Zavvari Fahime, Nahavandi Arezo
Department of Physiology, Faculty of Medicine, Iran University of Medical Science, Tehran, Iran.
Department of Physiology, Faculty of Medicine, Iran University of Medical Science, Tehran, Iran; Department of Neuroscience, Faculty of Advanced Technologies in Medicine, Iran University of Medical Science, Tehran, Iran; Neuroscience Research Center, Iran University of Medical Science, Tehran, Iran.
Physiol Behav. 2020 Dec 1;227:113140. doi: 10.1016/j.physbeh.2020.113140. Epub 2020 Aug 19.
Axonal transport deficit is a key mechanism involved in neurodegenerative conditions. Fluoxetine, a commonly used antidepressant for treatment of depression, is known to regulate several important structural and neurochemical aspects of hippocampal functions. However, the mechanisms underlying these effects are still poorly understood. This study aimed to investigate the effects of chronic fluoxetine treatment on axonal transport in the hippocampus of rat stress-induced model of depression.
We have analyzed the effects of chronic fluoxetine treatment (20 mg/kg/day, 24 days) on immobility behavior (forced swimming test), hippocampal iNOS (inflammatory factor) expression (RT-PCR) as well as hippocampal BDNF, kinesin and dynein expression (RT-PCR) and hippocampal neuronal survival (Nissl staining).
This study provided evidence that fluoxetine could effectively suppress iNOS expression following unpredictable chronic mild stress (P < 0.01), increase hippocampal BDNF (P < 0.01), kinesin (P < 0.05) and dynein (P < 0.01) gene expression, and control neuronal death in CA1 (P < 0.01) and CA3 regions (P < 0.01) of the hippocampus and thereby improve immobility behavior (P < 0.001).
Based on the findings of this study, we concluded the neuroprotective effect of fluoxetine may be due to its ability to improve axonal transmission, followed by increased energy supply and neurotrophin concentration and function.
轴突运输缺陷是神经退行性疾病的关键机制。氟西汀是一种常用的治疗抑郁症的抗抑郁药,已知其可调节海马功能的几个重要结构和神经化学方面。然而,这些作用的潜在机制仍知之甚少。本研究旨在探讨慢性氟西汀治疗对大鼠应激诱导抑郁症模型海马轴突运输的影响。
我们分析了慢性氟西汀治疗(20毫克/千克/天,24天)对不动行为(强迫游泳试验)、海马诱导型一氧化氮合酶(炎症因子)表达(逆转录-聚合酶链反应)以及海马脑源性神经营养因子、驱动蛋白和动力蛋白表达(逆转录-聚合酶链反应)和海马神经元存活(尼氏染色)的影响。
本研究提供的证据表明,氟西汀可有效抑制不可预测的慢性轻度应激后的诱导型一氧化氮合酶表达(P<0.01),增加海马脑源性神经营养因子(P<0.01)、驱动蛋白(P<0.05)和动力蛋白(P<0.01)基因表达,并控制海马CA1区(P<0.01)和CA3区(P<0.01)的神经元死亡,从而改善不动行为(P<0.001)。
基于本研究的结果,我们得出结论,氟西汀的神经保护作用可能是由于其改善轴突传递的能力,随后增加能量供应以及神经营养因子浓度和功能。