Tang Qi, Chen Sitan, Rizvi Syed Arif Hussain, Qu Jiaojiao, Wang Li, Wang Senye, Ma Changyang, Liu Lijun, Kang Wenyi
National R&D Center for Edible Fungus Processing Technology, Henan University, Kaifeng, China.
Pakistan Agricultural Research Council, Islamabad, Pakistan.
Front Nutr. 2022 Jan 20;8:826957. doi: 10.3389/fnut.2021.826957. eCollection 2021.
In this study, we isolated and identified four compounds in Royle, and they were Delbrunine (), 4--α-D-Glucosyl benzoic acid (), Kaempferol 3--β-D-glucopyranoside 7--α-L-rhamnopyranoside () and Eldeline (). Furthermore, the anti-inflammatory activity of these compounds was screened in RAW264.7 cells. The results showed that the anti-inflammatory activities of compounds and were weak, and , had good anti-inflammatory activity. The macrophage inflammation model was established by lipopolysaccharide (LPS). Then, the anti-inflammatory activity was evaluated by ELISA kits, qRT-PCR experiment and western blot experiment. And the anti-oxidative stress activity was assessed by flow cytometry. The results showed that compounds , could significantly inhibit the elevation of inflammatory factors nitric oxide (NO), tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6), and also had obvious inhibitory effects on the production of inducible nitric oxide synthase (iNOS) and cyclooxygenase 2 (COX-2). In addition, compounds and could effectively inhibit the overexpression of reactive oxygen species (ROS) in RAW264.7 cells that activated by LPS. These results indicated that compounds and may exert anti-inflammatory and anti-oxidative stress effects through the NF-κB signaling pathway.
在本研究中,我们从罗伊尔(Royle)中分离并鉴定出四种化合物,它们分别是德尔布鲁宁(Delbrunine)、4--α-D-葡萄糖基苯甲酸(4--α-D-Glucosyl benzoic acid)、山奈酚3--β-D-吡喃葡萄糖苷7--α-L-鼠李糖苷(Kaempferol 3--β-D-glucopyranoside 7--α-L-rhamnopyranoside)和埃尔德林(Eldeline)。此外,在RAW264.7细胞中筛选了这些化合物的抗炎活性。结果表明,化合物 和 的抗炎活性较弱,而 、 具有良好的抗炎活性。通过脂多糖(LPS)建立巨噬细胞炎症模型。然后,通过ELISA试剂盒、qRT-PCR实验和蛋白质免疫印迹实验评估抗炎活性。并通过流式细胞术评估抗氧化应激活性。结果表明,化合物 、 可显著抑制炎症因子一氧化氮(NO)、肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)的升高,对诱导型一氧化氮合酶(iNOS)和环氧化酶2(COX-2)的产生也有明显的抑制作用。此外,化合物 和 可有效抑制LPS激活的RAW264.7细胞中活性氧(ROS)的过度表达。这些结果表明,化合物 和 可能通过NF-κB信号通路发挥抗炎和抗氧化应激作用。