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首页> 外文期刊>Neurochemical journal >The Effects of Short-Term Stress and Long-Term Fluoxetine Treatment on the Expression of Apoptotic Proteins in the Brain
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The Effects of Short-Term Stress and Long-Term Fluoxetine Treatment on the Expression of Apoptotic Proteins in the Brain

机译:短期应激和长期氟西汀治疗对大脑中凋亡蛋白表达的影响

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摘要

The effects of 2- or 8-week-long daily treatment with fluoxetine at a dose of 7.26–7.70 mg/kg given with drinking water and short-term forced-swim stress on the levels of mRNAs of anti- and pro-apoptotic proteins, that is, Bcl-xL and Bax, respectively, were studied in the brains of adult male rats using the RT-PCR method. Antiapoptotic effects of stress on the expression of these proteins were observed in the hippocampus of rats that were not treated with fluoxetine and in the midbrain after 2 weeks of the antidepressant treatment. Pro-apoptotic effects of stress were revealed in the frontal cortex of animals that were not treated with fluoxetine and after 2 weeks of fluoxetine treatment. An 8-week-long fluoxetine treatment resulted in an increase in the basal Bax expression in the hippocampus and in anti-apoptotic effects in the neocortex, which were more clearly seen after stress. The observed interaction of the effects of stress and fluoxetine on the expression of proteins of neuronal survival and plasticity may provide anti- or proapoptotic action of the antidepressant on the cells of the emotiogenic structures of the brain.
机译:用富含氟西汀的氟西汀(7.26-7.70mg / kg)的2-周或8周长的每日治疗的影响饮用水和短期强迫游泳压力对抗凋亡蛋白的MRNA水平的影响,即使用RT-PCR方法在成年雄性大鼠的大脑中研究了Bcl-XL和Bax。在抗抑郁药物治疗2周后,在未在未治疗的大鼠和中脑中未处理过的大鼠的大鼠和中脑的大鼠中抗菌对这些蛋白质表达的影响。在不含氟西汀和氟西汀治疗后2周后未治疗的动物的额外皮质促进应激的促凋亡效应。 8周长的氟西汀治疗导致海马的基础蟾蜍表达和Neocortex中的抗凋亡作用增加,在压力后更清楚地看到。所观察到应力和氟西汀影响对神经元存活和可塑性蛋白质表达的影响可以提供抗抑郁药对脑的脑部感应结构细胞的抗抑郁或促凋亡作用。

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