Lee Dahae, Hong Sukyong, Jung Kiwon, Choi Sungyoul, Kang Ki Sung
Department of Preventive Medicine, College of Korean Medicine, Gachon University, Seongnam 13120, Republic of Korea.
College of Pharmacy, CHA University, Sungnam 13844, Republic of Korea.
Plants (Basel). 2022 Dec 16;11(24):3552. doi: 10.3390/plants11243552.
The suppressive effects of flavonoids on macrophage-associated adipocyte inflammation in a differentiated murine preadipocyte cell line (3T3-L1) co-cultured with a murine macrophage cell line (RAW264.7) were evaluated. Extracellular lipid accumulation was investigated via Oil Red O staining. The expression levels of adipogenesis- and inflammation-associated proteins, including CCAAT/enhancer-binding protein (C/EBP)-α, inducible nitric oxide synthase (iNOS), C/EBPβ, peroxisome proliferator-activated receptor γ (PPARγ), and cyclooxygenase-2 (COX-2), were determined via Western blotting. Proinflammatory cytokines, including monocyte chemoattractant protein 1 (MCP-1) and interleukin-6 (IL-6), were assessed using enzyme-linked immunosorbent assay kits. We found that silybin, formononetin, and diosmetin inhibited lipid accumulation and production of proinflammatory cytokines in the co-cultures of 3T3-L1 and RAW264.7 cells. Moreover, they inhibited the protein expression of PPARγ, C/EBPα, COX-2, C/EBPβ, and iNOS in the co-cultures of 3T3-L1 and RAW264.7 cells. These data support that silybin, formononetin, and diosmetin inhibit macrophage-associated adipocyte inflammation and lipid accumulation.
评估了黄酮类化合物对与小鼠巨噬细胞系(RAW264.7)共培养的分化小鼠前脂肪细胞系(3T3-L1)中巨噬细胞相关脂肪细胞炎症的抑制作用。通过油红O染色研究细胞外脂质积累。通过蛋白质免疫印迹法测定脂肪生成和炎症相关蛋白的表达水平,包括CCAAT/增强子结合蛋白(C/EBP)-α、诱导型一氧化氮合酶(iNOS)、C/EBPβ、过氧化物酶体增殖物激活受体γ(PPARγ)和环氧化酶-2(COX-2)。使用酶联免疫吸附测定试剂盒评估促炎细胞因子,包括单核细胞趋化蛋白1(MCP-1)和白细胞介素-6(IL-6)。我们发现水飞蓟宾、芒柄花素和香叶木素在3T3-L1和RAW264.7细胞共培养物中抑制脂质积累和促炎细胞因子的产生。此外,它们在3T3-L1和RAW264.7细胞共培养物中抑制PPARγ、C/EBPα、COX-2、C/EBPβ和iNOS的蛋白表达。这些数据支持水飞蓟宾、芒柄花素和香叶木素抑制巨噬细胞相关脂肪细胞炎症和脂质积累。