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环境温度对雄性猴子中3,4-亚甲基二氧甲基苯丙胺诱导的体温调节异常及药代动力学的影响。

Ambient temperature effects on 3,4-methylenedioxymethamphetamine-induced thermodysregulation and pharmacokinetics in male monkeys.

作者信息

Banks Matthew L, Sprague Jon E, Kisor David F, Czoty Paul W, Nichols David E, Nader Michael A

机构信息

Department of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston-Salem, NC, USA.

出版信息

Drug Metab Dispos. 2007 Oct;35(10):1840-5. doi: 10.1124/dmd.107.016261. Epub 2007 Jul 19.

Abstract

Changes in ambient temperature are known to alter both the hyperthermic and the serotonergic consequences of 3,4-methylenedioxymethamphetamine (MDMA). Metabolism of MDMA has been suggested to be a requisite for these neurotoxic effects, whereas the hyperthermic response is an important contributing variable. The aim of the present study was to investigate the interaction between ambient temperature, MDMA-induced thermodysregulation, and its metabolic disposition in monkeys. MDMA (1.5 mg/kg i.v.) was administered noncontingently at cool (18 degrees C; n = 5), room (24 degrees C; n = 7), and warm (31 degrees C; n = 7) ambient temperatures. For 240 min following MDMA administration, core temperature was recorded and blood samples were collected for analysis of MDMA and its metabolites 3,4-dihydroxymethamphetamine (HHMA), 3,4-dihydroxyamphetamine, and 3,4-methylenedioxyamphetamine (MDA). A dose of 1.5 mg/kg MDMA induced a hypothermic response at 18 degrees C, a hyperthermic response at 31 degrees C, and did not significantly change core temperature at 24 degrees C. Regardless of ambient temperature, plasma MDMA concentrations reached maximum within 5 min, and HHMA was a major metabolite. Curiously, the approximate elimination half-life (t(1/2)) of MDMA at 18 degrees C (136 min) and 31 degrees C (144 min) was increased compared with 24 degrees C (90 min) and is most likely because of volume of distribution changes induced by core temperature alterations. At 18 degrees C, there was a significantly higher MDA area under the concentration-time curve (AUC) and a trend for a lower HHMA AUC compared with 24 degrees C and 31 degrees C, suggesting that MDMA disposition was altered. Overall, induction of hypothermia in a cool environment by MDMA may alter its disposition. These results could have implications for MDMA-induced serotonergic consequences.

摘要

已知环境温度的变化会改变3,4-亚甲基二氧甲基苯丙胺(摇头丸)的高温和血清素能效应。有人认为摇头丸的代谢是这些神经毒性作用的必要条件,而高温反应是一个重要的促成变量。本研究的目的是调查环境温度、摇头丸诱导的体温调节障碍及其在猴子体内的代谢处置之间的相互作用。在凉爽(18摄氏度;n = 5)、室温(24摄氏度;n = 7)和温暖(31摄氏度;n = 7)的环境温度下,非连续静脉注射摇头丸(1.5毫克/千克)。在注射摇头丸后的240分钟内,记录核心体温并采集血样,用于分析摇头丸及其代谢物3,4-二羟基甲基苯丙胺(HHMA)、3,4-二羟基苯丙胺和3,4-亚甲基二氧苯丙胺(MDA)。1.5毫克/千克的摇头丸剂量在18摄氏度时引起体温过低反应,在31摄氏度时引起体温过高反应,在24摄氏度时未显著改变核心体温。无论环境温度如何,血浆摇头丸浓度在5分钟内达到最大值,HHMA是主要代谢物。奇怪的是,与24摄氏度(90分钟)相比,摇头丸在18摄氏度(136分钟)和31摄氏度(144分钟)时的近似消除半衰期(t(1/2))增加,这很可能是由于核心体温变化引起的分布容积改变。在18摄氏度时,与24摄氏度和31摄氏度相比,MDA浓度-时间曲线下面积(AUC)显著更高,而HHMA AUC有降低趋势,表明摇头丸的处置发生了改变。总体而言,摇头丸在凉爽环境中诱导体温过低可能会改变其处置。这些结果可能对摇头丸诱导的血清素能效应有影响。

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