A novel animal model of symptomatic neuroma for assessing neuropathic pain

IF 2.5 4区 医学 Q3 NEUROSCIENCES
Ipek Berberoglu , Scott W. Sabbagh , Paul S. Cederna , Stephen W.P. Kemp
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引用次数: 0

Abstract

Introduction

Following amputation, peripheral nerves lack distal targets for regeneration, often resulting in symptomatic neuromas and debilitating neuropathic pain. Animal models can establish a practical method for symptomatic neuroma formation for better understanding of neuropathic pain pathophysiology through behavioral and histological assessments. We created a clinically translatable animal model of symptomatic neuroma to mimic neuropathic pain in patients and assess sexual differences in pain behaviors.

Methods

Twenty-two male and female rats were randomly assigned to one of two experimental groups: (1) neuroma surgery, or (2) sham surgery. For the neuroma experimental group, the tibial nerve was transected in the thigh, and the proximal segment was placed under the skin for mechanical testing at the site of neuroma. For the sham surgery, rats underwent tibial nerve isolation without transection. Behavioral testing consisted of neuroma-site pain, mechanical allodynia, cold allodynia, and thermal hyperalgesia at baseline, and then weekly over 8 weeks.

Results

Male and female neuroma rats demonstrated significantly higher neuroma-site pain response compared to sham groups starting at weeks 3 and 4, indicating symptomatic neuroma formation. Weekly assessment of mechanical and cold allodynia among neuroma groups showed a significant difference in pain behavior compared to sham groups (p < 0.001). Overall, males and females did not display significant differences in their pain responses. Histology revealed a characteristic neuroma bulb at week 8, including disorganized axons, fibrotic tissue, Schwann cell displacement, and immune cell infiltration.

Conclusion

This novel animal model is a useful tool to investigate underlying mechanisms of neuroma formation and neuropathic pain.

用于评估神经病理性疼痛的新型无症状神经瘤动物模型。
导言:截肢后,周围神经缺乏远端再生靶点,往往会导致无症状神经瘤和令人衰弱的神经病理性疼痛。动物模型可以为症状性神经瘤的形成建立一种实用的方法,从而通过行为学和组织学评估更好地了解神经病理性疼痛的病理生理学。我们创建了一种可临床转化的症状性神经瘤动物模型,以模拟患者的神经病理性疼痛,并评估疼痛行为的性别差异:22只雌雄大鼠被随机分配到两个实验组中的一个:(1) 神经瘤手术组,或 (2) 假手术组。对于神经瘤实验组,在大腿上横断胫神经,并将其近端置于皮下,在神经瘤部位进行机械测试。在假手术中,大鼠接受了胫神经离断术,但没有进行横断。行为测试包括基线神经瘤部位疼痛、机械异感、冷异感和热超痛,然后在8周内每周进行一次测试:结果:从第3周和第4周开始,雄性和雌性神经瘤大鼠的神经瘤部位疼痛反应明显高于假神经瘤组,这表明有症状的神经瘤已经形成。每周对神经瘤组进行的机械痛觉和冷觉过敏评估显示,与假神经瘤组相比,神经瘤组大鼠的疼痛行为有显著差异(p 结论:这种新型动物模型是一种有用的工具,可用于治疗神经瘤:这种新型动物模型是研究神经瘤形成和神经病理性疼痛潜在机制的有用工具。
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来源期刊
Neuroscience Letters
Neuroscience Letters 医学-神经科学
CiteScore
5.20
自引率
0.00%
发文量
408
审稿时长
50 days
期刊介绍: Neuroscience Letters is devoted to the rapid publication of short, high-quality papers of interest to the broad community of neuroscientists. Only papers which will make a significant addition to the literature in the field will be published. Papers in all areas of neuroscience - molecular, cellular, developmental, systems, behavioral and cognitive, as well as computational - will be considered for publication. Submission of laboratory investigations that shed light on disease mechanisms is encouraged. Special Issues, edited by Guest Editors to cover new and rapidly-moving areas, will include invited mini-reviews. Occasional mini-reviews in especially timely areas will be considered for publication, without invitation, outside of Special Issues; these un-solicited mini-reviews can be submitted without invitation but must be of very high quality. Clinical studies will also be published if they provide new information about organization or actions of the nervous system, or provide new insights into the neurobiology of disease. NSL does not publish case reports.
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