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首页> 外文期刊>Pharmacology, Biochemistry and Behavior >Spontaneous and evoked pain-associated behaviors in a rat model of neuropathic pain respond differently to drugs with different mechanisms of action
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Spontaneous and evoked pain-associated behaviors in a rat model of neuropathic pain respond differently to drugs with different mechanisms of action

机译:在神经性疼痛大鼠模型中,自发性和诱发性疼痛相关行为对具有不同作用机制的药物的反应不同

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Given that patients with neuropathic pain suffer a mixture of spontaneous and evoked pain symptoms, we assessed the effects of drugs with different mechanism of action on spontaneous and evoked pain-associated behaviors in a rat model of neuropathic pain induced by chronic constriction injury (CCI) of the sciatic nerve. Frequent aberrant limb movement on the operated side was measured to assess spontaneous pain-associated behavior, and mechanical allodynia and thermal hyperalgesia were evaluated to assess evoked pain-associated behaviors. These three types of behavior were assessed after administration of the following drugs: pregabalin (alpha 2 delta-subunit ligand), morphine (mu-opioid receptor agonist), perampanel (alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid [AMPA] receptor antagonist), clonidine, dexmedetomidine (alpha 2-adrenoceptor agonists), and diclofenac (non-steroidal anti-inflammatory drug [NSAID]). Pregabalin at an oral dose of 10 or 30 mg/kg significantly alleviated frequent aberrant limb movement and mechanical allodynia, but not thermal. hyperalgesia. Morphine at a subcutaneous dose of 1 or 3 mg/kg significantly improved all three types of behavior. Perampanel at an oral dose of 1 mg/kg attenuated only frequent aberrant limb movement. Intraperitoneal administration of clonidine (0.01 or 0.03 mg/kg) and dexmedetomidine (0.03 mg/kg) significantly improved all three types of behavior, while diclofenac did not relieve any of the behaviors. Pregabalin, clonidine, and dexmedetomidine significantly decreased motor performance at doses close to analgesic doses in the rotarod test. The present study demonstrates that responses to spontaneous and evoked pain symptoms in neuropathic pain condition differ depending on a drug's mechanism of action. The selection and application of drugs according to the specific symptoms would be considered for the medication of patients with neuropathic pain. (C) 2015 Elsevier Inc. All rights reserved.
机译:鉴于患有神经性疼痛的患者同时患有自发性和诱发性疼痛症状,我们在慢性收缩性损伤(CCI)诱发的神经性疼痛的大鼠模型中评估了具有不同作用机制的药物对自发性和诱发性疼痛相关行为的影响坐骨神经测量手术侧肢体的频繁异常运动来评估自发性疼痛相关行为,并评估机械性异常性疼痛和热痛觉过敏以评估诱发的疼痛相关行为。服用以下药物后,对这三种行为进行了评估:普瑞巴林(普瑞巴林)(α2δ亚基配体),吗啡(μ阿片受体激动剂),perampanel(α-氨基-3-羟基-5-甲基-5-甲基-4-异恶唑丙酸[AMPA]受体拮抗剂),可乐定,右美托咪定(α2肾上腺素受体激动剂)和双氯芬酸(非甾体类抗炎药[NSAID])。普瑞巴林口服剂量为10或30 mg / kg可以显着缓解频繁的肢体异常运动和机械性异常性疼痛,但不能缓解热性疼痛。痛觉过敏。皮下注射1或3 mg / kg吗啡可显着改善所有三种行为。 Perampanel口服剂量为1 mg / kg只会减弱频繁的异常肢体运动。腹膜内给予可乐定(0.01或0.03 mg / kg)和右美托咪定(0.03 mg / kg)可以显着改善这三种类型的行为,而双氯芬酸不能缓解任何行为。普罗巴林,可乐定和右美托咪定在轮状试验中以接近镇痛剂量的剂量显着降低运动表现。本研究表明,在神经性疼痛条件下,对自发性和诱发性疼痛症状的反应取决于药物的作用机制。对于神经性疼痛患者,应考虑根据具体症状选择和应用药物。 (C)2015 Elsevier Inc.保留所有权利。

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