Anti-obesity Effect of the Flavonoid Rich Fraction from Mulberry Leaf Extract

脂肪酸合酶 芦丁 甘油三酯 脂肪细胞 脂肪组织 内分泌学 脂联素 内科学 过氧化物酶体增殖物激活受体 脂肪生成 甾醇调节元件结合蛋白 化学 生物 胰岛素抵抗 生物化学 受体 胰岛素 甾醇 脂质代谢 医学 胆固醇 抗氧化剂
作者
Eun Ji Go,Byeong Ryeol Ryu,Su Jin Yang,Jong Suep Baek,Su Ji Ryu,Hyun Bok Kim,Jung Dae Lim
出处
期刊:The Korean Journal of Medicinal Crop Science [Korean Society of Medicinal Crop Science]
卷期号:28 (6): 395-411 被引量:5
标识
DOI:10.7783/kjmcs.2020.28.6.395
摘要

Background: This study investigated the anti-obesity effect of the flavonoid rich fraction (FRF) and its constituent, rutin obtained from the leaf of Morus alba L., on the lipid accumulation mechanism in 3T3-L1 adipocyte and C57BL/6 mouse models.BRMethods and Results: In Oil Red O staining, FRF (1,000 ㎍/㎖) treatments showed inhibition rate of 35.39% in lipid accumulation compared to that in the control. AdipoRedTM assay indicated that the triglyceride content in 3T3-L1 adipocytes treated with FRF (1,000 ㎍/㎖) was reduced to 23.22%, and free glycerol content was increased to 106.04% that of the control. FRF and its major constituent, rutin affected mRNA gene expression. Rutin contributed to the inhibition of Sterol regulatory element binding protein-1c (SREBP-1c) gene expression, and inhibited the transcription factors SREBP-1c, peroxisome proliferator-activated receptor gamma (PPAR-γ), CCAAT/enhancer binding protein α (C/EBPα), fatty acid synthase (FAS) and acetyl-CoA carboxylase (ACC). In addition, the effect of FRF administration on obesity development in C57BL/6 mice fed high-fat diet (HFD) was investigated. FRF suppressed weight gain, and reduced liver triglyceride and leptin secretion. FRF exerted potential anti-inflammatory effects by improving insulin resistance and adiponectin levels, and could thus be used to help counteract obesity. The mRNA expressions of PPAR-γ, FAS, ACC, and CPT-1 were determined in liver tissue. Quantitative real-time PCR analysis was also performed to evaluate the expression of IL-1β, IL-6, and TNF-α in epididymal adipose tissue. Compared to the control group, mice fed the HFD showed the up-regulation in PPAR-γ, FAS, IL-6, and TNF-α genes, and down-regulation in CPT1 gene expression. FRF treatement markedly reduced the expression of PPAR-γ, FAS, IL-6, and TNF-α compared to those in HFD control, whereas increased the expression level of CPT1.BRConclusions: These results suggest that the FRF and its major active constituent, rutin, can be used as effective anti-obesity agents.

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