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利坦色林在戒酒慢性酒精中毒者中的药代动力学

Ritanserin pharmacokinetics in abstinent chronic alcoholics.

作者信息

Estévez F, Giusti M, Monti J

机构信息

Department of Pharmacology and Therapeutics, Medicine School, University Hospital, Montevideo, Uruguay.

出版信息

Medicina (B Aires). 1995;55(1):39-44.

PMID:7565034
Abstract

Ritanserin is a thymosthenic agent with an extensive hepatic metabolism and long elimination half life in healthy volunteers. It has been used in abstinent chronic alcoholic patients showing an interesting performance in this condition. Ritanserin pharmacokinetics has only been evaluated in single dose healthy volunteer studies and, on the other hand, chronic use of the drug in alcoholic patients during withdrawal period could be anticipated. Therefore, the objective of the present study, is to assess the cumulating kinetics of the serotonin antagonist during chronic administration. Ten abstinent alcoholic patients were included in an open study. The drug was administered at a daily dose of 10 mg for 28 days and the active phase was preceded by a seven-day wash out period with placebo. Blood samples were taken on the 1st, and 28th, day of treatment, 24 hours after taking the drug. Urine samples were taken during the night before the second and 28th dose. Plasma and urine ritanserin concentration was measured by high performance liquid chromatography. Very large variations in initial and steady state concentrations (CV = 65 and 52% respectively) were found, which is reflected in the large variability of the calculated pharmacokinetic parameters. Ritanserin cumulation factor (R) was 6.9 +/- 8.3 (mean+SEM). Two patients showing extensive accumulation had prolonged elimination half lives (433 and 279 hours) that are explained mostly by an expansion of the volume of distribution and, to a lesser extent, by diminished clearance.

摘要

利坦色林是一种具有强大肝脏代谢能力且在健康志愿者体内消除半衰期较长的兴奋胸腺剂。它已被用于戒酒的慢性酒精中毒患者,在这种情况下表现出有趣的效果。利坦色林的药代动力学仅在单剂量健康志愿者研究中进行过评估,另一方面,可以预期在戒酒期慢性使用该药物治疗酒精中毒患者。因此,本研究的目的是评估血清素拮抗剂在慢性给药期间的累积动力学。十名戒酒的酒精中毒患者被纳入一项开放性研究。药物以每日10毫克的剂量给药28天,在活跃期之前有一个为期七天的安慰剂洗脱期。在治疗的第1天和第28天服药后24小时采集血样。在第二次和第28次服药前的夜间采集尿样。通过高效液相色谱法测量血浆和尿液中的利坦色林浓度。发现初始浓度和稳态浓度有非常大的变化(分别为CV = 65%和52%),这反映在计算出的药代动力学参数的巨大变异性上。利坦色林累积因子(R)为6.9 +/- 8.3(平均值±标准误)。两名显示出大量蓄积的患者消除半衰期延长(分别为433小时和279小时),这主要是由于分布容积扩大,在较小程度上是由于清除率降低所致。

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