含有花青素的紫甘薯(Ipomoea batatas L.)共生酸奶通过抑制白色脂肪细胞特异性基因抑制3T3-L1脂肪生成。

Q2 Medicine
Journal of Experimental Pharmacology Pub Date : 2023-05-22 eCollection Date: 2023-01-01 DOI:10.2147/JEP.S405433
Eko Fuji Ariyanto, Widad Aghnia Shalannandia, Uci Ary Lantika, Taufik Muhammad Fakih, Dwi Syah Fitra Ramadhan, Arini Nurisydayanti Gumilar, Farhan Khalil Permana, Anisa Nadia Rahmah, Nur Atik, Astrid Feinisa Khairani
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引用次数: 0

摘要

目的:探讨含花青素的紫甘薯合生酸奶(PSPY)对3T3-L1脂肪细胞分化的影响及其基本分子机制。方法:通过分子对接模拟,观察和鉴定生物活性化合物与靶蛋白之间的亲和力和相互作用。本研究中使用了含有MDI(异丁基甲基黄嘌呤、地塞米松和胰岛素)的培养基,这是一种刺激脂肪生成的混合物。使用3-[4,5-二甲基噻唑-2-基]-2.5二苯基溴化四氮唑(MTT)测定法评估酸奶产品的毒性作用可能性。从接种后24小时至MDI诱导分化的第11天,将0.25%、0.5%、1%和5%(v/v)的普通或紫甘薯酸奶上清液给予3T3-L1前脂肪细胞培养基。分化诱导后第11天,分别使用RT-qPCR和油红O染色分析mRNA表达和脂质积聚。结果:计算机研究表明,花青素衍生的化合物具有抑制过氧化物酶体增殖物激活受体γ(PPAR-γ)的潜力,PPAR-γ是白色脂肪生成的主要调节因子。含有PSPY的花青素显著抑制Pparg、Adipoq、Slc2a4和Pgc1a的表达。PSPY在1%和5%浓度下显著抑制Pparg,而在0.25%浓度下,与对照相比,PSPY显著抑制Adipoq的表达。从0.25%浓度的PSPY开始观察到对Slc2a4和Pgc1a的显著抑制。在纯酸奶的处理中也观察到了脂肪生成基因的抑制;然而,效果相对低于PSPY。用1%和5%PSPY处理的组也显示出对脂质积聚的抑制作用。结论:本研究通过抑制Pparg及其下游基因Adipoq和Slc2a4,证明了PSPY对白色脂肪细胞分化的抑制作用,表明该酸奶具有作为肥胖管理和预防功能性食品的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Anthocyanin-Containing Purple Sweet Potato (<i>Ipomoea batatas L</i>.) Synbiotic Yogurt Inhibited 3T3-L1 Adipogenesis by Suppressing White Adipocyte-Specific Genes.

Anthocyanin-Containing Purple Sweet Potato (<i>Ipomoea batatas L</i>.) Synbiotic Yogurt Inhibited 3T3-L1 Adipogenesis by Suppressing White Adipocyte-Specific Genes.

Anthocyanin-Containing Purple Sweet Potato (<i>Ipomoea batatas L</i>.) Synbiotic Yogurt Inhibited 3T3-L1 Adipogenesis by Suppressing White Adipocyte-Specific Genes.

Anthocyanin-Containing Purple Sweet Potato (Ipomoea batatas L.) Synbiotic Yogurt Inhibited 3T3-L1 Adipogenesis by Suppressing White Adipocyte-Specific Genes.

Purpose: We unravel the effect of anthocyanin-containing purple sweet potato synbiotic yogurt (PSPY) on 3T3-L1 adipocyte differentiation and its fundamental molecular mechanisms.

Methods: Molecular docking simulation was performed to observe and identify the affinity and interaction between bioactive compounds and targeted proteins. MDI (isobutylmethylxanthine, dexamethasone, and insulin)-containing medium, a cocktail that stimulates adipogenesis, was used in this study. The toxic effect possibility of the yogurt product was evaluated using 3-[4, 5-dimethylthiazol-2-yl]-2.5 diphenyl tetrazolium bromide (MTT) assay. A 0.25%, 0.5%, 1%, and 5% (v/v) plain or purple sweet potato yogurt supernatant was given to 3T3-L1 preadipocyte culture medium from 24 h after seeding until day 11 of MDI-induced differentiation. The mRNA expression and lipid accumulation were analyzed using RT-qPCR and Oil red O staining, respectively, on day 11 after differentiation induction.

Results: In silico study suggested that anthocyanin-derived compounds have the potential to inhibit peroxisome proliferator activated receptor gamma (PPAR-γ), a master regulator for white adipogenesis. Anthocyanin-containing PSPY significantly suppressed the expression of Pparg, Adipoq, Slc2a4, and Pgc1a. PSPY significantly suppressed Pparg with 1% and 5% concentrations, while with a concentration of 0.25%, PSPY significantly suppressed Adipoq expression as compared to control. Significant inhibition of Slc2a4 and Pgc1a was observed starting from a 0.25% concentration of PSPY. The suppression of adipogenic genes was also observed with the treatment of plain yogurt; however, the effects were relatively lower than the PSPY. The group treated with 1% and 5% of PSPY also showed inhibition effects on lipid accumulation.

Conclusion: This study demonstrated PSPY inhibition effect on white adipocyte differentiation through suppression of Pparg and its downstream genes, Adipoq and Slc2a4, indicating the potential of this yogurt as a functional food for obesity management and prevention.

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来源期刊
Journal of Experimental Pharmacology
Journal of Experimental Pharmacology Medicine-Pharmacology (medical)
CiteScore
7.40
自引率
0.00%
发文量
43
审稿时长
16 weeks
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