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氢氧化镁对甲苯磺丁脲和氯磺丙脲吸收及疗效的影响。

Effect of magnesium hydroxide on the absorption and efficacy of tolbutamide and chlorpropamide.

作者信息

Kivistö K T, Neuvonen P J

机构信息

Department of Pharmacology, University of Turku, Finland.

出版信息

Eur J Clin Pharmacol. 1992;42(6):675-9. doi: 10.1007/BF00265936.

Abstract

The effect of magnesium hydroxide on the absorption and efficacy of tolbutamide and chlorpropamide was examined in a total of 32 healthy volunteers in two separate, randomized parallel-group studies, with 16 subjects in each study. After an overnight fast, the first group of 8 volunteers ingested 500 mg tolbutamide or 250 mg chlorpropamide with 150 ml water, and the second group the same doses of the active drugs with 150 ml water containing 850 mg magnesium hydroxide. Magnesium hydroxide increased the area under the plasma tolbutamide concentration-time curve (AUC) from 0 to 1 h and from 0 to 2 h by 5-fold and 2.5-fold, respectively. The peak plasma concentration, peak time and total AUC were not significantly altered. The incremental insulin area and the decremental glucose area from 0 to 1.5 h were significantly larger in the magnesium hydroxide group than in the controls. The maximum insulin response to tolbutamide was increased fourfold by coadministration of magnesium hydroxide, and it occurred about 1 h earlier than in the control group. In addition, the maximum fall in plasma glucose concentration was attained about 1 h earlier in the antacid group. A tendency to an increased rate of chlorpropamide absorption was observed after magnesium hydroxide, but it did not appear to affect the insulin and glucose responses to chlorpropamide. It is concluded that magnesium hydroxide increased the early bioavailability of tolbutamide, resulting in enhanced insulin and glucose responses. A tendency toward accelerated chlorpropamide absorption by magnesium hydroxide was also observed, but the efficacy of chlorpropamide was unaffected.

摘要

在两项独立的随机平行组研究中,共32名健康志愿者参与,每项研究16名受试者,考察了氢氧化镁对甲苯磺丁脲和氯磺丙脲吸收及疗效的影响。经过一夜禁食后,第一组8名志愿者服用500 mg甲苯磺丁脲或250 mg氯磺丙脲加150 ml水,第二组服用相同剂量的活性药物加150 ml含850 mg氢氧化镁的水。氢氧化镁使血浆甲苯磺丁脲浓度-时间曲线下0至1小时和0至2小时的面积分别增加了5倍和2.5倍。血浆峰值浓度、达峰时间和总曲线下面积无显著变化。氢氧化镁组0至1.5小时的胰岛素增量面积和葡萄糖减量面积显著大于对照组。同时服用氢氧化镁使甲苯磺丁脲的最大胰岛素反应增加了四倍,且比对照组提前约1小时出现。此外,抗酸剂组血浆葡萄糖浓度的最大降幅也提前约1小时出现。观察到氢氧化镁后氯磺丙脲吸收速率有增加的趋势,但似乎不影响氯磺丙脲对胰岛素和葡萄糖的反应。结论是,氢氧化镁增加了甲苯磺丁脲的早期生物利用度,从而增强了胰岛素和葡萄糖反应。还观察到氢氧化镁有加速氯磺丙脲吸收的趋势,但氯磺丙脲的疗效未受影响。

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