Reinberg A
Int J Clin Pharmacol Res. 1986;6(1):33-44.
Chronopharmacology involves the investigation of drug effects as a function of biological time and the investigation of drug effects on rhythm characteristics. Three new concepts must be considered: (a) the chronokinetics of a drug, embracing rhythmic (circadian) changes in drug bioavailability (or pharmacokinetics) and its excretion (urinary among others); (b) the chronaesthesia of a biosystem to a drug, i.e. circadian changes in the susceptibility of any biosystem to a drug (including organ systems, parasites, etc.); skin and bronchial chronaesthesia to various agents have been documented in man; and (c) the chronergy of a drug, taking into consideration its chronokinetics and the chronaesthesia of the involved organismic biosystems. The term chronergy includes rhythmic changes in the overall effects and in the effectiveness of some drugs. Clinical chronopharmacology is useful for solving problems of drug optimization, i.e. enhancing the desired efficiency of a drug and reducing its undesired effects. Circadian rhythms can be demonstrated in various effects of drugs on sleep, anaesthesia and related processes. For example, in the rat the duration of sleep induced by substances such as pentobarbital, hexobarbital, Althesin (alphaxadone and alphadoline in castor oil) is circadian system stage-dependent. Time-dependent changes of liver enzymes (e.g. hexobarbital oxidase) play a role in these circadian rhythms. The clinical chronopharmacokinetics of benzodiazepines have been documented in man. Chronopharmacologic methods can be used to study desired and undesired hypnotic effects of substances. Such is the case of new antihistamines (anti-H1), which do not induce sleepiness, in either acute or chronic administration. Pertinent also is the problem of intolerance to shift-work. Intolerant shift-workers are subject to internal desynchronization between at least two rhythms (e.g. activity-rest cycle and body temperature). Clinically these workers suffer from sleep disturbances, persistent fatigue and are regular users of sleeping pills, which is also a symptom of intolerance. However, over the long-term, these drugs are of no help to intolerant shift-workers.
时辰药理学涉及研究药物效应作为生物时间的函数,以及研究药物对节律特征的影响。必须考虑三个新概念:(a) 药物的时辰动力学,包括药物生物利用度(或药代动力学)及其排泄(包括尿液排泄等)的节律性(昼夜节律)变化;(b) 生物系统对药物的时辰感受性,即任何生物系统对药物的敏感性的昼夜节律变化(包括器官系统、寄生虫等);人体皮肤和支气管对各种药物的时辰感受性已有文献记载;(c) 药物的时辰效能,考虑到其时辰动力学和所涉及的机体生物系统的时辰感受性。时辰效能一词包括某些药物的总体效应和有效性的节律性变化。临床时辰药理学有助于解决药物优化问题,即提高药物的预期疗效并减少其不良作用。药物对睡眠、麻醉及相关过程的各种效应中可显示出昼夜节律。例如,在大鼠中,戊巴比妥、己巴比妥、阿尔thesin(蓖麻油中的阿法沙朵和阿法多林)等物质诱导的睡眠时间是依赖于昼夜节律系统阶段的。肝酶(如己巴比妥氧化酶)的时间依赖性变化在这些昼夜节律中起作用。苯二氮䓬类药物的临床时辰药代动力学在人体中已有文献记载。时辰药理学方法可用于研究药物的预期和非预期催眠作用。新型抗组胺药(抗H1)就是如此,无论急性还是慢性给药都不会引起嗜睡。轮班工作不耐受问题也与此相关。不耐受轮班工作者至少在两种节律(如活动-休息周期和体温)之间会出现内部不同步。临床上,这些工作者会出现睡眠障碍、持续疲劳,并且经常服用安眠药,这也是不耐受的一种症状。然而,从长期来看,这些药物对不耐受轮班工作者并无帮助。