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来自[来源未提及]的常春藤皂苷元促进3T3-L1脂肪细胞中的脂肪褐变。

Hederagenin from Promotes Fat Browning in 3T3-L1 Adipocytes.

作者信息

Choi Seung Min, Lee Ho Seon, Lim Sung Ho, Choi Gayoung, Choi Chang-Ik

机构信息

Integrated Research Institute for Drug Development, College of Pharmacy, Dongguk University-Seoul, Goyang 10326, Republic of Korea.

出版信息

Plants (Basel). 2024 Oct 4;13(19):2789. doi: 10.3390/plants13192789.

Abstract

The prevalence of obesity is increasing globally, with approximately 700 million obese people worldwide. Currently, regulating energy homeostasis by increasing energy expenditure is attracting attention as a strategy for treating obesity. White adipose tissue is known to play a role in accumulating energy by storing excess energy, while brown adipose tissue expends energy and maintains body temperature. Thus, the browning of white adipose tissue has been shown to be effective in controlling obesity. () has been widely used as a traditional medicine for various diseases. In several previous studies, hederagenin (HDG) from has demonstrated many biological activities. In this study, we investigated the antiobesity effect of HDG on fat browning in 3T3-L1 adipocytes. Consequent to HDG treatment, a reduction in lipid accumulation was measured through oil red O staining. In addition, this study investigated that HDG increases energy expenditure by upregulating the expression of several targets related to thermogenesis, including uncoupling protein 1 (UCP1). This process involves inhibiting lipogenesis via the adenosine monophosphate-activated protein kinase (AMPK) signaling pathway and promoting lipolysis through the protein kinase A (PKA) pathway. HDG is expected to be effective in promoting fat browning, indicating its potential as a natural antiobesity candidate.

摘要

全球肥胖症的患病率正在上升,全球约有7亿肥胖人口。目前,通过增加能量消耗来调节能量平衡作为一种治疗肥胖症的策略正受到关注。已知白色脂肪组织通过储存多余能量在能量积累中起作用,而棕色脂肪组织消耗能量并维持体温。因此,白色脂肪组织的褐色化已被证明对控制肥胖有效。()已被广泛用作治疗各种疾病的传统药物。在先前的几项研究中,来自的常春藤皂苷元(HDG)已显示出许多生物活性。在本研究中,我们研究了HDG对3T3-L1脂肪细胞脂肪褐色化的抗肥胖作用。HDG处理后,通过油红O染色测量脂质积累的减少。此外,本研究还调查了HDG通过上调包括解偶联蛋白1(UCP1)在内的几个与产热相关靶点的表达来增加能量消耗。这个过程包括通过腺苷单磷酸激活蛋白激酶(AMPK)信号通路抑制脂肪生成,并通过蛋白激酶A(PKA)通路促进脂肪分解。HDG有望有效促进脂肪褐色化,表明其作为天然抗肥胖候选物的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4a6/11478623/c1766ac0cf15/plants-13-02789-g001.jpg

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