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蛇床子素,一种天然香豆素,对纤维肌痛模型小鼠的保护作用:靶向致炎细胞因子和 MAO-A。

Protective Effect of Esculetin, Natural Coumarin in Mice Model of Fibromyalgia: Targeting Pro-Inflammatory Cytokines and MAO-A.

机构信息

Department of Pharmaceutical Sciences, Guru Nanak Dev University, Amritsar, Punjab, India.

出版信息

Neurochem Res. 2020 Oct;45(10):2364-2374. doi: 10.1007/s11064-020-03095-y. Epub 2020 Jul 16.

DOI:10.1007/s11064-020-03095-y
PMID:32676949
Abstract

Fibromyalgia is a refractory syndrome characterized by chronic wayward pain and complex co-morbid psychological trepidation. The current treatments have a limited role and proper clinical benefits are far from satisfactory. Naturally occurring coumarins such as osthole are known to have analgesic and anti-inflammatory activities. Therefore, the current investigation was designed to explore the potential of natural coumarin esculetin (2.5, 5, and 10 mg/kg) in mitigating reserpine-induced fibromyalgia in Swiss albino mice. Esculetin is a 6,7 dihydroxy-coumarin obtained from various plant sources such as Aesculus hippocastanum L, Ceratostigma willmottianum, Citrus limonia, etc. Reserpine (0.5 mg/kg/day s.c.) treatment for first 3 days, significantly altered the behavior of mice as evidenced by reduced paw withdrawal threshold in pressure application measurement (PAM) test and electronic von-Frey (eVF) test, increased immobility time in forced swim test (FST), increased latency to reach the platform in Morris water maze (MWM) test and reduced number of square crossed in the open field test (OFT). These behavioral deficits with reserpine treatment were integrated with a reduced level of serotonin (5-HT), reduced glutathione (GSH), along with an increase in monoamine oxidase-A (MAO-A) activity, pro-inflammatory cytokines (IL-1β, TNF-α), thiobarbituric acid reactive substances (TBARS) and glutamate level. Esculetin (10 mg/kg/day i.p) treatment for 5 days, significantly abrogated reserpine induced behavioral and biochemical alterations. Whereas, no significant improvement was observed with lower doses of esculetin i.e. 2.5 and 5 mg/kg.

摘要

纤维肌痛是一种难治性综合征,其特征为慢性不定部位疼痛和复杂的合并心理恐惧。目前的治疗方法作用有限,临床效果远不理想。已知天然香豆素如蛇床子素具有镇痛和抗炎作用。因此,本研究旨在探讨天然香豆素七叶灵(2.5、5 和 10mg/kg)减轻瑞士白化小鼠利血平诱导的纤维肌痛的潜力。七叶灵是一种 6,7-二羟基香豆素,可从多种植物来源获得,如欧洲七叶树、土木香、酸橙等。利血平(0.5mg/kg/天 sc)治疗前 3 天,显著改变了小鼠的行为,表现在压力应用测量(PAM)试验和电子 von-Frey(eVF)试验中, paw withdrawal threshold 降低,强迫游泳试验(FST)中不动时间增加,水迷宫试验(MWM)中到达平台的潜伏期增加,旷场试验(OFT)中穿越方格的次数减少。这些与利血平治疗相关的行为缺陷与 5-羟色胺(5-HT)水平降低、谷胱甘肽(GSH)降低、单胺氧化酶-A(MAO-A)活性升高、促炎细胞因子(IL-1β、TNF-α)、硫代巴比妥酸反应物质(TBARS)和谷氨酸水平升高有关。七叶灵(10mg/kg/天 ip)治疗 5 天,显著减轻了利血平诱导的行为和生化改变。而较低剂量的七叶灵(2.5 和 5mg/kg)则没有明显改善。

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