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首页> 外文期刊>Chemico-biological interactions >Herb-drug interaction of silymarin or silibinin on the pharmacokinetics of trazodone in rats
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Herb-drug interaction of silymarin or silibinin on the pharmacokinetics of trazodone in rats

机译:水飞蓟素或水飞蓟宾的药药相互作用对曲唑酮的大鼠药代动力学

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摘要

Silymarin, one of the most popular herbal medicines, has been widely used for its hepatoprotective effects. This study investigates the effects of repeated dose of silymarin and its major ingredient, silibinin, on the pharmacokinetics of the antidepressant trazodone. Treatment groups included vehicle control group, concomitant silymarin at 1.0 g/kg dose, and four 7-day repeated dose induction groups of 0.5 and 1.0 g/kg silymarin and 0.175 and 0.35 g/kg silibinin. Microdialysis coupled with high performance liquid chromatography (HPLC) was used to simultaneously monitor blood and bile concentrations of trazodone in the rats. Results indicate that pretreatment with an extremely high dose of 1.0 g/kg silymarin significantly decreases trazodone's area under concentration curve (AUC), distribution half-life (t 1/2,α), elimination half-life (t 1/2,β), and mean residence time (MRT). In conclusion, the present study finds no marked effects of silymarin and silibinin on the pharmacokinetics of trazodone under normal daily doses and the relative safety of taking the herb with trazodone.
机译:水飞蓟素是最受欢迎的草药之一,因其具有保肝作用而被广泛使用。这项研究调查了反复服用水飞蓟素及其主要成分水飞蓟宾对抗抑郁药物曲唑酮的药代动力学的影响。治疗组包括媒介物对照组,1.0 g / kg剂量的水飞蓟素和四个7天重复剂量诱导组,分别为0.5和1.0 g / kg水飞蓟素以及0.175和0.35 g / kg水飞蓟宾。微透析结合高效液相色谱法(HPLC)用于同时监测大鼠中曲唑酮的血液和胆汁浓度。结果表明,以1.0 g / kg的高剂量水飞蓟素进行预处理可显着降低曲唑酮的浓度曲线下面积(AUC),分布半衰期(t 1/2,α),消除半衰期(t 1/2,β) ),以及平均停留时间(MRT)。总之,本研究发现水飞蓟素和水飞蓟宾对正常日剂量下曲唑酮的药代动力学没有显着影响,并且与曲唑酮一起服用该草药相对安全。

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