Li Dak Sum Yip Yio Chin R&D Centre for Chinese Medicine, The Chinese University of Hong Kong, Hong Kong, China.
School of Life Sciences, The Chinese University of Hong Kong, Hong Kong, China.
Int J Mol Sci. 2023 Jul 18;24(14):11600. doi: 10.3390/ijms241411600.
Obesity is defined as a dampness-heat syndrome in traditional Chinese medicine. Coptidis Rhizoma is an herb used to clear heat and eliminate dampness in obesity and its complications. Berberine (BBR), the main active compound in Coptidis Rhizoma, shows anti-obesity effects. Peroxisome proliferator-activated receptors (PPARs) are a group of nuclear receptor proteins that regulate the expression of genes involved in energy metabolism, lipid metabolism, inflammation, and adipogenesis. However, whether PPARs are involved in the anti-obesity effect of BBR remains unclear. As such, the aim of this study was to elucidate the role of PPARs in BBR treatment on obesity and the underlying molecular mechanisms. Our data showed that BBR produced a dose-dependent regulation of the levels of PPARγ and PPARδ but not PPARα. The results of gene silencing and specific antagonist treatment demonstrated that PPARδ is key to the effect of BBR. In 3T3L1 preadipocytes, BBR reduced lipid accumulation; in high-fat-diet (HFD)-induced obese mice, BBR reduced weight gain and white adipose tissue mass and corrected the disturbed biochemical parameters, including lipid levels and inflammatory and oxidative markers. Both the in vitro and in vivo efficacies of BBR were reversed by the presence of a specific antagonist of PPARδ. The results of a mechanistic study revealed that BBR could activate PPARδ in both 3T3L1 cells and HFD mice, as evidenced by the significant upregulation of PPARδ endogenous downstream genes. After activating by BBR, the transcriptional functions of PPARδ were invoked, exhibiting negative regulation of CCAAT/enhancer-binding protein α (Cebpα) and Pparγ promoters and positive mediation of heme oxygenase-1 (Ho-1) promoter. In summary, this is the first report of a novel anti-obesity mechanism of BBR, which was achieved through the PPARδ-dependent reduction in lipid accumulation.
肥胖在中医学中被定义为湿热证。黄连是一种用于清除肥胖及其并发症中的热和湿的草药。小檗碱(BBR)是黄连中的主要活性化合物,具有抗肥胖作用。过氧化物酶体增殖物激活受体(PPARs)是一组核受体蛋白,可调节参与能量代谢、脂质代谢、炎症和脂肪生成的基因表达。然而,PPARs 是否参与 BBR 的抗肥胖作用尚不清楚。因此,本研究旨在阐明 PPARs 在 BBR 治疗肥胖及其潜在分子机制中的作用。我们的数据表明,BBR 对 PPARγ和 PPARδ水平具有剂量依赖性的调节作用,但对 PPARα没有调节作用。基因沉默和特异性拮抗剂处理的结果表明,PPARδ 是 BBR 作用的关键。在 3T3L1 前脂肪细胞中,BBR 减少了脂质积累;在高脂肪饮食(HFD)诱导的肥胖小鼠中,BBR 减轻了体重增加和白色脂肪组织质量,并纠正了紊乱的生化参数,包括脂质水平以及炎症和氧化标志物。在存在 PPARδ 特异性拮抗剂的情况下,BBR 的体外和体内疗效均被逆转。机制研究的结果表明,BBR 可以在 3T3L1 细胞和 HFD 小鼠中激活 PPARδ,这表现为 PPARδ 内源性下游基因的显著上调。在被 BBR 激活后,PPARδ 的转录功能被调用,表现为对 CCAAT/增强子结合蛋白α(Cebpα)和 Pparγ 启动子的负调节以及对血红素加氧酶-1(Ho-1)启动子的正调节。总之,这是首次报道 BBR 通过 PPARδ 依赖性减少脂质积累来实现的新型抗肥胖机制。