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甲基苯丙胺和大鼠的核心体温:环境温度、剂量以及 D2 受体阻滞剂的作用。

Methamphetamine and core temperature in the rat: ambient temperature, dose, and the effect of a D2 receptor blocker.

机构信息

Psychology Department, University of Mississippi, 207 Peabody Building, University, MS 38677, USA

出版信息

Psychopharmacology (Berl). 2013 Aug;228(4):551-61. doi: 10.1007/s00213-013-3059-z. Epub 2013 Jun 4.

Abstract

RATIONALE

Methamphetamine (METH) induces hyperthermia in warm and hypothermia in cool environments. Our first goal was to further study the role of ambient temperature in METH's effect on core temperature in rats. Previously, these effects were primarily demonstrated in high doses; we extended this investigation to the low-dose range (1 mg/kg METH). Our second goal was to identify the role of the D2 receptor in METH's effects in cool ambient temperatures.

METHOD

Rats received METH (saline, 1, 5, and 10 mg/kg), raclopride (saline, 0.3, 0.6, and 1.2 mg/kg), or a combination (all doses of raclopride combined with 10 mg/kg METH). Treatments occurred in ambient temperatures of 18, 24, or 30 °C.

RESULTS AND CONCLUSIONS

Consistent with prior research, 5 and 10 mg/kg METH caused hyperthermia or hypothermia in a dose- and ambient temperature-dependent manner (60 min after METH). In contrast, 1 mg/kg produced similar levels of hyperthermia at all ambient temperatures. These findings suggest that a threshold METH dose exists; below this dose, METH still changes core temperature, but CNS control over temperature regulation is left intact. In our experiments regarding D2 blockade, raclopride decreased METH-induced core temperature at 30 and 24 °C (60 min after METH), consistent with previous findings. We extended these findings by demonstrating that in a cool ambient temperature (18 °C), raclopride pretreatment also lowered the core temperature response to METH. Although the D2 receptor is known to mediate hypothermia, the combination of METH and D2 blockade suggests a complex mediation of the core temperature response, perhaps involving neurotransmitter interactions.

摘要

背景

甲基苯丙胺(METH)在温暖环境中会引起体温升高,在寒冷环境中会引起体温降低。我们的首要目标是进一步研究环境温度在大鼠 METH 对核心温度影响中的作用。此前,这些影响主要在高剂量下表现出来;我们将这一研究扩展到低剂量范围(1mg/kg METH)。我们的第二个目标是确定 D2 受体在 METH 在寒冷环境温度下的作用中的作用。

方法

大鼠接受 METH(生理盐水、1、5 和 10mg/kg)、雷氯必利(生理盐水、0.3、0.6 和 1.2mg/kg)或两者的组合(所有雷氯必利剂量与 10mg/kg METH 组合)。在环境温度为 18、24 或 30°C 下进行处理。

结果与结论

与之前的研究一致,5 和 10mg/kg METH 以剂量和环境温度依赖的方式导致体温升高或降低(METH 后 60 分钟)。相比之下,1mg/kg 在所有环境温度下产生相似水平的体温升高。这些发现表明存在一个 METH 剂量阈值;低于该剂量,METH 仍会改变核心温度,但中枢神经系统对体温调节的控制仍然完整。在我们关于 D2 阻断的实验中,雷氯必利降低了 30 和 24°C 时 METH 引起的核心温度(METH 后 60 分钟),这与之前的发现一致。我们通过证明在寒冷的环境温度(18°C)下,雷氯必利预处理也降低了 METH 引起的核心温度反应,扩展了这些发现。尽管 D2 受体已知介导体温降低,但 METH 和 D2 阻断的组合表明核心温度反应的复杂介导作用,可能涉及神经递质相互作用。

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