Westerlund T, Vuorinen V, Kirvelä O, Röyttä M
Department of Anaesthesiology, University of Turku, Turku University Hospital, Finland.
Reg Anesth Pain Med. 1999 Jul-Aug;24(4):294-302.
The variability and predictability of neurolytic neural blocks were studied using an experimental rat sciatic nerve model. The goal of the study was to compare endoneurial and clinical responses to commonly used neurolytic agents.
The sciatic nerves of 80 rats were treated either with intra- or perineural injections of 7% phenol-aqua, anhydrous glycerol, or 5% phenol-glycerol. Lidocaine and saline injections were used as controls. Muscle function and trophic changes of the hind limbs were evaluated, and samples for morphologic analysis were taken 1, 2, 4, and 8 weeks after the injections.
Intra- and perineural injections of 7% phenol-aqua resulted in gross endoneural damage of the sciatic nerve and hind limb paresis. Perineural 5% phenol-glycerol and anhydrous glycerol injections caused subperineural damage with slight paresis; gross endoneural damage and noticeable paresis were present only after intraneural injections. When 7% phenol-aqua was compared to other neurolytic agents, the differences in the lesion size (P < .0001) were statistically significant after perineural injections. Regeneration occurred in a stereotypic fashion in all neurolytic groups. Axonal sprouts were noted at the injured area 2 weeks after intraneural and 1 week after perineural injections. Motor function had partially recovered at 8 weeks.
There were no differences in the effects of clinically used neurolytic agents after intraneural injections. Although the perineurally applied 7% phenol-aqua induced marked endoneural damage, the destructive effect of glycerol and phenol-glycerol injections seemed to be prevented by the perineurium; phenol-glycerol and glycerol treatments induced subperineural damage only after perineural injections. The ability to penetrate the perineurium favors the use of 7% phenol-aqua in peripheral perineural blocks when complete neurolysis is the goal.
使用实验性大鼠坐骨神经模型研究神经溶解神经阻滞的变异性和可预测性。本研究的目的是比较神经内膜和临床对常用神经溶解剂的反应。
80只大鼠的坐骨神经接受神经内或神经周注射7%苯酚水溶液、无水甘油或5%苯酚甘油治疗。利多卡因和盐水注射用作对照。评估后肢的肌肉功能和营养变化,并在注射后1、2、4和8周采集用于形态学分析的样本。
神经内和神经周注射7%苯酚水溶液导致坐骨神经严重的神经内膜损伤和后肢轻瘫。神经周注射5%苯酚甘油和无水甘油引起神经周下损伤并伴有轻微轻瘫;仅在神经内注射后才出现严重的神经内膜损伤和明显的轻瘫。当将7%苯酚水溶液与其他神经溶解剂进行比较时,神经周注射后病变大小的差异(P <.0001)具有统计学意义。所有神经溶解组均以刻板的方式发生再生。神经内注射后2周和神经周注射后1周在损伤区域可见轴突芽。8周时运动功能部分恢复。
神经内注射后临床使用的神经溶解剂的效果无差异。虽然神经周应用7%苯酚水溶液会引起明显的神经内膜损伤,但神经束膜似乎可防止甘油和苯酚甘油注射的破坏作用;仅在神经周注射后,苯酚甘油和甘油治疗才会引起神经周下损伤。当以完全神经溶解为目标时,穿透神经束膜的能力有利于在周围神经周阻滞中使用7%苯酚水溶液。