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Effect of epidural polydeoxyribonucleotide in a rat model of lumbar foraminal stenosis
BACKGROUND: We aimed to investigate the effect of epidural polydeoxyribonucleotide (PDRN) on mechanical allodynia and motor dysfunction in a rat model of lumbar foraminal stenosis (LFS). METHODS: This study was conducted in two stages, using male Sprague-Dawley rats. The rats were randomly divided i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Pain Society
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494961/ https://www.ncbi.nlm.nih.gov/pubmed/34593657 http://dx.doi.org/10.3344/kjp.2021.34.4.394 |
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author | Lee, Ho-Jin Ju, Jiyoun Choi, Eunjoo Nahm, Francis Sahngun Choe, Ghee Young Lee, Pyung Bok |
author_facet | Lee, Ho-Jin Ju, Jiyoun Choi, Eunjoo Nahm, Francis Sahngun Choe, Ghee Young Lee, Pyung Bok |
author_sort | Lee, Ho-Jin |
collection | PubMed |
description | BACKGROUND: We aimed to investigate the effect of epidural polydeoxyribonucleotide (PDRN) on mechanical allodynia and motor dysfunction in a rat model of lumbar foraminal stenosis (LFS). METHODS: This study was conducted in two stages, using male Sprague-Dawley rats. The rats were randomly divided into eight groups. In the first stage, the groups were as follows vehicle (V), sham (S), and epidural PDRN at 5 (P5), 8 (P8), and 10 (P10) mg/kg; and in the second stage, they were as follows intraperitoneal PDRN 8 mg/kg, epidural 3,7-dimethyl-1-propargilxanthine (DMPX) (0.1 mg/kg), and DMPX (0.1 mg/kg). The LFS model was established, except for the S group. After an epidural injection of the test solutions, von Frey and treadmill tests were conducted for 3 weeks. Subsequently, histopathologic examinations were conducted in the V, S, P5, and P10 groups. RESULTS: A total of 65 rats were included. The P8 and P10 groups showed significant recovery from mechanical allodynia and motor dysfunction at all time points after drug administration compared to the V group. These effects were abolished by concomitant administration of DMPX. On histopathological examination, no epineurial inflammation or fibrosis was observed in the epidural PDRN groups. CONCLUSIONS: Epidural injection of PDRN significantly improves mechanical allodynia and motor dysfunction in a rat model of LFS, which is mediated by the spinal adenosine A(2A) receptor. The present data support the need for further research to determine the role of epidural PDRN in spinal stenosis treatment. |
format | Online Article Text |
id | pubmed-8494961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Korean Pain Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-84949612021-10-13 Effect of epidural polydeoxyribonucleotide in a rat model of lumbar foraminal stenosis Lee, Ho-Jin Ju, Jiyoun Choi, Eunjoo Nahm, Francis Sahngun Choe, Ghee Young Lee, Pyung Bok Korean J Pain Experimental Research Articles BACKGROUND: We aimed to investigate the effect of epidural polydeoxyribonucleotide (PDRN) on mechanical allodynia and motor dysfunction in a rat model of lumbar foraminal stenosis (LFS). METHODS: This study was conducted in two stages, using male Sprague-Dawley rats. The rats were randomly divided into eight groups. In the first stage, the groups were as follows vehicle (V), sham (S), and epidural PDRN at 5 (P5), 8 (P8), and 10 (P10) mg/kg; and in the second stage, they were as follows intraperitoneal PDRN 8 mg/kg, epidural 3,7-dimethyl-1-propargilxanthine (DMPX) (0.1 mg/kg), and DMPX (0.1 mg/kg). The LFS model was established, except for the S group. After an epidural injection of the test solutions, von Frey and treadmill tests were conducted for 3 weeks. Subsequently, histopathologic examinations were conducted in the V, S, P5, and P10 groups. RESULTS: A total of 65 rats were included. The P8 and P10 groups showed significant recovery from mechanical allodynia and motor dysfunction at all time points after drug administration compared to the V group. These effects were abolished by concomitant administration of DMPX. On histopathological examination, no epineurial inflammation or fibrosis was observed in the epidural PDRN groups. CONCLUSIONS: Epidural injection of PDRN significantly improves mechanical allodynia and motor dysfunction in a rat model of LFS, which is mediated by the spinal adenosine A(2A) receptor. The present data support the need for further research to determine the role of epidural PDRN in spinal stenosis treatment. The Korean Pain Society 2021-10-01 2021-10-01 /pmc/articles/PMC8494961/ /pubmed/34593657 http://dx.doi.org/10.3344/kjp.2021.34.4.394 Text en © The Korean Pain Society, 2021 https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Experimental Research Articles Lee, Ho-Jin Ju, Jiyoun Choi, Eunjoo Nahm, Francis Sahngun Choe, Ghee Young Lee, Pyung Bok Effect of epidural polydeoxyribonucleotide in a rat model of lumbar foraminal stenosis |
title | Effect of epidural polydeoxyribonucleotide in a rat model of lumbar foraminal stenosis |
title_full | Effect of epidural polydeoxyribonucleotide in a rat model of lumbar foraminal stenosis |
title_fullStr | Effect of epidural polydeoxyribonucleotide in a rat model of lumbar foraminal stenosis |
title_full_unstemmed | Effect of epidural polydeoxyribonucleotide in a rat model of lumbar foraminal stenosis |
title_short | Effect of epidural polydeoxyribonucleotide in a rat model of lumbar foraminal stenosis |
title_sort | effect of epidural polydeoxyribonucleotide in a rat model of lumbar foraminal stenosis |
topic | Experimental Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8494961/ https://www.ncbi.nlm.nih.gov/pubmed/34593657 http://dx.doi.org/10.3344/kjp.2021.34.4.394 |
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