Furst A
Health Phys. 1987 May;52(5):527-30. doi: 10.1097/00004032-198705000-00001.
A biological, physiological or biochemical response to a drug at a low dose may be completely opposite to that response when a larger dose is administered. Also, a response to a single dose of an agent may shortly afterwards be completely reversed. These observations are as old as the use of medicinal preparations or alcoholic beverages. The term "pharmacological inversions" can be used to describe these phenomena. A subset of the dose-response relationship is that of "hormesis." This term, "hormesis," is often used to denote the beneficial response of an organism to a low dose of a physical or chemical agent and a detrimental response to a much larger dose. Many, but not all, of the pharmacological inversions can serve as prototypes of hormesis. Examples of the dose-time effect or the dose-response relationship (which may include the phenomenon of hormesis) can be found among these agents: alcoholic beverages, anesthetic gases, barbiturates, some tranquilizers, many vitamins, caffeine, nicotine, salicylates, enzyme inducers and some toxic metals.
药物低剂量时的生物学、生理学或生化反应可能与大剂量给药时的反应完全相反。此外,对单一剂量药物的反应可能在不久后就完全逆转。这些观察结果与药用制剂或酒精饮料的使用历史一样悠久。“药理学倒置”一词可用于描述这些现象。剂量反应关系的一个子集是“兴奋效应”。“兴奋效应”这个术语通常用于表示生物体对低剂量物理或化学制剂的有益反应以及对大得多剂量的有害反应。许多(但不是全部)药理学倒置可作为兴奋效应的原型。在这些制剂中可以找到剂量-时间效应或剂量-反应关系(可能包括兴奋效应现象)的例子:酒精饮料、麻醉气体、巴比妥类药物、一些镇静剂、许多维生素、咖啡因、尼古丁、水杨酸盐、酶诱导剂和一些有毒金属。