Zavadil A P, Ross R J, Calil H M, Linnoila M, Blombery P, Jimerson D C, Kopin I J, Potter W Z
Life Sci. 1984 Sep 3;35(10):1061-8. doi: 10.1016/0024-3205(84)90070-5.
Eleven normal volunteers were given an acute and two chronic doses of desipramine (DMI). The plasma norepinephrine (NE), 3-methoxy-4-hydroxyphenylglycol (MHPG), and dihydroxyphenylglycol (DHPG) concentrations were measured before and during drug administration. DMI reduced plasma concentrations of MHPG by 13% and DHPG by 17%. After two weeks of drug administration, the MHPG/NE ratio was reduced, and there was a significant negative correlation with the concurrent drug concentration. These results suggest that DMI: (1) reduces the turnover of NE; and (2) diminishes the oxidative deamination of NE. In addition, the drug concentration response relationship indicates that the effects of uptake inhibition may not be maximal until concentrations in the apparent therapeutic range are achieved.
11名正常志愿者接受了一次急性剂量和两次慢性剂量的地昔帕明(DMI)。在给药前和给药期间测量了血浆去甲肾上腺素(NE)、3-甲氧基-4-羟基苯乙二醇(MHPG)和二羟基苯乙二醇(DHPG)的浓度。DMI使MHPG的血浆浓度降低了13%,使DHPG降低了17%。给药两周后,MHPG/NE比值降低,且与同时的药物浓度呈显著负相关。这些结果表明,DMI:(1)降低NE的周转率;(2)减少NE的氧化脱氨作用。此外,药物浓度反应关系表明,直到达到明显治疗范围内的浓度,摄取抑制作用可能才达到最大。