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Biomed Res ; 36(1): 47-54, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25749150

RESUMO

This study investigated the effect of bergamot essential oil (BEO) or linalool, a major volatile component of BEO, on the nociceptive response to formalin. Plantar subcutaneous injection of BEO or linalool into the ipsilateral hindpaw reduced both the first and late phases of the formalin-induced licking and biting responses in mice. Plantar subcutaneous injection of BEO or linalool into the contralateral hindpaw did not yield an antinociceptive effect, suggesting that the antinociceptive effect of BEO or linalool in the formalin test occurred peripherally. Intraperitoneal and plantar subcutaneous injection pretreatment with naloxone hydrochloride, an opioid receptor antagonist, significantly attenuated both BEO- and linalool-induced antinociception. Pretreatment with naloxone methiodide, a peripherally acting opioid receptor antagonists, also significantly antagonized the antinociceptive effects of BEO and linalool. Our results provide evidence for the involvement of peripheral opioids in antinociception induced by BEO and linalool. These results suggest that activation of peripheral opioid receptors may play an important role in reducing formalin-induced nociception.


Assuntos
Analgésicos/farmacologia , Monoterpenos/farmacologia , Nociceptividade/efeitos dos fármacos , Óleos de Plantas/farmacologia , Receptores Opioides/metabolismo , Monoterpenos Acíclicos , Animais , Membro Posterior , Injeções Subcutâneas , Masculino , Camundongos , Naloxona/análogos & derivados , Naloxona/farmacologia , Antagonistas de Entorpecentes/farmacologia , Nociceptividade/fisiologia , Medição da Dor , Compostos de Amônio Quaternário/farmacologia
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