Smith D E, Lau H S
J Pharm Sci. 1983 Nov;72(11):1298-302. doi: 10.1002/jps.2600721116.
Four male unanesthetized dogs each weighing 22.0-29.0 kg received 0.250 mg/kg iv of bumetanide before (treatment I) and after (treatment II) indomethacin pretreatment. Lactated Ringer's solution was administered intravenously throughout both treatments at a flow rate of 2 ml/min to avoid fluid and electrolyte depletion. Unchanged bumetanide and indomethacin concentrations were analyzed using high-performance liquid chromatography. Sodium was measured by flame photometry and creatinine by colorimetry. Indomethacin pretreatment did not significantly change the pharmacokinetics of bumetanide, affecting neither the total amount of drug nor time course of drug delivered into the urine. In contrast, indomethacin pretreatment resulted in a dramatic reduction in the 4-hr sodium excretion and urine volume. Therefore, a pharmacokinetic interaction may be eliminated as a possible mechanism for the attenuation, by indomethacin, of the natriuretic and diuretic response of bumetanide. Instead, it appears that indomethacin diminishes the response to bumetanide via prostaglandin inhibition.
四只体重在22.0 - 29.0千克之间的未麻醉雄性犬,在吲哚美辛预处理前(治疗I)和预处理后(治疗II)静脉注射布美他尼,剂量为0.250毫克/千克。在两种治疗过程中,均以2毫升/分钟的流速静脉输注乳酸林格氏液,以避免液体和电解质耗竭。使用高效液相色谱法分析未变化的布美他尼和吲哚美辛浓度。通过火焰光度法测量钠,通过比色法测量肌酐。吲哚美辛预处理并未显著改变布美他尼的药代动力学,既不影响药物总量,也不影响药物进入尿液的时间进程。相比之下,吲哚美辛预处理导致4小时钠排泄量和尿量显著减少。因此,药代动力学相互作用可能被排除为吲哚美辛减弱布美他尼利钠和利尿反应的一种可能机制。相反,吲哚美辛似乎通过抑制前列腺素而减弱对布美他尼的反应。