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环境温度的微小变化会导致大鼠体内3,4-亚甲基二氧甲基苯丙胺(摇头丸)诱导的5-羟色胺神经毒性及核心体温发生巨大变化。

Small changes in ambient temperature cause large changes in 3,4-methylenedioxymethamphetamine (MDMA)-induced serotonin neurotoxicity and core body temperature in the rat.

作者信息

Malberg J E, Seiden L S

机构信息

University of Chicago, Department of Pharmacological and Physiological Sciences, Chicago, Illinois 60637, USA.

出版信息

J Neurosci. 1998 Jul 1;18(13):5086-94. doi: 10.1523/JNEUROSCI.18-13-05086.1998.

Abstract

The amphetamine derivative 3,4-methylenedioxymethamphetamine (MDMA) is a drug of abuse and has been shown to be neurotoxic to 5-HT terminals in many species. MDMA-engendered neurotoxicity has been shown to be affected by both ambient temperature and core body temperature. We now report that small (2 degreesC) changes in ambient temperature produce changes in core temperature in MDMA-treated rats, but the same changes in ambient temperature do not affect core temperature of saline-treated animals. Furthermore, increases in core temperature of MDMA-treated animals increase neurotoxicity. Rats were given MDMA (20 or 40 mg/kg) or saline and placed in an ambient temperature of 20, 22, 24, 26, 28, or 30 degreesC using a novel temperature measurement apparatus that controls ambient temperature +/-0.5 degrees C. Two weeks after MDMA treatment, the rats were killed, and regional 5-HT and 5-hydroxyindole acetic acid levels were analyzed as a measure of neurotoxicity. Rats treated with MDMA at 20 and 22 degrees C showed a hypothermic core temperature response. Treatment with MDMA at 28 and 30 degreesC produced a hyperthermic response. At ambient temperatures of 20-24 degrees C, neurotoxicity was not observed in the frontal cortex, somatosensory cortex, hippocampus, or striatum. At ambient temperatures of 26-30 degrees C, neurotoxicity was seen and correlated with core temperature in all regions examined. These data indicate that ambient temperature has a significant affect on MDMA neurotoxicity, core temperature, and thermoregulation in rats. This finding has implications on both the temperature dependence of the mechanism of MDMA neurotoxicity and human use because fatal hyperthermia is associated with MDMA use in humans.

摘要

苯丙胺衍生物3,4-亚甲基二氧基甲基苯丙胺(MDMA)是一种滥用药物,已被证明对许多物种的5-羟色胺(5-HT)终末具有神经毒性。已表明MDMA引起的神经毒性受环境温度和核心体温的影响。我们现在报告,环境温度的微小(2℃)变化会使MDMA处理的大鼠的核心体温发生变化,但相同的环境温度变化不会影响生理盐水处理动物的核心体温。此外,MDMA处理动物的核心体温升高会增加神经毒性。使用一种能将环境温度控制在±0.5℃的新型温度测量装置,给大鼠注射MDMA(20或40mg/kg)或生理盐水,并将其置于20、22、24、26、28或30℃的环境温度中。MDMA处理两周后,处死大鼠,分析5-HT和5-羟吲哚乙酸水平以衡量神经毒性。在20和22℃下用MDMA处理的大鼠表现出核心体温降低的反应。在28和30℃下用MDMA处理产生体温过高的反应。在20-24℃的环境温度下,在额叶皮质、体感皮质、海马体或纹状体中未观察到神经毒性。在26-30℃的环境温度下,在所检查的所有区域均观察到神经毒性,且与核心体温相关。这些数据表明,环境温度对大鼠的MDMA神经毒性、核心体温和体温调节有显著影响。这一发现对MDMA神经毒性机制的温度依赖性以及人类使用都有影响,因为致命性体温过高与人类使用MDMA有关。

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