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首页> 外文期刊>Scientific reports. >Nonthermal plasma treated solution inhibits adipocyte differentiation and lipogenesis in 3T3-L1 preadipocytes via ER stress signal suppression
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Nonthermal plasma treated solution inhibits adipocyte differentiation and lipogenesis in 3T3-L1 preadipocytes via ER stress signal suppression

机译:非热血浆处理溶液通过ER应力信号抑制抑制3T3-L1前脂肪细胞中的脂肪细胞分化和脂肪生成

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The accumulation and differentiation of adipocytes contribute to the development of obesity and metabolic diseases. It is well-known that interactions of transcription factors such as peroxisome proliferator-activated receptor gamma (PPARγ), CCAAT/enhancer binding protein α (C/EBPα), and endoplasmic reticulum (ER) stress are required for adipogenesis. Recently, use of nonthermal atmospheric plasma (NTP) is expanding from the biomedical field into various other fields. In this study, we investigated whether nonthermal plasma-treated solution (NTS) has an inhibitory effect on adipogenesis and elucidated its mechanisms. Our results demonstrated that NTS significantly inhibited pre-adipocyte differentiation into adipocytes based on Oil Red O staining and triglyceride accumulation. Moreover, NTS treatment suppressed the mRNA and protein expression levels of key adipogenic transcription factors, and adipocyte-specific genes. NTS also down-regulated endoplasmic reticulum stress-related proteins. Consistent with in vitro studies, an animal study using a mouse model of diet-induced obesity showed that NTS treatment reduced body weight and fat, ER stress/UPR, triglyceride, and adipogenic marker level without altering food intake. These findings indicate that NTS inhibits adipogenic differentiation, and provide a mechanistic explanation of the inhibitory effect of NTS on adipogenesis. Taken together, our results suggest that NTS might be useful to treat obesity and obesity-related diseases.
机译:脂肪细胞的积累和分化有助于肥胖和代谢疾病的发展。众所周知,转录因子的相互作用如过氧化物体增殖物激活的受体γ(PPARγ),CCAAT / Enhancer结合蛋白α(C /EBPα)和内质网(ER)应力是脂肪组织所必需的。最近,使用非热大气等离子体(NTP)从生物医学领域扩展到各种其他领域。在这项研究中,我们研究了非热血浆治疗溶液(NTS)是否对脂肪发生具有抑制作用并阐明了其机制。我们的研究结果表明,基于油红O染色和甘油三酯积累,NTS显着抑制进入脂肪细胞的脂肪细胞分化。此外,NTS治疗抑制了关键脂肪转录因子和脂肪细胞特异性基因的mRNA和蛋白表达水平。 NTS也调节了下调的内质网应激相关蛋白质。与体外研究一致,使用饮食诱导肥胖的小鼠模型的动物研究表明,NTS治疗减少体重和脂肪,ER应激/ UPR,甘油三酯和脂肪生成标记水平,而不改变食物摄入量。这些发现表明,NTS抑制脂肪生成分化,并提供了对NTS对脂肪发生的抑制作用的机制解释。我们的结果表明,NTS可能有助于治疗肥胖和肥胖有关的疾病。

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