非酒精性脂肪肝
自噬
转录组
脂肪肝
脂质代谢
胰岛素抵抗
生物
信号转导
代谢途径
药理学
碳水化合物代谢
机制(生物学)
内分泌学
胰高血糖素
藜藜
疾病
脂肪酸代谢
内科学
生物化学
体内
胰岛素
过氧化物酶体增殖物激活受体
脂联素
胰岛素受体
肝病
新陈代谢
细胞生物学
医学
脂肪变性
mTORC1型
β氧化
作者
Yuelin Zhang,Zhengting Liang,Jiaxian Liu,Xianjie Zhen,Ruijie Liu,Xiaohong Luo,Guangjian Jiang
摘要
The beneficial effects of quinoa on metabolic diseases have been extensively investigated. In this context, we sought to study the efficacy of quinoa in a nonalcoholic fatty liver disease (NAFLD) mouse model and its underlying mechanism of action. Male ICR mice were fed a high-fat diet for 12 weeks to establish a NAFLD model, followed by 6 weeks of quinoa intervention. The mechanism by which quinoa improves NAFLD was explored using network pharmacology analysis and transcriptome sequencing analysis. Finally, combined with in vivo experiments for verification. Quinoa significantly improved liver damage, abnormal glucose and lipid metabolism, and insulin resistance in NAFLD mice. The results of network pharmacology and transcriptomics indicate that the Ras-PLD signaling pathway and autophagy are key pathways. Quinoa significantly regulates the expression of Ras, Raf, Mek, Erk, and autophagy-related proteins in liver tissue. Meanwhile, quinoa regulates the expression of HNF4A, ACOX2, and glucagon in the liver and pancreas. Our results suggest that quinoa may improve NAFLD by inhibiting the Ras-PLD signaling pathway and activating autophagy, regulating glucose and lipid metabolism and insulin resistance.
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