Department of Psychiatry and Psychotherapy, Friedrich-Alexander-University Erlangen-Nürnberg, Erlangen, Germany.
J Psychopharmacol. 2019 Dec;33(12):1533-1539. doi: 10.1177/0269881119862529. Epub 2019 Jul 22.
Neuropeptide Y (NPY) has anxiolytic effects and facilitates extinction of cued and contextual fear in rodents, thereby acting as a resilience factor against exaggerated fear responses after adverse events. We investigated whether NPY influences acquisition, expression and extinction of social fear in a mouse model of social fear conditioning (SFC).
NPY was administered intracerebroventricularly before SFC or before social fear extinction with or without prior administration of Y1 and/or Y2 receptor antagonists.
We show that NPY affects SFC-induced social fear in a time point-dependent manner. When administered before SFC, NPY did not affect acquisition, expression and extinction of social fear. However, when administered before social fear extinction, NPY reduced expression of social fear via simultaneous activation of Y1 and Y2 receptors. As such, neither the Y1 receptor antagonist BIBO3304 trifluoroacetate nor the Y2 receptor antagonist BIIE0246 was able to block the effects of NPY completely. However, when administered in combination, they completely blocked the effects of NPY on social fear expression.
These findings have important clinical implications, as they suggest that although medication strategies aimed at increasing brain NPY activity are unlikely to prevent the formation of aversive memories after a traumatic social experience, they might improve the recovery from a traumatic social experience by reducing the expression of social fear.
神经肽 Y(NPY)具有抗焦虑作用,并促进啮齿动物条件性恐惧的消退,从而成为对抗不良事件后过度恐惧反应的恢复力因素。我们研究了 NPY 是否会影响社交恐惧条件反射(SFC)小鼠模型中社会恐惧的获得、表达和消退。
在 SFC 之前或社交恐惧消退之前,通过脑室内给予 NPY,同时给予或不给予 Y1 和/或 Y2 受体拮抗剂。
我们表明,NPY 以时间依赖性的方式影响 SFC 诱导的社会恐惧。当给予 SFC 之前,NPY 不影响社会恐惧的获得、表达和消退。然而,当给予社交恐惧消退之前,NPY 通过同时激活 Y1 和 Y2 受体来减少社会恐惧的表达。因此,Y1 受体拮抗剂 BIBO3304 三氟乙酸盐和 Y2 受体拮抗剂 BIIE0246 均不能完全阻断 NPY 的作用。然而,当联合给予时,它们完全阻断了 NPY 对社会恐惧表达的影响。
这些发现具有重要的临床意义,因为它们表明,尽管旨在增加大脑 NPY 活性的药物治疗策略不太可能防止创伤性社交经历后产生厌恶记忆,但通过减少社会恐惧的表达,它们可能有助于从创伤性社交经历中恢复。