Jaffe R A, Rowe M A
Department of Anesthesia, Stanford University School of Medicine, California 94305, USA.
Anesth Analg. 1996 Oct;83(4):776-81. doi: 10.1097/00000539-199610000-00021.
The local anesthetic effects of opioids have been demonstrated in both clinical and laboratory studies. Clinically, both meperidine and sufentanil can produce segmental sensory anesthesia. However, previous studies of the effects of opioids on nerve conduction have all made use of peripheral nerve preparations and yielded conflicting results. In the present study we describe the local anesthetic effects of phenylpiperidine opioids on individual dorsal root axons, the probable target for intrathecal local anesthetics. Dorsal roots were removed from anesthetized adult male rats and maintained in vitro. Standard single fiber recording techniques were used to isolate activity in the individual axons. Drug exposure was accomplished by perfusing the isolated dorsal root with an artificial cerebrospinal fluid containing the study drug at a clinically relevant concentration. Steady-state drug effects were measured after 15-30 min of exposure and compared to control measurements in the same preparation. Meperidine (705 microM) blocked conduction in 61.5% of 39 myelinated and unmyelinated axons, and significantly reduced conduction velocity in the remaining unblocked axons. These effects were not naloxone reversible. Fentanyl (0.6 microM and 3 microM) and sufentanil (1.04 microM) failed to affect the nerve conduction in any dorsal root axon. The discrepancy between laboratory and clinical observations is discussed. We suggest that the site of conduction block may occur at the proximal end of the dorsal root as it passes through the dorsal root entry zone, an anatomically unique segment of the primary sensory pathway with decreased conduction safety for action potential propagation.
阿片类药物的局部麻醉作用已在临床和实验室研究中得到证实。在临床上,哌替啶和舒芬太尼均可产生节段性感觉麻醉。然而,先前关于阿片类药物对神经传导影响的研究均采用外周神经标本,结果相互矛盾。在本研究中,我们描述了苯基哌啶类阿片药物对单个背根轴突的局部麻醉作用,背根轴突可能是鞘内局部麻醉药的作用靶点。从麻醉的成年雄性大鼠身上取出背根并进行体外保存。使用标准的单纤维记录技术分离单个轴突的活动。通过用含有临床相关浓度研究药物的人工脑脊液灌注分离的背根来实现药物暴露。暴露15 - 30分钟后测量稳态药物效应,并与同一标本中的对照测量结果进行比较。哌替啶(705微摩尔)使39条有髓和无髓轴突中的61.5%传导阻滞,并使其余未阻滞轴突的传导速度显著降低。这些效应不能被纳洛酮逆转。芬太尼(0.6微摩尔和3微摩尔)和舒芬太尼(1.04微摩尔)未影响任何背根轴突的神经传导。讨论了实验室观察结果与临床观察结果之间的差异。我们认为传导阻滞部位可能发生在背根穿过背根入区的近端,背根入区是初级感觉通路中一个解剖学上独特的节段,动作电位传播的传导安全性降低。