Suppr超能文献

局部和静脉内利多卡因对损伤传入神经纤维持续活动的影响。

Effect of local and intravenous lidocaine on ongoing activity in injured afferent nerve fibers.

机构信息

Physiologisches Institut, Christian-Albrechts-Universität zu Kiel, Kiel, Germany Division of Neurological Pain Research and Therapy, Department of Neurology, Christian-Albrechts-Universität zu Kiel, Kiel, Germany.

出版信息

Pain. 2011 Jul;152(7):1562-1571. doi: 10.1016/j.pain.2011.02.046. Epub 2011 Apr 6.

Abstract

Lidocaine applied systemically or locally attenuates neuropathic pain in patients. Here we tested the hypothesis that ectopic activity in injured afferent A- or C-fibers is suppressed by lidocaine. In rats the sural nerve (skin nerve) or lateral gastrocnemius-soleus nerve (muscle nerve) was crushed. Four to 11 days after crush lesion afferent fibers were isolated from the lesioned nerves in bundles rostral to the injury site. Ongoing ectopic activity was recorded from 75 A-fibers (muscle N=43, skin N=32) and 69 C-fibers (muscle N=30, skin N=39). Most afferent fibers were functionally characterized by their responses to mechanical and thermal (mostly heat) stimuli applied at or distal to the nerve injury site. Low-threshold cold-sensitive cutaneous C-fibers were excluded from the analysis. Lidocaine was either applied to the nerve at or distal to the injury site in concentrations of 1 to 1000 μg/mL or injected i.v. in doses of 0.09 to 9 mg/kg (skin) or 0.047 to 4.7 mg/kg (muscle). Local application of lidocaine depressed ectopic activity in A- and C-fibers dose-dependently. Depression was weaker in C- than in A-fibers. Intravenous application of lidocaine depressed ongoing ectopic activity in A- and C-fibers dose-dependently. Responses to heat or mechanical stimulation of the injured nerve were not suppressed at the highest concentrations of lidocaine. The results support the hypothesis that decrease of neuropathic pain following local or systemic application of a local anesthetic is related to decrease of ectopic ongoing activity in injured afferent nerve fibers.

摘要

利多卡因全身或局部应用可减轻患者的神经性疼痛。在这里,我们检验了这样一个假设,即损伤传入 A 或 C 纤维的异位活动被利多卡因抑制。在大鼠中,切断腓肠神经(皮肤神经)或外侧比目鱼肌-跟腱神经(肌肉神经)。在损伤后 4 到 11 天,从损伤部位近端的损伤神经中分离出传入纤维束。从 75 根 A 纤维(肌肉 N=43,皮肤 N=32)和 69 根 C 纤维(肌肉 N=30,皮肤 N=39)中记录到持续的异位活动。大多数传入纤维的功能特征是对机械和热(主要是热)刺激的反应,这些刺激施加在神经损伤部位或其远端。低阈值冷敏感皮肤 C 纤维不包括在分析中。利多卡因应用于损伤部位或其远端的神经,浓度为 1 至 1000μg/ml,或静脉内注射 0.09 至 9mg/kg(皮肤)或 0.047 至 4.7mg/kg(肌肉)。利多卡因的局部应用剂量依赖性地抑制 A 和 C 纤维的异位活动。C 纤维的抑制作用弱于 A 纤维。静脉内给予利多卡因剂量依赖性地抑制 A 和 C 纤维的持续异位活动。在利多卡因的最高浓度下,对损伤神经的热或机械刺激的反应没有被抑制。这些结果支持这样的假设,即局部或全身应用局部麻醉剂后神经性疼痛的减轻与损伤传入神经纤维异位持续活动的减少有关。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验