首页> 外文期刊>Journal of Pharmacological and Toxicological Methods >Accuracy of repeated blood sampling in rats: a new technique applied in pharmacokinetic/pharmacodynamic studies of the interaction between warfarin and co-enzyme Q10.
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Accuracy of repeated blood sampling in rats: a new technique applied in pharmacokinetic/pharmacodynamic studies of the interaction between warfarin and co-enzyme Q10.

机译:大鼠重复采血的准确性:一种新技术,用于华法林与辅酶Q10之间相互作用的药代动力学/药效学研究。

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In the past, combined pharmacokinetic/pharmacodynamic (PK/PD) modeling studies of oral anticoagulants in rats have been hampered by the technical problems of blood sampling. In the present study, a semi-micromethod of preparing serial plasma samples for accurate assessment of the prothrombin times (PT) and clotting factor VII activity (CFA) in rats is proposed. The method consists of orbital bleeding, blood sample weighing, gravity calculation and buffer volume adjustment. No significant differences of CFA (percentage normal) were found between citrate-diluted and undiluted plasma. This technique was employed to examine the possibility of PK/PD interaction between warfarin and Co-enzyme Q10 (CoQ10). Rats were given a single oral dose (1.5 mg/kg) of warfarin either alone or on day 4 of an 8-day oral dosing regimen of 10 mg/kg CoQ10 daily. Serial plasma and serum samples, which were subjected to respectively measurements of the anticoagulant effects and concentrations of warfarin and its main metabolites, were obtained over a 96-h period following warfarin administration. All rats survived the whole experiment and maintained a stable condition except for a marked hematocrit decrease. CoQ10 significantly augmented warfarin metabolism but showed little effect on the absorption of warfarin. CoQ10 alone had no apparent effect on either the PT or CFA. The concomitant administration of CoQ10 and warfarin does not significantly affect the anticoagulant effect of warfarin. In conclusion, the proposed serial orbital bleeding technique in rats to prepare an accurate citrate-diluted plasma for PT and CFA measurement is rapid and reliable.
机译:过去,大鼠口服抗凝剂的药代动力学/药效学(PK / PD)组合模型研究受到血液采样技术问题的阻碍。在本研究中,提出了制备连续血浆样品以精确评估大鼠凝血酶原时间(PT)和凝血因子VII活性(CFA)的半微量方法。该方法包括眼眶出血,血样称重,重力计算和缓冲液体积调整。柠檬酸盐稀释血浆和未稀释血浆之间的CFA(正常百分数)无显着差异。使用该技术来检查华法林与辅酶Q10(CoQ10)之间PK / PD相互作用的可能性。单独或在每天10 mg / kg CoQ10的8天口服给药方案的第4天给大鼠口服华法林单次口服剂量(1.5 mg / kg)。在服用华法林后的96小时内,分别获得了血浆和血清样品,分别测定了华法林及其主要代谢产物的抗凝作用和浓度。除明显的血细胞比容降低外,所有大鼠在整个实验中均存活并保持稳定状态。辅酶Q10显着增强了华法林的代谢,但对华法林的吸收几乎没有影响。单独的辅酶Q10对PT或CFA均无明显影响。辅酶Q10和华法林的同时给药对华法林的抗凝作用没有明显影响。总之,拟议的大鼠连续眼眶出血技术可制备出准确的柠檬酸稀释的血浆用于PT和CFA的测定,这种方法快速可靠。

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