胰岛素抵抗
胰岛素
安普克
氧化应激
糖尿病
内分泌学
链脲佐菌素
内科学
医学
药理学
蛋白激酶A
化学
激酶
生物化学
作者
Zhuozhou Hu,Jing Zhou,Liang Han,Xiangxiang Li,Chun Li,Tongyu Wu,Jingjing Liu,Wenyang Zhao,Jia Kang,Xinping Chen
出处
期刊:Life Sciences
[Elsevier]
日期:2022-09-01
卷期号:304: 120725-120725
被引量:2
标识
DOI:10.1016/j.lfs.2022.120725
摘要
Diabetes mellitus (DM) is a major global health threat characterized by insulin resistance. A new tactic to ameliorate insulin resistance, thereby reversing the exacerbation of DM, is urgently needed. The work is aiming to provide a new strategy for DM treatment as well as to identify new targets.C57BL/6 N mice were raised with high-fat diet (HFD) and infused with streptozotocin (STZ) to induce diabetes. The blood glucose, serum insulin, blood lipid and oxidative stress were detected. In vitro insulin resistance model experiment has been made to examine the molecular mechanisms underlying anti-diabetic effect of potential active chemicals in human hepatocellular carcinoma cells (HepG2).Acyclovir, an antiviral nucleotide analog, alleviates insulin resistance by reducing blood lipids as well as oxidative stress and elevating insulin sensitivity on diabetic mice, which is in accord with results in the insulin resistance model of HepG2 cells. Mechanically, acyclovir stimulates pyruvate kinase M1 (PKM1) directly to activate adenosine 5'-monophosphate (AMP)-activated protein kinase (AMPK)/Sirtuin1 (SIRT1) signaling pathway, thus improving insulin resistance.The present study supports that acyclovir should be translated to remedy DM, and PKM1 might be a valuable target to develop new medicines.
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