首页> 外文期刊>Neuroreport >L-Tetrahydropalmatine alleviates mechanical hyperalgesia in models of chronic inflammatory and neuropathic pain in mice
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L-Tetrahydropalmatine alleviates mechanical hyperalgesia in models of chronic inflammatory and neuropathic pain in mice

机译:L-四氢巴马汀缓解小鼠慢性炎性和神经性疼痛模型中的机械性痛觉过敏

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摘要

Chronic pain is categorized as inflammatory and neuropathic, and there are common mechanisms underlying the generation of each pain state. Such pain is difficult to treat and the treatment at present is inadequate. Corydalis yanhusuo is a traditional Chinese medicine with demonstrated analgesic efficacy in humans. The potential antihyperalgesic effect of its active component is L-tetrahydropalmatine (L-THP). L-THP has been used for the treatment of headache and other mild pain. However, little is known about its analgesic effect on chronic pain and its mechanism. Here, we report that L-THP exerts remarkable antihyperalgesic effects on neuropathic and inflammatory pain in animal models. Neuropathic hypersensitivity was induced by segmental spinal nerve ligation and inflammatory hypersensitivity was induced by an intraplantar injection of complete Freund's adjuvant. To determine the receptor mechanism underlying the antihyperalgesic actions of L-THP, we used SCH23390, an antagonist of a dopamine D1 receptor, in an attempt to block the antihyperalgesic effects of L-THP. We found that L-THP (1-4 mg/kg, i.p.) produced a dose-dependent antihyperalgesic effect in spinal nerve ligation and complete Freund's adjuvant models. The antihyperalgesic effects of L-THP were abolished by a dopamine D1 receptor antagonist SCH23390 (0.02 mg/kg). Furthermore, L-THP (4 mg/kg, i.p.) did not influence motor function. These findings suggest that L-THP may ameliorate mechanical hyperalgesia by enhancing dopamine D1 receptor-mediated dopaminergic transmission. Copyright (C) 2016 Wolters Kluwer Health, Inc. All rights reserved.
机译:慢性疼痛分为炎症性和神经性,每种疼痛状态的产生都有共同的机制。这种疼痛难以治疗,目前的治疗还不够。延胡索是一种传统的中药,对人具有镇痛作用。其活性成分的潜在止痛作用是L-四氢巴马汀(L-THP)。 L-THP已用于治疗头痛和其他轻度疼痛。然而,关于其对慢性疼痛的镇痛作用及其机理知之甚少。在这里,我们报道L-THP对动物模型的神经性和炎性疼痛具有显着的抗痛觉过敏作用。节段性脊髓神经结扎可诱发神经性超敏反应,足底内注射完全弗氏佐剂可诱发炎症性超敏反应。为了确定L-THP的抗痛觉过敏作用的受体机制,我们使用了多巴胺D1受体的拮抗剂SCH23390,试图阻止L-THP的抗痛觉过敏作用。我们发现L-THP(1-4 mg / kg,i.p.)在脊髓神经结扎和完整的Freund佐剂模型中产生了剂量依赖性的抗痛觉过敏作用。多巴胺D1受体拮抗剂SCH23390(0.02 mg / kg)消除了L-THP的抗痛觉过敏作用。此外,L-THP(4 mg / kg,腹膜内)不影响运动功能。这些发现表明,L-THP可通过增强多巴胺D1受体介导的多巴胺能传递来改善机械性痛觉过敏。版权所有(C)2016 Wolters Kluwer Health,Inc.保留所有权利。

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