Nishimura N, Naora K, Hirano H, Iwamoto K
Department of Pharmacy, Shimane Medical University Hospital, Japan.
Am J Chin Med. 1999;27(3-4):355-63. doi: 10.1142/S0192415X99000409.
The effects of Sho-saiko-to on the pharmacokinetics of tolbutamide were investigated in rats. After intravenous administration of tolbutamide (5 mg/kg), no significant change in the pharmacokinetics of tolbutamide was observed in both groups of single and multiple (7 days) pre-administration of Sho-saiko-to (500 mg/kg). In the study of single oral administration of tolbutamide (50 mg/kg), co-administration of Sho-saiko-to tended to accelerate the initial absorption rate of tolbutamide. The area under the plasma concentration-time curve of tolbutamide after oral administration was significantly reduced by Sho-saiko-to. Subsequently, a significant decrease was observed in the oral bioavailability of this drug when Sho-saiko-to was given concomitantly. These findings suggest that Sho-saiko-to reduces the bioavailability of tolbutamide after oral administration in rats, and that this change is not related to hepatic metabolism.
在大鼠中研究了小柴胡汤对甲苯磺丁脲药代动力学的影响。静脉注射甲苯磺丁脲(5mg/kg)后,单次和多次(7天)预先给予小柴胡汤(500mg/kg)的两组中,均未观察到甲苯磺丁脲药代动力学有显著变化。在单次口服甲苯磺丁脲(50mg/kg)的研究中,同时给予小柴胡汤有加速甲苯磺丁脲初始吸收速率的趋势。小柴胡汤显著降低了口服给药后甲苯磺丁脲的血浆浓度-时间曲线下面积。随后,当同时给予小柴胡汤时,观察到该药物的口服生物利用度显著降低。这些发现表明,小柴胡汤降低了大鼠口服给药后甲苯磺丁脲的生物利用度,且这种变化与肝脏代谢无关。