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830纳米激光照射可诱导大鼠中小直径背根神经节神经元形成静脉曲张,降低线粒体膜电位并阻断快速轴浆运输:对830纳米激光镇痛作用的启示

830 nm laser irradiation induces varicosity formation, reduces mitochondrial membrane potential and blocks fast axonal flow in small and medium diameter rat dorsal root ganglion neurons: implications for the analgesic effects of 830 nm laser.

作者信息

Chow Roberta T, David Monique A, Armati Patricia J

机构信息

Castle Hill Medical Centre, Discipline of Medicine, The University of Sydney, Sydney, Australia.

出版信息

J Peripher Nerv Syst. 2007 Mar;12(1):28-39. doi: 10.1111/j.1529-8027.2007.00114.x.

DOI:10.1111/j.1529-8027.2007.00114.x
PMID:17374099
Abstract

We report the formation of 830 nm (cw) laser-induced, reversible axonal varicosities, using immunostaining with beta-tubulin, in small and medium diameter, TRPV-1 positive, cultured rat DRG neurons. Laser also induced a progressive and statistically significant decrease (p<0.005) in MMP in mitochondria in and between static axonal varicosities. In cell bodies of the neuron, the decrease in MMP was also statistically significant (p<0.05), but the decrease occurred more slowly. Importantly we also report for the first time that 830 nm (cw) laser blocked fast axonal flow, imaged in real time using confocal laser microscopy and JC-1 as mitotracker. Control neurons in parallel cultures remained unaffected with no varicosity formation and no change in MMP. Mitochondrial movement was continuous and measured along the axons at a rate of 0.8 microm/s (range 0.5-2 microm/s), consistent with fast axonal flow. Photoacceptors in the mitochondrial membrane absorb laser and mediate the transduction of laser energy into electrochemical changes, initiating a secondary cascade of intracellular events. In neurons, this results in a decrease in MMP with a concurrent decrease in available ATP required for nerve function, including maintenance of microtubules and molecular motors, dyneins and kinesins, responsible for fast axonal flow. Laser-induced neural blockade is a consequence of such changes and provide a mechanism for a neural basis of laser-induced pain relief. The repeated application of laser in a clinical setting modulates nociception and reduces pain. The application of laser therapy for chronic pain may provide a non-drug alternative for the management of chronic pain.

摘要

我们报告了在培养的中小直径、TRPV-1阳性大鼠背根神经节(DRG)神经元中,使用β-微管蛋白免疫染色法,形成830纳米(连续波)激光诱导的可逆性轴突膨体。激光还导致静态轴突膨体内外线粒体膜电位(MMP)逐渐且具有统计学意义地降低(p<0.005)。在神经元的细胞体中,MMP的降低也具有统计学意义(p<0.05),但降低过程较为缓慢。重要的是,我们还首次报告,830纳米(连续波)激光阻断了快速轴突运输,这是使用共聚焦激光显微镜和JC-1作为线粒体追踪剂实时成像观察到的。平行培养的对照神经元未受影响,未形成膨体,MMP也无变化。线粒体沿着轴突持续移动,速率为0.8微米/秒(范围为0.5 - 2微米/秒),这与快速轴突运输一致。线粒体膜中的光感受器吸收激光,并将激光能量转化为电化学变化,引发细胞内事件的二级级联反应。在神经元中,这导致MMP降低,同时神经功能所需的可用三磷酸腺苷(ATP)减少,包括维持微管和分子马达(动力蛋白和驱动蛋白)所需的ATP,这些分子马达负责快速轴突运输。激光诱导的神经阻滞是这些变化的结果,并为激光诱导的疼痛缓解提供了神经学基础机制。在临床环境中重复应用激光可调节伤害性感受并减轻疼痛。激光疗法用于慢性疼痛的治疗可能为慢性疼痛的管理提供一种非药物替代方法。

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