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Mechanism studies underlying the alleviatory effects of isoliquiritigenin on abnormal glucolipid metabolism triggered by type 2 diabetes
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Zi-yi CHEN, Xiao-xue YANG, Wen-wen DING, Dou-dou WANG, Ping HE*, Ying LIU*
Acta Pharmaceutica Sinica | 2024, 59(1) : 105 - 118
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Acta Pharmaceutica Sinica | 2024, 59(1): 105-118
Original Articles
Mechanism studies underlying the alleviatory effects of isoliquiritigenin on abnormal glucolipid metabolism triggered by type 2 diabetes
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Zi-yi CHEN, Xiao-xue YANG, Wen-wen DING, Dou-dou WANG, Ping HE*, Ying LIU*
Affiliations
  • School of Life Sciences, Beijing University of Chinese Medicine, Beijing 102488, China
Published: 2024-01-12 doi: 10.16438/j.0513-4870.2023-0520
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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.

isoliquiritigenin  /  type 2 diabetes mellitus  /  glucose and lipid metabolism disorder  /  gluconeogenesis  /  lipid metabolism
Zi-yi CHEN, Xiao-xue YANG, Wen-wen DING, Dou-dou WANG, Ping HE, Ying LIU. Mechanism studies underlying the alleviatory effects of isoliquiritigenin on abnormal glucolipid metabolism triggered by type 2 diabetes[J]. Acta Pharmaceutica Sinica, 2024 , 59 (1) : 105 -118 . DOI: 10.16438/j.0513-4870.2023-0520
Year 2024 volume 59 Issue 1
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doi: 10.16438/j.0513-4870.2023-0520
  • Receive Date:2023-04-27
  • Online Date:2025-11-28
  • Published:2024-01-12
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  • Received:2023-04-27
  • Revised:2023-09-05
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    School of Life Sciences, Beijing University of Chinese Medicine, Beijing 102488, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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