T. Cường, Giang Huy Diệm, T. T. Doan, N. Huy, N. Phuong, Hoàng Thế Hưng
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引用次数: 5
摘要
维地内酯具有抗炎症性肝炎、抗肝毒活性和胰蛋白酶抑制作用等生物活性。然而,到目前为止,关于维地内酯在调节宿主过度炎症反应过程中,对酶酶生诱导的信号通路的作用还没有深入的研究。在这里,我们证明了维地内酯在调节酶蛋白诱导的小鼠骨髓源性巨噬细胞(bmdm)炎症反应中起重要作用。韦地内酯预处理能显著抑制肿瘤坏死因子-α (TNF)-α)、白细胞介素(IL)-6)和IL- 12p40的分泌(30µg/mL, P < 0.001)。此外,经30µg/mL的维德内酯预处理后,zymosan诱导的超氧化物生成、NADPH氧化酶(P < 0.001)、BMDMs中p47phox的磷酸化显著降低。总的来说,这些数据表明维地内酯减少了酶生酶诱导的炎症反应。此外,体内wedelolactone (30 mg/kg)通过抑制全身炎症细胞因子水平,明显地从zymosan诱导的休克中恢复过来。
Wedelolactone from Vietnamese Eclipta prostrata (L) L. Protected Zymosan-induced shock in Mice
Wedelolactone is known to have biological activities such as anti-inflammation hepatitis, anti-hepatotoxic activity, and trypsin inhibitory effect. However, up to date, there has not been any deep study on the role of wedelolactone for zymosan-induced signaling pathways in the process of regulating the excessive inflammatory responses in host. Here, we demonstrated that wedelolactone plays an essential role for regulation of zymosan-induced inflammatory responses in murine bone marrow-derived macrophages (BMDMs). The zymosan-mediated secretion of tumor necrosis factor-α (TNF)-α), interleukin (IL)-6), and IL12p40 but not IL-10 in BMDMs was significantly inhibited by pre-treatment with wedelolactone (30 µg/mL, P < 0.001). Furthermore, zymosan-induced supreoxide generation, NADPH oxidase (P < 0.001), phosphorylation of p47phox in BMDMs were significantly reduced by pre-treatment of wedelolactone (30 µg/mL). Collectively, these data indicated that wedelolactone reduced zymosan-induced inflammatory responses. Moreover, in-vivo wedelolactone (30 mg/kg) was significantly rescued from zymosan-induced shock through inhibition of systemic inflammatory cytokine levels.