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The effect of human mesenchymal stem cell injection on pain behavior in chronic post-ischemia pain mice
BACKGROUND: Neuropathic pain (NP) is considered a clinically incurable condition despite various treatment options due to its diverse causes and complicated disease mechanisms. Since the early 2000s, multipotent human mesenchymal stem cells (hMSCs) have been used in the treatment of NP in animal mod...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Pain Society
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944374/ https://www.ncbi.nlm.nih.gov/pubmed/31888314 http://dx.doi.org/10.3344/kjp.2020.33.1.23 |
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author | Yoo, Sie Hyeon Lee, Sung Hyun Lee, Seunghwan Park, Jae Hong Lee, Seunghyeon Jin, Heecheol Park, Hue Jung |
author_facet | Yoo, Sie Hyeon Lee, Sung Hyun Lee, Seunghwan Park, Jae Hong Lee, Seunghyeon Jin, Heecheol Park, Hue Jung |
author_sort | Yoo, Sie Hyeon |
collection | PubMed |
description | BACKGROUND: Neuropathic pain (NP) is considered a clinically incurable condition despite various treatment options due to its diverse causes and complicated disease mechanisms. Since the early 2000s, multipotent human mesenchymal stem cells (hMSCs) have been used in the treatment of NP in animal models. However, the effects of hMSC injections have not been studied in chronic post-ischemia pain (CPIP) mice models. Here, we investigated whether intrathecal (IT) and intrapaw (IP) injections of hMSCs can reduce mechanical allodynia in CPIP model mice. METHODS: Seventeen CPIP C57/BL6 mice were selected and randomized into four groups: IT sham (n = 4), IT stem (n = 5), IP sham (n = 4), and IP stem (n = 4). Mice in the IT sham and IT stem groups received an injection of 5 μL saline and 2 × 10(4) hMSCs, respectively, while mice in the IP sham and IP stem groups received an injection of 5 μL saline and 2 × 10(5) hMSCs, respectively. Mechanical allodynia was assessed using von Frey filaments from pre-injection to 30 days post-injection. Glial fibrillary acidic protein (GFAP) expression in the spinal cord and dorsal root ganglia were also evaluated. RESULTS: IT and IP injections of hMSCs improved mechanical allodynia. GFAP expression was decreased on day 25 post-injection compared with the sham group. Injections of hMSCs improved allodynia and GFAP expression was decreased compared with the sham group. CONCLUSIONS: These results suggested that hMSCs may be also another treatment modality in NP model by ischemia-reperfusion. |
format | Online Article Text |
id | pubmed-6944374 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Korean Pain Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-69443742020-01-09 The effect of human mesenchymal stem cell injection on pain behavior in chronic post-ischemia pain mice Yoo, Sie Hyeon Lee, Sung Hyun Lee, Seunghwan Park, Jae Hong Lee, Seunghyeon Jin, Heecheol Park, Hue Jung Korean J Pain Original Article BACKGROUND: Neuropathic pain (NP) is considered a clinically incurable condition despite various treatment options due to its diverse causes and complicated disease mechanisms. Since the early 2000s, multipotent human mesenchymal stem cells (hMSCs) have been used in the treatment of NP in animal models. However, the effects of hMSC injections have not been studied in chronic post-ischemia pain (CPIP) mice models. Here, we investigated whether intrathecal (IT) and intrapaw (IP) injections of hMSCs can reduce mechanical allodynia in CPIP model mice. METHODS: Seventeen CPIP C57/BL6 mice were selected and randomized into four groups: IT sham (n = 4), IT stem (n = 5), IP sham (n = 4), and IP stem (n = 4). Mice in the IT sham and IT stem groups received an injection of 5 μL saline and 2 × 10(4) hMSCs, respectively, while mice in the IP sham and IP stem groups received an injection of 5 μL saline and 2 × 10(5) hMSCs, respectively. Mechanical allodynia was assessed using von Frey filaments from pre-injection to 30 days post-injection. Glial fibrillary acidic protein (GFAP) expression in the spinal cord and dorsal root ganglia were also evaluated. RESULTS: IT and IP injections of hMSCs improved mechanical allodynia. GFAP expression was decreased on day 25 post-injection compared with the sham group. Injections of hMSCs improved allodynia and GFAP expression was decreased compared with the sham group. CONCLUSIONS: These results suggested that hMSCs may be also another treatment modality in NP model by ischemia-reperfusion. The Korean Pain Society 2020-01 2020-01-01 /pmc/articles/PMC6944374/ /pubmed/31888314 http://dx.doi.org/10.3344/kjp.2020.33.1.23 Text en © The Korean Pain Society, 2020 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/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Yoo, Sie Hyeon Lee, Sung Hyun Lee, Seunghwan Park, Jae Hong Lee, Seunghyeon Jin, Heecheol Park, Hue Jung The effect of human mesenchymal stem cell injection on pain behavior in chronic post-ischemia pain mice |
title | The effect of human mesenchymal stem cell injection on pain behavior in chronic post-ischemia pain mice |
title_full | The effect of human mesenchymal stem cell injection on pain behavior in chronic post-ischemia pain mice |
title_fullStr | The effect of human mesenchymal stem cell injection on pain behavior in chronic post-ischemia pain mice |
title_full_unstemmed | The effect of human mesenchymal stem cell injection on pain behavior in chronic post-ischemia pain mice |
title_short | The effect of human mesenchymal stem cell injection on pain behavior in chronic post-ischemia pain mice |
title_sort | effect of human mesenchymal stem cell injection on pain behavior in chronic post-ischemia pain mice |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6944374/ https://www.ncbi.nlm.nih.gov/pubmed/31888314 http://dx.doi.org/10.3344/kjp.2020.33.1.23 |
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