Department of Anesthesiology and Center for Pain Research, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
Reg Anesth Pain Med. 2012 Jul-Aug;37(4):403-9. doi: 10.1097/AAP.0b013e3182485965.
There is increasing clinical use of adjuvant drugs to prolong the duration of local anesthetic-induced block of peripheral nerves. However, the mechanistic understanding regarding drug interactions between these compounds in the periphery is quite limited. Accordingly, we undertook this study to determine whether selected adjuvant drugs are efficacious in blocking action potential propagation in peripheral nerves at concentrations used clinically and whether these drugs influence peripheral nerve block produced by local anesthetics.
Isolated rat sciatic nerves were used to assess (1) the efficacy of buprenorphine, clonidine, dexamethasone, or midazolam, alone and in combination, on action potential propagation; and (2) their influence on the blocking actions of local anesthetics ropivacaine and lidocaine. Compound action potentials (CAPs) from A- and C-fibers were studied before and after drug application.
At estimated clinical concentrations, neither buprenorphine nor dexamethasone affected either A- or C-waves of the CAP. Clonidine produced a small but significant attenuation of the C-wave amplitude. Midazolam attenuated both A- and C-wave amplitudes, but with greater potency on the C-wave. The combination of clonidine, buprenorphine, and dexamethasone had no influence on the potency or duration of local anesthetic- or midazolam-induced block of A- and C-waves of the CAP.
These results suggest that the reported clinical efficacy of clonidine, buprenorphine, and dexamethasone influences the actions of local anesthetics via indirect mechanisms. Further identification of these indirect mechanisms may enable the development of novel approaches to achieve longer-duration, modality-specific peripheral nerve block.
越来越多的临床医生使用辅助药物来延长外周神经局部麻醉阻滞的持续时间。然而,对于这些化合物在周围环境中的药物相互作用的机制理解相当有限。因此,我们进行了这项研究,以确定选定的辅助药物在临床上使用的浓度下是否能有效阻断周围神经动作电位的传播,以及这些药物是否会影响局部麻醉药产生的周围神经阻滞。
使用分离的大鼠坐骨神经来评估 (1) 布比卡因、可乐定、地塞米松或咪达唑仑单独和联合应用对动作电位传播的效果;以及 (2) 它们对罗哌卡因和利多卡因局部麻醉剂阻断作用的影响。在药物应用前后研究 A-和 C-纤维的复合动作电位 (CAP)。
在估计的临床浓度下,布比卡因或地塞米松均不影响 CAP 的 A-或 C-波。可乐定轻微但显著地衰减了 C-波幅度。咪达唑仑衰减了 A-和 C-波的幅度,但对 C-波的作用更强。可乐定、布比卡因和地塞米松的组合对局部麻醉药或咪达唑仑诱导的 CAP 的 A-和 C-波的阻滞效力和持续时间没有影响。
这些结果表明,报告的可乐定、布比卡因和地塞米松的临床疗效通过间接机制影响局部麻醉剂的作用。进一步确定这些间接机制可能为实现更长时间、特定模式的周围神经阻滞开辟新的途径。