Aripiprazole: The antiallodynic and antihyperalgesic effects in chronic constriction injury-induced neuropathic pain and reserpine-induced fibromyalgia with possible mechanisms

IF 4.6 2区 医学 Q1 NEUROSCIENCES
Yagmur Okcay , Özlem Aykaç , Rana Arslan , Nurcan Bektas
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Abstract

Neuropathic pain, caused by peripheral or central nerve damage, and fibromyalgia, a chronic musculoskeletal disorder, require complex treatment approaches. This study evaluated the antiallodynic and antihyperalgesic effects of aripiprazole (1, 5, and 10 mg/kg, i. p.) in rats with chronic constriction injury-induced neuropathic pain and reserpine-induced fibromyalgia in female Sprague-Dawley rats, using electronic von Frey and Hargreaves tests. Dopaminergic, serotonergic, and opioidergic systems' roles were assessed through pre-treatment with sulpiride (50 mg/kg), WAY 100635 (1 mg/kg), and naloxone (1 mg/kg), respectively. The effect of aripiprazole was compared with 30 mg/kg pregabalin in the neuropathic pain model and 30 mg/kg duloxetine in the fibromyalgia model. Aripiprazole demonstrated significant antiallodynic and antihyperalgesic activity in both models. It did not change locomotor activity at a dose of 1 mg/kg but caused a decrease at a dose of 5 mg/kg. Dopamine D2, serotonin 5-HT1A, and opioidergic receptors contributed to aripiprazole's effects at varying levels. This study highlights the potential use of aripiprazole for managing neuropathic pain and fibromyalgia by targeting multiple receptor systems. The findings demonstrate the potential use of aripiprazole alone or as an adjuvant in the treatments of neuropathic pain and fibromyalgia.
阿立哌唑对慢性收缩损伤性神经性疼痛和利血平性纤维肌痛的抗异动和抗痛觉作用及其可能的机制
由周围或中枢神经损伤引起的神经性疼痛,以及纤维肌痛,一种慢性肌肉骨骼疾病,需要复杂的治疗方法。本研究通过电子von Frey和Hargreaves实验,评估阿立哌唑(1、5和10 mg/kg,每日1次)对雌性Sprague-Dawley大鼠慢性收缩损伤性神经性疼痛和利血平性纤维肌痛的抗allodyan和抗过敏作用。通过分别使用舒必利(50 mg/kg)、WAY 100635 (1 mg/kg)和纳洛酮(1 mg/kg)预处理,评估多巴胺能、血清素能和阿片能系统的作用。比较阿立哌唑与30 mg/kg普瑞巴林在神经性疼痛模型中的作用和30 mg/kg度洛西汀在纤维肌痛模型中的作用。阿立哌唑在两种模型中均表现出显著的抗异速动力学和抗过敏活性。在1 mg/kg剂量下,它没有改变运动活动,但在5 mg/kg剂量下,它会导致运动活动减少。多巴胺D2、5-羟色胺5-HT1A和阿片能受体对阿立哌唑的作用有不同程度的影响。这项研究强调了阿立哌唑通过靶向多受体系统来治疗神经性疼痛和纤维肌痛的潜在用途。研究结果表明,阿立哌唑单独使用或作为辅助治疗神经性疼痛和纤维肌痛的潜在用途。
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来源期刊
Neuropharmacology
Neuropharmacology 医学-神经科学
CiteScore
10.00
自引率
4.30%
发文量
288
审稿时长
45 days
期刊介绍: Neuropharmacology publishes high quality, original research and review articles within the discipline of neuroscience, especially articles with a neuropharmacological component. However, papers within any area of neuroscience will be considered. The journal does not usually accept clinical research, although preclinical neuropharmacological studies in humans may be considered. The journal only considers submissions in which the chemical structures and compositions of experimental agents are readily available in the literature or disclosed by the authors in the submitted manuscript. Only in exceptional circumstances will natural products be considered, and then only if the preparation is well defined by scientific means. Neuropharmacology publishes articles of any length (original research and reviews).
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