首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >The effects of the beta 1 antagonist, metoprolol, on methamphetamine-induced changes in core temperature in the rat
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The effects of the beta 1 antagonist, metoprolol, on methamphetamine-induced changes in core temperature in the rat

机译:β1拮抗剂,美托洛尔对大鼠核心温度变化的β1拮抗剂的影响

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Methamphetamine (METH) results in hyperthermia or hypothermia depending on environmental conditions. Here we studied the role of the beta 1 adrenergic receptor in mediating METH's temperature effects. Core temperature measurements were made telemetrically over a 7.5 h session, two days/week, in test chambers regulated at either 18 degrees C, 24 degrees C, or 30 degrees C ambient temperature. Rats were treated with the beta 1 antagonist metoprolol (5.0, 10.0, and 15.0 mg/kg) alone (Experiment 1), or in combination with 5.0 mg/kg METH (Experiment 2). In experiment 3, we combined a lower dose range of metoprolol (0.75, 1.5, and 3.0 mg/kg) with 5.0 mg/kg Amu at 18 degrees C and 30 degrees C. Confirming prior findings, METH alone resulted in hyperthermia in warm (30) and hypothermia in cool environments (18 degrees C). Metoprolol alone induced small but significant increases in core temperature. In combination, however, metoprolol reduced METH-induced changes in core temperature. Specifically, at 30 degrees C, 3.0, 5.0, 10.0, and 15.0 mg/kg metoprolol decreased METH-induced hyperthermia; at 18 degrees C, all six doses of metoprolol enhanced METH-induced hypothermia. Our metoprolol findings suggest that one component of METH's temperature effects involves increasing core temperature at all ambient conditions via beta 1 receptors. Since beta receptors are involved in brown adipose tissue (BAT)-mediated thermogenesis, skeletal muscle-mediated thermogenesis, heart rate, and the metabolism of glucose and lipids, we discuss each of these as possible mechanisms for metoprolol's effects on METH-induced changes in core temperature. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
机译:根据环境条件,甲基苯丙胺(甲基)导致高温或体温过低。在这里,我们研究了β1肾上腺素能受体在介导甲基温度效应中的作用。核心温度测量在7.5小时/周的7.5小时/周,在18℃,24℃或30摄氏度环境温度下调节的测试室。用β1拮抗剂美托洛尔(5.0,10.0和15.0mg / kg)用β1拮抗剂甲酚(实验1)或与5.0mg / kg甲基甲基(实验2)组合进行大鼠。在实验3中,我们将较低剂量的富含剂量范围(0.75,1.5和3.0mg / kg)组合在18摄氏度和30摄氏度下的5.0mg / kg Amu中。确认先前发现,单独导致温暖的热疗( 30)凉爽环境中的耐低温(18℃)。甲型托洛尔单独诱导核心温度的小但显着增加。然而,组合,美托洛尔降低了核心温度的甲基诱导的变化。具体地,在30摄氏度,3.0,5.0,10.0和15.0mg / kg富金属托洛尔下降,降低了甲状腺炎的甲状腺炎;在18℃下,所有六剂甲型托洛尔增强了甲状腺炎的体温过低。我们的富洛洛尔调查结果表明,甲基温效应的一个组分涉及通过β1受体在所有环境条件下增加核心温度。由于β受体涉及棕色脂肪组织(蝙蝠)介导的热生成,骨骼肌介导的热生成,心率和葡萄糖和脂质的代谢,我们将这些中的每一个作为氟托洛尔对甲基诱导变化的影响的可能机制核心温度。 (c)2015 Elsevier Ireland Ltd.保留所有权利。

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