首页> 美国卫生研究院文献>Biomolecules Therapeutics >Saucerneol F a New Lignan Isolated from Saururus chinensis Attenuates Degranulation via Phospholipase Cγ 1 Inhibition and Eicosanoid Generation by Suppressing MAP Kinases in Mast Cells
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Saucerneol F a New Lignan Isolated from Saururus chinensis Attenuates Degranulation via Phospholipase Cγ 1 Inhibition and Eicosanoid Generation by Suppressing MAP Kinases in Mast Cells

机译:Saucerneol F一种新的木质素从Saururus chinensis中分离出来通过抑制肥大细胞中的MAP激酶通过磷脂酶Cγ1抑制和类二十烷酸生成来减轻成粒作用。

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摘要

During our on-going studies to identify bioactive compounds in medicinal herbs, we found that saucerneol F (SF), a naturally occurring sesquilignan isolated from Saururus chinensis (S. chinensis), showed in vitro anti-inflammatory activity. In this study, we examined the effects of SF on the generation of 5-lipoxygenase (5-LO) dependent leukotriene C4 (LTC4), cyclooxygenase-2 (COX-2) dependent prostaglandin D2 (PGD2), and on phospholipase Cγ1 (PLCγ1)-mediated degranulation in SCF-induced mouse bone marrow-derived mast cells (BMMCs). SF inhibited eicosanoid (PGD2 and LTC4) generation and degranulation dose-dependently. To identify the molecular mechanisms underlying the inhibition of eicosanoid generation and degranulation by SF, we examined the effects of SF on the phosphorylation of PLCγ1, intracellular Ca2+ influx, the translocation of cytosolic phospholipase A2 (cPLA2) and 5-LO, and on the phosphorylation of MAP kinases (MAPKs). SF was found to reduce intracellular Ca2+ influx by inhibiting PLCγ1 phosphorylation and suppressing the nuclear translocations of cPLA2 and 5-LO via the phosphorylations of MAPKs, including extracellular signal-regulated protein kinase-1/2 (ERK1/2), c-Jun N-terminal kinase (JNK), and p38. Taken together, these results suggest that SF may be useful for regulating mast cell-mediated inflammatory responses by inhibiting degranulation and eicosanoid generation.
机译:在我们正在进行的用于鉴定草药中生物活性化合物的研究中,我们发现,从Saururus chinensis(S. chinensis)分离出的天然存在的芝麻草素sauceneol F(SF)具有体外抗炎活性。在这项研究中,我们检查了SF对5-脂氧合酶(5-LO)依赖性白三烯C4(LTC4),环氧合酶2(COX-2)依赖性前列腺素D2(PGD2)和磷脂酶Cγ1(PLCγ1)生成的影响SCF诱导的小鼠骨髓肥大细胞(BMMC)介导的脱粒。 SF剂量依赖性地抑制类花生酸(PGD2和LTC4)的产生和脱粒。为了确定SF抑制类花生酸生成和脱粒的分子机制,我们研究了SF对PLCγ1磷酸化,细胞内Ca 2 + 内流,胞质磷脂酶A2(cPLA2)易位的影响。和5-LO,以及MAP激酶(MAPK)的磷酸化。发现SF通过抑制PLCγ1磷酸化并通过MAPK的磷酸化抑制cPLA2和5-LO的核易位来减少细胞内Ca 2 + 流入,包括细胞外信号调节蛋白激酶-1/2( ERK1 / 2),c-Jun N末端激酶(JNK)和p38。综上,这些结果表明,SF可能通过抑制脱颗粒和类花生酸的产生而用于调节肥大细胞介导的炎症反应。

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