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大鼠周围神经损伤后的神经性疼痛:一种使用坐骨神经夹闭的模型。

Neuropathic pain after peripheral nerve injury in rats: a model using sciatic nerve clamping.

作者信息

Kumagai Michio, Sugino Shigekazu, Murakami Toru, Obata Hideaki, Yamauchi Masanori

机构信息

Department of Anesthesiology and Perioperative Medicine, Tohoku University Graduate School of Medicine, Seiryo-Machi 2-1, Aoba-Ku, Sendai, Miyagi, 980-8575, Japan.

Department of Anesthesiology, Saitama Medical University Saitama Medical Center, Kawagoe, Kamoda 1981, Saitama, 350-8550, Japan.

出版信息

J Anesth. 2025 Oct;39(5):815-820. doi: 10.1007/s00540-025-03541-7. Epub 2025 Aug 2.

Abstract

Various preclinical rodent models have been established and utilized to elucidate the mechanisms underlying neuropathic pain. However, the utility of existing major models faces challenges, such as reproducibility and surgical complexity. Here, we introduce a new rat model of neuropathic pain created by simply clamping the sciatic nerve for 10 min. First, we investigated pain-related behavior in 12 male Wistar rats after surgery to clamp the sciatic nerve that induced mechanical allodynia for 21 days and thermal hyperalgesia for 7 days (2-way ANOVA compared with sham-operated rats, p < 0.01). We observed only small interindividual differences in response to stimuli among the rats after sciatic nerve clamp surgery. The L5 dorsal root ganglion and spinal dorsal horn of the other 14 rats were subsequently sectioned and stained for Atf3 and Iba-1 immunoreactivity, respectively. Compared with sham surgery, nerve clamping induced peripheral and central sensitization (Mann-Whitney U test, p < 0.01). This new preclinical rat model of neuropathic pain offers procedural simplicity and high reproducibility.

摘要

已经建立并利用了各种临床前啮齿动物模型来阐明神经性疼痛的潜在机制。然而,现有主要模型的实用性面临挑战,如可重复性和手术复杂性。在此,我们介绍一种新的神经性疼痛大鼠模型,该模型通过简单地钳夹坐骨神经10分钟创建。首先,我们在12只雄性Wistar大鼠钳夹坐骨神经手术后调查疼痛相关行为,该手术诱导机械性异常性疼痛持续21天,热痛觉过敏持续7天(与假手术大鼠相比,双向方差分析,p < 0.01)。我们观察到坐骨神经钳夹手术后大鼠对刺激的反应仅存在微小的个体间差异。随后,对另外14只大鼠的L5背根神经节和脊髓背角分别进行切片,并进行Atf3和Iba-1免疫反应性染色。与假手术相比,神经钳夹诱导了外周和中枢敏化(曼-惠特尼U检验,p < 0.01)。这种新的临床前神经性疼痛大鼠模型具有操作简单和高可重复性的特点。

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