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Sciatic nerve injury following analgesic drug injection in rats: A histopathological examination

OBJECTIVE: Sciatic nerve neuropathy can be observed following intramuscular gluteal injections. The histopathological examination of sciatic nerve damage following intramuscular injection in the gluteal region for acute pain treatment is not feasible in humans due to the inability to dissect and exa...

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Autores principales: Bostan, Habib, Cabalar, Murat, Altinay, Serdar, Kalkan, Yildiray, Tumkaya, Levent, Kanat, Ayhan, Balik, Sabri, Erkut, Adem, Altuner, Dudu, Salihoglu, Ziya, Kocer, Abdulkadir
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kare Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323560/
https://www.ncbi.nlm.nih.gov/pubmed/30688928
http://dx.doi.org/10.14744/nci.2017.28190
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author Bostan, Habib
Cabalar, Murat
Altinay, Serdar
Kalkan, Yildiray
Tumkaya, Levent
Kanat, Ayhan
Balik, Sabri
Erkut, Adem
Altuner, Dudu
Salihoglu, Ziya
Kocer, Abdulkadir
author_facet Bostan, Habib
Cabalar, Murat
Altinay, Serdar
Kalkan, Yildiray
Tumkaya, Levent
Kanat, Ayhan
Balik, Sabri
Erkut, Adem
Altuner, Dudu
Salihoglu, Ziya
Kocer, Abdulkadir
author_sort Bostan, Habib
collection PubMed
description OBJECTIVE: Sciatic nerve neuropathy can be observed following intramuscular gluteal injections. The histopathological examination of sciatic nerve damage following intramuscular injection in the gluteal region for acute pain treatment is not feasible in humans due to the inability to dissect and examine the nerve tissue. To overcome this issue, we used a rat model for demonstrating damage to the sciatic nerve tissue after the application of commonly used drug injections. METHODS: We investigated possible damage following the intramuscular injection of diclofenac, lornoxicam, morphine, and pethidine in a rat model based on histopathological characteristics such as myelin degeneration, axon degeneration, epineurium degeneration, fibrosis, epineurium thickening, perineurium thickening, lymphocyte infiltration, vacuolization, and edema. RESULTS: All the analgesic drugs used in our study induced histopathological changes in the sciatic nerve. Anti-S100 positivity, showing nerve damage, was found to be the lowest in the group treated with diclofenac. Neurotoxic effects of diclofenac on the sciatic nerve were greater than those of the other drugs used in the study. Lornoxicam induced the least histopathological changes in the nerve. CONCLUSION: Diclofenac induced severe nerve damage not only after direct injection in the sciatic nerve but also after injection in the area around the nerve. Thus, we recommend restricting the use of intramuscular gluteal injections of diclofenac. Intramuscular use of morphine and pethidine should also be overviewed.
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spelling pubmed-63235602019-01-25 Sciatic nerve injury following analgesic drug injection in rats: A histopathological examination Bostan, Habib Cabalar, Murat Altinay, Serdar Kalkan, Yildiray Tumkaya, Levent Kanat, Ayhan Balik, Sabri Erkut, Adem Altuner, Dudu Salihoglu, Ziya Kocer, Abdulkadir North Clin Istanb Original Article OBJECTIVE: Sciatic nerve neuropathy can be observed following intramuscular gluteal injections. The histopathological examination of sciatic nerve damage following intramuscular injection in the gluteal region for acute pain treatment is not feasible in humans due to the inability to dissect and examine the nerve tissue. To overcome this issue, we used a rat model for demonstrating damage to the sciatic nerve tissue after the application of commonly used drug injections. METHODS: We investigated possible damage following the intramuscular injection of diclofenac, lornoxicam, morphine, and pethidine in a rat model based on histopathological characteristics such as myelin degeneration, axon degeneration, epineurium degeneration, fibrosis, epineurium thickening, perineurium thickening, lymphocyte infiltration, vacuolization, and edema. RESULTS: All the analgesic drugs used in our study induced histopathological changes in the sciatic nerve. Anti-S100 positivity, showing nerve damage, was found to be the lowest in the group treated with diclofenac. Neurotoxic effects of diclofenac on the sciatic nerve were greater than those of the other drugs used in the study. Lornoxicam induced the least histopathological changes in the nerve. CONCLUSION: Diclofenac induced severe nerve damage not only after direct injection in the sciatic nerve but also after injection in the area around the nerve. Thus, we recommend restricting the use of intramuscular gluteal injections of diclofenac. Intramuscular use of morphine and pethidine should also be overviewed. Kare Publishing 2018-05-29 /pmc/articles/PMC6323560/ /pubmed/30688928 http://dx.doi.org/10.14744/nci.2017.28190 Text en Copyright: © 2018 by Istanbul Northern Anatolian Association of Public Hospitals http://creativecommons.org/licenses/by-nc-sa/4.0 This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License
spellingShingle Original Article
Bostan, Habib
Cabalar, Murat
Altinay, Serdar
Kalkan, Yildiray
Tumkaya, Levent
Kanat, Ayhan
Balik, Sabri
Erkut, Adem
Altuner, Dudu
Salihoglu, Ziya
Kocer, Abdulkadir
Sciatic nerve injury following analgesic drug injection in rats: A histopathological examination
title Sciatic nerve injury following analgesic drug injection in rats: A histopathological examination
title_full Sciatic nerve injury following analgesic drug injection in rats: A histopathological examination
title_fullStr Sciatic nerve injury following analgesic drug injection in rats: A histopathological examination
title_full_unstemmed Sciatic nerve injury following analgesic drug injection in rats: A histopathological examination
title_short Sciatic nerve injury following analgesic drug injection in rats: A histopathological examination
title_sort sciatic nerve injury following analgesic drug injection in rats: a histopathological examination
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6323560/
https://www.ncbi.nlm.nih.gov/pubmed/30688928
http://dx.doi.org/10.14744/nci.2017.28190
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