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木犀草素-7-O-葡萄糖苷通过抑制激活的鼠骨髓来源肥大细胞中丝裂原活化蛋白激酶和磷酯酶 Cγ1 的磷酸化来抑制白三烯 C(4)的产生和脱颗粒。

Luteolin-7-O-glucoside suppresses leukotriene C(4) production and degranulation by inhibiting the phosphorylation of mitogen activated protein kinases and phospholipase Cγ1 in activated mouse bone marrow-derived mast cells.

机构信息

College of Pharmacy, Yeungnam University, Gyeongsan 712–749, Republic of Korea.

出版信息

Biol Pharm Bull. 2011;34(7):1032-6. doi: 10.1248/bpb.34.1032.

Abstract

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.

摘要

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。

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