Department of Zoology, Faculty of Science, Engineering & Technology, PB X1, Mthatha, 5117, Eastern Cape Province, South Africa,
Inflammation. 2015 Feb;38(1):61-9. doi: 10.1007/s10753-014-0007-y.
Acetylation and methylation semisynthesis of oleanolic acid (OA) isolated from Syzygium aromaticum L. yielded two compounds: 3-acetoxyoleanolic acid (3-AOA) and 3-acetoxy, 28-methylester oleanolic acid (3-A,28-MOA). Anti-inflammatory properties of these compounds were assessed using the serotonin and fresh egg albumin-induced inflammatory test models in male Wistar rats weighing 250-300 g. Furthermore, erythrocyte membrane-stabilizing property of these compounds was evaluated in the heat- and hypotonicity-induced in vitro hemolysis test models. The two semisynthetic compounds significantly (p < 0.05) inhibited albumin-induced inflammation better than OA and indomethacin from 1-5 h post administration. Both compounds were membrane stabilizing in heat-induced hemolysis test while only 3-AOA showed membrane-stabilizing effects in a hypotonic milieu. Semisynthesis of OA yielded two compounds which had better in vivo anti-inflammatory and in vitro membrane-stabilizing properties.
从丁香 Syzygium aromaticum L. 中分离得到的齐墩果酸(OA)进行乙酰化和甲基化半合成,得到两种化合物:3-乙酰氧基齐墩果酸(3-AOA)和 3-乙酰氧基,28-甲酯齐墩果酸(3-A,28-MOA)。使用雄性 Wistar 大鼠体重 250-300g 的 5-羟色胺和新鲜卵白蛋白诱导的炎症测试模型评估这些化合物的抗炎特性。此外,还在热和低渗诱导的体外溶血测试模型中评估了这些化合物对红细胞膜稳定的特性。这两种半合成化合物在给药后 1-5 小时内显著(p < 0.05)抑制了卵白蛋白诱导的炎症,优于 OA 和吲哚美辛。两种化合物在热诱导的溶血试验中均具有膜稳定作用,而只有 3-AOA 在低渗环境中显示出膜稳定作用。OA 的半合成产生了两种具有更好的体内抗炎和体外膜稳定特性的化合物。