Department of Agricultural Biotechnology and Research Institute for Agriculture and Life Sciences, Republic of Korea.
Food Funct. 2019 May 22;10(5):2958-2969. doi: 10.1039/c9fo00334g.
Cacao (Theobroma cacao) has a significant polyphenol content and has been reported to elicit anti-obesity effects. Previous studies have focused on the properties of cacao extract and procyanidins, while the potential mechanisms have not been fully elucidated. Here, we investigated the inhibitory effects of procyanidin metabolites on adipogenic cocktail-induced adipogenesis and lipogenesis in 3T3-L1 preadipocytes. It was observed that 5-(3',4'-dihydroxyphenyl)-γ-valerolactone (DHPV), a major procyanidin metabolite, exhibited the greatest inhibitory effects on adipogenesis and lipogenesis. DHPV dose-dependently reduced the expression levels of proteins involved in adipogenesis including peroxisome proliferator-activated receptor γ (PPAR γ) and CCAT/enhancer-binding protein α (C/EBP α), as well as lipogenesis-related factors such as fatty acid synthase and acetyl-CoA carboxylase. These inhibitory effects were primarily due to G1 phase arrest and the suppression of cell proliferation during mitotic clonal expansion, the early stage of adipogenesis. In an extensive kinase array, DHPV directly suppressed activation of the CDK2/cyclin O complex, and inhibited the phosphorylation of C/EBP β, which is responsible for the induction of PPAR γ and C/EBP α. Taken together, these findings suggest that DHPV is a highly biologically active compound with potential anti-obesity effects and works by inhibiting the intracellular lipid content and cell differentiation.
可可(Theobroma cacao)含有丰富的多酚,据报道具有抗肥胖作用。以前的研究主要集中在可可提取物和原花青素的特性上,而潜在的机制尚未完全阐明。在这里,我们研究了原花青素代谢物对 3T3-L1 前脂肪细胞中脂肪生成鸡尾酒诱导的脂肪生成和脂肪生成的抑制作用。观察到 5-(3',4'-二羟基苯基)-γ-缬草酸(DHPV),一种主要的原花青素代谢物,对脂肪生成和脂肪生成表现出最大的抑制作用。DHPV 剂量依赖性地降低了参与脂肪生成的蛋白质的表达水平,包括过氧化物酶体增殖物激活受体 γ(PPARγ)和 CCAT/增强子结合蛋白 α(C/EBPα),以及脂肪生成相关因子,如脂肪酸合酶和乙酰辅酶 A 羧化酶。这些抑制作用主要是由于 G1 期停滞和有丝分裂克隆扩张过程中细胞增殖的抑制,这是脂肪生成的早期阶段。在广泛的激酶阵列中,DHPV 直接抑制 CDK2/周期蛋白 O 复合物的激活,并抑制 C/EBPβ的磷酸化,C/EBPβ负责诱导 PPARγ和 C/EBPα。总之,这些发现表明 DHPV 是一种具有潜在抗肥胖作用的高度生物活性化合物,通过抑制细胞内脂质含量和细胞分化起作用。