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Effects of oxidative stress on the pharmacokinetics and hepatic metabolism of atazanavir in rats

机译:氧化应激对阿扎那韦大鼠药代动力学和肝代谢的影响

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We studied the effects of oxidative stress (OS) on the pharmacokinetics of atazanavir (ATV), particularly the distribution of ATV in the plasma and its metabolism in hepatic microsomes, using a rat model of ferric-nitrilotriacetate-induced OS (OS rats). The areas under the plasma concentration-time curves for intravenous bolus, oral, and intraportal administration of ATV in the OS rats were significantly greater than those in the control rats, whereas blood clearance of ATV after intravenous bolus injection in the OS rats (0.94 +- 0.04 L/h/kg) was approximately half of that in the control rats (2.08 +- 0.20 L/h/kg). Moreover, the intrinsic clearance (CL_(int)), which is determined by in vitro metabolic studies using hepatic microsomal fractions of rats, was approximately 43% lower in the OS rats (0.489 +- 0.017 mL/min/mg protein) than in the control rats (0.851 +- 0.004 mL/min/mg protein). ATV concentrations in both the plasma-bound fraction and erythrocytes of the OS rats were significantly greater than those in the control rats. These results suggest that the hepatic metabolism of ATV may be reduced in patients under OS.
机译:我们使用亚铁三乙酸铁诱导的OS大鼠模型(OS大鼠)研究了氧化应激(OS)对阿扎那韦(ATV)药代动力学的影响,特别是血浆中ATV的分布及其在肝微粒体中的代谢。 OS大鼠静脉推注,口服和门内给予ATV的血浆浓度-时间曲线下面积显着大于对照大鼠,而OS大鼠静脉推注后ATV的血液清除率(0.94 + -0.04 L / h / kg)约为对照组大鼠(2.08±-0.20 L / h / kg)的一半。此外,通过使用大鼠肝微粒体部分进行的体外代谢研究确定的固有清除率(CL_(int))比OS大鼠降低了约43%(0.489±0.017 mL / min / mg蛋白质)。对照大鼠(0.851±0.004mL / min / mg蛋白质)。 OS大鼠血浆结合部分和红细胞中的ATV浓度均显着高于对照组大鼠。这些结果表明在OS下患者中ATV的肝代谢可能降低。

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