Huupponen R, Viinamäki O, Lammintausta R
Int J Clin Pharmacol Ther Toxicol. 1981 Jan;19(1):6-8.
The proposed ADH-releasing capacity of chlorpropamide was tested after intravenous administration of the drug to nine healthy fasted volunteers. When compared with the placebo experiment, no evidence for increased ADH release was found. On the contrary, the AVP values measured after chlorpropamide injection were slightly lower during the first 2 h than after the saline injection. Serum chlorpropamide concentration was also measured. After a rapid distribution phase, a slow elimination phase followed. The calculated t 1/2 for distribution phase was 1.00 +/- 0.26 hrs (mean +/- s.e.m.).
对9名健康禁食志愿者静脉注射氯磺丙脲后,测试了该药物拟释放抗利尿激素(ADH)的能力。与安慰剂实验相比,未发现抗利尿激素释放增加的证据。相反,注射氯磺丙脲后最初2小时内测得的精氨酸加压素(AVP)值略低于注射生理盐水后。还测量了血清氯磺丙脲浓度。在快速分布阶段之后,接着是缓慢消除阶段。计算得出的分布相半衰期(t1/2)为1.00 +/- 0.26小时(平均值 +/- 标准误)。