Fear-learning is altered in a mouse neuropathic pain model.

IF 2.5 Q2 CLINICAL NEUROLOGY
Frontiers in pain research (Lausanne, Switzerland) Pub Date : 2025-08-29 eCollection Date: 2025-01-01 DOI:10.3389/fpain.2025.1648374
Neda Assareh, Eddy E Sokolaj, Saima Sadia, Kristen E Anderson, Caitlin Frith, Olivia B Walls, Vanessa A Mitchell, Christopher W Vaughan, Bryony L Winters
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引用次数: 0

Abstract

Background: While chronic neuropathic pain is characterised by abnormal pain signs, such as allodynia, highly disabling co-morbidities, such as anxiety and depression, have a major impact. It is thought that these co-morbidities arise from learning maladaptations related to inappropriate associations between pain and stimulus/environmental cues. However, the impact of animal neuropathic pain models on the interactions between fear-learning, pain and anxiety are poorly understood, particularly during early stages prior to establishment of anxiety.

Methods: We examined the impact of fear-conditioning on fear, anxiety-like behaviours and cold/mechanical allodynia in the mouse sciatic nerve chronic constriction injury (CCI) model of neuropathic pain, at an early post-injury time point.

Results: At 2 weeks post-surgery, CCI and sham operated mice displayed similar acquisition of fear-like freezing responses to a paired audio-tone/footshock fear-conditioning paradigm. On the following day, CCI mice displayed greater freezing than sham mice in response to the same context and subsequent tone presentations. While CCI and sham mice display similar anxiety-like behaviour in the light-dark box and open field, these were increased by fear-conditioning in CCI but not mice. Finally, CCI but not sham surgery produced cold and mechanical allodynia, however, these were unaffected by fear-conditioning.

Conclusions: These findings indicate that a neuropathic pain model enhances learned context/cue evoked fear behaviours at an early stage following nerve-injury. Furthermore, fear-conditioning enhances anxiety-like behaviour, before such behaviour is normally developed. Thus, fear-conditioning induces exaggerated fear-learning which triggers enhanced fear and anxiety, even during early stages of chronic neuropathic pain.

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在小鼠神经性疼痛模型中,恐惧学习被改变。
背景:虽然慢性神经性疼痛的特征是异常疼痛体征,如异常性疼痛,但高度致残性合并症,如焦虑和抑郁,具有重要影响。人们认为,这些合并症是由于疼痛和刺激/环境线索之间不适当的关联引起的学习适应不良。然而,动物神经性疼痛模型对恐惧学习、疼痛和焦虑之间相互作用的影响知之甚少,特别是在焦虑建立之前的早期阶段。方法:在损伤后早期的小鼠坐骨神经慢性收缩损伤(CCI)神经性疼痛模型中,研究恐惧条件反射对恐惧、焦虑样行为和冷/机械异常痛的影响。结果:术后2周,CCI小鼠和假手术小鼠对配对音频/脚震恐惧调节模式表现出相似的恐惧样冻结反应。第二天,CCI小鼠对相同情境和随后的音调呈现的反应比假手术小鼠表现出更大的冻结。虽然CCI小鼠和假小鼠在明暗箱和开阔场地中表现出相似的焦虑样行为,但CCI小鼠的恐惧条件反射增加了这些行为,而小鼠则没有。最后,CCI而非假手术产生冷性和机械性异常痛,然而,这些不受恐惧条件反射的影响。结论:这些发现表明神经性疼痛模型在神经损伤后的早期阶段增强了习得性情境/线索诱发的恐惧行为。此外,恐惧条件反射会在类似焦虑的行为正常发展之前增强这种行为。因此,即使在慢性神经性疼痛的早期阶段,恐惧条件反射诱导了夸大的恐惧学习,从而引发了增强的恐惧和焦虑。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.10
自引率
0.00%
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审稿时长
13 weeks
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