Lomax P, Daniel K A
Department of Pharmacology, School of Medicine, University of California, Los Angeles.
Pharmacology. 1990;40(2):103-9. doi: 10.1159/000138648.
The laboratory rat is being developed as a model to determine whether abuse of cocaine constitutes a risk factor in the pathogenesis of stress or exertion-induced heatstroke. Under thermoneutral conditions (Ta 20 degrees C) cocaine (10-40 mg/kg i.p.) caused a dose-dependent fall in core temperature ranging from 0.45 +/- 0.18 to 1.77 +/- 0.26 degrees C. When the ambient temperature (Ta) was increased to 35 degrees C, cocaine (10-40 mg/kg i.p.) led to a dose-dependent hyperthermia (0.3 +/- 0.08 to 1.43 +/- 0.43 degrees C). Repeated injection of cocaine (40 mg/kg at Ta 20 degrees C or 20 mg/kg at Ta 40 degrees C) on days 1, 3, 8, 15, and 23 did not alter the magnitude of the temperature change compared to that following the first injection, i.e., neither tolerance nor potentiation occurred.
实验室大鼠正被开发成一种模型,以确定滥用可卡因是否构成应激或运动诱导中暑发病机制中的一个风险因素。在热中性条件下(环境温度20摄氏度),可卡因(腹腔注射10 - 40毫克/千克)导致核心体温呈剂量依赖性下降,范围为0.45±0.18至1.77±0.26摄氏度。当环境温度(Ta)升至35摄氏度时,可卡因(腹腔注射10 - 40毫克/千克)导致剂量依赖性体温过高(0.3±0.08至1.43±0.43摄氏度)。在第1、3、8、15和23天重复注射可卡因(在环境温度20摄氏度时为40毫克/千克,或在环境温度40摄氏度时为20毫克/千克),与首次注射后的温度变化幅度相比,并未改变温度变化的幅度,即既未出现耐受性也未出现增强作用。