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醋氨酚在神经病理性疼痛大鼠模型中的抗伤害作用。

The antinociceptive effect of acetaminophen in a rat model of neuropathic pain.

机构信息

Department of Anesthesiology and Pain Medicine, School of Medicine, The Catholic University of Korea, Seoul, South Korea.

出版信息

Kaohsiung J Med Sci. 2012 May;28(5):251-8. doi: 10.1016/j.kjms.2011.11.003. Epub 2012 Feb 22.

Abstract

Acetaminophen is one of the most popular and widely used analgesics for the treatment of pain and fever but few studies have evaluated its effects on neuropathic pain. This study examined the effect of acetaminophen on thermal hyperalgesia, mechanical and cold allodynia in a rat model of neuropathic pain. Male Sprague-Dawley rats were prepared by tightly ligating the left L5 and L6 spinal nerves to produce a model of neuropathic pain. Sixty neuropathic rats were assigned randomly into six groups. Normal saline and acetaminophen (25, 50, 100, 200 and 300 mg/kg) were administered intraperitoneally to these individual groups. Thermal hyperalgesia, mechanical and cold allodynia were examined at preadministration and at 15, 30, 60, 90, 120, 180, 240 and 360 min after administering the drug. Mechanical allodynia was quantified by measuring the paw withdrawal threshold to stimuli with von Frey filaments. Cold allodynia was quantified by measuring the frequency of foot lift after applying 100% acetone. Thermal hyperalgesia was quantified by measuring the thermal withdrawal threshold. The rotarod performance was measured to detect any drug-induced adverse effects, such as drowsiness. The hepatic and renal adverse effect was also assessed by measuring the serum levels of aspartate aminotransferase, alanine aminotransferase, blood urea nitrogen and creatinine. The paw withdrawal thresholds to mechanical stimuli and the thermal withdrawal threshold were increased significantly and withdrawal frequencies to cold stimuli were reduced by acetaminophen administration in a dose-dependent manner. Acetaminophen reduces thermal hyperalgesia, mechanical and cold allodynia in a rat model of neuropathic pain, and might be useful for managing neuropathic pain.

摘要

对乙酰氨基酚是治疗疼痛和发热最常用和广泛使用的镇痛药之一,但很少有研究评估其对神经病理性疼痛的影响。本研究检查了对乙酰氨基酚对神经病理性疼痛大鼠模型中热痛觉过敏、机械和冷感觉异常的影响。雄性 Sprague-Dawley 大鼠通过紧紧结扎左 L5 和 L6 脊神经制备神经病理性疼痛模型。将 60 只神经病理性大鼠随机分为 6 组。分别给正常生理盐水和对乙酰氨基酚(25、50、100、200 和 300mg/kg)腹腔注射。在给药前和给药后 15、30、60、90、120、180、240 和 360 分钟时检查热痛觉过敏、机械和冷感觉异常。机械感觉异常通过测量 Von Frey 纤维刺激时的足部退缩阈值来量化。冷感觉异常通过测量施加 100%丙酮后抬脚的频率来量化。热痛觉过敏通过测量热撤退阈值来量化。通过旋转棒测试来检测任何药物引起的不良反应,如嗜睡。还通过测量血清天冬氨酸转氨酶、丙氨酸转氨酶、血尿素氮和肌酐来评估肝肾功能的不良反应。乙酰氨基酚给药呈剂量依赖性地显著增加机械刺激的足部退缩阈值和热撤退阈值,并且减少冷刺激的撤退频率。乙酰氨基酚可减轻神经病理性疼痛大鼠模型中的热痛觉过敏、机械和冷感觉异常,可能对治疗神经病理性疼痛有用。

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