental compression injury of the rat sciatic nerve |
title_sort | influence of galantamine on peripheral nerve degeneration after experimental compression injury of the rat sciatic nerve |
topic | Experimental Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10493531/ https://www.ncbi.nlm.nih.gov/pubmed/35485563 http://dx.doi.org/10.14744/tjtes.2020.56573 |
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