Li Hongdi, Tang Shouyan
School of Sports Training, Wuhan Sports University, Wuhan 430079, China.
School of Sports Science, Lingnan Normal University, Zhanjiang 524033, China.
Obes Res Clin Pract. 2021 Sep-Oct;15(5):485-490. doi: 10.1016/j.orcp.2021.08.003. Epub 2021 Aug 28.
Adipose tissues have essential roles on energy homeostasis and the development of metabolic syndrome and obesity, they have become critical targets for treating obesity and metabolic disorders. Baicalin is a flavonoid that derived from the root of Scutellaria baicalensis, and it has been reported to take part in the regulation of adipocyte function. All these highlighted the potential of baicalin in the regulation of fat accumulation and obesity. Yet the impact of baicalin on thermogenic function of adipocytes remains to be deciphered.
This study aims to explore the anti-obesity effects of baicalin.
MATERIALS & METHODS: The level of mRNA was detected by qRT-PCR and the protein expression level was examined by western blot. H&E staining was used for the observation of the structure of adipose tissue. Serum triglyceride and insulin levels were detected by commercial test kits.
Our data demonstrated that baicalin up-regulates the expression of UCP1 and PGC1a in a dose-dependent manner in vitro. Baicalin also increases ERK phosphorylation, and the increased expression of UCP1 and PGC1a in adipocytes could be inhibited by an ERK inhibitor, U0126. Moreover, dietary baicalin ameliorates high fat diet (HFD)-induced obesity without affecting food intake. In addition, dietary baicalin inhibits adipocyte hypertrophy and enhances thermogenic gene program in sWAT and intrascapular brown adipose tissue (iBAT) in vivo.
DISCUSSION & CONCLUSION: Baicalin prevents HFD-induced obesity partially through promoting adipocyte thermogenesis. Baicalin may be a promising compound against human obesity and related metabolic diseases.
脂肪组织在能量稳态以及代谢综合征和肥胖症的发展过程中发挥着重要作用,已成为治疗肥胖症和代谢紊乱的关键靶点。黄芩苷是一种从黄芩根部提取的黄酮类化合物,据报道它参与脂肪细胞功能的调节。所有这些都凸显了黄芩苷在调节脂肪堆积和肥胖方面的潜力。然而,黄芩苷对脂肪细胞产热功能的影响仍有待阐明。
本研究旨在探讨黄芩苷的抗肥胖作用。
采用qRT-PCR检测mRNA水平,通过蛋白质免疫印迹法检测蛋白质表达水平。采用苏木精-伊红染色观察脂肪组织的结构。使用商用试剂盒检测血清甘油三酯和胰岛素水平。
我们的数据表明,黄芩苷在体外以剂量依赖的方式上调UCP1和PGC1α的表达。黄芩苷还能增加ERK磷酸化,而ERK抑制剂U0126可抑制脂肪细胞中UCP1和PGC1α表达的增加。此外,饮食中的黄芩苷可改善高脂饮食(HFD)诱导的肥胖,且不影响食物摄入量。此外,饮食中的黄芩苷在体内可抑制皮下白色脂肪组织(sWAT)和肩胛间棕色脂肪组织(iBAT)中的脂肪细胞肥大,并增强产热基因程序。
黄芩苷部分通过促进脂肪细胞产热来预防HFD诱导的肥胖。黄芩苷可能是一种有前景的抗人类肥胖及相关代谢疾病的化合物。