Key Laboratory for Modernization of Qiandongnan Miao & Dong Medicine, Qiandongnan Traditional Medicine Research & Development Center, Kaili University, 3 Kaiyuan Road, Kaili, Guizhou, 556011, People's Republic of China.
Key Laboratory for Modernization of Qiandongnan Miao & Dong Medicine, Qiandongnan Traditional Medicine Research & Development Center, Kaili University, 3 Kaiyuan Road, Kaili, Guizhou, 556011, People's Republic of China.
Eur J Pharmacol. 2021 Mar 15;895:173869. doi: 10.1016/j.ejphar.2021.173869. Epub 2021 Jan 14.
The purpose of this study was to investigate the analgesic interaction between matrine and paracetamol in an acetic acid-induced writhing model in mice. Fifty percent effective dose (ED) values of the individual drugs were determined, and the different proportions of matrine and paracetamol were assayed using the isobolographic method. Our study demonstrated that both of matrine and paracetamol dose-dependently inhibited the writhing response evoked by acetic acid, and the ED values and their 95% confidence intervals against these tonic pain were 21.10 (17.86-24.92) mg/kg and 61.30 (50.71-74.10) mg/kg for matrine and paracetamol, respectively. At the fixed ratios of 1:1, 1:3 and 3:1, the experimental ED values of matrine and paracetamol combinations and their 95% confidence intervals were 10.52 (5.14-21.55) mg/kg, 9.13 (4.46-18.70) mg/kg and 4.98 (4.17-5.95) mg/kg, respectively, their theoretical ED values and 95% confidence intervals were 41.20 (36.31-46.74) mg/kg, 51.25 (44.19-59.44) mg/kg and 31.15 (27.25-35.60) mg/kg, and the experimental ED values of matrine and paracetamol combination were significantly lower than their calculated theoretical ED values (all P < 0.01), as revealed by isobolographic analysis. Furthermore, the experimental regression line was also significantly different from the calculated additive equal-effect line over the range of the tested doses (all P < 0.01). Our results suggest that the combination of matrine with paracetamol exerts analgesic synergistic interactions in a mouse acetic acid-induced writhing model, thereby offering a possible therapeutic alternative for the clinical management of inflammatory pain.
本研究旨在探讨苦参碱和扑热息痛在醋酸诱导的小鼠扭体模型中的镇痛相互作用。测定了两种药物的 50%有效剂量(ED)值,并采用等比图形分析法测定了苦参碱和扑热息痛的不同比例。结果表明,苦参碱和扑热息痛均能剂量依赖性地抑制醋酸引起的扭体反应,其对这些强直性疼痛的 ED 值及其 95%置信区间分别为 21.10(17.86-24.92)mg/kg 和 61.30(50.71-74.10)mg/kg。在固定比例为 1:1、1:3 和 3:1 时,苦参碱和扑热息痛联合用药的实验 ED 值及其 95%置信区间分别为 10.52(5.14-21.55)mg/kg、9.13(4.46-18.70)mg/kg 和 4.98(4.17-5.95)mg/kg,其理论 ED 值及其 95%置信区间分别为 41.20(36.31-46.74)mg/kg、51.25(44.19-59.44)mg/kg 和 31.15(27.25-35.60)mg/kg,苦参碱和扑热息痛联合用药的实验 ED 值明显低于其理论计算的 ED 值(均 P<0.01),等比图形分析结果显示。此外,在测试剂量范围内,实验回归线与计算的相加等效应线也显著不同(均 P<0.01)。结果表明,苦参碱与扑热息痛在醋酸诱导的小鼠扭体模型中具有协同镇痛作用,为临床治疗炎性疼痛提供了一种可能的治疗选择。