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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Effects of 3,4-methylenedioxymethamphetamine and related amphetamines on autonomic and behavioral thermoregulation.
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Effects of 3,4-methylenedioxymethamphetamine and related amphetamines on autonomic and behavioral thermoregulation.

机译:3,4-亚甲基二氧基甲基苯丙胺和相关苯丙胺对自主和行为温度调节的影响。

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摘要

3,4-Methylenedioxymethamphetamine (MDMA, 'ecstasy') and related amphetamines such as para-methoxyamphetamine (PMA) disrupt normal thermoregulation in humans and rats. Behavior, an important component of thermoregulation in mammals, has not been investigated with respect to these drugs. This is surprising as harm minimization depends on appropriate thermoregulatory behavior by drug users. The effects of MDMA (10 mg/kg), PMA (10 mg/kg) and d-amphetamine (2 mg/kg) were therefore studied in Sprague-Dawley rats, with telemetry implants measuring core body temperature (T(C)), locomotor activity and heart rate. Rats were administered an amphetamine or saline and confined to an ambient temperature of 21, 30 or 15 degrees C for 30 min, before being able to choose their preferred temperature (T(P)) on a thermally graded runway (11-41 degrees C). Confinement at 21 degrees C had little effect on T(C) in any group. At 30 degrees C MDMA and PMA increased T(C) compared to saline (p<0.001). MDMA treated animals behaviorally overcompensated for this effect (p<0.01). Locomotor activity after MDMA treatment was significantly elevated compared with saline (p<0.01). In contrast, at 15 degrees C MDMA administration resulted in a lower T(C) than saline (p<0.001). MDMA and PMA disrupt autonomic components of thermoregulation, while behavioral components are disrupted to a lesser extent. These results highlight differences in thermoregulatory responses to individual drugs, which were only evident when behavior was measured, and this may be important in assessing their risk.
机译:3,4-亚甲二氧基甲基苯丙胺(MDMA,摇头丸)和相关的苯丙胺如对甲氧基苯丙胺(PMA)破坏了人类和大鼠的正常体温调节。行为,是哺乳动物体内温度调节的重要组成部分,尚未针对这些药物进行过研究。这是令人惊讶的,因为危害最小化取决于药物使用者的适当体温调节行为。因此,在Sprague-Dawley大鼠中研究了MDMA(10 mg / kg),PMA(10 mg / kg)和d-苯异丙胺(2 mg / kg)的作用,并使用遥测植入物测量核心体温(T(C))。运动能力和心率。给大鼠服用苯丙胺或盐水,并在21、30或15摄氏度的环境温度下封闭30分钟,然后才能在热梯度跑道(11-41摄氏度)上选择其首选温度(T(P)) )。在任何组中,将温度限制在21摄氏度对T(C)的影响都很小。与盐水相比,在30摄氏度时,MDMA和PMA的T(C)增加(p <0.001)。用MDMA处理的动物在行为上对此效果过度补偿(p <0.01)。与盐水相比,MDMA处理后的自发活动显着提高(p <0.01)。相反,在15摄氏度下,MDMA给药导致的T(C)低于生理盐水(p <0.001)。 MDMA和PMA破坏了温度调节的自主成分,而行为成分受到的破坏程度较小。这些结果突显了对单个药物的温度调节反应的差异,只有在测量行为时才明显,这对于评估其风险可能很重要。

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