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甲基异梭林-3-O-β-D-吡喃葡萄糖苷对脂肪细胞-巨噬细胞共培养中肥胖诱导的炎症反应的双重有益作用

Dual Beneficial Effects of Methylnissolin-3-O-β-d-Glucopyranoside on Obesity-Induced Inflammatory Responses in Adipocyte-Macrophage Co-Culture.

作者信息

Lee Dahae, Wu Xiaohua, Lange Ingo, Cao Shugeng, Kang Ki Sung

机构信息

College of Korean Medicine, Gachon University, Seongnam 13120, Korea.

Department of Pharmaceutical Sciences, Daniel K. Inouye College of Pharmacy, University of Hawai'i at Hilo, Hilo, HI 96720, USA.

出版信息

Plants (Basel). 2022 Jun 28;11(13):1715. doi: 10.3390/plants11131715.

Abstract

Methylnissolin-3-O-β-d-glucopyranoside (MNG) is a pterocarpan analog, which protects EA.hy926 cells against oxidative damage through the Nrf2/HO-1 pathway. However, the effects of MNG on obesity-induced inflammatory responses in adipocyte-macrophage co-culture remain unclear. A differentiated murine preadipocyte cell line (3T3-L1) was co-cultured with a murine macrophage cell line (RAW264.7). Intracellular lipid accumulation was determined using Oil Red O staining. Western blotting was performed to investigate the expression of adipogenesis- and inflammation-associated proteins. Cell culture supernatants were assayed using ELISA kits to measure the levels of proinflammatory cytokines such as interleukin 6 (IL-6) and monocyte chemoattractant protein-1 (MCP-1). MNG inhibited lipid accumulation and the production of IL-6 and MCP-1 in the 3T3-L1 and RAW264.7 cell co-culture. Moreover, MNG inhibited the protein expression of CCAAT/enhancer-binding protein alpha (C/EBPα), C/EBPβ, peroxisome proliferator-activated receptor γ (PPARγ), cyclooxygenase 2 (COX-2), and inducible nitric oxide synthase (iNOS) under the same co-culture conditions. MNG also inhibited IL-6 and MCP-1 production compared with the co-culture control. These findings demonstrate that MNG inhibited lipid accumulation and inflammatory response by downregulating IL-6 and MCP-1 production and protein expression of C/EBPβ, C/EBPα, PPARγ, COX-2, and iNOS in co-culture conditions with 3T3-L1 and RAW264.7 cells. These results suggest that MNG may be beneficial in preventing obesity-related inflammatory status.

摘要

甲基异黄酮-3-O-β-D-吡喃葡萄糖苷(MNG)是一种紫檀素类似物,它通过Nrf2/HO-1途径保护EA.hy926细胞免受氧化损伤。然而,MNG对脂肪细胞-巨噬细胞共培养中肥胖诱导的炎症反应的影响仍不清楚。将分化的小鼠前脂肪细胞系(3T3-L1)与小鼠巨噬细胞系(RAW264.7)共培养。使用油红O染色测定细胞内脂质积累。进行蛋白质印迹以研究脂肪生成和炎症相关蛋白的表达。使用ELISA试剂盒检测细胞培养上清液,以测量促炎细胞因子如白细胞介素6(IL-6)和单核细胞趋化蛋白-1(MCP-1)的水平。MNG抑制3T3-L1和RAW264.7细胞共培养中脂质积累以及IL-6和MCP-1的产生。此外,在相同的共培养条件下,MNG抑制CCAAT/增强子结合蛋白α(C/EBPα)、C/EBPβ、过氧化物酶体增殖物激活受体γ(PPARγ)、环氧化酶2(COX-2)和诱导型一氧化氮合酶(iNOS)的蛋白表达。与共培养对照相比,MNG也抑制IL-6和MCP-1的产生。这些发现表明,在与3T3-L1和RAW264.7细胞共培养的条件下,MNG通过下调IL-6和MCP-1的产生以及C/EBPβ、C/EBPα、PPARγ、COX-2和iNOS的蛋白表达来抑制脂质积累和炎症反应。这些结果表明,MNG可能有助于预防肥胖相关的炎症状态。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e3d5/9269391/2a691337fe4f/plants-11-01715-g001.jpg

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