酮发生
基因敲除
脂质代谢
脂肪生成
碳水化合物代谢
内科学
内分泌学
胰岛素抵抗
糖酵解
胰岛素
甘油三酯
糖异生
化学
下调和上调
体内
新陈代谢
生物
胆固醇
生物化学
医学
基因
酮体
生物技术
作者
Shilpa R. Nagarajan,Eilidh Livingstone,Thomas Monfeuga,Lara C. Lewis,Shahul Hameed Liyakath Ali,Anandhakumar Chandran,David Dearlove,Matt J. Neville,Lingyan Chen,Cyrielle Maroteau,Maxwell A. Ruby,Leanne Hodson
标识
DOI:10.1016/j.metabol.2023.155563
摘要
We have demonstrated using human in vitro and in vivo models that MLX inhibition favored lipid catabolism over anabolism and increased glucose production, despite increased glycolysis and phosphorylation of Akt, suggesting a metabolic mechanism that involves futile cycling.
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