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Evidence for the Participation of ATP-sensitive Potassium Channels in the Antinociceptive Effect of Curcumin
BACKGROUND: It has been reported that curcumin, the main active compound of Curcuma longa, also known as turmeric, exhibits antinociceptive properties. The aim of this study was to examine the participation of ATP-sensitive potassium channels (K(ATP) channels) and, in particular, that of the L-argin...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Pain Society
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3468798/ https://www.ncbi.nlm.nih.gov/pubmed/23091682 http://dx.doi.org/10.3344/kjp.2012.25.4.221 |
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author | De Paz-Campos, Marco Antonio Chávez-Piña, Aracely Evangelina Ortiz, Mario I Castañeda-Hernández, Gilberto |
author_facet | De Paz-Campos, Marco Antonio Chávez-Piña, Aracely Evangelina Ortiz, Mario I Castañeda-Hernández, Gilberto |
author_sort | De Paz-Campos, Marco Antonio |
collection | PubMed |
description | BACKGROUND: It has been reported that curcumin, the main active compound of Curcuma longa, also known as turmeric, exhibits antinociceptive properties. The aim of this study was to examine the participation of ATP-sensitive potassium channels (K(ATP) channels) and, in particular, that of the L-arginine-nitric oxide-cyclic GMP-K(ATP) channel pathway, in the antinociceptive effect of curcumin. METHODS: Pain was induced by the intraplantar injection of 1% formalin in the right hind paw of Wistar rats. Formalin-induced flinching behavior was interpreted as an expression of nociception. The antinociceptive effect of oral curcumin was explored in the presence and absence of local pretreatment with L-NAME, an inhibitor of nitric oxide synthase, ODQ, an inhibitor of soluble guanylyl cyclase, and glibenclamide, a blocker of K(ATP) channels. RESULTS: Oral curcumin produced a dose-dependent antinociceptive effect in the 1% formalin test. Curcumin-induced antinociception was not altered by local L-NAME or ODQ, but was significantly impaired by glibenclamide. CONCLUSIONS: Our results confirm that curcumin is an effective antinociceptive agent. Curcumin-induced antinociception appears to involve the participation of K(ATP) channels at the peripheral level, as local injection of glibenclamide prevented its effect. Activation of K(ATP) channels, however, does not occur by activation of the L-arginine-nitric oxide-cGMP-K(ATP) channel pathway. |
format | Online Article Text |
id | pubmed-3468798 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Korean Pain Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-34687982012-10-22 Evidence for the Participation of ATP-sensitive Potassium Channels in the Antinociceptive Effect of Curcumin De Paz-Campos, Marco Antonio Chávez-Piña, Aracely Evangelina Ortiz, Mario I Castañeda-Hernández, Gilberto Korean J Pain Original Article BACKGROUND: It has been reported that curcumin, the main active compound of Curcuma longa, also known as turmeric, exhibits antinociceptive properties. The aim of this study was to examine the participation of ATP-sensitive potassium channels (K(ATP) channels) and, in particular, that of the L-arginine-nitric oxide-cyclic GMP-K(ATP) channel pathway, in the antinociceptive effect of curcumin. METHODS: Pain was induced by the intraplantar injection of 1% formalin in the right hind paw of Wistar rats. Formalin-induced flinching behavior was interpreted as an expression of nociception. The antinociceptive effect of oral curcumin was explored in the presence and absence of local pretreatment with L-NAME, an inhibitor of nitric oxide synthase, ODQ, an inhibitor of soluble guanylyl cyclase, and glibenclamide, a blocker of K(ATP) channels. RESULTS: Oral curcumin produced a dose-dependent antinociceptive effect in the 1% formalin test. Curcumin-induced antinociception was not altered by local L-NAME or ODQ, but was significantly impaired by glibenclamide. CONCLUSIONS: Our results confirm that curcumin is an effective antinociceptive agent. Curcumin-induced antinociception appears to involve the participation of K(ATP) channels at the peripheral level, as local injection of glibenclamide prevented its effect. Activation of K(ATP) channels, however, does not occur by activation of the L-arginine-nitric oxide-cGMP-K(ATP) channel pathway. The Korean Pain Society 2012-10 2012-10-04 /pmc/articles/PMC3468798/ /pubmed/23091682 http://dx.doi.org/10.3344/kjp.2012.25.4.221 Text en Copyright © The Korean Pain Society, 2012 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 non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article De Paz-Campos, Marco Antonio Chávez-Piña, Aracely Evangelina Ortiz, Mario I Castañeda-Hernández, Gilberto Evidence for the Participation of ATP-sensitive Potassium Channels in the Antinociceptive Effect of Curcumin |
title | Evidence for the Participation of ATP-sensitive Potassium Channels in the Antinociceptive Effect of Curcumin |
title_full | Evidence for the Participation of ATP-sensitive Potassium Channels in the Antinociceptive Effect of Curcumin |
title_fullStr | Evidence for the Participation of ATP-sensitive Potassium Channels in the Antinociceptive Effect of Curcumin |
title_full_unstemmed | Evidence for the Participation of ATP-sensitive Potassium Channels in the Antinociceptive Effect of Curcumin |
title_short | Evidence for the Participation of ATP-sensitive Potassium Channels in the Antinociceptive Effect of Curcumin |
title_sort | evidence for the participation of atp-sensitive potassium channels in the antinociceptive effect of curcumin |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3468798/ https://www.ncbi.nlm.nih.gov/pubmed/23091682 http://dx.doi.org/10.3344/kjp.2012.25.4.221 |
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