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侧隔核内注射神经肽 Y Y2 受体激动剂 NPY(13-36)可差异调节雄性长爪沙鼠的不同防御行为。

Lateral septal infusions of the neuropeptide Y Y2 receptor agonist, NPY(13-36) differentially affect different defensive behaviors in male, Long Evans rats.

机构信息

Centre for Neuroscience Studies, Queen's University, 62 Arch Street, Kingston, Ontario, Canada K7L 3N6.

出版信息

Physiol Behav. 2013 Feb 17;110-111:20-9. doi: 10.1016/j.physbeh.2012.12.011. Epub 2012 Dec 28.

Abstract

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.

摘要

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。

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