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褐藻通过下调 PPARγ 对 3T3-L1 脂肪细胞发挥抗氧化和抗脂肪生成作用。

Brown Algae Exert Anti-Oxidative and Anti-AdipogenicEffects on 3T3-L1 Adipocytes by Downregulating PPARγ.

机构信息

School of Food Science and Biotechnology, Kyungpook National University, Daegu 41566, Korea.

Department of Integrative Biology, Kyungpook National University, Daegu 41566, Korea.

出版信息

Medicina (Kaunas). 2020 Nov 24;56(12):634. doi: 10.3390/medicina56120634.

Abstract

, belonging to the family Sargassaceae, has been reported to have various biological effects such as anti-tyrosinase activity and anti-inflammation. However, the anti-obesity effect of has not yet been reported. The effects of extract (SME) on 3T3-L1 adipocytes were screened by3-(4,5)-dimethylthiazo-2-yl-2,5-diphenyltetrazolium bromide (MTT), Oil red O staining, western blot, and Real-time reverse transcription polymerase chain reaction analyses. : Here, we show that SME had potent 2,2'-azinobis-3-ehtlbezothiazoline-6-sulfonic acid radical decolorization (ABTS) and 2,2-diphenyl-1-picrylhydrazyl (DPPH) antioxidant activity with half maximal inhibitory concentration (IC50) value of 0.2868 ± 0.011 mg/mL and 0.2941 ± 0.014 mg/mL, respectively. In addition, SME significantly suppressed lipid accumulation and differentiation of 3T3-L1 preadipocytes, as shown by Oil Red O staining results. SME attenuated the expression of adipogenic- and lipogenic-related genes such as peroxisome proliferator-activated receptor gamma (PPARγ), CCAAT-enhancer-binding protein alpha (C/EBPα), CCAAT-enhancer-binding protein delta (C/EBPδ), adiponectin, adipose triglyceride lipase (ATGL), fatty acid synthase (FAS), hormone-sensitive lipase (HSL), and lipoprotein lipase (LPL). These findings suggest that SME may have therapeutic implications for developing a new anti-obesity agent.

摘要

裙带菜属于马尾藻科,已被报道具有多种生物活性,如抑制酪氨酸酶活性和抗炎作用。然而,裙带菜的抗肥胖作用尚未见报道。本文采用 3-(4,5)-二甲基噻唑-2-基-2,5-二苯基四氮唑溴盐(MTT)、油红 O 染色、western blot 和实时逆转录聚合酶链反应分析筛选裙带菜提取物(SME)对 3T3-L1 脂肪细胞的作用。结果表明:SME 具有较强的 2,2'-偶氮双(3-乙基苯并噻唑啉-6-磺酸)自由基脱色(ABTS)和 2,2-二苯基-1-苦基肼(DPPH)抗氧化活性,半数最大抑制浓度(IC50)值分别为 0.2868±0.011mg/mL 和 0.2941±0.014mg/mL。此外,SME 显著抑制 3T3-L1 前脂肪细胞的脂质积累和分化,油红 O 染色结果显示。SME 下调了过氧化物酶体增殖物激活受体γ(PPARγ)、CCAAT 增强子结合蛋白α(C/EBPα)、CCAAT 增强子结合蛋白δ(C/EBPδ)、脂联素、脂肪甘油三酯脂肪酶(ATGL)、脂肪酸合成酶(FAS)、激素敏感脂肪酶(HSL)和脂蛋白脂肪酶(LPL)等脂肪生成和脂肪生成相关基因的表达。这些发现表明,SME 可能对开发新型抗肥胖药物具有治疗意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b9b4/7760913/680308be902d/medicina-56-00634-g001.jpg

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