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κ-Opioid receptor participates of NSAIDs peripheral antinociception

2016; Elsevier BV; Volume: 622; Linguagem: Inglês

10.1016/j.neulet.2016.04.029

1872-7972

Lívia Caroline Resende Silva, Marina Gomes Miranda e Castor, Larissa Caldeira Navarro, Thiago Roberto Lima Romero, Igor Dimitri Gama Duarte,

Anesthesia and Pain Management

NSAIDs represent some of the most widely prescribed drugs for relief of short-term fever, pain and inflammation. The participation of the opioid system in the peripheral is poorly understood. The aim of this study was evaluate the role of opioid system in the peripheral antinociception by diclofenac and dipyrone. To test this hypothesis, opioid receptor antagonists were evaluated using the rat paw pressure test, in which pain sensitivity is increased by intraplantar injection of prostaglandin E2 (PGE2, 2 μg). Diclofenac (20 μg/paw) and Dipyrone (40 μg/paw) administered locally into the right paw elicited an antinociceptive effect. It was used naloxone (50 μg/paw), a non-selective opioid receptor antagonist, which antagonized peripheral antinociception induced by diclofenac and dipyrone. Selectively, it was evaluated the μ-, δ- and κ-opioid receptor antagonists, respectively, clocinnamox (40 μg/paw), naltrindole (50 μg/paw) and nor-binaltorphimine (20, 40 and 80 μg/paw). Our data indicated that only the κ-opioid antagonist was capable to reverse the peripheral antinociception by NSAIDs. The present results provide evidence that the opioid system participated in the diclofenac and dipyrone-induced peripheral antinociception by indirect activation of κ-opioid receptor probable by release of endogenous opioids such as dynorphins.