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环丙沙星对健康受试者茶碱药代动力学的影响。

The effect of ciprofloxacin on theophylline pharmacokinetics in healthy subjects.

作者信息

Batty K T, Davis T M, Ilett K F, Dusci L J, Langton S R

机构信息

Department of Pharmacy, Fremantle Hospital, Western Australia.

出版信息

Br J Clin Pharmacol. 1995 Mar;39(3):305-11. doi: 10.1111/j.1365-2125.1995.tb04453.x.

Abstract
  1. The mechanism of the interaction between ciprofloxacin and theophylline was investigated in nine healthy subjects. 2. Subjects were given a single oral dose of theophylline (3.4 mg kg-1), before and after 60 h of ciprofloxacin therapy at a dose of 500 mg twice daily. 3. Ciprofloxacin reduced the oral clearance of theophylline by 19% (-7.73 +/- 6.42 ml kg-1 h-1 (95% confidence limits -12.66, -2.79)). Some subjects (group A, n = 4) showed little decrease in clearance (mean 4.4%; -1.6 +/- 0.7 ml kg-1 h-1 (-2.6, 0.5)), whereas others (group B, n = 5) showed a marked decrease (mean 30%; -12.7 +/- 3.7 ml kg-1 h-1 (-17.2, -8.1)). 4. Comparing groups A and B, the decrease in oral clearance of theophylline in group B could not be ascribed to differences in the AUC of ciprofloxacin. Group A subjects showed only slight inhibition of 1-demethylation (-12.8 +/- 5.5% (-21.5, -4.0)), while group B subjects showed a significantly greater inhibition of 1-demethylation (-49.9 +/- 9.8% (-62.1, -37.7)), 3-demethylation (-44.8 +/- 8.6% (-55.4, -34.1)) and 8-hydroxylation (-27.0 +/- 3.7% (-31.6, -22.4)). 5. The results suggest that inter-individual variability in the inhibition of theophylline metabolism by ciprofloxacin can be attributed to inter-individual differences in the level of CYP1A2 expression and/or in the degree of inhibition of hepatic CYP1A2 and CYP3A4. 6. The interaction between ciprofloxacin and theophylline can be clinically significant.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 在9名健康受试者中研究了环丙沙星与茶碱之间的相互作用机制。2. 在每日两次给予500 mg环丙沙星治疗60小时前后,受试者口服单剂量茶碱(3.4 mg/kg)。3. 环丙沙星使茶碱的口服清除率降低了19%(-7.73±6.42 ml/kg/h(95%置信区间-12.66,-2.79))。一些受试者(A组,n = 4)清除率降低很少(平均4.4%;-1.6±0.7 ml/kg/h(-2.6,0.5)),而其他受试者(B组,n = 5)则显著降低(平均30%;-12.7±3.7 ml/kg/h(-17.2,-8.1))。4. 比较A组和B组,B组茶碱口服清除率的降低不能归因于环丙沙星的AUC差异。A组受试者仅表现出对1-去甲基化的轻微抑制(-12.8±5.5%(-21.5,-4.0)),而B组受试者对1-去甲基化(-49.9±9.8%(-62.1,-37.7))、3-去甲基化(-44.8±8.6%(-55.4,-34.1))和8-羟基化(-27.0±3.7%(-31.6,-22.4))的抑制作用明显更强。5. 结果表明,环丙沙星对茶碱代谢抑制的个体间差异可归因于CYP1A2表达水平和/或肝脏CYP1A2及CYP3A4抑制程度的个体间差异。6. 环丙沙星与茶碱之间的相互作用在临床上可能具有重要意义。(摘要截断于250字)

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