Punjab University College of Pharmacy, University of the Punjab, Lahore, Punjab, Pakistan.
Department of Pharmacology, Faculty of Pharmacy, The Islamia University, Bahawalpur, Punjab, Pakistan.
Inflammopharmacology. 2021 Apr;29(2):483-497. doi: 10.1007/s10787-020-00761-z. Epub 2020 Oct 16.
Asphodelus tenuifolius is traditionally used in the management of rheumatic pain and inflamed body parts. The current study validated its traditional use as an anti-arthritic and anti-inflammatory agent using a series of in vivo models. Carrageenan and histamine-induced acute oedema models were employed to study the effects of n-hexane (n-HeAT) and ethanolic (EeAT) extracts on acute inflammatory mediators and were found to inhibit oedema formation in a dose-dependent manner. Formalin and complete Freund's adjuvant (CFA) were injected into the hind paw of rats for the induction of arthritis. In the formalin model both n-HeAT and EeAT showed significantly better (p < 0.05) anti-oedema effects from day 6 onward. In CFA model rats were treated on 8th day of induction with extracts at the doses of 250, 500, and 750 mg/kg respectively. Piroxicam (10 mg/kg) and normal saline (10 mL/kg) were used as positive and negative controls respectively. Both n-HeAT and EeAT significantly (p < 0.05) decreased arthritis development in a time-dependent manner and at 28th day extent of inflammation was even less than that observed at day 8. The arthritic score was measured at day 12, 16, 20, 24, and 28 and was observed to be significantly less (p < 0.05) in animals treated with 750 mg/kg of n-HeAT and EeAT, respectively. Joint inflammation (p < 0.01), bone erosion (p < 0.001) and, pannus formation (p < 0.01) were significantly declined in A. tenuifolius treatment groups. Radiographic evaluations (X-ray) were conducted to check bone integrity and extent of inflammation and were observed to be diminished at day 28 in A. tenuifolius extracts treated groups. HPLC was performed to screen the phytochemical profile of n-HeAT and EeAT and were found to contain flavonoids and phenolic compounds. Quantitative real-time polymerase chain reaction (qPCR) was performed to detect effects of n-HeAT and EeAT treatments on inflammatory markers i.e., IL-4, IL-6, IL-10, COX-2, NF-κB, and I-κB using blood samples. ELISA assays were performed for the detection of levels of C-reactive proteins, respectively. Significant downregulation of TNF-α, IL-4, IL-6, IL-1β, COX-2, NF-κB with simultaneous upregulation of IL-10 and I-κB was observed in n-HeAT and EeAT treatment groups. ELISA assays also showed significant (p < 0.05) down-modulation in the serum levels of CRP and TNF-α. Both extracts showed relatively weak antioxidant activities as compared with ascorbic acid in in vitro assay. Based on findings of the current study it is concluded that A. tenuifolius has anti-inflammatory and anti-arthritic effects and thus has potential to be used as an adjunct to standard NSAIDs therapy.Graphic abstract.
文殊兰传统上用于治疗风湿疼痛和发炎的身体部位。本研究使用一系列体内模型验证了其作为抗关节炎和抗炎剂的传统用途。采用角叉菜胶和组胺诱导的急性水肿模型研究 n-己烷 (n-HeAT) 和乙醇 (EeAT) 提取物对急性炎症介质的影响,结果表明提取物呈剂量依赖性抑制水肿形成。向大鼠后爪注射甲醛和完全弗氏佐剂 (CFA) 以诱导关节炎。在甲醛模型中,n-HeAT 和 EeAT 从第 6 天开始均表现出明显更好的 (p<0.05) 抗水肿作用。在 CFA 模型中,在诱导后的第 8 天分别以 250、500 和 750mg/kg 的剂量用提取物处理大鼠。吡罗昔康 (10mg/kg) 和生理盐水 (10mL/kg) 分别用作阳性和阴性对照。n-HeAT 和 EeAT 均显著 (p<0.05) 降低关节炎的发展,呈时间依赖性,在第 28 天,炎症的严重程度甚至低于第 8 天。在第 12、16、20、24 和 28 天测量关节炎评分,用 750mg/kg 的 n-HeAT 和 EeAT 治疗的动物的关节炎评分明显降低 (p<0.05)。关节炎症 (p<0.01)、骨侵蚀 (p<0.001) 和滑膜形成 (p<0.01) 在文殊兰治疗组中明显减少。进行 X 射线照相评估以检查骨完整性和炎症程度,并在第 28 天观察到文殊兰提取物处理组的炎症程度降低。进行高效液相色谱法 (HPLC) 筛选 n-HeAT 和 EeAT 的植物化学成分,并发现其含有类黄酮和酚类化合物。采用实时定量聚合酶链反应 (qPCR) 检测 n-HeAT 和 EeAT 处理对炎症标志物即白细胞介素-4 (IL-4)、白细胞介素-6 (IL-6)、白细胞介素-10 (IL-10)、环氧化酶-2 (COX-2)、核因子-κB (NF-κB) 和 I-κB 的影响,采用血液样本。采用酶联免疫吸附试验 (ELISA) 分别检测 C-反应蛋白的水平。n-HeAT 和 EeAT 处理组观察到 TNF-α、IL-4、IL-6、IL-1β、COX-2、NF-κB 的下调和 IL-10 和 I-κB 的上调。ELISA 检测还显示,血清 CRP 和 TNF-α 的水平显著降低 (p<0.05)。与体外试验中的抗坏血酸相比,两种提取物的抗氧化活性均相对较弱。基于当前研究的结果,可以得出结论,文殊兰具有抗炎和抗关节炎作用,因此有可能被用作标准 NSAIDs 治疗的辅助药物。