Chabal Charles, Russell Lisa C, Burchiel Kim J
Department of Anesthesiology, University of Washington School of Medicine, Seattle, WAU.S.A. Department of Neurological Surgery, University of Washington School of Medicine, Seattle, WAU.S.A. Veterans Administration Medical Center, Seattle, WAU.S.A.
Pain. 1989 Sep;38(3):333-338. doi: 10.1016/0304-3959(89)90220-0.
The effects of intravenously administered subanesthetic concentrations of lidocaine, tocainide, and mexiletine on spontaneously active fibers (SAFs) originating in 7-day-old rat sciatic neuromas were studied. Control injections of normal saline caused no decrease in SAF or discharge rate. Lidocaine and tocainide given in incremental doses of 5, 10, 15, 20 and up to 25 mg/kg caused nearly all observed SAFs to stop firing. Mexiletine given in doses of 3, 5, 7, 10 and up to 15 mg/kg showed similar results at lower doses. All agents decreased the sensitivity of SAF to mechanical stimulation. No conduction blockade occurred at these doses of intravenously administered local anesthetics. The demonstrated reduction in firing rate of SAF may explain the pain relief observed in clinical trials of these orally available agents.
研究了静脉注射低于麻醉浓度的利多卡因、妥卡尼和美西律对7日龄大鼠坐骨神经瘤自发活动纤维(SAFs)的影响。注射生理盐水作为对照,未导致SAFs或放电率降低。以5、10、15、20直至25mg/kg的递增剂量给予利多卡因和妥卡尼,几乎使所有观察到的SAFs停止放电。以3、5、7、10直至15mg/kg的剂量给予美西律,在较低剂量时显示出类似结果。所有药物均降低了SAFs对机械刺激的敏感性。在这些静脉注射局部麻醉药的剂量下未发生传导阻滞。SAFs放电率的降低可能解释了这些口服药物在临床试验中观察到的疼痛缓解现象。