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用稀释蜂毒进行穴位刺激(蜂针疗法)可增强鞘内可乐定在啮齿动物福尔马林试验和神经病理性疼痛模型中的镇痛效果。

Acupoint stimulation with diluted bee venom (apipuncture) potentiates the analgesic effect of intrathecal clonidine in the rodent formalin test and in a neuropathic pain model.

作者信息

Yoon Seo-Yeon, Roh Dae-Hyun, Kwon Young-Bae, Kim Hyun-Woo, Seo Hyoung-Sig, Han Ho-Jae, Lee Hye-Jung, Beitz Alvin J, Lee Jang-Hern

机构信息

Department of Veterinary Physiology, College of Veterinary Medicine and BK21 Program for Veterinary Science, Seoul National University, Seoul, South Korea.

出版信息

J Pain. 2009 Mar;10(3):253-63. doi: 10.1016/j.jpain.2008.09.002. Epub 2008 Nov 17.

Abstract

UNLABELLED

Although intrathecal (i.t.) administration of the alpha(2)-adrenoceptor agonist clonidine has a pronounced analgesic effect, the clinical use of clonidine is limited by its side effects. Previously, our laboratory has demonstrated that the subcutaneous injection of diluted bee venom (DBV) into an acupoint (termed apipuncture) produces significant analgesic effect in various pain animal models. The present study was designed to examine whether DBV injection into the Zusanli acupoint (ST-36) could enhance lower-dose clonidine-induced analgesic effects without the development of hypotension, bradycardia, or sedation. In the mouse formalin test, DBV injection produced a dramatic leftward shift in the dose-response curve for clonidine-induced analgesia. In a rat neuropathic pain model i.t. clonidine dose dependently suppressed chronic constriction injury (CCI)-induced mechanical allodynia and thermal hyperalgesia, and this clonidine-induced analgesic effect was significantly potentiated by apipuncture pretreatment. DBV apipuncture alone or in combination with a low dose of i.t. clonidine produced an analgesic effect similar to that of the high dose of clonidine, but without significant side effects. The analgesic effect produced by the combination of i.t. clonidine and apipuncture was completely blocked by pretreatment with an alpha(2)-adrenoceptor antagonist. These data show that DBV-apipuncture significantly enhances clonidine-induced analgesia and suggest that a combination of low dose clonidine with acupuncture therapy represents a novel strategy for pain management that could eliminates clonidine's side effects.

PERSPECTIVE

This study demonstrated that intrathecal clonidine-induced analgesia is significantly enhanced when it is combined with chemical acupuncture treatment. The administration of low-dose clonidine in combination with acupuncture produced a potent analgesic effect without significant side effects and thus represents a potential novel strategy for the management of chronic pain.

摘要

未标记

尽管鞘内注射α₂肾上腺素能受体激动剂可乐定具有显著的镇痛作用,但其临床应用因副作用而受到限制。此前,我们实验室已证明,将稀释的蜂毒(DBV)皮下注射到穴位(称为蜂针疗法)在各种疼痛动物模型中产生显著的镇痛效果。本研究旨在探讨将DBV注射到足三里穴位(ST-36)是否能增强低剂量可乐定诱导的镇痛作用,同时不产生低血压、心动过缓或镇静作用。在小鼠福尔马林试验中,DBV注射使可乐定诱导镇痛的剂量反应曲线显著左移。在大鼠神经病理性疼痛模型中,鞘内注射可乐定剂量依赖性地抑制慢性压迫损伤(CCI)诱导的机械性异常性疼痛和热痛觉过敏,而这种可乐定诱导的镇痛作用通过蜂针疗法预处理得到显著增强。单独的DBV蜂针疗法或与低剂量鞘内可乐定联合使用产生的镇痛效果与高剂量可乐定相似,但无明显副作用。鞘内可乐定与蜂针疗法联合产生的镇痛作用被α₂肾上腺素能受体拮抗剂预处理完全阻断。这些数据表明,DBV蜂针疗法显著增强了可乐定诱导的镇痛作用,并表明低剂量可乐定与针灸疗法联合是一种可消除可乐定副作用的新型疼痛管理策略。

观点

本研究表明,鞘内可乐定诱导的镇痛作用在与化学针灸治疗联合时显著增强。低剂量可乐定与针灸联合给药产生了强效镇痛作用且无明显副作用,因此代表了一种潜在的慢性疼痛管理新策略。

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