首页|异甘草素改善2型糖尿病异常糖脂代谢机制研究

异甘草素改善2型糖尿病异常糖脂代谢机制研究

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异甘草素(isoliquiritigenin,ISL)是甘草中的一种查尔酮类化合物,具有良好的抗炎和抗氧化等药理活性。课题组前期研究发现,ISL具有改善2型糖尿病(type 2 diabetes mellitus,T2DM)糖脂代谢紊乱的潜力,因此本文拟解析其作用机制。体内实验采用高脂高糖饮食结合腹腔注射链脲佐菌素的方法处理C57BL/6J小鼠,构建T2DM小鼠模型,动物福利和实验过程均遵循北京中医药大学实验动物伦理委员会的规定;体外实验以人肝癌HepG2细胞作为实验细胞系,采用棕榈酸钠(sodium palmitate,SP)诱导构建胰岛素抵抗(insulin resistance,IR)细胞模型。考察ISL对小鼠体重、空腹血糖、肝脏组织病理变化的作用效果,同时利用酶联免疫吸附法(enzyme-linked immune sorbent assay,ELISA)及实时荧光定量 PCR法(real-time quantitative PCR,RT-qPCR)等检测 ISL 对糖脂代谢关键靶点的调控作用,并利用分子对接和分子动力学模拟对ISL与关键靶点的相互作用进行检验。结果显示:ISL可显著降低T2DM小鼠空腹血糖水平,降低糖异生途径关键酶丙酮酸羧化酶(pyruvate carboxylase,PC)、磷酸烯醇式丙酮酸羧化酶(phosphoenolpyruvate carboxykinase,PEPCK)和果糖-1,6-二磷酸酶(fructose-1,6-bisphosphatase,FBP)的转录水平和蛋白活性,下调转录因子肝细胞核因子4α(hepatocyte nuclear factor 4α,HNF4α)与cAMP反应元件结合蛋白(cAMP response element binding protein,CREB)的转录和蛋白水平,从而抑制T2DM小鼠肝脏糖异生;ISL可降低肝脏总胆固醇(total cholesterol,TC)和甘油三酯(triglycerides,TG)含量,上调脂质摄取、脂肪酸氧化和脂质输出相关基因的转录水平,下调脂质合成相关基因的转录水平。综上,ISL可抑制T2DM小鼠肝脏糖异生,促进脂质分解,抑制脂质合成,改善T2DM引起的糖脂代谢紊乱。
Mechanism studies underlying the alleviatory effects of isoliquiritigenin on abnormal glucolipid metabolism triggered by type 2 diabetes
Isoliquiritigenin(ISL)is an active chalcone compound isolated from licorice.It possesses anti-inflammatory and anti-oxidative activities.In our previous study,we uncovered a great potential of ISL in treatment of type 2 diabetes mellitus(T2DM).Therefore,this study aims to reveal the mechanism underlying the alleviatory effects of ISL on T2DM-induced glycolipid metabolism disorder.High-fat-high-sugar diet(HFD)combined with intraperitoneal injection of streptozotocin(STZ)were used to establish T2DM mice model.All animal experiments were carried out with approval of the Committee of Ethics at Beijing University of Chinese Medicine.HepG2 cells were used in in vitro experiments,and sodium palmitate(SP)was applied to establish insulin resistance(IR)model cells.The effects of ISL on body weight,fasting blood glucose levels,and pathological changes in the livers of mice were examined.Enzyme-linked immune sorbent assay(ELISA)and real-time quantitative PCR(RT-qPCR)were applied to detect the regulatory effects of ISL on key targets involved in glucolipid metabolism.Additionally,molecular docking and analytical dynamics simulation methods were used to analyze the interaction between ISL and key target protein.The results indicate that ISL significantly downregulates the transcriptional levels and inhibits the activities of key enzymes involved in gluconeogenesis,including pyruvate carboxylase(PC),phosphoenolpyruvate carboxykinase(PEPCK),and fructose-1,6-bisphosphatase(FBP).It also downregulates the transcriptional and protein levels of hepatocyte nuclear factor 4α(HNF4α)and cAMP response element binding protein(CREB),the two transcriptional factors involved in gluconeogenesis.Thus,ISL inhibits hepatic gluconeogenesis in T2DM mice.In addition,ISL reduces total cholesterol(TC)and triglyceride(TG)levels in the livers of T2DM mice.Moreover,ISL downregulates the mRNA levels of lipogenesis genes and upregulates those of genes involved in fatty acid oxidation,lipid uptake,and lipid export.In conclusion,ISL suppresses hepatic gluconeogenesis,promotes lipolysis,and restrains lipogenesis in T2DM mice,thereby improving the abnormal glycolipid metabolism caused by T2DM.

isoliquiritigenintype 2 diabetes mellitusglucose and lipid metabolism disordergluconeogenesislipid metabolism

陈姿伊、杨晓雪、丁文文、汪逗逗、何平、刘颖

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北京中医药大学生命科学学院,北京 102488

异甘草素 2型糖尿病 糖脂代谢紊乱 糖异生 脂代谢

北京中医药大学研究生自主科研课题

90011461220416

2024

药学学报
中国药学会 中国医学科学院药物研究所

药学学报

CSTPCD北大核心
影响因子:1.274
ISSN:0513-4870
年,卷(期):2024.59(1)
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