慢性社会压力诱导对厌恶的广泛性超敏感:一个具有理解和治疗负价障碍翻译效度的小鼠模型

IF 4.6 2区 医学 Q1 NEUROSCIENCES
Giulia Poggi , Adrián Portalés , Mélisse Robert , Céline Hofer , Sophie Schmid , Diana Kúkeľová , Hannes Sigrist , Stefan Just , Bastian Hengerer , Christopher R. Pryce
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引用次数: 0

摘要

RDoC框架关注的是精神障碍中功能失调的神经行为过程,并与转化研究相适应。对厌恶/威胁的广泛性超敏感在各种压力相关情绪障碍中很常见;增加巴甫洛夫厌恶学习记忆(PAL, PAM)为其研究提供了一种翻译范式。在这里,我们提出了一个小鼠模型的发展和应用,以研究广义超敏感厌恶/威胁。在雄性成年小鼠中,相对于对照组(CON),长期暴露于社会厌恶(慢性社会压力,CSS)导致音调-脚震动条件冻结行为的获得和表达增加。CSS小鼠的神经行为状态的改变可能与杏仁核的结构-功能改变有关:在CSS小鼠中,PAL和PAM冻结行为的升高与表达即时早期基因蛋白c-Fos的外侧/基底杏仁核谷氨酸神经元的减少同时发生。目前的一种抗抑郁药,SSRI艾司西酞普兰,通过亚慢性给药逆转了CSS小鼠过度的PAM冻结行为。应用该模型研究了3种具有新的作用机制的化合物:吲哚胺双加氧酶1 (IDO 1)抑制、生长抑素受体4 (SSTR4)激动作用和瞬时受体电位规范通道4和5 (TRPC4/5)抑制。对于每一种,都有证据表明CSS小鼠中过量PAL和/或PAM的衰减。TRPC4/5通道抑制的临床前验证有助于决定研究并准确预测临床疗效,以减少杏仁核和对厌恶的情绪反应来衡量。未来的工作将集中于(反向)转化研究,以解决应激引起的杏仁核反应性和厌恶处理的变化,其潜在的病因病理生理原因和神经药理学反应性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Chronic social stress induces generalized hyper-sensitivity to aversion: A mouse model with translational validity for understanding and treating negative valence disorders

Chronic social stress induces generalized hyper-sensitivity to aversion: A mouse model with translational validity for understanding and treating negative valence disorders
The RDoC framework focuses on neurobehavioral processes often dysfunctional in mental disorders and commensurate with translational research. Generalized hyper-sensitivity to aversion/threat is common in various stress-related emotional disorders; increased Pavlovian aversion learning-memory (PAL, PAM) provides a translational paradigm for its study. Here we present the development and application of a mouse model for the study of generalized hyper-sensitivity to aversion/threat. In male adult mice, chronic exposure to social aversion (chronic social stress, CSS) leads, relative to controls (CON), to increased acquisition and expression of tone-footshock conditioned freezing behavior. The altered neurobehavioral state of CSS mice is expected to involve structure-function changes in amygdala: in CSS mice, higher levels of both PAL and PAM freezing behavior co-occurred with fewer lateral/basal amygdala glutamate neurons expressing the immediate early-gene protein c-Fos. A current antidepressant, SSRI escitalopram, reversed excessive PAM freezing behavior in CSS mice with sub-chronic dosing. The model was applied to investigate 3 compounds with novel mechanisms of action: indoleamine dioxygenase 1 (IDO 1) inhibition, somatostatin receptor 4 (SSTR4) agonism, and transient receptor potential canonical channels 4 and 5 (TRPC4/5) inhibition. For each, there was evidence for attenuation of excessive PAL and/or PAM in CSS mice. Preclinical validation of TRPC4/5 channels inhibition contributed to the decision to investigate, and accurately predicted, clinical efficacy, measured as reduced amygdala and emotional reactivities to aversion in major depressive disorder. Future work will focus on (back-)translational studies that address stress-induced changes in amygdala reactivity and aversion processing, their underlying etio-pathophysiological causes, and neuropharmacological responsiveness.
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来源期刊
Neuropharmacology
Neuropharmacology 医学-神经科学
CiteScore
10.00
自引率
4.30%
发文量
288
审稿时长
45 days
期刊介绍: Neuropharmacology publishes high quality, original research and review articles within the discipline of neuroscience, especially articles with a neuropharmacological component. However, papers within any area of neuroscience will be considered. The journal does not usually accept clinical research, although preclinical neuropharmacological studies in humans may be considered. The journal only considers submissions in which the chemical structures and compositions of experimental agents are readily available in the literature or disclosed by the authors in the submitted manuscript. Only in exceptional circumstances will natural products be considered, and then only if the preparation is well defined by scientific means. Neuropharmacology publishes articles of any length (original research and reviews).
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