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大鼠罗哌卡因坐骨神经阻滞消退过程中的短暂热痛觉过敏。

Transient heat hyperalgesia during resolution of ropivacaine sciatic nerve block in the rat.

机构信息

Department of Anesthesiology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.

出版信息

Reg Anesth Pain Med. 2011 May-Jun;36(3):220-4. doi: 10.1097/AAP.0b013e3182176f5a.

Abstract

BACKGROUND

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).

METHODS

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.

RESULTS

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.

CONCLUSIONS

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.

摘要

背景

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)。

方法

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。

结果

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。

结论

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。

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