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Antinociceptive effects of gabapentin & its mechanism of action in experimental animal studies

BACKGROUND & OBJECTIVES: Several studies have shown the possible analgesic effects of gabapentin, widely used as an antiepileptic. Thus, clinical studies have been carried out especially for neuropathic syndroms. This study was undertaken to investigate experimentally whether gabapentin has anal...

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Autores principales: Kilic, Fatma Sultan, Sirmagul, Basar, Yildirim, Engin, Oner, Setenay, Erol, Kevser
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401692/
https://www.ncbi.nlm.nih.gov/pubmed/22771591
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author Kilic, Fatma Sultan
Sirmagul, Basar
Yildirim, Engin
Oner, Setenay
Erol, Kevser
author_facet Kilic, Fatma Sultan
Sirmagul, Basar
Yildirim, Engin
Oner, Setenay
Erol, Kevser
author_sort Kilic, Fatma Sultan
collection PubMed
description BACKGROUND & OBJECTIVES: Several studies have shown the possible analgesic effects of gabapentin, widely used as an antiepileptic. Thus, clinical studies have been carried out especially for neuropathic syndroms. This study was undertaken to investigate experimentally whether gabapentin has analgesic effects in mice and rats. METHODS: The mice were divided into 10 groups (n=7) with various treatments to assess central and peripheral antinociceptive activity of gabapentin. Hot plate, tail clip and tail flick tests were applied for the investigation of central antinociceptive activity and the writhing test was applied for the investigation of peripheral antinociceptive activity. In addition, we also evaluated the levels of PGE(2) and nNOS on perfused hippocampus slices of rats. RESULTS: Gabapentin showed a peripheral antinociceptive effect at all doses and a central antinociceptive effect at 30mg/kg dose. While the L-NAME and cyproheptadine changed the central and peripheral effects of gabapentin, naloxone did not change these effects. In vitro studies showed that gabapentin significantly increased nNOS level. PGE(2) and nNOS were found to have an important role in the antinociceptive effects of gabapentin at all doses and its combinations with L-NAME, cyproheptadine, indomethacine, and naloxone. As expected, PGE(2) levels decreased in all groups, while nNOS levels increased, which is believed to be an adaptation mechanism. INTERPRETATION & CONCLUSIONS: Our findings indicate that arachidonate, nitrergic and serotonergic systems play an important role in the antinociceptive activity of gabapentin except for the opioidergic system. Additionally, this effect occured centrally and peripherally. These effects were also mediated by nNOS and PGE2.
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spelling pubmed-34016922012-07-26 Antinociceptive effects of gabapentin & its mechanism of action in experimental animal studies Kilic, Fatma Sultan Sirmagul, Basar Yildirim, Engin Oner, Setenay Erol, Kevser Indian J Med Res Original Article BACKGROUND & OBJECTIVES: Several studies have shown the possible analgesic effects of gabapentin, widely used as an antiepileptic. Thus, clinical studies have been carried out especially for neuropathic syndroms. This study was undertaken to investigate experimentally whether gabapentin has analgesic effects in mice and rats. METHODS: The mice were divided into 10 groups (n=7) with various treatments to assess central and peripheral antinociceptive activity of gabapentin. Hot plate, tail clip and tail flick tests were applied for the investigation of central antinociceptive activity and the writhing test was applied for the investigation of peripheral antinociceptive activity. In addition, we also evaluated the levels of PGE(2) and nNOS on perfused hippocampus slices of rats. RESULTS: Gabapentin showed a peripheral antinociceptive effect at all doses and a central antinociceptive effect at 30mg/kg dose. While the L-NAME and cyproheptadine changed the central and peripheral effects of gabapentin, naloxone did not change these effects. In vitro studies showed that gabapentin significantly increased nNOS level. PGE(2) and nNOS were found to have an important role in the antinociceptive effects of gabapentin at all doses and its combinations with L-NAME, cyproheptadine, indomethacine, and naloxone. As expected, PGE(2) levels decreased in all groups, while nNOS levels increased, which is believed to be an adaptation mechanism. INTERPRETATION & CONCLUSIONS: Our findings indicate that arachidonate, nitrergic and serotonergic systems play an important role in the antinociceptive activity of gabapentin except for the opioidergic system. Additionally, this effect occured centrally and peripherally. These effects were also mediated by nNOS and PGE2. Medknow Publications & Media Pvt Ltd 2012-05 /pmc/articles/PMC3401692/ /pubmed/22771591 Text en Copyright: © The Indian Journal of Medical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kilic, Fatma Sultan
Sirmagul, Basar
Yildirim, Engin
Oner, Setenay
Erol, Kevser
Antinociceptive effects of gabapentin & its mechanism of action in experimental animal studies
title Antinociceptive effects of gabapentin & its mechanism of action in experimental animal studies
title_full Antinociceptive effects of gabapentin & its mechanism of action in experimental animal studies
title_fullStr Antinociceptive effects of gabapentin & its mechanism of action in experimental animal studies
title_full_unstemmed Antinociceptive effects of gabapentin & its mechanism of action in experimental animal studies
title_short Antinociceptive effects of gabapentin & its mechanism of action in experimental animal studies
title_sort antinociceptive effects of gabapentin & its mechanism of action in experimental animal studies
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3401692/
https://www.ncbi.nlm.nih.gov/pubmed/22771591
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