Drug-Drug Interaction Between Amlodipine And Clarithromycin In Hypertension Rabbits

Rana Mahmood Ahmad,, Zahraa Kadhim Lafi,, H. Alshaikhli
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Abstract

This study is the first to examine the possibility of pharmacokinetic interaction in blood circulation using amlodipine and clarithromycin as representatives in hypertension rabbits and identify changes. The current study design required rabbits (n=6) for Pharmacokinetics. In group A, rabbits without treatment were used as control. In group B, were administration of a single dose of amlodipine (0.21mg/kg.BW) for 24 hours. Group C, were administered with a single dose of amlodipine (0.21mg/kg/BW.) and clarithromycin (22 mg/kg/BW.) each 6 hr. for 24 hour. The blood samples were collected from (B and C) groups at time intervals of zero, 1, 2, 3, 4, 6, 8, 12, 24, 36, 48, 60, 72, 96, 120, 144 hours and the drug concentrations were estimated using a spectrophotometer and estimated blood pressure using blood pressure cuff with Doppler ultrasound transducer. An increase in C max and AUC in group C (3.52 μg/ml and 130 μg/ml*h) respectively, indicates the improved bioavailability of amlodipine in the presence of clarithromycin compared with group B (2.03 μg/ml and 96.10 μg/ml*h) respectively. Furthermore, reduction in (CL) with an elevation of (Vd) in the presence of clarithromycin (54.94 L/kg/hr. and 4994 L/kg) in group C respectively, compared with group B (74.31 L/kg/hr and 3715 L/kg) respectively. We studied the influence of clarithromycin on the pharmacodynamics of amlodipine in hypertension rabbits. Interaction of amlodipine with multiple doses of clarithromycin produced a high reduction in blood pressure at 9 after administration and the blood pressure continues redaction. In conclusion, the combination of amlodipine with clarithromycin led to the enhancement of the bioavailability of amlodipine by inhibiting the CYP3A4 enzyme leading to producing a hypotension effect with peak plasma concentration effect in hypertension rabbits.
氨氯地平与克拉霉素在家兔高血压中的相互作用
本研究首次以氨氯地平和克拉霉素为代表,探讨高血压家兔血液循环中药代动力学相互作用的可能性,并确定其变化。目前的研究设计需要兔(n=6)进行药代动力学研究。A组以未经处理的家兔为对照。B组给予单剂量氨氯地平(0.21mg/kg.BW) 24小时。C组患者给予单剂量氨氯地平(0.21mg/kg/BW.)和克拉霉素(22 mg/kg/BW.),每6小时一次。24小时。B组和C组分别于0、1、2、3、4、6、8、12、24、36、48、60、72、96、120、144小时采血,用分光光度计测定药物浓度,用带多普勒超声换能器的血压袖带测定血压。C组的cmax和AUC升高(分别为3.52 μg/ml和130 μg/ml*h),表明克拉霉素存在下氨氯地平的生物利用度较B组(分别为2.03 μg/ml和96.10 μg/ml*h)有所提高。此外,在克拉霉素存在下(Vd)升高时(CL)降低(54.94 L/kg/hr)。与B组(74.31 L/kg/hr和3715 L/kg)相比,C组分别为74.31 L/kg和4994 L/kg。研究克拉霉素对高血压家兔氨氯地平药效学的影响。氨氯地平与多剂量克拉霉素的相互作用在给药后9点血压大幅降低,血压继续降低。综上所述,氨氯地平与克拉霉素联用可抑制高血压家兔的CYP3A4酶,从而提高氨氯地平的生物利用度,产生具有血药浓度峰效应的降压作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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