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Pilot study on the effects of low intensity focused ultrasound in a swine model of neuropathic pain.低强度聚焦超声对猪神经性疼痛模型影响的初步研究。
J Neurosurg. 2021 Apr 16;135(5):1508-1515. doi: 10.3171/2020.9.JNS202962. Print 2021 Nov 1.
2
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Low Intensity Focused Ultrasound Modulation of Vincristine Induced Neuropathy.低强度聚焦超声对长春新碱诱导的神经病变的调节作用
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Reg Anesth Pain Med. 2020 Apr;45(4):287-292. doi: 10.1136/rapm-2019-101141. Epub 2020 Jan 29.
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建立家猪腓总神经损伤模型用于转化性神经性疼痛治疗研究

Development of a common peroneal nerve injury model in domestic swine for the study of translational neuropathic pain treatments.

作者信息

Hellman Abigail, Maietta Teresa, Clum Alicia, Byraju Kanakaharini, Raviv Nataly, Staudt Michael D, Jeannotte Erin, Nalwalk Julia, Belin Sophie, Poitelon Yannick, Pilitsis Julie G

机构信息

2Neuroscience and Experimental Therapeutics, and.

Departments of1Neurosurgery and.

出版信息

J Neurosurg. 2021 Apr 16;135(5):1516-1523. doi: 10.3171/2020.9.JNS202961. Print 2021 Nov 1.

DOI:10.3171/2020.9.JNS202961
PMID:33862596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8521549/
Abstract

OBJECTIVE

To date, muscular and bone pain have been studied in domestic swine models, but the only neuropathic pain model described in swine is a mixed neuritis model. Common peroneal nerve injury (CPNI) neuropathic pain models have been utilized in both mice and rats.

METHODS

The authors developed a swine surgical CPNI model of neuropathic pain. Behavioral outcomes were validated with von Frey filament testing, thermal sensitivity assessments, and social and motor scoring. Demyelination of the nerve was confirmed through standard histological assessment. The contralateral nerve served as the control.

RESULTS

CPNI induced mechanical and thermal allodynia (p < 0.001 [n = 10] and p < 0.05 [n = 4], respectively) and increased pain behavior, i.e., guarding of the painful leg (n = 12). Myelin protein zero (P0) staining revealed demyelination of the ligated nerve upstream of the ligation site.

CONCLUSIONS

In a neuropathic pain model in domestic swine, the authors demonstrated that CPNI induces demyelination of the common peroneal nerve, which the authors hypothesize is responsible for the resulting allodynic pain behavior. As the anatomical features of domestic swine resemble those of humans more closely than previously used rat and mouse models, utilizing this swine model, which is to the authors' knowledge the first of its kind, will aid in the translation of experimental treatments to clinical trials.

摘要

目的

迄今为止,已经在家猪模型中研究了肌肉和骨骼疼痛,但猪中描述的唯一神经病理性疼痛模型是混合神经炎模型。小鼠和大鼠均已使用腓总神经损伤(CPNI)神经病理性疼痛模型。

方法

作者建立了一种猪手术CPNI神经病理性疼痛模型。通过von Frey细丝测试、热敏感性评估以及社交和运动评分来验证行为结果。通过标准组织学评估确认神经脱髓鞘。对侧神经作为对照。

结果

CPNI分别诱发了机械性和热性痛觉过敏(分别为p < 0.001 [n = 10]和p < 0.05 [n = 4]),并增加了疼痛行为,即对患侧腿部的保护(n = 12)。髓磷脂蛋白零(P0)染色显示结扎部位上游结扎神经的脱髓鞘。

结论

在一个家猪神经病理性疼痛模型中,作者证明CPNI诱发了腓总神经的脱髓鞘,作者推测这是导致痛觉过敏疼痛行为的原因。由于家猪的解剖特征比以前使用的大鼠和小鼠模型更接近人类,利用这种据作者所知是首例的猪模型,将有助于将实验性治疗转化为临床试验。