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Analgesic Effect of Intrathecal Gabapentin in a Rat Model of Persistent Muscle Pain
OBJECTIVE: To evaluate the analgesic effect of intrathecal gabapentin therapy on secondary hyperalgesia in a rat model of persistent muscle pain. METHODS: Intrathecal catheters were implanted into rats. Mechanical secondary hyperalgesia was induced by repeated intramuscular injections of acidic solu...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Academy of Rehabilitation Medicine
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221397/ https://www.ncbi.nlm.nih.gov/pubmed/25379498 http://dx.doi.org/10.5535/arm.2014.38.5.682 |
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author | Kang, Tae-Wook Sohn, Min Kyun Park, Noh Kyoung Ko, Sang Hyung Cho, Kyoung Jin Beom, Jaewon Kang, Sangkuk |
author_facet | Kang, Tae-Wook Sohn, Min Kyun Park, Noh Kyoung Ko, Sang Hyung Cho, Kyoung Jin Beom, Jaewon Kang, Sangkuk |
author_sort | Kang, Tae-Wook |
collection | PubMed |
description | OBJECTIVE: To evaluate the analgesic effect of intrathecal gabapentin therapy on secondary hyperalgesia in a rat model of persistent muscle pain. METHODS: Intrathecal catheters were implanted into rats. Mechanical secondary hyperalgesia was induced by repeated intramuscular injections of acidic solution into the gastrocnemius muscle. Gabapentin was administrated intrathecally. Rats were allocated to control and experimental (gabapentin 30, 100, 300, and 1,000 µg) group. After gabapentin administration, mechanical withdrawal threshold was measured every 15 minutes and the motor function was measured 30 minutes later. RESULTS: Mechanical hyperalgesia was evoked after the second acidic buffer injection. There was a significant improvement on the mechanical threshold after administration of 100, 300, and 1,000 µg gabapentin compared to pre-injection and the control group. The analgesic effect continued for 105, 135, and 210 minutes, respectively. To discern side effects, motor function was measured. Motor function was preserved in both groups after gabapentin administration, except for rats who received 1,000 µg gabapentin. CONCLUSION: Intrathecal gabapentin administration produces dose-dependent improvements in mechanical hyperalgesia in a persistent muscle pain rat model. This implicates the central nervous system as having a strong influence on the development of persistent mechanical hyperalgesia. These results are helpful in understanding the pathophysiology of secondary hyperalgesia and in the treatment of patients with chronic muscle pain. |
format | Online Article Text |
id | pubmed-4221397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Korean Academy of Rehabilitation Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-42213972014-11-06 Analgesic Effect of Intrathecal Gabapentin in a Rat Model of Persistent Muscle Pain Kang, Tae-Wook Sohn, Min Kyun Park, Noh Kyoung Ko, Sang Hyung Cho, Kyoung Jin Beom, Jaewon Kang, Sangkuk Ann Rehabil Med Original Article OBJECTIVE: To evaluate the analgesic effect of intrathecal gabapentin therapy on secondary hyperalgesia in a rat model of persistent muscle pain. METHODS: Intrathecal catheters were implanted into rats. Mechanical secondary hyperalgesia was induced by repeated intramuscular injections of acidic solution into the gastrocnemius muscle. Gabapentin was administrated intrathecally. Rats were allocated to control and experimental (gabapentin 30, 100, 300, and 1,000 µg) group. After gabapentin administration, mechanical withdrawal threshold was measured every 15 minutes and the motor function was measured 30 minutes later. RESULTS: Mechanical hyperalgesia was evoked after the second acidic buffer injection. There was a significant improvement on the mechanical threshold after administration of 100, 300, and 1,000 µg gabapentin compared to pre-injection and the control group. The analgesic effect continued for 105, 135, and 210 minutes, respectively. To discern side effects, motor function was measured. Motor function was preserved in both groups after gabapentin administration, except for rats who received 1,000 µg gabapentin. CONCLUSION: Intrathecal gabapentin administration produces dose-dependent improvements in mechanical hyperalgesia in a persistent muscle pain rat model. This implicates the central nervous system as having a strong influence on the development of persistent mechanical hyperalgesia. These results are helpful in understanding the pathophysiology of secondary hyperalgesia and in the treatment of patients with chronic muscle pain. Korean Academy of Rehabilitation Medicine 2014-10 2014-10-30 /pmc/articles/PMC4221397/ /pubmed/25379498 http://dx.doi.org/10.5535/arm.2014.38.5.682 Text en Copyright © 2014 by Korean Academy of Rehabilitation Medicine http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kang, Tae-Wook Sohn, Min Kyun Park, Noh Kyoung Ko, Sang Hyung Cho, Kyoung Jin Beom, Jaewon Kang, Sangkuk Analgesic Effect of Intrathecal Gabapentin in a Rat Model of Persistent Muscle Pain |
title | Analgesic Effect of Intrathecal Gabapentin in a Rat Model of Persistent Muscle Pain |
title_full | Analgesic Effect of Intrathecal Gabapentin in a Rat Model of Persistent Muscle Pain |
title_fullStr | Analgesic Effect of Intrathecal Gabapentin in a Rat Model of Persistent Muscle Pain |
title_full_unstemmed | Analgesic Effect of Intrathecal Gabapentin in a Rat Model of Persistent Muscle Pain |
title_short | Analgesic Effect of Intrathecal Gabapentin in a Rat Model of Persistent Muscle Pain |
title_sort | analgesic effect of intrathecal gabapentin in a rat model of persistent muscle pain |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4221397/ https://www.ncbi.nlm.nih.gov/pubmed/25379498 http://dx.doi.org/10.5535/arm.2014.38.5.682 |
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