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Platelet-Rich Plasma Injection in Burn Scar Areas Alleviates Neuropathic Scar Pain
Objective: No effective treatments have yet been developed for burn-induced neuropathic pain. Platelet-rich plasma (PRP) has been reported to ameliorate various types of inflammation pain. However, the effect of PRP on burn-induced neuropathic pain is unclear. Methods: Burn-induced neuropathic pain...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820853/ https://www.ncbi.nlm.nih.gov/pubmed/29483815 http://dx.doi.org/10.7150/ijms.22563 |
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author | Huang, Shu-Hung Wu, Sheng-Hua Lee, Su-Shin Lin, Yun-Nan Chai, Chee-Yin Lai, Chung-Sheng Wang, Hui-Min David |
author_facet | Huang, Shu-Hung Wu, Sheng-Hua Lee, Su-Shin Lin, Yun-Nan Chai, Chee-Yin Lai, Chung-Sheng Wang, Hui-Min David |
author_sort | Huang, Shu-Hung |
collection | PubMed |
description | Objective: No effective treatments have yet been developed for burn-induced neuropathic pain. Platelet-rich plasma (PRP) has been reported to ameliorate various types of inflammation pain. However, the effect of PRP on burn-induced neuropathic pain is unclear. Methods: Burn-induced neuropathic pain Sprague-Dawley rat model was confirmed using a mechanical response test 4 weeks after the burn injuries were sustained, following which PRP was injected in the scar area. The rats were divided into four groups (n = 6) as following: Group A, Sham; Group B, Sham + PRP; Group C, Burn; and Group D, Burn + PRP. Four weeks after the PRP injection, the animals were subjected to behavior tests and then sacrificed; specimens were collected for inflammation tests, Masson's trichrome stain and chromosome 10 (PTEN) in the injured skin; and PTEN, phosphorylated mammalian target of rapamycin (p-mTOR), p38, nuclear factor κB (NFκB), chemokine (CC motif) ligand 2 (CCL2), and CCL2 cognate receptor (CCR2) in spinal cord dorsal horns through immunohistochemistry and immunofluorescence staining. Results: PRP significantly alleviated allodynia in burn-induced neuropathic pain 4 weeks after treatment, and PTEN expression in the skin and spinal cord were significantly increased in group D compared with the group C. p-PTEN, p-mTOR, and CCL2 expression in neuron cells; p-p38 and p-NFκB expression in microglia; and p-JNK and p-NFκB activation in spinal astrocytes decreased significantly in the group D compared with the group C. Conclusions: PRP is effective in treating burn-induced neuropathic pain and may be used in clinical practice. |
format | Online Article Text |
id | pubmed-5820853 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-58208532018-02-26 Platelet-Rich Plasma Injection in Burn Scar Areas Alleviates Neuropathic Scar Pain Huang, Shu-Hung Wu, Sheng-Hua Lee, Su-Shin Lin, Yun-Nan Chai, Chee-Yin Lai, Chung-Sheng Wang, Hui-Min David Int J Med Sci Research Paper Objective: No effective treatments have yet been developed for burn-induced neuropathic pain. Platelet-rich plasma (PRP) has been reported to ameliorate various types of inflammation pain. However, the effect of PRP on burn-induced neuropathic pain is unclear. Methods: Burn-induced neuropathic pain Sprague-Dawley rat model was confirmed using a mechanical response test 4 weeks after the burn injuries were sustained, following which PRP was injected in the scar area. The rats were divided into four groups (n = 6) as following: Group A, Sham; Group B, Sham + PRP; Group C, Burn; and Group D, Burn + PRP. Four weeks after the PRP injection, the animals were subjected to behavior tests and then sacrificed; specimens were collected for inflammation tests, Masson's trichrome stain and chromosome 10 (PTEN) in the injured skin; and PTEN, phosphorylated mammalian target of rapamycin (p-mTOR), p38, nuclear factor κB (NFκB), chemokine (CC motif) ligand 2 (CCL2), and CCL2 cognate receptor (CCR2) in spinal cord dorsal horns through immunohistochemistry and immunofluorescence staining. Results: PRP significantly alleviated allodynia in burn-induced neuropathic pain 4 weeks after treatment, and PTEN expression in the skin and spinal cord were significantly increased in group D compared with the group C. p-PTEN, p-mTOR, and CCL2 expression in neuron cells; p-p38 and p-NFκB expression in microglia; and p-JNK and p-NFκB activation in spinal astrocytes decreased significantly in the group D compared with the group C. Conclusions: PRP is effective in treating burn-induced neuropathic pain and may be used in clinical practice. Ivyspring International Publisher 2018-01-08 /pmc/articles/PMC5820853/ /pubmed/29483815 http://dx.doi.org/10.7150/ijms.22563 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Research Paper Huang, Shu-Hung Wu, Sheng-Hua Lee, Su-Shin Lin, Yun-Nan Chai, Chee-Yin Lai, Chung-Sheng Wang, Hui-Min David Platelet-Rich Plasma Injection in Burn Scar Areas Alleviates Neuropathic Scar Pain |
title | Platelet-Rich Plasma Injection in Burn Scar Areas Alleviates Neuropathic Scar Pain |
title_full | Platelet-Rich Plasma Injection in Burn Scar Areas Alleviates Neuropathic Scar Pain |
title_fullStr | Platelet-Rich Plasma Injection in Burn Scar Areas Alleviates Neuropathic Scar Pain |
title_full_unstemmed | Platelet-Rich Plasma Injection in Burn Scar Areas Alleviates Neuropathic Scar Pain |
title_short | Platelet-Rich Plasma Injection in Burn Scar Areas Alleviates Neuropathic Scar Pain |
title_sort | platelet-rich plasma injection in burn scar areas alleviates neuropathic scar pain |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5820853/ https://www.ncbi.nlm.nih.gov/pubmed/29483815 http://dx.doi.org/10.7150/ijms.22563 |
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