普伐他汀与格列齐特在动物模型中的相互作用

S. Satyanarayana, M. Chandrasekhar, O. Gouda, K. E. Kumar
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引用次数: 5

摘要

目前的研究计划在大鼠和家兔中评估格列齐特(降糖)在普伐他汀(降血脂)存在下的安全性。对正常和四氧嘧啶诱导的糖尿病大鼠进行了口服剂量格列齐特、普伐他汀及其联合用药的研究。同样,在正常家兔中进行的研究是口服剂量的格列齐特和普伐他汀,并在两种治疗之间有足够的洗脱期。在不同时间间隔采集大鼠和家兔的血样,分析血清格列齐特水平。格列齐特在正常大鼠和糖尿病大鼠中产生降糖/抗高血糖活性,在2小时和8小时后达到峰值,在正常家兔中产生降糖活性,在3小时后达到峰值。普伐他汀对正常大鼠/糖尿病大鼠/正常家兔的血糖水平有轻微的降低。普伐他汀对正常大鼠/糖尿病大鼠/正常家兔的降糖作用增强。普伐他汀使家兔血清胰岛素水平升高。普伐他汀的存在显著改变了家兔血清格列齐特水平和药动学参数。观察到的相互作用似乎是代谢和排泄水平的药代动力学相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug-Drug Interaction between Pravastatin and Gliclazide in Animal Models
The present study is planned to evaluate the safety of gliclazide (antidiabetic) therapy in the presence of pravastatin (antihyperlipidemic) in rats and rabbits. Studies in normal and alloxan-induced diabetic rats were conducted with oral doses of gliclazide, pravastatin, and their combination. Similarly, studies in normal rabbits were conducted with oral doses of gliclazide, pravastatin, and their combination with adequate washout periods in between the treatments. Blood samples were collected from rats and rabbits at different time intervals and were analyzed for blood serum gliclazide levels. Gliclazide produced hypoglycaemic/antihyperglycaemic activity in normal and diabetic rats with peak activity after 2 hours and 8 hours and hypoglycaemic activity in normal rabbits with peak activity after 3 hours. Pravastatin alone produced minor reduction in blood glucose levels in normal rats/diabetic rats/normal rabbits. Pravastatin increased the hypoglycaemic effect of gliclazide in normal rats/diabetic rats/normal rabbits when administered together. The serum insulin levels were increased with pravastatin treatment in rabbits. The serum gliclazide levels and pharmacokinetic parameters of gliclazide were altered significantly in presence of pravastatin in rabbits. The interaction observed appears to be pharmacokinetic interaction at metabolic and excretion levels.
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