Cui Yongming, Ao Mingzhang, Li Wei, Hu Jing, Yu Longjiang
College of Life Science and Technology, Institute of Resource Biology and Biotechnology, Huazhong University of Science & Technology, Wuhan 430074, China.
Z Naturforsch C J Biosci. 2008 May-Jun;63(5-6):361-5. doi: 10.1515/znc-2008-5-609.
Licochalcone A was isolated from the roots of Glycyrrhiza inflata and evaluated for its anti-inflammatory activity in xylene-induced mice ear edema and carrageenan-induced paw edema tests. At the same time, the inhibition of prostaglandin biosynthesis by licochalcone A was also studied in lipopolysaccharide (LPS)-induced mouse macrophage cells. At 5 mg/ ear, licochalcone A showed remarkable effects against acute inflammation induced by xylene, and at the doses of 2.5, 5, 10 mg/kg (p.o.), licochalcone A reduced significantly paw edema induced by carrageenan compared to the control at the fourth hour. Both COX-2 activity and expression were significantly inhibited by licochalcone A at all the test doses. Therefore, licochalcone A could be a useful compound for the development of new anti-inflammatory agents.
光甘草定从胀果甘草根中分离得到,并在二甲苯诱导的小鼠耳肿胀和角叉菜胶诱导的爪肿胀试验中对其抗炎活性进行了评估。同时,还在脂多糖(LPS)诱导的小鼠巨噬细胞中研究了光甘草定对前列腺素生物合成的抑制作用。在5mg/耳剂量下,光甘草定对二甲苯诱导的急性炎症显示出显著效果,在2.5、5、10mg/kg(口服)剂量下,与对照组相比,光甘草定在第4小时显著减轻了角叉菜胶诱导的爪肿胀。在所有测试剂量下,光甘草定都显著抑制了COX-2的活性和表达。因此,光甘草定可能是开发新型抗炎药物的有用化合物。