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Rapid, transient, and dose-dependent expression of Hsp70 messenger RNA in the rat brain after morphine treatment

机译:吗啡处理后大鼠脑中Hsp70信使RNA的快速,瞬时和剂量依赖性表达

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摘要

Induction of Hsp70 in the brain has been reported after intake of drugs of abuse like amphetamine and lysergic acid diethylamide. In this investigation, gene expression of Hsp70 and other heat shock genes in the rat brain was studied in response to morphine. Twenty milligrams per kilogram morphine intraperitoneally resulted in a marked induction of Hsp70 messenger RNA (mRNA) expression in the frontal cortex with a maximum increase of 13.2-fold after 2 hours. A moderate increase of Hsp27 mRNA expression (6.7-fold) could be observed after 4 hours, whereas mRNA expression of Hsp90 and of the constitutive Hsc70 did not exceed a mean factor of 1.8-fold during the 24 hours interval. The increase in Hsp70 mRNA was dose dependent, showing a significant elevation after doses ranging from 10 to 50 mg/kg morphine. In situ hybridization revealed enhanced Hsp70 mRNA expression mainly in cortical areas, in the hippocampus, in the paraventricular and supraoptic nuclei of the hypothalamus, in the locus coeruleus, as well in the pineal body. The double in situ hybridization technique revealed increased Hsp70 mRNA expression mainly in VGLUT1-positive neurons and to a lesser extent in olig1-positive oligodendroglia. Immunohistochemistry revealed a marked increase of Hsp70 protein in neuronal cells and blood vessels after 12 hours. In contrast to animal experiments, morphine did not increase Hsp70 mRNA expression in vitro in μ-opioid receptor (MOR1)–expressing human embryonic kidney 293 cells, suggesting no direct MOR1-mediated cellular effect. To exclude a body temperature–related morphine effect on Hsp70 mRNA expression, the temperature was recorded. Five to 20 mg/kg resulted in hyperthermia (maximum 40.6°), whereas a high dose (50 mg/kg) that produced the highest mRNA induction, showed a clear hypothermia (minimum 37.2°C). These findings argue against the possibility that Hsp70 induction by morphine is caused by its effect on body temperature. It may be speculated that increased expression of Hsp70 after morphine application protects brain structures against potentially hazardous effects of opiates.
机译:据报道,摄入苯丙胺和麦角酸二乙酰胺等滥用药物后,大脑中会诱导Hsp70诱导。在这项研究中,研究了大鼠脑中Hsp70和其他热休克基因对吗啡的响应。腹膜内每公斤20毫克吗啡导致额叶皮层中Hsp70信使RNA(mRNA)表达的明显诱导,2小时后最大增加13.2倍。在4小时后,可以观察到Hsp27 mRNA表达的中等增加(6.7倍),而在24小时间隔内,Hsp90和组成型Hsc70的mRNA表达没有超过平均1.8倍。 Hsp70 mRNA的增加是剂量依赖性的,剂量在10至50 mg / kg吗啡后显示出明显的升高。原位杂交揭示增强的Hsp70 mRNA表达主要在皮层区域,海马,下丘脑室旁和视上核,蓝斑轨迹以及松果体中。双原位杂交技术显示,Hsp70 mRNA表达主要在VGLUT1阳性神经元中增加,而在olig1阳性少突胶质细胞中表达较少。免疫组织化学显示12小时后神经元细胞和血管中Hsp70蛋白显着增加。与动物实验相反,吗啡在体外在表达μ阿片受体(MOR1)的人类胚胎肾293细胞中不增加Hsp70 mRNA的表达,表明没有直接的MOR1介导的细胞作用。为了排除与体温有关的吗啡对Hsp70 mRNA表达的影响,记录了温度。 5至20 mg / kg导致体温过高(最高40.6°),而产生最高mRNA诱导的高剂量(50 mg / kg)显示出明显的体温过低(最低37.2°C)。这些发现反驳了吗啡诱导Hsp70的原因是其对体温的影响。可以推测,吗啡应用后Hsp70表达的增加保护了大脑结构免受鸦片的潜在危险影响。

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