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Differential effects of environment-induced changes in body temperature on modafinil’s actions against methamphetamine-induced striatal toxicity in mice

机译:环境引起的体温变化对莫达非尼抵抗甲基苯丙胺引起的小鼠纹状体毒性的作用的不同影响

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摘要

Methamphetamine (METH) exposure can produce hyperthermia that might lead to toxicity and death. Modafinil is a wake-promoting compound that is also been prescribed off-label to treat METH dependence. Modafinil has shown neuroprotective properties against METH harmful effects in animal models. The goal of the present study was to test if the prevention of hyperthermia might play a role on the neuroprotective actions of modafinil against METH toxicity using various ambient temperatures. METH was administered to female C57BL/6 mice in a binge regimen: 4 × 5 mg/kg , 2h apart; modafinil (90mg/kg) was injected twice, 1h before first and fourth METH injections. Drugs were given at cold ambient temperature (14 °C) or hot ambient temperature (29 °C). Body temperature was measured during treatments. Brains were dissected out six days after treatments and processed for TH, DAT, GFAP and c-Fos immunohistochemistry. Exposure to hot ambient temperature exacerbated METH toxicity evidenced by sriatal reductions in TH and DAT and increased GFAP immmunoreactivity. Modafinil counteracted reductions in TH and DAT, but failed to block astroglial activation. At both ambient temperatures tested modafinil did induce increments in GFAP, but the magnitude was significantly lower than the one induced by METH. Both drugs induced increases in c-Fos positive nuclei; modafinil did not block this effect. Our results suggest that protective effects of modafinil against METH-induced neurotoxicity may be dependent, in part, to its hypothermic effects. Nevertheless, modafinil maintained some protective properties on METH-induced alterations in the striatum at different ambient temperatures.
机译:甲基苯丙胺(METH)暴露会产生热疗,可能导致毒性和死亡。莫达非尼(Modafinil)是一种促醒化合物,也已开处方用于治疗METH依赖性。莫达非尼在动物模型中显示出对METH有害作用的神经保护特性。本研究的目的是测试在各种环境温度下,高温的预防是否可能对莫达非尼的抗METH毒性的神经保护作用起作用。以暴食方案对雌性C57BL / 6小鼠施用METH:4×5 mg / kg,间隔2小时;在第一次和第四次METH注射前1小时,两次注射莫达非尼(90mg / kg)。在低温环境温度(14°C)或高温环境温度(29°C)下给药。在治疗期间测量体温。治疗后六天解剖大脑,并进行TH,DAT,GFAP和c-Fos免疫组织化学处理。暴露于炎热的环境中会加剧THM和DAT的降低以及GFAP免疫反应性的增加,从而证明METH的毒性加剧。莫达非尼抵消了TH和DAT的降低,但未能阻止星形胶质细胞的激活。在两种环境温度下,莫达非尼的确能引起GFAP的增加,但幅度明显低于甲基苯丙胺诱导的幅度。两种药物均可诱导c-Fos阳性细胞核的增加。莫达非尼没有阻止这种作用。我们的结果表明,莫达非尼对METH诱导的神经毒性的保护作用可能部分取决于其低温效应。然而,莫达非尼在不同的环境温度下,对甲基苯丙胺诱导的纹状体改变具有一定的保护作用。

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