Total flavonoids of Broussonetia papyrifera alleviate non-alcohol fatty liver disease via regulating Nrf2/AMPK/mTOR signaling pathways

IF 3.9 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochimica et biophysica acta. Molecular and cell biology of lipids Pub Date : 2024-04-20 DOI:10.1016/j.bbalip.2024.159497
Qi Wang , Yunfei Wei , Yeling Wang , Ziyang Yu , Haiyan Qin , Lilei Zhao , Jiaqi Cheng , Bingyu Shen , Meiyu Jin , Haihua Feng
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Abstract

Backgrounds

Non-alcoholic fatty liver disease (NAFLD) is one of the most prevalent chronic liver diseases. The leaves of Broussonetia papyrifera contain a large number of flavonoids, which have a variety of biological functions.

Methods

In vitro experiments, free fatty acids were used to stimulate HepG2 cells. NAFLD model was established in vivo in mice fed with high fat diet (HFD) or intraperitoneally injected with Tyloxapol (Ty). At the same time, Total flavonoids of Broussonetia papyrifera (TFBP) was used to interfere with HepG2 cells or mice.

Results

The results showed that TFBP significantly decreased the lipid accumulation induced by oil acid (OA) with palmitic acid (PA) in HepG2 cells. TFBP decreased the total cholesterol (TC), the triglyceride (TG), low-density lipoprotein cholesterol (LDL-C), and increased high-density lipoprotein cholesterol (HDLC) in serum. TFBP could also effectively inhibit the generation of reactive oxygen species (ROS) and restrained the level of myeloperoxidase (MPO), and enhance the activity of superoxide dismutase (SOD) to alleviate the injury from oxidative stress in the liver. Additionally, TFBP activated nuclear factor erythroid-2-related factor 2 (Nrf2) pathway to increasing the phosphorylation of AMP-activated protein kinase (AMPK). Meanwhile, protein levels of mTORC signaling pathway were evidently restrained with the treatment of TFBP.

Conclusion

Our experiments proved that TFBP has the therapeutic effect in NAFLD, and the activation of Nrf2 and AMPK signaling pathways should make sense.

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纸莎草总黄酮通过调节 Nrf2/AMPK/mTOR 信号通路缓解非酒精性脂肪肝
背景非酒精性脂肪肝(NAFLD)是最常见的慢性肝病之一。方法在体外实验中,用游离脂肪酸刺激 HepG2 细胞。在体内建立非酒精性脂肪肝模型,给小鼠喂食高脂饮食(HFD)或腹腔注射泰乐菌素(Ty)。结果表明,TFBP 能显著降低油酸(OA)与棕榈酸(PA)诱导的 HepG2 细胞脂质积累。TFBP 能降低血清中的总胆固醇(TC)、甘油三酯(TG)和低密度脂蛋白胆固醇(LDL-C),并能升高高密度脂蛋白胆固醇(HDLC)。TFBP 还能有效抑制活性氧(ROS)的生成,抑制髓过氧化物酶(MPO)的水平,提高超氧化物歧化酶(SOD)的活性,从而缓解肝脏氧化应激损伤。此外,TFBP 还能激活核因子红细胞-2 相关因子 2(Nrf2)通路,增加 AMP 激活蛋白激酶(AMPK)的磷酸化。结论我们的实验证明,TFBP 对非酒精性脂肪肝有治疗作用,而 Nrf2 和 AMPK 信号通路的激活应该是有意义的。
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来源期刊
CiteScore
11.00
自引率
2.10%
发文量
109
审稿时长
53 days
期刊介绍: BBA Molecular and Cell Biology of Lipids publishes papers on original research dealing with novel aspects of molecular genetics related to the lipidome, the biosynthesis of lipids, the role of lipids in cells and whole organisms, the regulation of lipid metabolism and function, and lipidomics in all organisms. Manuscripts should significantly advance the understanding of the molecular mechanisms underlying biological processes in which lipids are involved. Papers detailing novel methodology must report significant biochemical, molecular, or functional insight in the area of lipids.
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