Reinberg A E
Bull Acad Natl Med. 1996 Mar;180(3):533-43; discussion 544-7.
The chronokinetics of a drug corresponds to dosing time-dependent and predictable (rhythmic) changes in parameters used to characterize its pharmacokinetics e.g. Cmax, t(max), t1/2, AUC, etc.) The chronesthesy or chronopharmacodynamics corresponds to circadian changes in susceptibility of target biosystems to this drug. The target system can be an organ or a tissue (skin, bronchial tree, etc.) as well as a receptor, a membrane, an enzymatic process. Both theoretical and practical implications of chronesthesy have been underestimated and even ignored. It is usually assumed that the constant level over time of a drug in the plasma should result in constant effects. Much experimental evidence have shown that this hypothesis must be rejected.
药物的时辰动力学对应于用于表征其药代动力学的参数(例如Cmax、t(max)、t1/2、AUC等)随给药时间的依赖性和可预测(节律性)变化。时辰感觉或时辰药效学对应于靶生物系统对该药物敏感性的昼夜变化。靶系统可以是一个器官或组织(皮肤、支气管树等)以及受体、膜、酶促过程。时辰感觉的理论和实际意义一直被低估甚至忽视。通常认为药物在血浆中随时间保持恒定水平应导致恒定效应。许多实验证据表明这一假设必须被摒弃。