College of Pharmacy, Yeungnam University, Gyeongsan 712–749, Republic of Korea.
Biol Pharm Bull. 2011;34(7):1032-6. doi: 10.1248/bpb.34.1032.
In this study, luteolin-7-O-glucoside (L7G), an herbal medicine isolated from Ailanthus altissima, inhibited 5-lipoxygenase (5-LOX)-dependent leukotriene C(4) (LTC(4)) production in bone marrow-derived mast cells (BMMCs) in a concentration-dependent manner with an IC(50) of 3.0 µM. To determine the action mechanism of L7G, we performed immunoblotting for cytosolic phospholipase A(2) (cPLA(2)) and mitogen-activated protein kinases (MAPKs) following c-kit ligand (KL)-induced activation of BMMCs with or without L7G. Inhibition of LTC(4) production by L7G was accompanied by a decrease in cPLA(2) phosphorylation, which occurred via the extracellular signal-regulated protein kinase-1/2 (ERK1/2) and p38 and c-Jun N-terminal kinase (JNK) pathways. In addition, L7G also attenuated mast cell degranulation in a dose-dependent manner (IC(50), 22.8 µM) through inhibition of phospholipase Cγ1 (PLCγ1) phosphorylation. Our results suggest that the anti-asthmatic activity of L7G may be mediated in part via the inhibition of LTC(4) generation and mast cell degranulation.
在这项研究中,从臭椿中分离得到的一种草药成分——木樨草素-7-O-葡萄糖苷(L7G),以浓度依赖的方式抑制骨髓来源的肥大细胞(BMMC)中 5-脂氧合酶(5-LOX)依赖性白三烯 C4(LTC4)的产生,其 IC50 为 3.0 μM。为了确定 L7G 的作用机制,我们在 c-kit 配体(KL)诱导 BMMC 激活后,进行了细胞质磷脂酶 A2(cPLA2)和丝裂原活化蛋白激酶(MAPKs)的免疫印迹分析,同时加入或不加入 L7G。L7G 抑制 LTC4 产生伴随着 cPLA2 磷酸化的减少,这是通过细胞外信号调节蛋白激酶-1/2(ERK1/2)和 p38 以及 c-Jun N-末端激酶(JNK)途径发生的。此外,L7G 还通过抑制磷脂酶 Cγ1(PLCγ1)磷酸化,以剂量依赖的方式减弱肥大细胞脱颗粒(IC50 为 22.8 μM)。我们的结果表明,L7G 的抗哮喘活性可能部分通过抑制 LTC4 的生成和肥大细胞脱颗粒来介导。