Centre for Neuroscience Studies, Queen's University, 62 Arch Street, Kingston, Ontario, Canada K7L 3N6.
Physiol Behav. 2013 Feb 17;110-111:20-9. doi: 10.1016/j.physbeh.2012.12.011. Epub 2012 Dec 28.
The lateral septum has been extensively implicated in regulating anxiety-related defensive behaviors in the rat. Neuropeptide Y (NPY) contributes to anxiety, likely through activity at the NPY Y1 and/or Y2 receptor binding sites. Although the lateral septum contains the highest density of Y2 receptors in brain, the involvement of this receptor in anxiety-related defensive behaviors is not clear. Thus, the purpose of the current study was to characterize lateral septal Y2 receptor contributions to rats' defensive responses to threat and/or potentially threatening environments. We investigated this by infusing the NPY Y2 agonist NPY13-36 into the lateral septum and testing rats across a battery of animal models of anxiety (Experiment 1). To verify the role of Y2 in mediating the observed effects, rats were pre-infused with the potent and highly selective Y2 antagonist BIIE 0246 prior to infusion with NPY13-36 (Experiment 2). Infusions of NPY13-36 into the lateral septum increased rats' open-arm exploration in the elevated plus-maze test (p<0.01) and decreased the proportion of rats' that buried (p<0.05) as well as their latency to initiate burying in the shock-probe burying test (p<0.01). By contrast, NPY13-36 did not affect either anxiety- or appetite-related responses in the novelty-induced suppression of feeding test (all ps>0.3; Experiment 1). Pre-treatment with the Y2 antagonist BIIE 0246 prevented the anxiolytic-like actions of NPY13-36 in the plus-maze but not in the shock-probe test (Experiment 2). Thus, it appears that the anxiolytic-like actions of lateral septal NPY13-36 are mediated by the Y2 receptor in a test-specific manner.
外侧隔核在调节大鼠焦虑相关防御行为方面起着广泛的作用。神经肽 Y(NPY)通过 NPY Y1 和/或 Y2 受体结合位点的活性有助于焦虑。尽管外侧隔核在大脑中含有最高密度的 Y2 受体,但该受体在焦虑相关防御行为中的参与尚不清楚。因此,本研究的目的是描述外侧隔核 Y2 受体对大鼠对威胁和/或潜在威胁环境的防御反应的贡献。我们通过将 NPY Y2 激动剂 NPY13-36 注入外侧隔核并在一系列焦虑动物模型中测试大鼠来研究这一点(实验 1)。为了验证 Y2 在介导观察到的效应中的作用,大鼠在注入 NPY13-36 之前预先注入了强效且高度选择性的 Y2 拮抗剂 BIIE 0246(实验 2)。将 NPY13-36 注入外侧隔核增加了高架十字迷宫测试中大鼠的开放臂探索(p<0.01),减少了大鼠埋藏的比例(p<0.05)以及它们开始在电击探头埋藏测试中埋藏的潜伏期(p<0.01)。相比之下,NPY13-36 并未影响新奇诱发的摄食抑制测试中的焦虑或食欲相关反应(所有 p 值均大于 0.3;实验 1)。Y2 拮抗剂 BIIE 0246 的预处理阻止了 NPY13-36 在高架十字迷宫中的抗焦虑作用,但在电击探头测试中没有(实验 2)。因此,外侧隔核 NPY13-36 的抗焦虑样作用似乎以特定于测试的方式通过 Y2 受体介导。