Department of Anesthesiology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Reg Anesth Pain Med. 2011 May-Jun;36(3):220-4. doi: 10.1097/AAP.0b013e3182176f5a.
Preliminary studies using perineural sciatic ropivacaine in rat demonstrated unexpected heat hyperalgesia after block resolution. To better characterize the time course relative to mechanical anesthesia-analgesia, we tested the hypothesis that ropivacaine 0.5% leads to transient heat hyperalgesia in rats independent of mechanical nociception. We also evaluated functional toxicity (eg, long-term hyperalgesia and/or tactile allodynia 2 weeks after injection).
Under surgical exposure, left sciatic nerve block was performed in 2 groups of adult male rats-ropivacaine (200 μL, 5 mg/mL; n = 14) versus vehicle (n = 11). The efficacy and duration of block were assessed with serial heat, mechanical (Randall-Selitto testing), and tactile (von Frey-like monofilaments) tests; motor-proprioceptive (rotating rod) and sedation tests were used at 1 and 7 hrs after injection. The presence of nerve injury was assessed by repeating the heat, tactile, and motor tests 12 to 14 days after injection.
Ropivacaine-induced anesthesia was fully manifest at 1 hr after injection. At 3 hrs after injection, heat hypersensitivity was present in the setting of resolved mechanical analgesia. All behavioral measures returned to baseline by 2 weeks after injection. There was no evidence of (i) behavioral sedation, (ii) persistent changes in heat or mechanical sensitivity, or (iii) persistent changes in proprioceptive-motor function at 12 to 14 days after injection.
Ropivacaine 0.5% induces transient heat hyperalgesia in the setting of resolved mechanical analgesia, further suggestive of modality and/or nociceptive fiber specificity. Whether this finding partially translates to "rebound pain" after patients' nerve blocks wear off requires further study.
初步研究表明,在大鼠中使用周围神经鞘内罗哌卡因后,阻滞消退时会出现意外的热痛觉过敏。为了更好地描述与机械感觉-镇痛相关的时间进程,我们假设 0.5%罗哌卡因可导致大鼠产生短暂的热痛觉过敏,而与机械伤害感受无关。我们还评估了功能毒性(例如,注射后 2 周出现长期痛觉过敏和/或触觉过敏)。
在手术暴露下,对两组成年雄性大鼠进行左侧坐骨神经阻滞:罗哌卡因(200 μL,5mg/mL;n = 14)和载体(n = 11)。使用连续的热、机械(Randall-Selitto 测试)和触觉(冯·弗雷样单丝)测试来评估阻滞的效果和持续时间;在注射后 1 小时和 7 小时使用运动-本体感觉(旋转棒)和镇静测试。在注射后 12 至 14 天重复使用热、触觉和运动测试,以评估神经损伤的存在。
罗哌卡因诱导的麻醉在注射后 1 小时完全显现。在注射后 3 小时,在机械镇痛消退的情况下出现热敏感性增加。所有行为测量在注射后 2 周内均恢复至基线。在注射后 12 至 14 天,没有出现以下情况:(i)行为镇静,(ii)热或机械敏感性持续变化,或(iii)本体感觉-运动功能持续变化。
0.5%罗哌卡因在机械镇痛消退的情况下会引起短暂的热痛觉过敏,这进一步提示了感觉方式和/或伤害感受纤维的特异性。这一发现是否部分转化为患者神经阻滞消退后的“反弹疼痛”,需要进一步研究。