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Efficacy of nerve growth factor antibody in a knee osteoarthritis pain model in mice
BACKGROUND: Nerve growth factor (NGF) is not only an important factor in nerve growth but also a major contributor to the production of inflammation. It has been reported that inhibiting NGF could reduce several types of pain in several animal models. Here, we aimed to clarify the efficacy of NGF an...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670727/ https://www.ncbi.nlm.nih.gov/pubmed/29100502 http://dx.doi.org/10.1186/s12891-017-1792-x |
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author | Miyagi, Masayuki Ishikawa, Tetsuhiro Kamoda, Hiroto Suzuki, Miyako Inoue, Gen Sakuma, Yoshihiro Oikawa, Yasuhiro Orita, Sumihisa Uchida, Kentaro Takahashi, Kazuhisa Takaso, Masashi Ohtori, Seiji |
author_facet | Miyagi, Masayuki Ishikawa, Tetsuhiro Kamoda, Hiroto Suzuki, Miyako Inoue, Gen Sakuma, Yoshihiro Oikawa, Yasuhiro Orita, Sumihisa Uchida, Kentaro Takahashi, Kazuhisa Takaso, Masashi Ohtori, Seiji |
author_sort | Miyagi, Masayuki |
collection | PubMed |
description | BACKGROUND: Nerve growth factor (NGF) is not only an important factor in nerve growth but also a major contributor to the production of inflammation. It has been reported that inhibiting NGF could reduce several types of pain in several animal models. Here, we aimed to clarify the efficacy of NGF antibody in a knee osteoarthritis (OA) pain model in mice. METHOD: Six-week-old male C57BR/J mice were used (n = 30). Ten mice comprised the control group, which received saline injection into the right knee joints; the other 20 mice comprised the experimental group, which received monoiodoacetate (MIA) injection into the right knee joints. Three weeks after surgery, the 20 experimental mice were randomly placed into treatment groups which received either sterile saline (non-treat group: 10 mg/kg, i.p.) or an anti-NGF antibody (anti-NGF group: 10 mg/kg, i.p.). Simultaneously, all mice received fluorogold (FG) retrograde neurotracer injection into their right joints. In a behavioral study, we evaluated gait using the CatWalk quantitative gait analysis system before surgery, 3 weeks after surgery (before treatment), 4 weeks after surgery (one week after surgery), and 5 weeks after surgery (2 weeks after surgery). In immunohistochemical analysis, the right dorsal root ganglia (DRGs) from the L4–L6 levels were resected 5 weeks after surgery (2 weeks after surgery). They were immunostained for calcitonin gene-related peptide (CGRP), and the number of FG-labeled or CGRP-immunoreactive (IR) DRG neurons was counted. RESULTS: On gait analysis using the CatWalk system, duty cycle, swing speed, and print area were decreased in non-treat group compared with those in control group and improved in the anti-NGF group compared with those in non-treat group. CGRP expression in DRGs was up-regulated in non-treat group compared with that in control group and suppressed in the anti-NGF group compared with that in non-treat group (both p < 0.05). CONCLUSIONS: MIA injection into the knee joint induced gait impairment and the up-regulation of CGRP in DRG neurons in a knee OA pain model in mice. Intraperitoneal injection of anti-NGF antibody suppressed this impairment of gait and up-regulation of CGRP in DRG neurons. These finding suggest that anti-NGF therapy might be valuable in the treatment of OA pain in the knee. |
format | Online Article Text |
id | pubmed-5670727 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-56707272017-11-15 Efficacy of nerve growth factor antibody in a knee osteoarthritis pain model in mice Miyagi, Masayuki Ishikawa, Tetsuhiro Kamoda, Hiroto Suzuki, Miyako Inoue, Gen Sakuma, Yoshihiro Oikawa, Yasuhiro Orita, Sumihisa Uchida, Kentaro Takahashi, Kazuhisa Takaso, Masashi Ohtori, Seiji BMC Musculoskelet Disord Research Article BACKGROUND: Nerve growth factor (NGF) is not only an important factor in nerve growth but also a major contributor to the production of inflammation. It has been reported that inhibiting NGF could reduce several types of pain in several animal models. Here, we aimed to clarify the efficacy of NGF antibody in a knee osteoarthritis (OA) pain model in mice. METHOD: Six-week-old male C57BR/J mice were used (n = 30). Ten mice comprised the control group, which received saline injection into the right knee joints; the other 20 mice comprised the experimental group, which received monoiodoacetate (MIA) injection into the right knee joints. Three weeks after surgery, the 20 experimental mice were randomly placed into treatment groups which received either sterile saline (non-treat group: 10 mg/kg, i.p.) or an anti-NGF antibody (anti-NGF group: 10 mg/kg, i.p.). Simultaneously, all mice received fluorogold (FG) retrograde neurotracer injection into their right joints. In a behavioral study, we evaluated gait using the CatWalk quantitative gait analysis system before surgery, 3 weeks after surgery (before treatment), 4 weeks after surgery (one week after surgery), and 5 weeks after surgery (2 weeks after surgery). In immunohistochemical analysis, the right dorsal root ganglia (DRGs) from the L4–L6 levels were resected 5 weeks after surgery (2 weeks after surgery). They were immunostained for calcitonin gene-related peptide (CGRP), and the number of FG-labeled or CGRP-immunoreactive (IR) DRG neurons was counted. RESULTS: On gait analysis using the CatWalk system, duty cycle, swing speed, and print area were decreased in non-treat group compared with those in control group and improved in the anti-NGF group compared with those in non-treat group. CGRP expression in DRGs was up-regulated in non-treat group compared with that in control group and suppressed in the anti-NGF group compared with that in non-treat group (both p < 0.05). CONCLUSIONS: MIA injection into the knee joint induced gait impairment and the up-regulation of CGRP in DRG neurons in a knee OA pain model in mice. Intraperitoneal injection of anti-NGF antibody suppressed this impairment of gait and up-regulation of CGRP in DRG neurons. These finding suggest that anti-NGF therapy might be valuable in the treatment of OA pain in the knee. BioMed Central 2017-11-03 /pmc/articles/PMC5670727/ /pubmed/29100502 http://dx.doi.org/10.1186/s12891-017-1792-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Miyagi, Masayuki Ishikawa, Tetsuhiro Kamoda, Hiroto Suzuki, Miyako Inoue, Gen Sakuma, Yoshihiro Oikawa, Yasuhiro Orita, Sumihisa Uchida, Kentaro Takahashi, Kazuhisa Takaso, Masashi Ohtori, Seiji Efficacy of nerve growth factor antibody in a knee osteoarthritis pain model in mice |
title | Efficacy of nerve growth factor antibody in a knee osteoarthritis pain model in mice |
title_full | Efficacy of nerve growth factor antibody in a knee osteoarthritis pain model in mice |
title_fullStr | Efficacy of nerve growth factor antibody in a knee osteoarthritis pain model in mice |
title_full_unstemmed | Efficacy of nerve growth factor antibody in a knee osteoarthritis pain model in mice |
title_short | Efficacy of nerve growth factor antibody in a knee osteoarthritis pain model in mice |
title_sort | efficacy of nerve growth factor antibody in a knee osteoarthritis pain model in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5670727/ https://www.ncbi.nlm.nih.gov/pubmed/29100502 http://dx.doi.org/10.1186/s12891-017-1792-x |
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