Medina-López Raúl, Vara-Gama Nancy, Soria-Arteche Olivia, Moreno-Rocha Luis A, López-Muñoz Francisco J
Departamento Sistemas Biologicos Universidad Autonoma Metropolitana-Xochimilco, Calz. del Hueso 1100, Col. Villa Quietud, Mexico City 04960, Mexico.
Laboratorio No. 7 "Dolor y Analgesia" del Departamento de Farmacobiologia, Cinvestav-Sede Sur, Calz. de los Tenorios No. 235, Col. Granjas Coapa, Mexico City 14330, Mexico.
Pharmaceutics. 2018 Jan 26;10(1):20. doi: 10.3390/pharmaceutics10010020.
The purpose of the present study was to determine whether caffeine modifies the pharmacokinetics and pharmacodynamics of ()-ketoprofen following oral administration in a gout-type pain model. 3.2 mg/kg of ()-ketoprofen alone and combined with 17.8 mg/kg of caffeine were administered to Wistar rats and plasma levels were determined between 0.5 and 24.0 h. Additionally, antinociception was evaluated based on the protocol of the PIFIR (pain-induced functional impairment in the rat) model before blood sampling between 0.5 and 4.0 h. Significant differences in C, AUC, and AUC values were observed with caffeine administration ( < 0.05). Also, significant differences in E, T, and AUC values were determined when comparing the treatments with and without caffeine ( < 0.05). By relating the pharmacokinetic and pharmacodynamic data, a counter-clockwise hysteresis loop was observed regardless of the administration of caffeine. When the relationship between AUCe and AUCp was fitted to the sigmoidal model, a satisfactory correlation was found (R² > 0.99) as well as significant differences in and values ( < 0.05). With caffeine, and values changed by 489.5% and 695.4%, respectively. The combination studied represents a convenient alternative for the treatment of pain when considering the advantages offered by using drugs with different mechanisms of action.
本研究的目的是确定在痛风型疼痛模型中,口服给药后咖啡因是否会改变()-酮洛芬的药代动力学和药效学。将3.2mg/kg的()-酮洛芬单独以及与17.8mg/kg咖啡因联合给予Wistar大鼠,并在0.5至24.0小时之间测定血浆水平。此外,在0.5至4.0小时之间采血前,根据PIFIR(大鼠疼痛诱导功能障碍)模型的方案评估抗伤害感受。给予咖啡因后,观察到C、AUC和AUC值有显著差异(<0.05)。此外,比较有咖啡因和无咖啡因的治疗时,E、T和AUC值也有显著差异(<0.05)。通过关联药代动力学和药效学数据,无论是否给予咖啡因,均观察到逆时针滞后环。当将AUCe和AUCp之间的关系拟合到S形模型时,发现有令人满意的相关性(R²>0.99)以及和值有显著差异(<0.05)。使用咖啡因时,和值分别变化了489.5%和695.4%。考虑到使用具有不同作用机制的药物所带来的优势,所研究的组合代表了一种方便的疼痛治疗替代方案。