National Research Laboratory of Lipid Metabolism & Atherosclerosis, Korea Research Institute of Bioscience and Biotechnology, Daejeon 305-806, Korea.
Biol Pharm Bull. 2010;33(6):1019-23. doi: 10.1248/bpb.33.1019.
Oxidized low-density lipoprotein (oxLDL) and reactive oxygen species (ROS) play key roles in the early stage of atherosclerosis. Nitric oxide (NO) and ROS are responsible for regulation of the transcriptional pathways of nuclear Factor-kappaB (NF-kappaB) and mitogen-activated protein kinase (MAPK), key regulators of cellular inflammatory and immune responses. Previously, we examined LDL-antioxidant activities of the nine flavonoids isolated from Sophora flavescens. Among these, two lavandulyl flavonoids, kurarinone (1) and kuraridin (2) inhibited inducible nitric oxide synthase (iNOS)-dependent NO production and ROS generation, and suppressed remarkably the expression of inflammatory cytokines, CCL2, tumor necrosis factor (TNF)-alpha, interleukin (IL)-1beta, and iNOS in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages. Moreover, compounds 1 and 2 attenuated NF-kappaB activation by inhibition of IkappaBalpha proteolysis and p65 nuclear translocation, as well as phosphorylation of extracellular signal-regulated kinase (ERK)1/2, c-Jun N-terminal kinase (JNK), and p38 MAP kinases.
氧化型低密度脂蛋白(oxLDL)和活性氧(ROS)在动脉粥样硬化的早期阶段发挥关键作用。一氧化氮(NO)和 ROS 负责调节核因子-κB(NF-κB)和丝裂原激活蛋白激酶(MAPK)的转录途径,这些是细胞炎症和免疫反应的关键调节剂。此前,我们研究了从苦参中分离得到的九种黄酮类化合物对 LDL 的抗氧化活性。其中,两种 lavandulyl 类黄酮,苦参酮(1)和苦参啶(2)抑制诱导型一氧化氮合酶(iNOS)依赖性 NO 产生和 ROS 生成,并显著抑制脂多糖(LPS)刺激的 RAW264.7 巨噬细胞中炎症细胞因子 CCL2、肿瘤坏死因子(TNF)-α、白细胞介素(IL)-1β和 iNOS 的表达。此外,化合物 1 和 2 通过抑制 IkappaBalpha 蛋白水解和 p65 核易位,以及细胞外信号调节激酶(ERK)1/2、c-Jun N 末端激酶(JNK)和 p38 MAP 激酶的磷酸化,减轻了 NF-κB 的激活。