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大鼠福尔马林试验中脊髓可乐定与利多卡因之间的抗伤害感受相互作用:等效线分析

Antinociceptive interaction between spinal clonidine and lidocaine in the rat formalin test: an isobolographic analysis.

作者信息

Hao S, Takahata O, Iwasaki H

机构信息

Department of Anesthesiology & Critical Care Medicine, Asahikawa Medical College, Asahikawa, Japan.

出版信息

Anesth Analg. 2001 Mar;92(3):733-8. doi: 10.1097/00000539-200103000-00034.

Abstract

UNLABELLED

Clinical and basic science studies suggest that spinal alpha-2-adrenergic receptor agonists and local anesthetics produce analgesia, but interaction between alpha-2-adrenergic receptor agonists and local anesthetics in the persistent pain model has not been examined. In the present study, using isobolographic analysis, we investigated the antinociceptive interaction of intrathecal clonidine and lidocaine in the rat formalin test. Sprague-Dawley rats were implanted with chronic lumbar intrathecal catheters, and were tested for paw flinch by formalin injection. Biphasic painful behavior was counted. Intrathecal clonidine (3-12 nmol) was administered 15 min before formalin, and intrathecal lidocaine (375-1850 nmol) was administered 5 min before formalin. To examine the interaction of intrathecal clonidine and lidocaine, an isobolographic design was used. Spinal administration of clonidine produced dose-dependent suppression of the biphasic responses in the formalin test. Spinal lidocaine resulted in dose-dependent transient motor dysfunction and the motor dysfunction recovered to normal at 10-15 min after administration. Spinal lidocaine produced dose-dependent suppression of phase-2 activity in the formalin test. Isobolographic analysis showed that the combination of intrathecal clonidine and lidocaine synergistically reduced Phase-2 activity. We conclude that intrathecal clonidine synergistically interacts with lidocaine in reducing the nociceptive response in the formalin test.

IMPLICATIONS

Preformalin administration of intrathecal clonidine and lidocaine dose-dependently produced antinociception in the formalin test. The combination of clonidine and lidocaine, synergistically produced suppression of nociceptive response in the persistent pain model.

摘要

未标记

临床和基础科学研究表明,脊髓α-2-肾上腺素能受体激动剂和局部麻醉药可产生镇痛作用,但在持续性疼痛模型中,α-2-肾上腺素能受体激动剂与局部麻醉药之间的相互作用尚未得到研究。在本研究中,我们使用等效应线图分析法,研究了鞘内注射可乐定和利多卡因在大鼠福尔马林试验中的抗伤害感受相互作用。将Sprague-Dawley大鼠植入慢性腰段鞘内导管,通过注射福尔马林测试 paw flinch。对双相疼痛行为进行计数。在注射福尔马林前15分钟鞘内注射可乐定(3-12 nmol),在注射福尔马林前5分钟鞘内注射利多卡因(375-1850 nmol)。为了研究鞘内可乐定和利多卡因的相互作用,采用了等效应线图设计。鞘内注射可乐定在福尔马林试验中产生剂量依赖性的双相反应抑制。鞘内利多卡因导致剂量依赖性的短暂运动功能障碍,给药后10-15分钟运动功能障碍恢复正常。鞘内利多卡因在福尔马林试验中产生剂量依赖性的第二相活动抑制。等效应线图分析表明,鞘内可乐定和利多卡因联合使用可协同降低第二相活动。我们得出结论,鞘内可乐定与利多卡因在降低福尔马林试验中的伤害感受反应方面具有协同相互作用。

启示

在福尔马林试验中,福尔马林注射前鞘内注射可乐定和利多卡因可剂量依赖性地产生抗伤害感受作用。可乐定和利多卡因联合使用,在持续性疼痛模型中协同产生伤害感受反应抑制作用。

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