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神经性疼痛会促使参与应激和抑郁的脑网络中的基因表达发生适应性变化。

Neuropathic pain promotes adaptive changes in gene expression in brain networks involved in stress and depression.

作者信息

Descalzi Giannina, Mitsi Vasiliki, Purushothaman Immanuel, Gaspari Sevasti, Avrampou Kleopatra, Loh Yong-Hwee Eddie, Shen Li, Zachariou Venetia

机构信息

Fishberg Department of Neuroscience, Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

出版信息

Sci Signal. 2017 Mar 21;10(471):eaaj1549. doi: 10.1126/scisignal.aaj1549.

Abstract

Neuropathic pain is a complex chronic condition characterized by various sensory, cognitive, and affective symptoms. A large percentage of patients with neuropathic pain are also afflicted with depression and anxiety disorders, a pattern that is also seen in animal models. Furthermore, clinical and preclinical studies indicate that chronic pain corresponds with adaptations in several brain networks involved in mood, motivation, and reward. Chronic stress is also a major risk factor for depression. We investigated whether chronic pain and stress affect similar molecular mechanisms and whether chronic pain can affect gene expression patterns that are involved in depression. Using two mouse models of neuropathic pain and depression [spared nerve injury (SNI) and chronic unpredictable stress (CUS)], we performed next-generation RNA sequencing and pathway analysis to monitor changes in gene expression in the nucleus accumbens (NAc), the medial prefrontal cortex (mPFC), and the periaqueductal gray (PAG). In addition to finding unique transcriptome profiles across these regions, we identified a substantial number of signaling pathway-associated genes with similar changes in expression in both SNI and CUS mice. Many of these genes have been implicated in depression, anxiety, and chronic pain in patients. Our study provides a resource of the changes in gene expression induced by long-term neuropathic pain in three distinct brain regions and reveals molecular connections between pain and chronic stress.

摘要

神经性疼痛是一种复杂的慢性疾病,其特征为各种感觉、认知和情感症状。很大一部分神经性疼痛患者还患有抑郁症和焦虑症,这种情况在动物模型中也可见。此外,临床和临床前研究表明,慢性疼痛与参与情绪、动机和奖赏的多个脑网络的适应性变化相关。慢性应激也是抑郁症的主要危险因素。我们研究了慢性疼痛和应激是否影响相似的分子机制,以及慢性疼痛是否会影响与抑郁症相关的基因表达模式。利用两种神经性疼痛和抑郁症的小鼠模型[ spared nerve injury (SNI)和慢性不可预测应激(chronic unpredictable stress, CUS)],我们进行了新一代RNA测序和通路分析,以监测伏隔核(nucleus accumbens, NAc)、内侧前额叶皮质(medial prefrontal cortex, mPFC)和导水管周围灰质(periaqueductal gray, PAG)中基因表达的变化。除了在这些区域发现独特的转录组图谱外,我们还鉴定了大量信号通路相关基因,在SNI和CUS小鼠中表达有相似变化。这些基因中有许多与人类患者的抑郁、焦虑和慢性疼痛有关。我们的研究提供了长期神经性疼痛在三个不同脑区诱导的基因表达变化的资源,并揭示了疼痛与慢性应激之间的分子联系。

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