Benbouzid Malika, Pallage Viviane, Rajalu Mathieu, Waltisperger Elisabeth, Doridot Stéphane, Poisbeau Pierrick, Freund-Mercier Marie José, Barrot Michel
Institut des Neurosciences Cellulaires et Intégratives, Centre National de Recherche Scientifique, Université de Strasbourg, 21 Rue René Descartes, 67084 Strasbourg Cedex, France.
Eur J Pain. 2008 Jul;12(5):591-9. doi: 10.1016/j.ejpain.2007.10.002. Epub 2007 Nov 19.
Because of its severity, chronicity, resistance to usual therapy and its consequences on quality of life, neuropathic pain represents a real clinical challenge. Fundamental research on this pathology uses metabolic, pharmacological or traumatic models in rodents that reproduce the characteristic human pain symptoms. In 1996, Mosconi and Kruger morphologically described a model of peripheral neuropathy in which a cuff of polyethylene tubing was placed around the sciatic nerve in rats. In the present study, we evaluated the behavioral consequences of this neuropathic pain model in C57Bl/6J mice which is the main genetic background used for studies in transgenic mice. A short cuff of polyethylene tubing was unilaterally placed around the main branch of the sciatic nerve. It induced an ipsilateral heat thermal hyperalgesia lasting around 3 weeks, and a sustained ipsilateral mechanical allodynia lasting at least 2 months. We showed that this neuropathic pain model is insensitive to ketoprofen, a non-steroidal anti-inflammatory drug. Morphine treatment acutely suppressed the mechanical allodynia, but tolerance to this effect rapidly developed. The analysis of video recordings revealed that most aspects of spontaneous behavior remained unaffected on the long term, excepted for a decrease in the time spent at social interaction for the neuropathic mice. Using the elevated plus-maze and the marble-burying test, we also showed that neuropathic mice develop an anxiety phenotype. Our data indicate that sciatic nerve cuffing in mice is a pertinent model for the study of nociceptive and emotional consequences of sustained neuropathic pain.
由于其严重性、慢性、对常规治疗的抗性及其对生活质量的影响,神经性疼痛是一个真正的临床挑战。对这种病症的基础研究使用啮齿动物的代谢、药理学或创伤模型,这些模型可重现人类疼痛的特征性症状。1996年,莫斯coni和克鲁格从形态学上描述了一种周围神经病变模型,即在大鼠坐骨神经周围放置一个聚乙烯管套。在本研究中,我们评估了这种神经性疼痛模型在C57Bl/6J小鼠中的行为后果,该小鼠是转基因小鼠研究中使用的主要遗传背景。在坐骨神经的主要分支周围单侧放置一个短的聚乙烯管套。它诱发了持续约3周的同侧热痛觉过敏,以及持续至少2个月的同侧机械性异常性疼痛。我们发现这种神经性疼痛模型对非甾体抗炎药酮洛芬不敏感。吗啡治疗可急性抑制机械性异常性疼痛,但很快就会产生耐受性。视频记录分析显示,除了神经性小鼠社交互动时间减少外,自发行为的大多数方面长期不受影响。使用高架十字迷宫和埋珠试验,我们还表明神经性小鼠会出现焦虑表型。我们的数据表明,小鼠坐骨神经套扎是研究持续性神经性疼痛的伤害性和情绪后果的相关模型。