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黄芩根中黄酮类化合物黄芩素的抗炎特性及体外对白三烯C4生物合成的抑制作用。

Anti-inflammatory properties and inhibition of leukotriene C4 biosynthesis in vitro by flavonoid baicalein from Scutellaria baicalensis georgy roots.

作者信息

Butenko I G, Gladtchenko S V, Galushko S V

机构信息

State Scientific Center of Drugs, Kharkov, Ukraine.

出版信息

Agents Actions. 1993;39 Spec No:C49-51. doi: 10.1007/BF01972717.

Abstract

Anti-inflammatory activity of baicalein (5,6,7-trioxyflavone-7-O-beta-D-glucuronide) was greater in the chronic inflammation model (rat adjuvant arthritis, ED50 = 120.6 mg/kg) than observed in the rat carrageenan-induced paw edema, ED50 > or = 200.0 mg/kg. A comparative study of the 5-lipoxygenase (5-LO) inhibitory activity of baicalein, BW 755 C, and hydroxamic acid arachidonate on leukotriene C4 (LTC4) biosynthesis by rat resident peritoneal macrophages stimulated with calcium ionophore (A 23186) showed that these drugs significantly inhibited LTC4 production, IC50: 9.5, 41.8, and 2.8 microM, respectively. This finding suggests that inhibition of the 5-LO pathway of arachidonic acid metabolism may be one of the mechanisms of baicalein's anti-inflammatory activity.

摘要

黄芩素(5,6,7 - 三羟基黄酮 - 7 - O - β - D - 葡萄糖醛酸苷)在慢性炎症模型(大鼠佐剂性关节炎,ED50 = 120.6 mg/kg)中的抗炎活性比在大鼠角叉菜胶诱导的爪肿胀模型(ED50≥200.0 mg/kg)中更强。一项关于黄芩素、BW 755 C和异羟肟酸花生四烯酸对钙离子载体(A 23186)刺激的大鼠腹腔巨噬细胞合成白三烯C4(LTC4)的5 - 脂氧合酶(5 - LO)抑制活性的比较研究表明,这些药物显著抑制LTC4的产生,IC50分别为:9.5、41.8和2.8 μM。这一发现表明,抑制花生四烯酸代谢的5 - LO途径可能是黄芩素抗炎活性的机制之一。

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