亚临界水提取尾藤可减少脂质积累和肥胖引起的炎症

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2023-03-15 DOI:10.4490/algae.2023.38.12.26
Laxmi Sen Thakuri, C. Park, Jin-woo Park, Hyeon-A Kim, D. Rhyu
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引用次数: 1

摘要

肥胖引起的炎症在胰岛素抵抗和2型糖尿病的发病机制中至关重要。在本研究中,我们在细胞模型(3T3-L1脂肪细胞和RAW 264.7巨噬细胞)中研究了根草(GC)对脂质积累和肥胖诱导的炎症变化或葡萄糖稳态的影响。GC样品分别在不同温度(90、150、210℃)下使用溶剂(水、甲醇、乙醇)和亚临界水(SW)进行提取。210°C时GCSW提取物(GCSW210)的总酚含量最高,且GCSW210能有效抑制脂质积累,显著降低3T3-L1脂肪细胞中过氧化物酶体增殖激活受体-γ、CCAAT/增强子结合蛋白-α、固醇调节元件结合蛋白-1c和脂肪酸合成酶的基因表达。此外,GCSW210有效下调RAW 264.7巨噬细胞中促炎细胞因子调控通路,包括丝裂原活化蛋白激酶、转录信号转导和激活因子、核因子-κB。在3T3-L1脂肪细胞和RAW 264.7巨噬细胞共培养中,GCSW210显著降低一氧化氮生成和白细胞介素-6水平,并以剂量依赖的方式改善葡萄糖摄取。这些发现表明,GCSW210通过减轻肥胖引起的脂肪细胞炎症来改善葡萄糖代谢,这可能被用作治疗肥胖和相关代谢疾病的可能治疗选择。
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Subcritical water extraction of Gracilaria chorda abbreviates lipid accumulation and obesity-induced inflammation
Obesity-induced inflammation is crucial in the pathogenesis of insulin resistance and type 2 diabetes. In this study, we investigated the effects of the Gracilaria chorda (GC) on lipid accumulation and obesity-induced inflammatory changes or glucose homeostasis in cell models (3T3-L1 adipocytes and RAW 264.7 macrophages). Samples of GC were extracted using solvents (water, methanol, and ethanol) and subcritical water (SW) at different temperatures (90, 150, and 210°C). The total phenolic content of GCSW extract at 210°C (GCSW210) showed the highest content compared to others, and GCSW210 highly inhibited lipid accumulation and significantly reduced gene expressions of peroxisome proliferatoractivated receptor-γ, CCAAT/enhancer-binding protein-α, sterol regulatory element-binding protein-1c, and fatty acid synthase in 3T3-L1 adipocytes. In addition, GCSW210 effectively downregulated the pro-inflammatory cytokine regulator pathways in RAW 264.7 macrophages, including mitogen-activated protein kinase, signal transducers and activators of transcription and nuclear factor-κB. In co-culture of 3T3-L1 adipocytes and RAW 264.7 macrophages, GCSW210 significantly reduced nitric oxide production and interleukin-6 levels, and improved glucose uptake with dose-dependent manner. These findings suggest that GCSW210 improves glucose metabolism by attenuating obesity-induced inflammation in adipocytes, which may be used as a possible treatment option for managing obesity and associated metabolic disorders.
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4.30%
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567
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