抽象来源: 肠肝肝脏。 2017年9月15日; 11(5):655-666。 PMID: 28651306“ Han,Eun-Jin Go,Juyeon Park,Hocheol Kim,Jae Gab Han,Oran Kwon,Ki Baik Hahm kyu-hyun hyun han Methods: Murine intestinal epithelial IEC-6 cells were pretreated with AM or TH before a脂多糖(LPS)引起的挑战。 Acute colitis was induced with 7 days of dextran sulfate sodium (DSS) in male C57BL/6 mice, and extracts of AM and TH were administered for 2 weeks before DSS administration. Results: In vitro studies demonstrated that AM or TH treatment reduced LPS-induced COX-2 and tumor坏死因子-αmRNA水平,但血红素加氧酶-1(HO-1)增加。 AM和TH的口服前分泌从DSS诱导的结肠炎中拯救了小鼠,通过通过失活的细胞外信号抑制炎症介质调节激酶和抑制核因子κB和信号传感器和转录3的激活剂,但对磺胺嗪的作用比提取物弱。抗炎活性是通过抑制巨噬细胞和T淋巴细胞浸润而发生的。与没有诱导HO-1的磺氮嗪不同,Th提取物具有显着的HO-1诱导性。 结论: