摘要
Ⅱ类组蛋白去乙酰化酶(HDACs)包括HDAC4、5、7和9,它们能够发生磷酸化作用和介导核质转位。HDACs在肝、脂肪组织中的糖脂代谢中发挥作用,可加重胰岛素抵抗程度和糖尿病进展。Ⅱ类HDACs抑制剂目前已成为研究热点,旨在抑制酶活性,改善代谢和胰岛素敏感性。
Class Ⅱ histone deacetylases (HDACs) include HDAC4, 5, 7 and 9, which are subject to phosphorylation, thereby regulating their nuclear and cytoplasmic translocation. They play a role in glycolipid metabolism in liver and adipose tissues, thus aggravating the degree of insulin resistance and the progression of diabetes. Inhibitors of class Ⅱ HDACs have become a hot research topic. They aim to inhibit enzymatic activities, improve metabolism and insulin sensitivity.
作者
赵航
马慧娟
宋光耀
ZHAO Hang;MA Hui-Juan;SONG Guang-Yao(Graduate School of Hebei Medical University,Shijiazhuang 050017,China;Department of Internal Medicine,Hebei Medical University,Shijiazhuang 050017,China;Endocrinology Department,Hebei General Hospital,Shijiazhuang 050051,China;Hebei Key Laboratory of Metabolic,Shijiazhuang 050017,China)
出处
《中国生物化学与分子生物学报》
CAS
CSCD
北大核心
2018年第12期1294-1298,共5页
Chinese Journal of Biochemistry and Molecular Biology
基金
Supported by Natural Science Foundation of Hebei Province(No.H2018307071)~~