Department of Clinical and Molecular Biomedicine, Section of Pharmacology and Biochemistry, Catania University, Catania, Italy.
Int J Neuropsychopharmacol. 2013 May;16(4):813-23. doi: 10.1017/S1461145712000612. Epub 2012 Jun 14.
These experiments were undertaken to assess the mechanisms underlying the antidepressant-like effects of the neurokinin-2 (NK(2)) receptor antagonist saredutant (SR48968) in rats tested in the forced swim test (FST), by analysing hippocampal brain-derived neurotrophic factor (BDNF) and plasma corticosterone [as index of hypothalamic-pituitary-adrenal (HPA) axis activity]. Male Wistar rats received three intraperitoneal injections over 24 h of vehicle, saredutant (5 mg/kg), citalopram (15 mg/kg), clomipramine (50 mg/kg). Rats were subjected to restraint stress (4 h) 24 h prior to the FST procedure. This stress procedure increased immobility and decreased swimming behaviour in the FST; furthermore, it lowered hippocampal BDNF protein expression and increased plasma corticosterone levels. Saredutant and clomipramine or citalopram, used here as positive controls, reduced the immobility time in the FST both under basal conditions and after stress exposure. This effect was not attributable to changes in locomotion, because locomotor activity was unchanged when assessed in the open field test. Pretreatment with para-cholorophenylalanine (150 mg/kg, 72 h and 48 h prior to FST) abolished the effect of citalopram and saredutant on immobility time. At neurochemical level, saredutant attenuated activation of HPA axis in stressed animals more than clomipramine or citalopram. The behavioural effects of saredutant support the hypothesis that NK(2) receptor activity is involved in stress-related disorders. These effects of saredutant may be related to normalization of the HPA axis. Moreover, saredutant increases BDNF expression in the hippocampus, confirming the role of NK(2) receptor blockade in BDNF activation following stressor application.
这些实验旨在评估神经激肽-2 (NK(2)) 受体拮抗剂沙瑞特坦 (SR48968) 在强迫游泳试验 (FST) 中测试的大鼠中抗抑郁样作用的机制,通过分析海马脑源性神经营养因子 (BDNF) 和血浆皮质酮 [作为下丘脑-垂体-肾上腺 (HPA) 轴活动的指标]。雄性 Wistar 大鼠在 24 小时内接受三次腹膜内注射载体、沙瑞特坦 (5mg/kg)、西酞普兰 (15mg/kg)、氯米帕明 (50mg/kg)。大鼠在 FST 程序前 24 小时接受束缚应激 (4 小时)。这种应激程序增加了 FST 中的不动性并减少了游泳行为;此外,它降低了海马 BDNF 蛋白表达并增加了血浆皮质酮水平。沙瑞特坦和氯米帕明或西酞普兰在这里用作阳性对照,在基础条件和应激暴露后均减少了 FST 中的不动时间。这种作用不是由于运动变化引起的,因为在开放场试验中评估时运动活动没有改变。预先用对氯苯丙氨酸 (150mg/kg,在 FST 前 72 小时和 48 小时) 处理消除了西酞普兰和沙瑞特坦对不动时间的影响。在神经化学水平上,沙瑞特坦对应激动物的 HPA 轴激活的抑制作用大于氯米帕明或西酞普兰。沙瑞特坦的行为作用支持 NK(2) 受体活性参与应激相关疾病的假说。沙瑞特坦的这些作用可能与 HPA 轴的正常化有关。此外,沙瑞特坦增加了海马体中的 BDNF 表达,证实了 NK(2) 受体阻断在应激后 BDNF 激活中的作用。