Guthrie S K, Heidt M, Pande A, Grunhaus L, Haskett R F, Hariharan M
College of Pharmacy, University of Michigan, Ann Arbor 48109-1065.
J Clin Psychopharmacol. 1992 Jun;12(3):191-6.
Ten depressed patients and eight control subjects received 1 mg of dexamethasone intravenously at two different time points. Depressed patients were studied when they were depressed and following an improvement in their depression. In control subjects the first and second studies were performed approximately 1 month apart. Dexamethasone and cortisol were determined at 0, 5, 15, and 30 minutes, then at 1, 1.2, 2, 3, 4, 5, 6, 7, 9, 12, 17, and 24 hours following dexamethasone administration. Data from each patient was fit using a computer to a two compartment pharmacokinetic model and area under the time versus plasma concentration curve, elimination half-life, and clearance were also determined. Depressed patients exhibited a slower dexamethasone clearance and a larger area under the curve than control subjects at the first time point, but not at the second time point. The groups did not differ significantly in any of the other pharmacokinetic parameters (including distribution half-life, elimination half-life, or volume of distribution) at either time point. The possible causes and implications of these findings are discussed.
十名抑郁症患者和八名对照受试者在两个不同时间点接受了1毫克静脉注射地塞米松。对抑郁症患者在抑郁状态时以及抑郁症状改善后进行了研究。对照受试者的首次和第二次研究相隔约1个月进行。在注射地塞米松后的0、5、15和30分钟,然后在1、1.2、2、3、4、5、6、7、9、12、17和24小时测定地塞米松和皮质醇。使用计算机将每位患者的数据拟合到二室药代动力学模型,并确定时间与血浆浓度曲线下面积、消除半衰期和清除率。在第一个时间点,抑郁症患者的地塞米松清除率较慢,曲线下面积比对照受试者大,但在第二个时间点并非如此。在两个时间点的任何其他药代动力学参数(包括分布半衰期、消除半衰期或分布容积)方面,两组均无显著差异。讨论了这些发现的可能原因和意义。