Nataraju A, Raghavendra Gowda C D, Rajesh R, Vishwanath B S
Department of Studies in Biochemistry, University of Mysore, Manasagangotri, Mysore-570 006, Karnataka, India.
Curr Top Med Chem. 2007;7(8):801-9. doi: 10.2174/156802607780487696.
Ursolic acid (3beta-hydroxy-urs-12-en-28-oic acid) isolated from many medicinal plants has diverse pharmacologically important properties, including strong anti-inflammatory activity. However its interaction with pro-inflammatory PLA2 is not known. Ursolic acid inhibited secretory PLA2 (sPLA2) enzymes purified from Vipera russelli, Naja naja venom and human pleural fluid and synovial fluid. IC50 values determined for these enzymes ranged from 12 to 18 microM. Group II secretory PLA2 from both venoms & human inflammatory source were found to be sensitive to inhibition in comparison with group I cobra venom sPLA2. Variation in Ca2+ concentration from 2.5-15 mM did not alter the level of inhibition. Similarly sPLA2 inhibition by ursolic acid is independent of substrate concentration. Ursolic acid interacts with purified venom sPLA2 enzymes and enhances relative fluorescence intensity in a dose dependent manner. In the presence of ursolic acid apparent shift in the far UV-CD spectra of sPLA2 was observed, indicating a direct interaction with the enzyme and formation of enzyme-ursolic acid complex. This complex results in irreversible inhibition of sPLA2 as evident by dialysis study. Inhibition of sPLA2 induced mouse paw edema and indirect hemolytic activity confirmed its sPLA2 inhibitory activity in vivo and in situ respectively. These studies revealed that the strong anti-inflammatory activity of ursolic acid is by inhibiting sPLA2 enzymes.
从多种药用植物中分离得到的熊果酸(3β - 羟基 - 乌苏 - 12 - 烯 - 28 - 酸)具有多种重要的药理特性,包括强大的抗炎活性。然而,其与促炎磷脂酶A2的相互作用尚不清楚。熊果酸可抑制从圆斑蝰蛇毒、眼镜蛇毒以及人胸腔积液和滑液中纯化得到的分泌型磷脂酶A2(sPLA2)。这些酶的半数抑制浓度(IC50)值在12至18微摩尔之间。与I组眼镜蛇毒sPLA2相比,来自蛇毒和人类炎症源的II组分泌型磷脂酶A2对抑制更为敏感。钙离子浓度在2.5 - 15毫摩尔范围内变化时,抑制水平未改变。同样,熊果酸对sPLA2的抑制作用与底物浓度无关。熊果酸与纯化的蛇毒sPLA2酶相互作用,并以剂量依赖的方式增强相对荧光强度。在存在熊果酸的情况下,观察到sPLA2的远紫外圆二色光谱出现明显偏移,表明其与该酶直接相互作用并形成酶 - 熊果酸复合物。透析研究表明,这种复合物导致sPLA2的不可逆抑制。抑制sPLA2可减轻小鼠爪肿胀和间接溶血活性,分别证实了其在体内和原位的sPLA2抑制活性。这些研究表明,熊果酸的强大抗炎活性是通过抑制sPLA2酶实现的。