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通过调节涉及 ERK1/2 和 Akt 信号通路的有丝分裂克隆扩张,抑制 3T3-L1 前脂肪细胞的脂肪生成。

Inhibits Adipogenesis of 3T3-L1 Preadipocytes via Modulation of Mitotic Clonal Expansion Involving ERK 1/2 and Akt Signaling Pathways.

机构信息

Department of Food Science and Biotechnology of Animal Resources, Konkuk University, Seoul 05029, Korea.

出版信息

Nutrients. 2020 Oct 3;12(10):3037. doi: 10.3390/nu12103037.

Abstract

The flower of contains various phenolic compounds with prophylactic properties. This study aimed to determine the anti-adipogenic effect of an flower aqueous extract (IAE) and its underlying mechanisms in the 3T3-L1 preadipocytes and to identify the phenolic compounds in the extract. Treatment with IAE inhibited the adipogenesis by showing a dose-dependent suppressed intracellular lipid accumulation and mitigated expression levels of lipogenesis- and adipogenesis-associated biomarkers including transcription factors. IAE exerted an anti-adipogenic effect through the modulation of the early phases of adipogenesis including mitotic clonal expansion (MCE). Treatment with IAE inhibited MCE by arresting the cell cycle at the G0/G1 phase and suppressing the activation of MCE-related transcription factors. Furthermore, IAE inhibited adipogenesis by regulating the extracellular signal-regulated kinase 1/2 and Akt signaling pathways. Protocatechuic acid, chlorogenic acid, kaempferol-3--glucoside, and 6-methoxyluteolin, which are reported to exhibit anti-adipogenic properties, were detected in IAE. Therefore, modulation of early phases of adipogenesis, especially MCE, is a key mechanism underlying the anti-adipogenic activity of IAE. In summary, the anti-obesity effects of IAE can be attributed to its phenolic compounds, and hence, IAE can be used for the development of anti-obesity products.

摘要

藏红花的花含有各种具有预防作用的酚类化合物。本研究旨在确定藏红花花水提物(IAE)对 3T3-L1 前体脂肪细胞的抗脂肪生成作用及其潜在机制,并鉴定提取物中的酚类化合物。IAE 处理表现出剂量依赖性抑制细胞内脂质积累,减轻脂肪生成和脂肪生成相关生物标志物(包括转录因子)的表达水平,从而抑制脂肪生成。IAE 通过调节包括有丝分裂克隆扩张(MCE)在内的脂肪生成早期阶段发挥抗脂肪生成作用。IAE 通过将细胞周期阻滞在 G0/G1 期并抑制与 MCE 相关的转录因子的激活来抑制 MCE。此外,IAE 通过调节细胞外信号调节激酶 1/2 和 Akt 信号通路来抑制脂肪生成。在 IAE 中检测到了已报道具有抗脂肪生成特性的原儿茶酸、绿原酸、山奈酚-3-O-β-葡萄糖苷和 6-甲氧基木犀草素。因此,调节脂肪生成的早期阶段,特别是 MCE,是 IAE 抗脂肪生成活性的关键机制。总之,IAE 的抗肥胖作用可归因于其酚类化合物,因此,IAE 可用于开发抗肥胖产品。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d7e/7599673/9bee1de9dff1/nutrients-12-03037-g001.jpg

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