Department of Pharmacology, Faculty of Pharmaceutical Sciences, Government College University Faisalabad, Faisalabad, 38000, Pakistan.
Riphah Institute of Pharmaceutical Sciences, Riphah International University, Lahore Campus, Lahore, 38000, Pakistan.
Inflammopharmacology. 2023 Dec;31(6):3167-3182. doi: 10.1007/s10787-023-01374-y. Epub 2023 Nov 14.
The current study aimed to find out the anti-arthritic activity and safety study of Coronopus didymus aqueous extract (CDAE) as well as its chemical characterization by HPLC-DAD. Safety study including acute and subacute toxicity studies of the plant aqueous extract was also performed. In complete Freund's adjuvant-induced arthritic model (CFA), 0.15 ml CFA was injected in the left hind paw at day 1 in all rats except normal rats. Treatment with CDAE at 200, 400, and 800 mg/kg and methotrexate (1 mg/kg) was administered at day 8 and continued till 28th day using oral gavage. The CDAE considerably (p < 0.05) reduced the paw swelling and arthritic score, and reinstated the body weight and blood parameters. The CDAE considerably modulated superoxide dismutase, catalase, reduced glutathione, and malondialdehyde level in liver homogenate in contrast to disease control. The CDAE at 400 mg/kg considerably reduced IL-6, IL -1β, COX-2, and NF-ĸβ, whereas elevated IL-10, IL-4, and I-kappa β as equated to disease and standard groups. The LD50 of CDAE > 2000 mg/kg. In subacute toxicity study, CDAE at 200-800 mg/kg did not exhibit clinical signs of toxicity, mortality, hematological, biochemical, and histological alteration in the liver heart, kidney, and lungs in contrast to the normal group. It was concluded that the presence of delphinidine-3-glucoside, diosmetin, 3-feruloyl-4,5-dicaffeoyl quinic acid, and gallic acid in CDAE might be accountable for its anti-arthritic activity and safe use for a long period.
本研究旨在探讨冠状毛茛水提物(CDAE)的抗关节炎活性和安全性,并通过高效液相色谱-二极管阵列检测法(HPLC-DAD)对其进行化学表征。还进行了植物水提物的急性和亚急性毒性研究。在完全弗氏佐剂诱导的关节炎模型(CFA)中,除正常大鼠外,所有大鼠于第 1 天在左后爪中注射 0.15 ml CFA。在第 8 天和第 28 天,通过口服灌胃给予 CDAE 200、400 和 800mg/kg 以及甲氨蝶呤(1mg/kg)治疗。CDAE 显著(p<0.05)降低了爪肿胀和关节炎评分,并恢复了体重和血液参数。与疾病对照组相比,CDAE 显著调节了肝匀浆中超氧化物歧化酶、过氧化氢酶、还原型谷胱甘肽和丙二醛水平。CDAE 以 400mg/kg 剂量显著降低了 IL-6、IL-1β、COX-2 和 NF-ĸB,而与疾病和标准组相比,IL-10、IL-4 和 I-κB 则升高。CDAE 的 LD50>2000mg/kg。在亚急性毒性研究中,与正常组相比,CDAE 以 200-800mg/kg 剂量未表现出毒性、死亡率、血液学、生化和肝、心、肾和肺组织学改变的临床症状。结论是 CDAE 中存在飞燕草定-3-葡萄糖苷、芫花素、3-阿魏酰-4,5-二咖啡酰奎宁酸和没食子酸可能是其抗关节炎活性和长期安全使用的原因。