Zhuang Shuting, Zhang Jieping, Lin Xiaohui, Wang Xiaoning, Yu Wenzhen, Shi Hong
College of Integrated Traditional Chinese and Western Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou, China.
Front Pharmacol. 2023 Feb 16;14:1112554. doi: 10.3389/fphar.2023.1112554. eCollection 2023.
Dendrobium mixture (DM) is a patented Chinese herbal medicine indicated which has anti-inflammatory and improved glycolipid metabolism. However, its active ingredients, targets of action, and potential mechanisms are still uncertain. Here, we investigate the role of DM as a prospective modulator of protection against non-alcoholic fatty liver disease (NAFLD) induced by type 2 diabetes mellitus (T2DM) and illustrate the molecular mechanisms potentially involved. The network pharmacology and TMT-based quantitative protomics analysis were conducted to identify potential gene targets of the active ingredients in DM against NAFLD and T2DM. DM was administered to the mice of DM group for 4 weeks, and mice (control group) and mice (model group) were gavaged by normal saline. DM was also given to Sprague-Dawley (SD) rats, and the serum was subjected to the palmitic acid-induced HepG2 cells with abnormal lipid metabolism. The mechanism of DM protection against T2DM-NAFLD is to improve liver function and pathological morphology by promoting peroxisome proliferator-activated receptor γ (PPARγ) activation, lowering blood glucose, improving insulin resistance (IR), and reducing inflammatory factors. In mice, DM reduced RBG, body weight, and serum lipids levels, and significantly alleviated histological damage of liver steatosis and inflammation. It upregulated the PPARγ corresponding to the prediction from the bioinformatics analysis. DM significantly reduced inflammation by activating PPARγ in both mice and palmitic acid-induced HepG2 cells.
石斛合剂(DM)是一种已获专利的中草药,具有抗炎和改善糖脂代谢的作用。然而,其活性成分、作用靶点和潜在机制仍不明确。在此,我们研究了DM作为2型糖尿病(T2DM)诱导的非酒精性脂肪性肝病(NAFLD)潜在保护调节剂的作用,并阐明了可能涉及的分子机制。通过网络药理学和基于TMT的定量蛋白质组学分析,确定了DM中活性成分针对NAFLD和T2DM的潜在基因靶点。对DM组小鼠给予DM 4周,对对照组小鼠和模型组小鼠灌胃生理盐水。对Sprague-Dawley(SD)大鼠也给予DM,并将血清作用于棕榈酸诱导的脂质代谢异常的HepG2细胞。DM对T2DM-NAFLD的保护机制是通过促进过氧化物酶体增殖物激活受体γ(PPARγ)活化、降低血糖、改善胰岛素抵抗(IR)和减少炎症因子来改善肝功能和病理形态。在小鼠中,DM降低了RBG、体重和血脂水平,并显著减轻了肝脏脂肪变性和炎症的组织学损伤。它上调了与生物信息学分析预测相对应的PPARγ。DM在小鼠和棕榈酸诱导的HepG2细胞中均通过激活PPARγ显著减轻了炎症。