脂质代谢
脂肪生成
安普克
甾醇调节元件结合蛋白
生物
信号转导
碳水化合物代谢
葡萄糖稳态
PI3K/AKT/mTOR通路
细胞生物学
脂肪酸合成
胰岛素抵抗
细胞信号
能量稳态
新陈代谢
生物化学
脂肪酸
内分泌学
转录因子
胰岛素
激酶
蛋白激酶A
受体
基因
作者
R. S. Lopes,Moema de Souza Santana,Carla Rios da Cruz,Rafael Bianchini Fulindi,Ana Maria Minarelli Gaspar,Paulo Inácio da Costa
标识
DOI:10.4025/actascibiolsci.v42i1.51151
摘要
The liver is primarily responsible for energy homeostasis and the regulation of lipid, carbohydrate and protein metabolism. Lipid metabolism consists of distributing lipids to peripheral tissues or ensuring their return to the liver to be reprocessed. Additionally, cellular metabolism is regulated by several molecules in different signaling pathways. Lipid homeostasis in the liver is mainly regulated by AKT, AMPK, SREBP, PPAR, and JNK. The PI3K/AKT/mTOR signaling pathway results in the biosynthesis of macromolecules and regulates lipogenesis and the expression of lipogenic genes. AMPK is an energy sensor that regulates metabolism and is activated when stored ATP is depleted, and it is responsible for the suppression of several key lipogenic factors in the liver related to cholesterol and fatty acid synthesis. SREBPs control lipogenic gene expression and cholesterol metabolism and act in the nutritional regulation of fatty acids and triglycerides. The continued activation of SREBPs is associated with cellular stress, inflammation and ultimately steatosis. PPARs are intrinsically important regulators of lipid metabolism. These genes are essential to various metabolic processes, especially lipid and glucose homeostasis, and can play a role in cell differentiation. JNK signaling is related to insulin resistance and its activation results in decreased mitochondrial activity and fat accumulation. Therefore, the study of cell signaling pathways related to lipid metabolism and liver function may help to identify abnormalities and develop strategies to manage and regulate metabolic disorders and resulting complications.
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