Nam Hyungwoo, Kerman Ilan A
Department of Anatomy and Neurobiology, University of Maryland School of Medicine, United States.
Department of Psychiatry and Behavioral Medicine, Virginia Tech Carilion School of Medicine, United States; School of Neuroscience, Virginia Tech, United States.
Physiol Behav. 2016 Oct 15;165:339-49. doi: 10.1016/j.physbeh.2016.08.020. Epub 2016 Aug 20.
The Wistar-Kyoto (WKY) rat is a widely used animal model of depression, which is characterized by dysregulation of noradrenergic signaling. We previously demonstrated that WKY rats show a unique behavioral profile on the forced swim test (FST), characterized by high levels of immobility upon initial exposure and a greater learning-like response by further increasing immobility upon re-exposure than the genetically related Wistar rats. In the current study we aimed to determine whether altered activation of brainstem noradrenergic cell groups contributes to this behavioral profile. We exposed WKY and Wistar rats, to either 5min of forced swim or to the standard two-day FST (i.e. 15min forced swim on Day 1, followed by 5min on Day 2). We then stained their brains for FOS/tyrosine hydroxylase double-immunocytochemistry to determine potential differences in the activation of the brainstem noradrenergic cell groups. We detected a relative hyperactivation in the locus coeruleus of WKY rats when compared to Wistars in response to both one- and two-day forced swim. In contrast, within the A2 noradrenergic cell group, WKY rats exhibited diminished levels of FOS across both days of the FST, suggesting their lesser activation. We followed up these observations by selectively lesioning the A2 neurons, using anti-dopamine-β-hydroxylase-conjugated saporin, in Wistar rats, which resulted in increased FST immobility on both days of the test. Together these data indicate that the A2 noradrenergic cell group regulates FST behavior, and that its hypoactivation may contribute to the unique behavioral phenotype of WKY rats.
Wistar-Kyoto(WKY)大鼠是一种广泛应用的抑郁症动物模型,其特征是去甲肾上腺素能信号失调。我们之前证明,WKY大鼠在强迫游泳试验(FST)中表现出独特的行为特征,其特点是初次暴露时不动时间较长,再次暴露时通过进一步增加不动时间表现出更强的类似学习的反应,这与基因相关的Wistar大鼠不同。在本研究中,我们旨在确定脑干去甲肾上腺素能细胞群的激活改变是否导致了这种行为特征。我们将WKY和Wistar大鼠暴露于5分钟的强迫游泳或标准的为期两天的FST(即第1天15分钟强迫游泳,第2天5分钟)。然后,我们对它们的大脑进行FOS/酪氨酸羟化酶双免疫细胞化学染色,以确定脑干去甲肾上腺素能细胞群激活的潜在差异。与Wistar大鼠相比,我们发现WKY大鼠在应对一天和两天的强迫游泳时,蓝斑中的相对激活增强。相反,在A2去甲肾上腺素能细胞群中,WKY大鼠在FST的两天中FOS水平均降低,表明其激活程度较低。我们通过在Wistar大鼠中使用抗多巴胺-β-羟化酶结合的皂草素选择性损伤A2神经元来跟进这些观察结果,这导致在测试的两天中FST不动时间增加。这些数据共同表明,A2去甲肾上腺素能细胞群调节FST行为,其激活不足可能导致WKY大鼠独特的行为表型。