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甲基苯丙胺对前速激肽原mRNA表达的长期突触后影响。

Long-term post-synaptic consequences of methamphetamine on preprotachykinin mRNA expression.

作者信息

Johnson-Davis Kamisha L, Hanson Glen R, Keefe Kristen A

机构信息

Department of Pharmacology and Toxicology, University of Utah, Salt Lake City, Utah 84112, USA.

出版信息

J Neurochem. 2002 Sep;82(6):1472-9. doi: 10.1046/j.1471-4159.2002.01095.x.

Abstract

Exposure to repeated high doses of methamphetamine produces long-term toxicity to central monoamine systems and alters striatonigral pathway function 3 weeks after exposure. To determine whether these changes in the striatonigral pathway persist for longer we examined neuropeptide mRNA expression in the striatum and cytochrome oxidase activity in the output nuclei of the basal ganglia after treatment with multiple high doses of methamphetamine. Rats exposed to multiple high doses of methamphetamine had significant depletion in dopamine and serotonin content, decreases in tyrosine hydroxylase immunoreactivity, and decreases in preprotachykinin mRNA expression, 6 and 12 weeks after methamphetamine treatment. Preprotachykinin mRNA expression was significantly reduced by approximately 20% in the middle striatum and approximately 32% in the caudal striatum, 6 weeks after treatment. Twelve weeks after treatment, preprotachykinin mRNA expression continued to be significantly reduced by approximately 20% in the middle striatum and approximately 14% in the caudal striatum. Cytochrome oxidase histochemical staining in the entopeduncular nucleus and substantia nigra pars reticulata was not significantly different from that in controls at either time point. These data suggest that neurotoxic regimens of methamphetamine induce changes in striatonigral neurons that persist for up to 3 months, although there is some recovery.

摘要

反复暴露于高剂量甲基苯丙胺会对中枢单胺系统产生长期毒性,并在暴露后3周改变纹状体黑质通路功能。为了确定纹状体黑质通路的这些变化是否会持续更长时间,我们在用多次高剂量甲基苯丙胺治疗后,检测了纹状体中神经肽mRNA表达以及基底神经节输出核中的细胞色素氧化酶活性。在甲基苯丙胺治疗后6周和12周,暴露于多次高剂量甲基苯丙胺的大鼠多巴胺和5-羟色胺含量显著减少,酪氨酸羟化酶免疫反应性降低,前速激肽原mRNA表达减少。治疗6周后,前速激肽原mRNA表达在纹状体中部显著降低约20%,在尾状纹状体中显著降低约32%。治疗12周后,前速激肽原mRNA表达在纹状体中部继续显著降低约20%,在尾状纹状体中显著降低约14%。在两个时间点,内苍白球核和黑质网状部的细胞色素氧化酶组织化学染色与对照组相比均无显著差异。这些数据表明,甲基苯丙胺的神经毒性方案会诱导纹状体黑质神经元发生变化,这些变化可持续长达3个月,尽管有一定程度的恢复。

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