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脆弱腊菊提取物通过调节白细胞介素-1β、肿瘤坏死因子-α、白细胞介素-6、核因子-κB、环氧化酶-2、白细胞介素-4 和白细胞介素-10 来减轻大鼠关节炎。

Launaea fragilis extract attenuated arthritis in rats through modulation of IL-1β, TNF-α, IL-6, NF-κB, COX-2, IL-4, and IL-10.

机构信息

Department of Pharmacology, Faculty of Pharmacy, The Islamia University of Bahawalpur, Bahawalpur, 63100, Punjab, Pakistan.

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, The Islamia University of Bahawalpur, Bahawalpur, 63100, Punjab, Pakistan.

出版信息

Inflammopharmacology. 2024 Aug;32(4):2427-2443. doi: 10.1007/s10787-024-01471-6. Epub 2024 May 7.

Abstract

Launaea fragilis (Asso) Pau is a Cholistan desert medicinal plant. Launaea species are used as traditional remedies against various inflammatory conditions. The current research was designed to evaluate the anti-nociceptive, anti-inflammatory, and anti-arthritic potential of ethanolic extract of L. fragilis (Et-LF). The plant extract was prepared by triple maceration. GC-MS screening explored the presence of various bioactive phytoconstituents including n-tetracosanol-1, 1-heptacosanol, and n-hexadecanoic acid. DPPH assay demonstrated the antioxidant potential of Et-LF. Safety profile data indicated that Et-LF was safe up to the oral dose of 5000 mg/kg in female rats. Anti-nociceptive activity of Et-LF was assessed in hot plate method and acetic acid-induced writhing model and the results suggested that Et-LF had significant analgesic effects in both animal models. Carrageenan, histamine, and serotonin-induced edema models were used to estimate the anti-inflammatory effects of Et-LF and were found to prevent paw edema development dose dependently. The anti-arthritic effect of Et-LF was estimated in CFA-induced arthritic rat model. Treatment with Et-LF 125, 250, 500 and flurbiprofen (FP) 10 mg/kg/day significantly attenuated the paw edema, reversed the reduced body weight, and restored the altered hematological parameters in arthritic rats. Gene expression studies revealed the significant downregulation of IL-1β, TNF-α, IL-6, NF‑κB, and COX-2, and upregulation of IL-4 and IL-10 in arthritic rats treated with various doses of plant extract. Histological evaluation of ankle joints showed that Et-LF mitigated pannus formation, infiltration of inflammatory cells, and fibrous connective tissue formation in the diseased rats. Thereof, it may be concluded that the recent study demonstrated the anti-nociceptive, anti-inflammatory, and anti-arthritic effects ascribed to the signifying presence of phytoconstituents in L. fragilis.

摘要

Launaea fragilis (Asso) Pau 是 Cholistan 沙漠药用植物。Launaea 物种被用作传统疗法,用于治疗各种炎症性疾病。本研究旨在评估 Launaea fragilis(Et-LF)乙醇提取物的抗伤害感受、抗炎和抗关节炎潜力。植物提取物通过三重浸提制备。GC-MS 筛选发现了各种生物活性植物成分,包括 n-二十四烷醇-1、1-十七烷醇和 n-十六烷酸。DPPH 测定法表明 Et-LF 具有抗氧化潜力。安全性数据表明,Et-LF 在雌性大鼠中口服剂量高达 5000mg/kg 时是安全的。Et-LF 的抗伤害感受活性通过热板法和醋酸诱导扭体模型进行评估,结果表明 Et-LF 在两种动物模型中均具有显著的镇痛作用。角叉菜胶、组胺和 5-羟色胺诱导的水肿模型用于评估 Et-LF 的抗炎作用,结果表明 Et-LF 可剂量依赖性地预防爪水肿的发展。在 CFA 诱导的关节炎大鼠模型中评估了 Et-LF 的抗关节炎作用。Et-LF 125、250、500mg/kg/天和氟比洛芬(FP)10mg/kg/天的治疗显著减轻了爪水肿,逆转了体重减轻,并恢复了关节炎大鼠改变的血液学参数。基因表达研究表明,关节炎大鼠用不同剂量的植物提取物治疗后,IL-1β、TNF-α、IL-6、NF-κB 和 COX-2 的表达显著下调,IL-4 和 IL-10 的表达上调。踝关节组织学评估表明,Et-LF 减轻了患病大鼠的滑膜增生、炎症细胞浸润和纤维结缔组织形成。因此,可以得出结论,最近的研究表明,Launaea fragilis 中存在的显著植物成分赋予了其抗伤害感受、抗炎和抗关节炎作用。

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