花生四烯酸
磷脂酶A2
炎症
药理学
白三烯B4
花生四烯酸5-脂氧合酶
前列腺素E2
脂质信号
消炎药
化学
卡拉胶
代谢物
二十烷酸
作用机理
生物化学
内分泌学
生物
酶
免疫学
体外
作者
Xiaobin Ren,Mingzhu Zhang,Lingxiang Chen,Wanli Zhang,Yu Huang,Huazhen Luo,Ling Li,Hongbing He
出处
期刊:Molecular Medicine Reports
[Spandidos Publications]
日期:2017-07-27
卷期号:16 (4): 4045-4053
被引量:22
标识
DOI:10.3892/mmr.2017.7104
摘要
The traditional Chinese medicine Yunnan Baiyao (YNB) has been reported to possess anti‑inflammatory properties, however its mechanism of action remains unclear. It was previously reported that YNB ameliorated depression of arachidonic acid (AA) levels in a rat model of collagen-induced arthritis. In the current study, the capacity of YNB to ameliorate inflammation was compared in carrageenan‑induced and AA‑induced acute inflammation of the rat paw with celecoxib and mizolastine, respectively (n=24 per group). The capacity of YNB to affect the phospholipase A2 (PLA2)/AA pathway (using reverse transcription‑quantitative polymerase chain reaction) and release of inflammatory lipid mediators (by ELISA) were investigated. Celecoxib ameliorated carrageenan‑induced paw edema, and mizolastine ameliorated AA‑induced rat paw edema. YNB alleviated paw edema and inhibited inflammatory cell infiltration in the two models. YNB inhibited production of 5‑LOX AA metabolite leukotriene B4 (LTB4), and suppressed expression of 5‑LOX, cytosolic PLA2 (cPLA2), 5‑LOX‑activating protein, and LTB4 receptor mRNA in the AA‑induced inflammation model (P<0.05). YNB Inhibited the production of the COX‑2 AA metabolite prostaglandin E2 (PGE2) and suppressed expression of COX‑2, cPLA2, PGE2 mRNA in the carrageenan‑induced inflammation mode (P<0.05). Taken together, the data suggest that modulation of COX and LOX pathways in AA metabolism represent a novel anti-inflammatory mechanism of YNB.
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