Pérez-Valenzuela Catherine, Gárate-Pérez Macarena F, Sotomayor-Zárate Ramón, Delano Paul H, Dagnino-Subiabre Alexies
Laboratory of Stress Neurobiology, Institute of Physiology, Center for Neurobiology and Brain Plasticity, Faculty of Sciences, Universidad de Valparaíso Valparaíso, Chile.
Laboratory of Neurochemistry and Neuropharmacology, Institute of Physiology, Center for Neurobiology and Brain Plasticity, Faculty of Sciences, Universidad de Valparaíso Valparaíso, Chile.
Front Neural Circuits. 2016 Dec 27;10:108. doi: 10.3389/fncir.2016.00108. eCollection 2016.
Chronic stress impairs auditory attention in rats and monoamines regulate neurotransmission in the primary auditory cortex (A1), a brain area that modulates auditory attention. In this context, we hypothesized that norepinephrine (NE) levels in A1 correlate with the auditory attention performance of chronically stressed rats. The first objective of this research was to evaluate whether chronic stress affects monoamines levels in A1. Male rats were subjected to chronic stress (restraint stress) and monoamines levels were measured by high performance liquid chromatographer (HPLC)-electrochemical detection. Chronically stressed rats had lower levels of NE in A1 than did controls, while chronic stress did not affect serotonin (5-HT) and dopamine (DA) levels. The second aim was to determine the effects of reboxetine (a selective inhibitor of NE reuptake) on auditory attention and NE levels in A1. Rats were trained to discriminate between two tones of different frequencies in a two-alternative choice task (2-ACT), a behavioral paradigm to study auditory attention in rats. Trained animals that reached a performance of ≥80% correct trials in the 2-ACT were randomly assigned to control and stress experimental groups. To analyze the effects of chronic stress on the auditory task, trained rats of both groups were subjected to 50 2-ACT trials 1 day before and 1 day after of the chronic stress period. A difference score (DS) was determined by subtracting the number of correct trials after the chronic stress protocol from those before. An unexpected result was that vehicle-treated control rats and vehicle-treated chronically stressed rats had similar performances in the attentional task, suggesting that repeated injections with vehicle were stressful for control animals and deteriorated their auditory attention. In this regard, both auditory attention and NE levels in A1 were higher in chronically stressed rats treated with reboxetine than in vehicle-treated animals. These results indicate that NE has a key role in A1 and attention of stressed rats during tone discrimination.
慢性应激会损害大鼠的听觉注意力,单胺类物质调节初级听觉皮层(A1)中的神经传递,A1是一个调节听觉注意力的脑区。在此背景下,我们假设A1中的去甲肾上腺素(NE)水平与慢性应激大鼠的听觉注意力表现相关。本研究的首要目标是评估慢性应激是否会影响A1中的单胺类物质水平。对雄性大鼠施加慢性应激(束缚应激),并通过高效液相色谱仪(HPLC)-电化学检测法测量单胺类物质水平。与对照组相比,慢性应激大鼠A1中的NE水平较低,而慢性应激并未影响血清素(5-HT)和多巴胺(DA)水平。第二个目标是确定瑞波西汀(一种NE再摄取的选择性抑制剂)对A1中听觉注意力和NE水平的影响。在双选任务(2-ACT)中训练大鼠区分两种不同频率的音调,这是一种研究大鼠听觉注意力的行为范式。在2-ACT中达到≥80%正确试验表现的训练动物被随机分配到对照组和应激实验组。为了分析慢性应激对听觉任务的影响,两组训练大鼠在慢性应激期前1天和后1天均进行50次2-ACT试验。通过用慢性应激方案实施前的正确试验次数减去之后的正确试验次数来确定差异分数(DS)。一个意外的结果是,接受赋形剂处理的对照大鼠和接受赋形剂处理的慢性应激大鼠在注意力任务中的表现相似,这表明对对照动物反复注射赋形剂具有应激性并使其听觉注意力下降。在这方面,接受瑞波西汀治疗的慢性应激大鼠的听觉注意力和A1中的NE水平均高于接受赋形剂处理的动物。这些结果表明,在音调辨别过程中,NE在应激大鼠的A1和注意力方面起着关键作用。