Díaz-Reval M Irene, Cárdenas Yolitzy, Huerta Miguel, Trujillo Xóchitl, Sánchez-Pastor Enrique Alejandro, González-Trujano María Eva, Virgen-Ortíz Adolfo, Pérez-Hernández M Gicela
Centro Universitario de Investigaciones Biomédicas, Universidad de Colima, Colima 28045, México.
Laboratorio de Neurofarmacología de Productos Naturales, Dirección de Investigaciones en Neurociencias, Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz, Ciudad de México 14370, México.
Pharmaceuticals (Basel). 2022 Jul 23;15(8):910. doi: 10.3390/ph15080910.
Pharmacological synergism is a current strategy for the treatment of pain. However, few studies have been explored to provide evidence of the possible synergism between a non-steroidal anti-inflammatory drug (NSAID) and a cannabinoid agonist, in order to establish which combinations might be effective to manage pain. The aim of this study was to explore the synergism between ibuprofen (IBU) and the synthetic cannabinoid WIN 55,212-2 (WIN) to improve pain relief by analyzing the degree of participation of the CB and CB cannabinoid receptors in the possible antinociceptive synergism using an experimental model of pain in Wistar rats. First, the effective dose thirty (ED) of IBU (10, 40, 80, and 160 mg/kg, subcutaneous) and WIN (3, 10, and 30 µg/p, intraplantar) were evaluated in the formalin test. Then, the constant ratio method was used to calculate the doses of IBU and WIN to be administered in combination (COMB) to determine the possible synergism using the isobolographic method. The participation of the CB and CB receptors was explored in the presence of the antagonists AM281 and AM630, respectively. The combination of these drugs produced a supra-additive response with an interaction index of 0.13. In addition, AM281 and AM630 antagonists reversed the synergistic effect in 45% and 76%, respectively, suggesting that both cannabinoid receptors are involved in this synergism, with peripheral receptors playing a relevant role. In conclusion, the combination of IBU + WIN synergism is mainly mediated by the participation of the CB receptor, which can be a good option for the better management of pain relief.
药理协同作用是目前治疗疼痛的一种策略。然而,很少有研究探讨非甾体抗炎药(NSAID)与大麻素激动剂之间可能存在的协同作用,以确定哪些组合可能有效控制疼痛。本研究的目的是通过使用Wistar大鼠疼痛实验模型,分析CB和CB大麻素受体在可能的抗伤害感受协同作用中的参与程度,探讨布洛芬(IBU)与合成大麻素WIN 55,212-2(WIN)之间的协同作用,以改善疼痛缓解。首先,在福尔马林试验中评估了IBU(10、40、80和160mg/kg,皮下注射)和WIN(3、10和30μg/p,足底注射)的半数有效剂量(ED)。然后,使用恒定比例法计算联合给药(COMB)时IBU和WIN的剂量,并用等效应线图法确定可能的协同作用。分别在拮抗剂AM281和AM630存在的情况下,探讨CB和CB受体的参与情况。这些药物的组合产生了超相加反应,相互作用指数为0.13。此外,AM281和AM630拮抗剂分别在45%和76%的程度上逆转了协同作用,表明两种大麻素受体均参与了这种协同作用,外周受体发挥了相关作用。总之,IBU + WIN的协同作用主要由CB受体的参与介导,这可能是更好地控制疼痛缓解的一个良好选择。