Jaehne Emily Joy, Salem Abdallah, Irvine Rodney James
Discipline of Pharmacology, School of Medical Sciences, University of Adelaide, Level 5 Medical School North, Adelaide, South Australia 5005, Australia.
Psychopharmacology (Berl). 2007 Sep;194(1):41-52. doi: 10.1007/s00213-007-0825-9. Epub 2007 May 27.
Cocaine, methamphetamine, 3,4-methylenedioxymethamphetamine (MDMA, ecstasy), and para-methoxyamphetamine (PMA) disrupt normal thermoregulation in humans, with PMA being associated with more severe cases of hyperthermia. Harm minimization advice on how to prevent overheating depends on appropriate thermoregulatory behavior by drug users.
The purpose of the current study was to establish dose-response relationships for the effects of a number of commonly used illicit stimulants and investigate the behavioral response to increased core temperature.
Sprague-Dawley rats with telemetry implants were administered either saline or 4, 12, 26, 40 or 80 micromol/kg of cocaine, methamphetamine, MDMA, or PMA and confined to an ambient temperature of 30 degrees C for 30 min, before being able to choose their preferred temperature on a thermally graded runway (11-41 degrees C).
The increased core temperature caused by administration of cocaine, methamphetamine, and MDMA treatment led to the animals seeking the cool end of the runway to correct their core temperature, although this did not occur in PMA-treated rats. The order of potency for increasing core temperature was methamphetamine >PMA = MDMA>cocaine. This differed to the slopes of the dose-response curves where MDMA and PMA showed the steepest slope for the doses used followed by methamphetamine then cocaine.
These results suggest that behavioral aspects of thermoregulation are important in assessing the potential of individual drugs to cause harmful increases in core temperature.
可卡因、甲基苯丙胺、3,4-亚甲基二氧甲基苯丙胺(摇头丸)和对甲氧基苯丙胺(PMA)会扰乱人体正常的体温调节,其中PMA与更严重的体温过高病例有关。关于如何预防过热的危害最小化建议取决于吸毒者适当的体温调节行为。
本研究的目的是确定多种常用非法兴奋剂作用的剂量反应关系,并研究对核心体温升高的行为反应。
给植入遥测装置的Sprague-Dawley大鼠注射生理盐水或4、12、26、40或80微摩尔/千克的可卡因、甲基苯丙胺、摇头丸或PMA,将其置于30摄氏度的环境温度下30分钟,然后让它们在温度梯度跑道(11-41摄氏度)上选择自己喜欢的温度。
注射可卡因、甲基苯丙胺和摇头丸治疗导致的核心体温升高,使动物们寻找跑道较凉爽的一端来调节核心体温,不过接受PMA治疗的大鼠没有出现这种情况。提高核心体温的效力顺序为甲基苯丙胺>PMA = 摇头丸>可卡因。这与剂量反应曲线的斜率不同,其中摇头丸和PMA在所使用的剂量下显示出最陡的斜率,其次是甲基苯丙胺,然后是可卡因。
这些结果表明,体温调节的行为方面对于评估个别药物导致核心体温有害升高的可能性很重要。