葛根芩连汤对2型糖尿病大鼠沙格列汀药动学和药效学的影响。

IF 1.7 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Chao Yu, Mingyu Cui, Yifeng Yin, Fengmei Zhu, Yue Sui, Xueying Yan, Yingli Gai
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引用次数: 0

摘要

葛根芩连汤(GQD)是一种经典的中药方剂,起源于上汉伦。中药临床常用GQD联合降糖药物(沙格列汀、萨克斯、二甲双胍)治疗2型糖尿病(T2DM)。然而,GQD与降糖药之间的草药相互作用(hdi)仍不清楚。为了确定联合用药的安全性,我们评估了GQD对2型糖尿病大鼠Sax药代动力学和药效学的影响。采用高效液相色谱法测定经GQD(冻干粉,1.35 g/kg)和未经GQD预处理的Sax (5 mg/kg)血浆浓度,并计算药代动力学参数。通过测定大鼠体重、OGTT、TC、TG、LDL-C、HDL-C、FBG、FINS、HOMA-IR、QUICKI、AST、ALT和肝脏系数,探讨GQD对Sax药效学的影响。无论是正常大鼠还是T2DM大鼠,联合用药组Sax的Cmax、AUC0-t、AUC0-∞均显著升高。药效学结果显示,各给药组大鼠体重均有所增加。FBG、TC、TG、LDL-C和HOMA-IR降低,HDL-C、FINS和QUICKI显著升高(p . 2)
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Influence of Gegenqinlian decoction on pharmacokinetics and pharmacodynamics of saxagliptin in type 2 diabetes mellitus rats

Influence of Gegenqinlian decoction on pharmacokinetics and pharmacodynamics of saxagliptin in type 2 diabetes mellitus rats

Gegenqinlian decoction (GQD) is a classic prescription of traditional Chinese medicine (TCM), which originated from Shanghanlun. The combination of GQD and hypoglycemic drugs (saxagliptin, Sax, metformin) is often used to treat Type 2 diabetes mellitus (T2DM) in TCM clinics. However, the herb–drug interactions (HDIs) between GQD and hypoglycemic drugs are still unclear. In order to determine the safety of the combination, we assessed the influences of GQD on the pharmacokinetics and pharmacodynamics of Sax in T2DM rats. The plasma concentration of Sax (5 mg/kg) pretreated with GQD (freeze-dried powder, 1.35 g/kg) or not was determined by high-performance liquid chromatography (HPLC), and pharmacokinetics parameters were calculated. The influence of GQD on the pharmacodynamics of Sax was investigated by detecting the levels of weight, (see abbreviations list) OGTT, TC, TG, LDL-C, HDL-C, FBG, FINS, HOMA-IR, QUICKI, AST, ALT, and the liver coefficient. The Cmax, AUC0-t,and AUC0-∞ of Sax increased significantly in the combination group whether in normal or T2DM rats. The results of pharmacodynamics showed that the weight of rats in each treatment group increased. FBG, TC, TG, LDL-C, and HOMA-IR decreased, HDL-C, FINS, and QUICKI increased significantly (p < 0.05) compared with the model control group. The result showed that the combination of GQD and Sax could not only improve the hypoglycemic effect but also increase the plasma exposure of Sax. The potential HDIs between GQD and Sax should be taken into consideration in clinics. Moreover, for the complexity of the human compared with experimental animals, as well as genetic differences, the in-depth study should be carried out to assess the uniformity of the pharmacokinetics and pharmacodynamics between rats and humans.

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来源期刊
CiteScore
3.60
自引率
0.00%
发文量
35
审稿时长
6-12 weeks
期刊介绍: Biopharmaceutics & Drug Dispositionpublishes original review articles, short communications, and reports in biopharmaceutics, drug disposition, pharmacokinetics and pharmacodynamics, especially those that have a direct relation to the drug discovery/development and the therapeutic use of drugs. These includes: - animal and human pharmacological studies that focus on therapeutic response. pharmacodynamics, and toxicity related to plasma and tissue concentrations of drugs and their metabolites, - in vitro and in vivo drug absorption, distribution, metabolism, transport, and excretion studies that facilitate investigations related to the use of drugs in man - studies on membrane transport and enzymes, including their regulation and the impact of pharmacogenomics on drug absorption and disposition, - simulation and modeling in drug discovery and development - theoretical treatises - includes themed issues and reviews and exclude manuscripts on - bioavailability studies reporting only on simple PK parameters such as Cmax, tmax and t1/2 without mechanistic interpretation - analytical methods
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