Pharmacological interactions of sulforaphane and gabapentin in a murine fibromyalgia-like pain model

IF 7.5 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL Biomedicine & Pharmacotherapy Pub Date : 2025-03-01 Epub Date: 2025-02-18 DOI:10.1016/j.biopha.2025.117929
Ik-Yahalcab Zamora-Díaz , María Eva González-Trujano , David Martínez-Vargas , G. Fernando Moreno-Pérez , Alberto Hernandez-Leon , Hugo Fernando Narváez-González , Rosa Ventura-Martínez , Francisco Pellicer , Francisco Javier López-Muñoz
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Abstract

Therapeutic management of a chronic painful syndrome such as fibromyalgia (FM) lacks effective and safe single or combined analgesics. Current medications such as gabapentin (GPB) or pregabalin are moderately effective but in the presence of several adverse effects. Natural products derived from cruciferous vegetables such as sulforaphane (SFN) produce neuroprotective effects due to their potent antioxidant and anti-inflammatory properties. However, it is unknown whether positive or negative pharmacological interactions may occur when GBP and SFN are combined. The aim of this study was to estimate the pharmacological interaction of GBP and SFN in FM-like pain induced in rats. Time course curves of antiallodynic and antihyperalgesic effects were constructed for both SFN (3.16, 31.6, and 100 mg/kg, i.p.) and GBP (10, 31.6, and 100 mg/kg, i.p.) by recording behavioral responses every 30 min and up to 4 h afterward, from which dose-response effects were also obtained to decide the dosage combination. An electrocorticographic (ECoG) recording in mice and docking analysis were also explored to explain the pharmacological interaction. Our results demonstrated significant and dose-dependent antiallodynic and antihyperalgesic effects in their individual administration. While a combination of intermediate doses of these drugs enhanced their effects producing the same level as that obtained by using only 1/3 of the individual dose in each case. The ECoG recording and docking analysis suggest that calcium channels could be partly involved in the drug interaction. This study provides preclinical evidence that SFN alone and in combination with GBP may be beneficial for relieving FM-like pain at certain doses.
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萝卜硫素和加巴喷丁在小鼠纤维肌痛样疼痛模型中的药理相互作用
慢性疼痛综合征如纤维肌痛(FM)的治疗管理缺乏有效和安全的单一或联合镇痛药。目前的药物,如加巴喷丁(GPB)或普瑞巴林是中等有效,但存在一些不良反应。从十字花科蔬菜中提取的天然产物,如萝卜硫素(SFN),由于其有效的抗氧化和抗炎特性,具有神经保护作用。然而,当GBP和SFN联合使用时,是否会发生积极或消极的药理相互作用尚不清楚。本研究的目的是评估GBP和SFN在大鼠fm样疼痛中的药理作用。通过记录每30 min和服药后4 h的行为反应,构建SFN(3.16、31.6和100 mg/kg, i.p.)和GBP(10、31.6和100 mg/kg, i.p.)抗allodyh和抗过敏作用的时间过程曲线,并由此得出剂量-反应效应,以确定给药组合。通过小鼠皮质电图(ECoG)记录和对接分析,也探讨了药物相互作用的解释。我们的研究结果显示了显著的剂量依赖性抗异动和抗痛觉作用。而这些药物的中间剂量的组合增强了它们的效果,产生的效果与在每种情况下只使用1/3的单个剂量所获得的效果相同。ECoG记录和对接分析提示钙通道可能部分参与了药物相互作用。本研究提供了临床前证据,证明SFN单独或联合GBP在一定剂量下可能有利于缓解fm样疼痛。
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来源期刊
CiteScore
11.90
自引率
2.70%
发文量
1621
审稿时长
48 days
期刊介绍: Biomedicine & Pharmacotherapy stands as a multidisciplinary journal, presenting a spectrum of original research reports, reviews, and communications in the realms of clinical and basic medicine, as well as pharmacology. The journal spans various fields, including Cancer, Nutriceutics, Neurodegenerative, Cardiac, and Infectious Diseases.
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