Martins Daniel F, Emer Aline A, Batisti A P, Donatello Nathalia, Carlesso Mariana G, Mazzardo-Martins Leidiane, Venzke Dalila, Micke Gustavo A, Pizzolatti Moacir G, Piovezan A P, dos Santos A R S
Experimental Neuroscience Laboratory (LaNEx), University of Southern Santa Catarina at Palhoça, Santa Catarina, Brazil; Postgraduate Program in Health Sciences, University of Southern Santa Catarina at Palhoça, Santa Catarina, Brazil.
Experimental Neuroscience Laboratory (LaNEx), University of Southern Santa Catarina at Palhoça, Santa Catarina, Brazil; Postgraduate Program in Health Sciences, University of Southern Santa Catarina at Palhoça, Santa Catarina, Brazil.
J Ethnopharmacol. 2015 Dec 4;175:30-8. doi: 10.1016/j.jep.2015.08.048. Epub 2015 Sep 4.
Cedrus atlantica essential oil (CaEO) presents analgesic and anti-inflammatory sedative properties. However, it remains unknown whether CaEO alleviates acute postoperative pain.
Here, we investigated the effect of CaEO on postoperative pain and its mechanisms related to the descending pain control in Swiss males mice induced by a plantar incision surgery (PIS) in the hindpaw.
Inhalation of CaEO (5', 30' or 60') markedly reduced mechanical hypersensitivity. This effect was prevented by pre-treatment with naloxone or p-chlorophenylalanine methyl ester (PCPA, 100mg/kg, i.p.)-induced depletion of serotonin. In addition, p-alpha-methyl-para-tyrosin (AMPT, 100mg/kg, i.p.)-induced depletion of norepinephrine, intraperitoneal injection of the α2-adrenergic receptor antagonist yohimbine (0.15 mg/kg, i.p.) or haloperidol (1mg/kg, i.p.) an antagonist of dopaminergic (D1 and D2) receptors prevented the effect of CaEO on hypersensitivity.
These findings suggest that CaEO alleviates postoperative pain by activating the descending pain modulation pathways on the opioidergic, serotonergic, noradrenergic (α2-adrenergic) and dopaminergic (dopamine D1 and D2 receptors) systems.
大西洋雪松精油(CaEO)具有镇痛、抗炎和镇静特性。然而,CaEO是否能减轻术后急性疼痛仍不清楚。
在此,我们研究了CaEO对术后疼痛的影响及其与后爪足底切口手术(PIS)诱导的瑞士雄性小鼠下行性疼痛控制相关的机制。
吸入CaEO(5分钟、30分钟或60分钟)显著降低了机械性超敏反应。用纳洛酮或对氯苯丙氨酸甲酯(PCPA,100mg/kg,腹腔注射)诱导的血清素耗竭预处理可阻止这种作用。此外,对α-甲基对酪氨酸(AMPT,100mg/kg,腹腔注射)诱导的去甲肾上腺素耗竭、腹腔注射α2-肾上腺素能受体拮抗剂育亨宾(0.15mg/kg,腹腔注射)或多巴胺能(D1和D2)受体拮抗剂氟哌啶醇(1mg/kg,腹腔注射)可阻止CaEO对超敏反应的作用。
这些发现表明,CaEO通过激活阿片能、血清素能、去甲肾上腺素能(α2-肾上腺素能)和多巴胺能(多巴胺D1和D2受体)系统上的下行性疼痛调制途径来减轻术后疼痛。