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Spatiotemporal dynamics of re-innervation and hyperinnervation patterns by uninjured CGRP fibers in the rat foot sole epidermis after nerve injury

机译:神经损伤后大鼠足底表皮中未损伤的CGRP纤维引起的再支配和超支配方式的时空动态

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摘要

The epidermis is innervated by fine nerve endings that are important in mediating nociceptive stimuli. However, their precise role in neuropathic pain is still controversial. Here, we have studied the role of epidermal peptidergic nociceptive fibers that are located adjacent to injured fibers in a rat model of neuropathic pain. Using the Spared Nerve Injury (SNI) model, which involves complete transections of the tibial and common peroneal nerve while sparing the sural and saphenous branches, mechanical hypersensitivity was induced of the uninjured lateral (sural) and medial (saphenous) area of the foot sole. At different time points, a complete foot sole biopsy was taken from the injured paw and processed for Calcitonin Gene-Related Peptide (CGRP) immunohistochemistry. Subsequently, a novel 2D-reconstruction model depicting the density of CGRP fibers was made to evaluate the course of denervation and re-innervation by uninjured CGRP fibers. The results show an increased density of uninjured CGRP-IR epidermal fibers on the lateral and medial side after a SNI procedure at 5 and 10 weeks. Furthermore, although in control animals the density of epidermal CGRP-IR fibers in the footpads was lower compared to the surrounding skin of the foot, 10 weeks after the SNI procedure, the initially denervated footpads displayed a hyper-innervation. These data support the idea that uninjured fibers may play a considerable role in development and maintenance of neuropathic pain and that it is important to take larger biopsies to test the relationship between innervation of injured and uninjured nerve areas.
机译:表皮被细神经末梢支配,这在介导伤害性刺激中很重要。但是,它们在神经性疼痛中的确切作用仍存在争议。在这里,我们研究了在神经性疼痛大鼠模型中邻近受损纤维的表皮肽能伤害感受纤维的作用。使用备用神经损伤(SNI)模型,该模型涉及胫骨和腓总神经的完整横断,同时保留腓肠和隐性分支,机械性超敏反应引起了脚底未损伤的外侧(眼部)和内侧(隐性)区域。在不同的时间点,从受伤的爪子上进行完整的足底活检,并进行降钙素基因相关肽(CGRP)免疫组织化学处理。随后,制作了一个描绘CGRP纤维密度的新型二维重建模型,以评估未损伤CGRP纤维去神经和再神经的过程。结果显示,在第5周和第10周进行SNI手术后,外侧和内侧未受伤的CGRP-IR表皮纤维的密度增加。此外,尽管在对照动物中,脚垫中的表皮CGRP-IR纤维的密度比脚周围的皮肤要低,但在SNI手术后10周,最初失神经的脚垫表现出了过度的神经支配。这些数据支持这样的想法,即未损伤的纤维可能在神经性疼痛的发展和维持中起重要作用,并且重要的是进行较大的活检以测试受伤和未损伤的神经区域的神经支配之间的关系。

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