Von Huben Stefani N, Lay Christopher C, Crean Rebecca D, Davis Sophia A, Katner Simon N, Taffe Michael A
1Molecular and Integrative Neurosciences Department, The Scripps Research Institute, La Jolla, CA 92037, USA.
Neuropsychopharmacology. 2007 Mar;32(3):673-81. doi: 10.1038/sj.npp.1301078. Epub 2006 Apr 12.
The ambient temperature (T(A)) under which rodents are exposed to (+/-)3,4-methylenedioxymethamphetamine (MDMA) affects the direction and magnitude of the body temperature response, and the degree of hypo/hyperthermia generated in subjects can modify the severity of lasting brain changes in 'neurotoxicity' models. The thermoregulatory effects of MDMA have not been well described in non-human primates and it is unknown if T(A) has the potential to affect acute hyperthermia and therefore other lasting consequences of MDMA. The objective of this study was to determine if the temperature alteration produced by MDMA in nonhuman primates depends on T(A) as it does in rats and mice. Body temperature and spontaneous home cage activity were monitored continuously in six male rhesus monkeys via radiotelemetry. The subjects were challenged intramuscularly with 0.56-2.4 mg/kg (+/-)MDMA under each of three T(A) conditions (18, 24, and 30 degrees C) in a randomized order. The temperature was significantly elevated following injection with all doses of MDMA under each ambient temperature. The magnitude of mean temperature change was approximately 1 degrees C in most conditions suggesting a closely controlled thermoregulatory response in monkeys across a range of doses and ambient temperatures. Activity levels were generally suppressed by MDMA; however, a 50% increase over vehicle was observed after 0.56 MDMA under the 30 degrees C condition. It is concluded that MDMA produces a similar degree of hyperthermia in rhesus monkeys across a range of T(A) conditions that result in hypothermia or exaggerated hyperthermia in rodents. Monkey temperature responses to MDMA appear to be more similar to humans than to rodents and therefore the monkey may offer an improved model of effects related to MDMA-induced hyperthermia.
啮齿动物接触3,4-亚甲基二氧甲基苯丙胺(摇头丸)时的环境温度(T(A))会影响体温反应的方向和幅度,并且在“神经毒性”模型中,受试者产生的体温过低/过高程度可改变持久脑变化的严重程度。摇头丸的体温调节作用在非人类灵长类动物中尚未得到充分描述,T(A)是否有可能影响急性体温过高以及摇头丸的其他持久后果尚不清楚。本研究的目的是确定摇头丸在非人类灵长类动物中产生的温度变化是否像在大鼠和小鼠中那样取决于T(A)。通过无线电遥测连续监测六只雄性恒河猴的体温和自发笼内活动。在三种T(A)条件(18、24和30摄氏度)下,以随机顺序对受试者进行肌肉注射0.56 - 2.4 mg/kg的(±)摇头丸。在每个环境温度下,注射所有剂量的摇头丸后体温均显著升高。在大多数情况下,平均温度变化幅度约为1摄氏度,这表明在一系列剂量和环境温度下,猴子的体温调节反应受到严格控制。活动水平通常受到摇头丸的抑制;然而,在30摄氏度条件下注射0.56剂量的摇头丸后,观察到活动水平比注射赋形剂后增加了50%。得出的结论是,在一系列导致啮齿动物体温过低或体温过高加剧的T(A)条件下,摇头丸在恒河猴中产生的体温过高程度相似。猴子对摇头丸的体温反应似乎比啮齿动物更类似于人类,因此猴子可能为与摇头丸诱导的体温过高相关的效应提供一个更好的模型。