Lambert L A, Lambert D H, Strichartz G R
Department of Anesthesia, Research Laboratories, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115.
Anesthesiology. 1994 May;80(5):1082-93. doi: 10.1097/00000542-199405000-00017.
Delivery of large doses of local anesthetics for spinal anesthesia by repeated injections or continuous infusion could expose the cauda equina to concentrations of drug that may be neurotoxic per se. We studied this possible neurotoxic effect by assessing recovery from conduction blockade of desheathed peripheral nerves after exposure to some of the local anesthetic solutions commonly used for spinal anesthesia.
The reversibility of conduction blockade was studied in desheathed bullfrog sciatic nerves, using the sucrose-gap method for recording compound action potentials, before and during exposure to local anesthetics and during drug washout. The nerves were exposed for 15 min to 5% or 1.5% lidocaine, with or without 7.5% dextrose; 0.5% tetracaine; or 0.75% bupivacaine (the latter two without dextrose). Some nerves were also bathed in 7.5% dextrose (without local anesthetic) or in 0.06% tetracaine, which in this preparation is equipotent to 5% lidocaine. After 15 min in the drug, the nerves were washed for 2-3 h and soaked in Ringer's solution overnight. Nerves exposed only to Ringer's solution served as controls. We also studied neuronal uptake and washout of radiolabeled lidocaine.
Exposure of nerves to 5% lidocaine, with or without 7.5% dextrose, or to 0.5% tetracaine resulted in irreversible total conduction blockade, whereas 1.5% lidocaine or 0.75% bupivacaine caused 25-50% residual block after the 2-3 h wash. Nerves exposed to Ringer's solution, 7.5% dextrose or 0.06% tetracaine had 0-10% residual block after 2-3 h wash. The action potential of all nerves declined after overnight soak to between 30-60% of the control value, except for those nerves exposed to 5% lidocaine or 0.5% tetracaine, which showed no activity. Exposure to 5% lidocaine for periods of only 4-5 min produced total, irreversible loss of conduction. The uptake by and washout of radiolabeled lidocaine from the nerves indicate that the maximum amount of residual drug after 2-4 min of exposure to 5% lidocaine and a 3-h wash should cause at most only 50% conduction block.
Solutions of 5% lidocaine and 0.5% tetracaine that have been associated with clinical cases of cauda equina syndrome after continuous spinal anesthesia caused irreversible conduction block in desheathed amphibian nerve. Whether these in vitro actions also occur in mammalian nerves in vivo is an important, clinically relevant question now under investigation in our laboratory.
通过重复注射或持续输注大剂量局部麻醉药进行脊髓麻醉,可能会使马尾神经暴露于本身可能具有神经毒性的药物浓度下。我们通过评估暴露于一些常用于脊髓麻醉的局部麻醉药溶液后去鞘外周神经传导阻滞的恢复情况,来研究这种可能的神经毒性作用。
在暴露于局部麻醉药之前、期间及药物冲洗期间,使用蔗糖间隙法记录复合动作电位,研究去鞘牛蛙坐骨神经传导阻滞的可逆性。将神经暴露于5%或1.5%利多卡因(含或不含7.5%葡萄糖)、0.5%丁卡因或0.75%布比卡因(后两种不含葡萄糖)15分钟。一些神经还浸泡于7.5%葡萄糖(不含局部麻醉药)或0.06%丁卡因中,在该制剂中其效力与5%利多卡因相当。在药物中暴露15分钟后,将神经冲洗2 - 3小时,并在林格氏液中浸泡过夜。仅暴露于林格氏液的神经作为对照。我们还研究了放射性标记利多卡因的神经元摄取和冲洗情况。
神经暴露于含或不含7.5%葡萄糖的5%利多卡因或0.5%丁卡因会导致不可逆的完全传导阻滞,而1.5%利多卡因或0.75%布比卡因在2 - 3小时冲洗后会导致25 - 50%的残余阻滞。暴露于林格氏液、7.5%葡萄糖或0.06%丁卡因的神经在2 - 3小时冲洗后残余阻滞为0 - 10%。过夜浸泡后,所有神经的动作电位均下降至对照值的30 - 60%,但暴露于5%利多卡因或0.5%丁卡因的神经无活动。仅暴露于5%利多卡因4 - 5分钟就会导致完全不可逆的传导丧失。放射性标记利多卡因从神经的摄取和冲洗表明,暴露于5%利多卡因2 - 4分钟并冲洗3小时后,残余药物的最大量最多应仅导致50%的传导阻滞。
连续脊髓麻醉后与马尾神经综合征临床病例相关的5%利多卡因和0.5%丁卡因溶液,在去鞘两栖动物神经中引起了不可逆的传导阻滞。这些体外作用在体内哺乳动物神经中是否也会发生,是我们实验室目前正在研究的一个重要的临床相关问题。