实验性神经瘤的自发电活动量是否被高估了?

K J Burchiel, L C Russell
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引用次数: 10

摘要

先前对实验性神经瘤的研究表明,在神经瘤中终止的一些轴突表现出自发和机械敏感性放电。由于这些自发放电似乎发生在潜在的伤害性轴突(A δ和C纤维),因此推测这种活动可能与周围神经损伤后发生的疼痛有关。我们实验室最近的结果揭示了先前神经瘤电生理研究中几个可能的错误来源。最值得注意的是,胆碱是一种肌肉麻痹剂,在之前的大多数实验性神经瘤研究中都使用过,它具有深刻的钾通道阻断特性,可能会增加受损轴突的自发活动。本研究旨在重新评估实验性神经瘤自发性活动的发生率,以及参与这些放电的纤维类型。选取44只雄性Sprague-Dawley大鼠,在进行急性神经生理记录实验前1-8周进行单侧隐窝轴切开术,另外6只大鼠进行急性对照记录。采用改进的微丝记录技术对所有动物进行记录,以确定传导速度(cv)和自发放电轴突的起源。在给药前后,对每条神经的自发放电进行了彻底的研究。自发性活动是罕见的,在急性切断隐神经,并没有显着影响给药胆碱。在1- 4周龄的实验性隐神经瘤大鼠中,自发性活动很少见,但经胆碱治疗后,自发性活动增加了12.75倍。与对照组的记录相比,加了胆碱的小鼠产生了更多的α - β和α - δ活性。在给药前后均未发现神经瘤中自发的c纤维活性。明显孤立的隐神经段的c -纤维自发放电在后肢内侧的筋膜、浅表血管和毛状皮肤上有接受野。我们的结论如下:(1)神经瘤只表现出罕见的自发放电,除非暴露于钾通道阻滞剂;(2)在远端神经瘤的隐神经中记录的所有c -纤维活动来源于血管、筋膜和其他感受野,而不是神经瘤;(3)这些数据与已知的临床现象一致,即神经瘤通常不会自发疼痛。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Has the amount of spontaneous electrical activity in experimental neuromas been overestimated?

Previous studies of experimental neuromas have indicated that some axons terminating in the neuroma exhibit both spontaneous and mechanosensitive discharges. Since these spontaneous discharges appear to occur in potentially nociceptive axons (A delta and C fibers), it has been speculated that this activity may relate to pain that occurs after peripheral nerve injury. Recent results from our laboratory have revealed several possible sources of error in prior electrophysiological studies of neuromas. Most notably, gallamine, a muscle-paralyzing agent that has been used in the majority of previous studies of experimental neuromas, has profound potassium-channel-blocking properties that may increase spontaneous activity in damaged axons. The present study was conducted to re-evaluate the incidence of spontaneous activity in experimental neuromas, and the fiber types involved in these discharges. A group of 44 male Sprague-Dawley rats underwent unilateral saphenous axotomy 1-8 weeks prior to acute neurophysiological recording experiments, and 6 additional rats underwent acute control recording procedures only. Recording was performed in all animals using a modification of the microfilament recording technique to determine the conduction velocities (CVs) and origins of spontaneously discharging axons. A thorough search for spontaneous discharges was made in each nerve both before and after the administration of gallamine. Spontaneous activity was rare in acutely severed saphenous nerve and was not significantly affected by gallamine administration. In rats with 1- to 4-week-old experimental saphenous neuromas, spontaneous activity was rare but was increased by a factor of 12.75 after gallamine treatment. Gallamine administration produced significantly more of both A alpha beta and A delta activity, compared to control recordings. No spontaneous C-fiber activity was found originating in neuromas either before or after gallamine. C-fiber spontaneous discharges in the apparently isolated saphenous nerve segment had receptive fields in fascia, superficial vasculature, and hairy skin of the medial hindlimb. Our conclusions are as follows: (1) Neuromas exhibit only rare spontaneous discharges unless exposed to potassium-channel-blocking agents; (2) all C-fiber activity recorded in saphenous nerve with a distal neuroma is derived from vascular, fascial, and other receptive fields rather than from the neuroma; (3) these data are consistent with known clinical phenomena in that neuromas are not usually spontaneously painful.

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