炎症是各种急慢性疾病发病的核心因素,包括阑尾炎、支气管炎、关节炎、癌症和神经系统疾病。非甾体抗炎药是治疗炎症性疾病的常用药物,长期使用会导致胃肠道出血、溃疡和更多问题。包括精油在内的植物治疗剂与低剂量合成药物相结合已被证明可以产生协同效应并减少合成药物的并发症。本研究旨在评估蓝桉精油单独使用以及与氟比洛芬联合使用的抗炎、镇痛和解热特性。GC-MS 分析用于筛选油的化学成分。进行体外抗炎测定(膜稳定测定)和体内急性炎症(角叉菜胶和组胺诱导的爪水肿)和慢性(棉球诱导的肉芽肿和完全弗氏佐剂诱导的关节炎)模型来检查抗炎作用特性。进行乙酸诱导的痛觉和酵母诱导的发热模型以检查镇痛和解热特性。进行 qRT-PCR 来研究治疗对炎症生物标志物表达的影响。对蓝桉精油的 GC-MS 分析表明存在桉树脑以及其他活性生物分子。 与单独使用 500 mg/kg蓝桉油和 10 mg/kg 氟比洛芬治疗组相比,500 + 10 mg/kg油药组合显示出显着(p < 0.05)更好的体外膜稳定效果。在所有体内模型中,与单独使用500 mg/kg蓝桉油相比,500 + 10 mg/kg 油药组合显示出显着(p < 0.05)更好的抗炎、镇痛和解热作用。500 + 10 mg/kg 油药组合治疗组与 10 mg/kg 氟比洛芬治疗组进行比较时,前者显示出显着(p < 0.05)更好的抗炎和解热作用,但镇痛模型中无显着差异。用10 mg/kg氟比洛芬治疗的动物组显示出比单独用500 mg/kg油治疗的组显着(p < 0.05)更好的抗炎和镇痛效果,而在解热效果方面没有显着差异。qRT-PCR 分析显示,与患病对照相比,用 500 + 10 mg/kg 油药组合治疗的动物血清样品中 IL-4 和 TNF-α 的表达显着下调(p < 0.05 )。关节炎)组。总体而言,目前的研究表明蓝桉精油与氟比洛芬联合使用比单独使用油和氟比洛芬表现出更好的抗炎、镇痛和解热作用,这归因于促炎生物标志物(IL-4和TNF-α)的下调。需要进一步的研究来制定稳定的剂型并检查其在不同炎症性疾病中的抗炎功效。
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Anti-inflammatory mechanisms of eucalyptol rich Eucalyptus globulus essential oil alone and in combination with flurbiprofen
Inflammation is the core contributor in the pathogenesis of various acute and chronic illness including appendicitis, bronchitis, arthritis, cancer and neurological diseases. NSAIDs, commonly used medications for inflammatory diseases, on prolonged use cause GI bleeding, ulcers and many more issues. Plant-based therapeutic agents including essential oils in combination with low-dose synthetic drugs have been shown to produce synergistic effects and reduce complications of synthetic drugs. This study was designed to evaluate the anti-inflammatory, analgesic and anti-pyretic properties of Eucalyptus globulus essential oil alone and in combination with flurbiprofen. GC–MS analysis was performed to screen chemical composition of oil. In vitro anti-inflammatory assay (membrane stabilization assay) and in vivo inflammatory acute (carrageenan and histamine-induced paw oedema) and chronic (cotton pellet-induced granuloma and Complete Freund’s adjuvant-induced arthritis) models were performed to check anti-inflammatory properties. Acetic acid-induced algesia and yeast-induced pyrexia models were performed to check analgesic and anti-pyretic properties. qRT-PCR was performed to study the effect of treatments on the expression of inflammatory biomarkers. GC–MS analysis of E. globulus essential oil showed the presence of eucalyptol along with other active biomolecules. 500 + 10 mg/kg of oil-drug combination showed significantly (p < 0.05) better in vitro membrane stabilization effects as compared with groups treated with 500 mg/kg of E. globulus oil and 10 mg/kg of Flurbiprofen alone. 500 + 10 mg/kg of oil-drug combination showed significantly (p < 0.05) better anti-inflammatory, analgesic and antipyretic effects as compared to 500 mg/kg of E. globulus oil alone in all in vivo models. When comparison was done between 500 + 10 mg/kg of oil-drug combination-treated and 10 mg/kg Flurbiprofen-treated group, the former group showed significantly (p < 0.05) better anti-inflammatory and anti-pyretic effects, but there were non-significant differences in the analgesic model. Animal group treated with 10 mg/kg of Flurbiprofen showed significantly (p < 0.05) better anti-inflammatory and analgesic effects than group treated with 500 mg/kg of oil alone while, there were non-significant differences in anti-pyretic effects. qRT-PCR analysis showed significant (p < 0.05) down-regulation in the expression of IL-4 and TNF-α in serum samples of animals treated with 500 + 10 mg/kg of oil-drug combination as compared to the diseased control (arthritic) group. Overall, the current research demonstrates that Eucalyptus globulus essential oil in combination with flurbiprofen showed better anti-inflammatory, analgesic and anti-pyretic effects than oil and flurbiprofen alone which is attributed to the down-regulation of pro-inflammatory biomarkers (IL-4 and TNF-α). Further studies are required to formulate a stable dosage form and to check the anti-inflammatory efficacy in different inflammatory disorders.