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菝葜多酚中的槲皮素、淫羊藿素和咖啡酸通过β3-AR/AMPK 信号通路刺激 3T3-L1 脂肪细胞向棕色样脂肪细胞分化。

Quercetin, Engelitin and Caffeic Acid of Smilax china L. Polyphenols, Stimulate 3T3-L1 Adipocytes to Brown-like Adipocytes Via β3-AR/AMPK Signaling Pathway.

机构信息

Jiangxi Key Laboratory of Natural Product and Functional Food, School of Food Science and Engineering, Jiangxi Agricultural University, 330045, Nanchang, Jiangxi Province, P.R. China.

出版信息

Plant Foods Hum Nutr. 2022 Dec;77(4):529-537. doi: 10.1007/s11130-022-00996-x. Epub 2022 Aug 20.

Abstract

The aim of the present study was to investigate the browning effects mechanism of Smilax china L. polyphenols (SCLP) and its monomer. In this study, polyphenols (SCLP, engeletin, quercetin and caffeic acid) markedly suppressed lipid accumulation. Polyphenols significantly up-graded the expression of protein kinase A (PKA), adipose triglyceride lipase (ATGL), peroxisome proliferators-activated receptors alpha (PPARα), carnitine palmitoyl transferase (CPT) and acyl-CoA oxidase (ACO) to promote lipolysis and β-oxidation. Moreover, polyphenols greatly enhanced mitochondrial biogenesis in adipocytes, as demonstrated by the expression of Nrf1 and Tfam were up-regulated. Furthermore, polyphenols treatment greatly up-regulated the browning program in adipocytes by increased brown-specific genes and proteins uncoupling protein 1 (UCP-1), peroxisome proliferator-activated receptor gamma coactivator-1 alpha (PGC-1α) and PR domain containing 16 (PRDM16), as well as beige-specific genes (Tmem26, Tbx1, CD137, Cited1), especially engeletin. Further research found that the brown-specific markers were decreased by antagonist treatment of AMPK or β3-AR, but polyphenols treatment reversed the effect of antagonists and improved the expression of UCP-1, PRDM16 and PGC-1α. In conclusion, these results indicated that polyphenols stimulate browning in adipocytes via activation of the β3-AR/AMPK signaling pathway, and SCLP and its monomer may be worth investigating to prevent obesity.

摘要

本研究旨在探讨菝葜多酚(SCLP)及其单体的褐色效应机制。在这项研究中,多酚(SCLP、engelin、槲皮素和咖啡酸)显著抑制脂肪积累。多酚显著上调蛋白激酶 A(PKA)、脂肪甘油三酯脂肪酶(ATGL)、过氧化物酶体增殖物激活受体α(PPARα)、肉碱棕榈酰转移酶(CPT)和酰基辅酶 A 氧化酶(ACO)的表达,以促进脂肪分解和β-氧化。此外,多酚大大增强了脂肪细胞中的线粒体生物发生,这表现为 Nrf1 和 Tfam 的表达上调。此外,多酚处理通过增加褐色特异性基因和蛋白解偶联蛋白 1(UCP-1)、过氧化物酶体增殖物激活受体γ共激活因子 1α(PGC-1α)和 PR 结构域包含蛋白 16(PRDM16),以及米色特异性基因(Tmem26、Tbx1、CD137、Cited1),来极大地促进脂肪细胞中的褐色化程序,特别是 engelin。进一步的研究发现,褐色特异性标志物的表达被 AMPK 或β3-AR 的拮抗剂处理所降低,但多酚处理逆转了拮抗剂的作用,并改善了 UCP-1、PRDM16 和 PGC-1α 的表达。总之,这些结果表明,多酚通过激活β3-AR/AMPK 信号通路刺激脂肪细胞中的褐色化,SCLP 及其单体可能值得研究以预防肥胖。

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