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Romero, T. R. L., & Duarte, I. D. G. (2012). N-Palmitoyl-ethanolamine (PEA) Induces Peripheral Antinociceptive Effect by ATP-Sensitive K+-Channel Activation. Journal of Pharmacological Sciences, 118(2), 156–160. Added by: Dr. Enrique Feoli (15/06/2020, 14:45) |
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| Resource type: Journal Article DOI: 10.1254/jphs.11150fp ID no. (ISBN etc.): 1347-8613 BibTeX citation key: Romero2012a View all bibliographic details  |
Categories: Mendeley, Mendeley Subcategories: Analgesia Creators: Duarte, Romero Collection: Journal of Pharmacological Sciences |
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| Abstract |
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Although the antinociceptive effects of N-palmitoyl-ethanolamine (PEA) were first characterized nearly 50 years ago, the identity of the mechanism that mediates these actions has not been elucidated. The present study investigated the contribution of K(+) channels on peripheral antinociception induced by the CB(2) agonist PEA. Nociceptive thresholds to mechanical paw stimulation of Wistar rats treated with intraplantar prostaglandin E(2) to induce hyperalgesia were measured, and other agents were also given by local injection. PEA (5, 10, and 20 µg/paw) elicited a local peripheral antinociceptive effect. This effect was antagonized by glibenclamide, a selective blocker of ATP-sensitive K(+) channels (20, 40, and 80 µg/paw). In addition, neither the voltage-dependent K(+) channel-specific blocker tetraethylammonium (30 µg/paw) nor the small and large conductance blockers of Ca(2+)-activated K(+) channels, dequalinium (50 µg/paw) and paxilline (20 µg/paw), respectively, were able to block the local antinociceptive effect of PEA. These results indicate that the activation of ATP-sensitive K(+) channels could be the mechanism that induces peripheral antinociception by PEA and that voltage-dependent K(+) channels and small and large conductance Ca(2+)-activated K(+) channels do not appear to be involved in this mechanism.
Added by: Dr. Enrique Feoli |