Lomax P, Daniel K A
Department of Pharmacology, University of California, Los Angeles.
Pharmacology. 1993;46(3):164-72. doi: 10.1159/000139042.
The laboratory rat has been used as an animal model to investigate the effects of cocaine on body temperature and to determine if abuse of the drug is a risk factor in the pathogenesis of exercise-induced heat stroke. Animals were trained to run on a treadmill which was enclosed so that the ambient temperature could be regulated. Exercise at ambient temperatures of 20 and 30 degrees C led to a similar rise in core temperature of approximately 1 degrees C, although the starting core temperature was higher in the rats at 30 degrees C (38.5 +/- 0.10 degrees C compared to 37.9 +/- 0.06 degrees C). Cocaine (20 mg/kg) led to a transient fall in core temperature in the 20 degrees C group; the temperature then rapidly recovered, so that after 60 min exercise there was no significant difference between these and the control animals. At the higher ambient temperature cocaine augmented the rise in core temperature during running, although the animals had regained thermal balance by 30 min and core temperature was maintained at 40.2 +/- 0.13 degrees C until the end of the exercise period. The dopamine D1 receptor antagonist SCH 23390 (0.1, 0.3 or 1.0 mg/kg) led to suppression of spontaneous motor activity so that the rats could be persuaded to exercise for only 30-45 min after treatment. Pretreatment with the antagonist did not affect the rise in core temperature induced by cocaine at 30 degrees C which again stabilized by 30 min at 40.0 +/- 0.12 degrees C.(ABSTRACT TRUNCATED AT 250 WORDS)
实验大鼠已被用作动物模型,以研究可卡因对体温的影响,并确定滥用该药物是否是运动性中暑发病机制中的一个风险因素。动物被训练在一个封闭的跑步机上跑步,以便能够调节环境温度。在20摄氏度和30摄氏度的环境温度下运动导致核心体温有相似的升高,约1摄氏度,尽管30摄氏度组大鼠的起始核心体温更高(38.5±0.10摄氏度,而20摄氏度组为37.9±0.06摄氏度)。可卡因(20毫克/千克)使20摄氏度组的核心体温出现短暂下降;随后体温迅速恢复,因此在运动60分钟后,这些大鼠与对照动物之间没有显著差异。在较高的环境温度下,可卡因加剧了跑步过程中核心体温的升高,尽管动物在30分钟时恢复了热平衡,并且核心体温在运动期结束前一直维持在40.2±0.13摄氏度。多巴胺D1受体拮抗剂SCH 23390(0.1、0.3或1.0毫克/千克)导致自发运动活动受到抑制,以至于给药后大鼠只能被说服运动30 - 45分钟。用拮抗剂预处理并不影响30摄氏度时可卡因诱导的核心体温升高,该体温在30分钟时再次稳定在40.0±0.12摄氏度。(摘要截选至250字)