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Isolation of Terpenoids from the Stem of Ficus aurantiaca Griff and their Effects on Reactive Oxygen Species Production and Chemotactic Activity of Neutrophils

机译:极光榕树茎中萜类化合物的分离及其对嗜中性粒细胞活性氧产生和趋化活性的影响

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摘要

Three new triterpenoids; namely 28,28,30-trihydroxylupeol (>1); 3,21,21,26-tetrahydroxy-lanostanoic acid (>2) and dehydroxybetulinic acid (>3) and seven known compounds; i.e., taraxerone (>4); taraxerol (>5); ethyl palmitate (>6); herniarin (>7); stigmasterol (>8); ursolic acid (>9) and acetyl ursolic acid (>10) were isolated from the stem of Ficus aurantiaca Griff. The structures of the compounds were established by spectroscopic techniques. The compounds were evaluated for their inhibitory effects on polymorphonuclear leukocyte (PMN) chemotaxis by using the Boyden chamber technique and on human whole blood and neutrophil reactive oxygen species (ROS) production by using a luminol-based chemiluminescence assay. Among the compounds tested, compounds >1–>4, >6 and >9 exhibited strong inhibition of PMN migration towards the chemoattractant N-formyl-methionyl-leucyl-phenylalanine (fMLP) with IC50 values of 6.8; 2.8; 2.5; 4.1; 3.7 and 3.6 μM, respectively, comparable to that of the positive control ibuprofen (6.7 μM). Compounds >2–>4, >6, >7 and >9 exhibited strong inhibition of ROS production of PMNs with IC50 values of 0.9; 0.9; 1.3; 1.1; 0.5 and 0.8 μM, respectively, which were lower than that of aspirin (9.4 μM). The bioactive compounds might be potential lead molecules for the development of new immunomodulatory agents to modulate the innate immune response of phagocytes.
机译:三种新的三萜;即28,28,30-trihydroxylupeol(> 1 ); 3,21,21,26-四羟基羊毛脂酸(> 2 )和脱羟基贝丁酸(> 3 )和7种已知化合物;即taraxerone(> 4 );蒲公英油(> 5 );棕榈酸乙酯(> 6 );疝气(> 7 ); stigmasterol(> 8 );从Ficus aurantiaca Griff的茎中分离得到乌索酸(> 9 )和乙酰乌索酸(> 10 )。化合物的结构通过光谱技术确定。使用Boyden室技术评估了这些化合物对多形核白细胞(PMN)趋化性的抑制作用,并使用基于鲁米诺的化学发光测定法评估了这些化合物对人全血和中性粒细胞活性氧(ROS)的抑制作用。在测试的化合物中,化合物> 1 – > 4 ,> 6 和> 9 对PMN向趋化剂的迁移具有强烈抑制作用N-甲酰基-甲硫酰基-亮氨酰-苯丙氨酸(fMLP),IC50值为6.8; 2.8; 2.5; 4.1;分别为3.7和3.6μM,与阳性对照布洛芬(6.7μM)相当。化合物> 2 – > 4 ,> 6 ,> 7 和> 9 对ROS表现出强烈的抑制作用生产IC50值为0.9的PMN; 0.9; 1.3; 1.1;分别为0.5和0.8μM,低于阿司匹林(9.4μM)。该生物活性化合物可能是潜在的先导分子,用于开发新的免疫调节剂来调节吞噬细胞的先天免疫应答。

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