Bertilsson L, Tomson T, Tybring G
J Clin Pharmacol. 1986 Jul-Aug;26(6):459-62. doi: 10.1002/j.1552-4604.1986.tb03558.x.
Drugs labeled with stable isotopes have been useful to study time-dependent changes in kinetics. Early studies suggested that carbamazepine (CBZ) may induce its own metabolism, but this could not be proved until tetradeuterium-labeled CBZ (CBZ-D4) was synthesized and then given to patients. CBZ-D4 was administered to three children during long-term treatment of epilepsy with CBZ. After 17 to 32 days of treatment, the plasma clearance of CBZ-D4 was doubled, but during the next four months, there was no further increase, indicating that autoinduction was complete within one month. Two patients with chronic alcoholism were treated with CBZ for five days. Half of the first dose of 600 mg was comprised of CBZ-D4. The half-life of this CBZ-D4 dose in the two patients (20 and 26 hr, respectively) was similar to the post-steady-state half-life of CBZ (23 hr in both patients) measured later. A single dose of CBZ given one week after the last maintenance dose had a longer half-life (46 and 45 hr, respectively), which probably is close to the disposition of the drug before starting the treatment with CBZ. This shows that autoinduction of CBZ metabolism was completed during the very first doses of CBZ. Autoinduction also disappeared rapidly after stopping the treatment. We have shown that it is mainly the epoxide-diol pathway that is induced, both during autoinduction and after induction with other antiepileptic agents.
标记有稳定同位素的药物对于研究动力学随时间的变化很有用。早期研究表明卡马西平(CBZ)可能诱导自身代谢,但直到合成了四氘代卡马西平(CBZ-D4)并给予患者后,这一点才得到证实。在三名儿童使用CBZ长期治疗癫痫期间给予了CBZ-D4。治疗17至32天后,CBZ-D4的血浆清除率增加了一倍,但在接下来的四个月中,没有进一步增加,这表明自身诱导在一个月内完成。两名慢性酒精中毒患者接受CBZ治疗五天。600毫克首剂的一半由CBZ-D4组成。该CBZ-D4剂量在两名患者中的半衰期(分别为20小时和26小时)与后来测得的CBZ稳态后半衰期(两名患者均为23小时)相似。在最后一次维持剂量一周后给予单剂量CBZ,其半衰期更长(分别为46小时和45小时),这可能接近开始使用CBZ治疗前药物的处置情况。这表明CBZ代谢的自身诱导在最初几剂CBZ期间就已完成。停止治疗后,自身诱导也迅速消失。我们已经表明,无论是在自身诱导期间还是在用其他抗癫痫药物诱导后,主要诱导的是环氧化物-二醇途径。