Department of Neurobiology, Weizmann Institute of Science, Rehovot 76100, Israel.
J Neurosci. 2011 Nov 30;31(48):17416-24. doi: 10.1523/JNEUROSCI.3087-11.2011.
Corticotropin-releasing factor receptor type 1 (CRFR1) plays a major role in the regulation of neuroendocrine and behavioral responses to stress and is considered a key mediator of anxiety behavior. The globus pallidus external (GPe), a main relay center within the basal ganglia that is primarily associated with motor and associative functions, is one of the brain nuclei with the highest levels of CRFR1 expression in the rodent brain. However, the role of CRFR1 in the GPe is yet unknown. In the present study, we used a lentiviral-based system of RNA interference to show that knockdown of CRFR1 mRNA expression in the GPe of adult mice induces a significant increase in anxiety-like behavior, as revealed by the light-dark transfer, open-field, and elevated plus-maze tests. This effect was further confirmed by pharmacological administration of the selective CRFR1 antagonist NBI 30775 (1.75 μg/side) directly into the GPe. In the marble-burying test, blockade of CRFR1 in the GPe increased the percentage of marbles buried and the duration of burying behavior. Additionally, we present evidence suggesting that the enkephalin system is involved in the effect of GPe-CRFR1 on anxiety-like behavior. In contrast to the well established anxiogenic role of CRFR1 in the extended amygdala, our data reveal a novel anxiolytic role for CRFR1 in the GPe.
促肾上腺皮质素释放因子受体 1(CRFR1)在调节神经内分泌和应激行为方面起着重要作用,被认为是焦虑行为的关键介导者。苍白球外部(GPe)是基底神经节的主要中继中心,主要与运动和联想功能有关,是啮齿动物大脑中 CRFR1 表达水平最高的脑核之一。然而,CRFR1 在 GPe 中的作用尚不清楚。在本研究中,我们使用基于慢病毒的 RNA 干扰系统表明,成年小鼠 GPe 中 CRFR1 mRNA 表达的敲低会导致焦虑样行为显著增加,这可以通过明暗转移、旷场和高架十字迷宫测试来揭示。这种效应通过将选择性 CRFR1 拮抗剂 NBI 30775(1.75 μg/侧)直接注射到 GPe 中进一步得到证实。在大理石埋藏试验中,GPe 中 CRFR1 的阻断增加了大理石埋藏的百分比和埋藏行为的持续时间。此外,我们提供的证据表明,脑啡肽系统参与了 GPe-CRFR1 对焦虑样行为的影响。与 CRFR1 在扩展杏仁核中确立的焦虑作用相反,我们的数据显示 CRFR1 在 GPe 中具有新的抗焦虑作用。