Department of Pharmacology, Faculty of Medicine, University of Malaya, 50603, Kuala Lumpur, Malaysia.
Division of Human Biology, School of Medicine, International Medical University, 57000, Kuala Lumpur, Malaysia.
Eur J Nutr. 2019 Feb;58(1):5-25. doi: 10.1007/s00394-018-1663-8. Epub 2018 Mar 14.
Obesity is a fast growing epidemic worldwide. During obesity, the increase in adipose tissue mass arise from two different mechanisms, namely, hyperplasia and hypertrophy. Hyperplasia which is the increase in adipocyte number is characteristic of severe obese patients. Recently, there has been much interest in targeting adipogenesis as therapeutic strategy against obesity. Flavonoids have been shown to regulate several pathways and affect a number of molecular targets during specific stages of adipocyte development.
Presently, we provide a review of key studies evaluating the effects of dietary flavonoids in different stages of adipocyte development with a particular emphasis on the investigations that explore the underlying mechanisms of action of these compounds in human or animal cell lines as well as animal models.
Flavonoids have been shown to regulate several pathways and affect a number of molecular targets during specific stages of adipocyte development. Although most of the studies reveal anti-adipogenic effect of flavonoids, some flavonoids demonstrated proadipogenic effect in mesenchymal stem cells or preadipocytes.
The anti-adipogenic effect of flavonoids is mainly via their effect on regulation of several pathways such as induction of apoptosis, suppression of key adipogenic transcription factors, activation of AMPK and Wnt pathways, inhibition of clonal expansion, and cell-cycle arrest.
肥胖是全球范围内迅速增长的流行病。在肥胖过程中,脂肪组织质量的增加来自两种不同的机制,即增生和肥大。增生是指脂肪细胞数量的增加,是严重肥胖患者的特征。最近,人们对将脂肪生成作为治疗肥胖的策略的靶向产生了浓厚的兴趣。类黄酮已被证明在脂肪细胞发育的特定阶段调节几种途径并影响许多分子靶标。
目前,我们提供了对评估饮食类黄酮在脂肪细胞发育不同阶段的作用的关键研究的综述,特别强调了探索这些化合物在人或动物细胞系以及动物模型中作用机制的研究。
类黄酮已被证明在脂肪细胞发育的特定阶段调节几种途径并影响许多分子靶标。尽管大多数研究显示类黄酮具有抗脂肪生成作用,但一些类黄酮在间充质干细胞或前脂肪细胞中显示出促脂肪生成作用。
类黄酮的抗脂肪生成作用主要是通过其对几种途径的调节作用,如诱导细胞凋亡、抑制关键的脂肪生成转录因子、激活 AMPK 和 Wnt 途径、抑制克隆扩张和细胞周期停滞。