Weetman D F, Crossfield C
Methods Find Exp Clin Pharmacol. 1982;4(2):99-103.
Prior administration of non-polar solvents was shown to prolong sleeping time in female mice induced with pentobarbitone sodium (37.5 mg/kg). The doses of solvents to double sleeping time were extrapolated from individual dose-response curves: they were (g/kg i.p.): dimethylformamide (DMF) 1.15: polyethyleneglycol 2.0: glycerol 0.66: dimethylsulphoxide 1.78: and sulpholone 1.26. The prolongation of sleeping time with DMF was not due to inhibition of hepatic microsomal enzymes because mice pretreated with SK & F 525A (40 mg/kg i.p.) did not exhibit a much greater solvent-induced effect than occurred in control (unpretreated) mice. DMF prolonged sleeping time in mice injected with thiopentone sodium (37.5 mg/kg i.v.), a drug known not to have its duration of narcotic effect determined by microsomal enzyme metabolism. It is concluded that prolongation of barbiturate-induced sleeping time in mice by DMF is not due to an inhibitory effect of the solvent on the hepatic microsomal enzymes.
先前的研究表明,给雌性小鼠腹腔注射戊巴比妥钠(37.5毫克/千克)后,预先给予非极性溶剂可延长其睡眠时间。使睡眠时间加倍的溶剂剂量是根据个体剂量反应曲线推算出来的:分别为(克/千克腹腔注射):二甲基甲酰胺(DMF)1.15、聚乙二醇2.0、甘油0.66、二甲基亚砜1.78和磺胺酮1.26。DMF延长睡眠时间并非由于抑制肝微粒体酶,因为预先腹腔注射SK&F 525A(40毫克/千克)的小鼠与未预先处理的对照小鼠相比,溶剂诱导的效应并没有显著增强。DMF可延长静脉注射硫喷妥钠(37.5毫克/千克)小鼠的睡眠时间,硫喷妥钠是一种已知其麻醉作用持续时间不由微粒体酶代谢决定的药物。由此得出结论,DMF延长巴比妥类药物诱导的小鼠睡眠时间并非由于该溶剂对肝微粒体酶有抑制作用。