Department of Surgery, Section of Plastic Surgery, The University of Michigan Health System, Ann Arbor, MI, United States.
Department of Surgery, Section of Plastic Surgery, The University of Michigan Health System, Ann Arbor, MI, United States.
Neurosci Lett. 2024 Jul 27;836:137896. doi: 10.1016/j.neulet.2024.137896. Epub 2024 Jul 11.
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.
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.
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.
This novel animal model is a useful tool to investigate underlying mechanisms of neuroma formation and neuropathic pain.
截肢后,外周神经失去了再生的远端靶标,常导致症状性神经瘤和使人虚弱的神经病理性疼痛。动物模型可以通过行为学和组织学评估,为更好地理解神经病理性疼痛病理生理学建立一种实用的症状性神经瘤形成方法。我们创建了一种具有临床转化潜力的症状性神经瘤动物模型,以模拟患者的神经病理性疼痛,并评估疼痛行为中的性别差异。
22 只雄性和雌性大鼠被随机分配到两个实验组之一:(1)神经瘤手术组,或(2)假手术组。对于神经瘤实验组,在大腿处切断胫神经,并将近端节段置于皮肤下,以在神经瘤部位进行机械测试。对于假手术,大鼠接受胫神经分离而不切断。行为学测试包括基线时和 8 周内每周的神经瘤部位疼痛、机械性痛觉过敏、冷感觉过敏和热痛觉过敏。
雄性和雌性神经瘤大鼠从第 3 周和第 4 周开始,与假手术组相比,神经瘤部位疼痛反应明显升高,表明形成了症状性神经瘤。神经瘤组的每周机械性和冷感觉过敏评估显示,与假手术组相比,疼痛行为存在显著差异(p<0.001)。总体而言,男性和女性在疼痛反应方面没有显著差异。组织学在第 8 周显示出典型的神经瘤球,包括轴突排列紊乱、纤维组织、施万细胞移位和免疫细胞浸润。
这种新的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。