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Molecular mechanism underlying the effects of licochalcone A on abnormal gluconeogenesis and endoplasmic reticulum stress induced by type 2 diabetes mellitus
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Wen-pu XU1, Jia-yu ZHANG1, Dou-dou WANG1, Wen-wen DING1, Zi-yi CHEN1, Yao XIAO2, *, Ying LIU1, *
Acta Pharmaceutica Sinica | 2024, 59(12) : 3291 - 3303
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Acta Pharmaceutica Sinica | 2024, 59(12): 3291-3303
Original Articles
Molecular mechanism underlying the effects of licochalcone A on abnormal gluconeogenesis and endoplasmic reticulum stress induced by type 2 diabetes mellitus
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Wen-pu XU1, Jia-yu ZHANG1, Dou-dou WANG1, Wen-wen DING1, Zi-yi CHEN1, Yao XIAO2, *, Ying LIU1, *
Affiliations
  • 1. School of Life Sciences, Beijing University of Chinese Medicine, Beijing 102488, China
  • 2. School of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing 102488, China
Published: 2024-12-12 doi: 10.16438/j.0513-4870.2024-0809
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The aim of this study is to investigate the molecular mechanism of licochalcone A (LCA) in alleviating abnormal gluconeogenesis and endoplasmic reticulum (ER) stress caused by type 2 diabetes mellitus (T2DM). In the in vivo study, 8-week-old male C57BL/6J mice were fed with a high-fat and high-sugar diet and injected intraperitoneally with streptozotocin (STZ) to establish a T2DM model. LCA (5 and 10 mg·kg-1) was administered at an interval of 3 days for 3 weeks with metformin (MET, 200 mg·kg-1) as a positive control drug. The animal experiment protocol was reviewed and approved by the Experimental Animal Ethics Committee of Beijing University of Chinese Medicine (approval number: BUCM-4-2021061701-2060). Human hepatoma cell line HepG2 was used as the experimental cell line for in vitro experiments. Sodium palmitate (SP) was used to induce the insulin resistance cell model and tunicamycin (TM) was applied to establish the ER stress cell model. Real-time quantitative polymerase chain reaction (RT-qPCR), enzyme-linked immunosorbent assay (ELISA) and Western blot (WB) were used to detect the mRNA and protein levels of gluconeogenesis and ER stress-related targets, respectively. Molecular docking and dynamics simulations were used to verify the interaction between LCA and key targets. The results showed that LCA inhibits gluconeogenesis by reducing phosphoenolpyruvate carboxykinase (PEPCK) and glucose-6-phosphatase (G6P) and increasing 6-phosphofructokinase-2/fructose-2, 6-bisphosphatase 3 (PFKFB3) at both the mRNA and protein levels, as well as suppressing the activity of pyruvate carboxylase (PC). Additionally, LCA alleviates ER stress by downregulating the transcription of eukaryotic initiation factor 2 subunit α (eIF2α), inositol-requiring enzyme 1α (IRE1α), X-box binding protein 1 (XBP1), c-Jun N-terminal kinase 1 (JNK1), and activating transcription factor 6α (ATF6α), inhibiting the transcription and protein expression of glucose-regulated protein 78 (GRP78), and suppressing the phosphorylation of protein kinase RNA-like endoplasmic reticulum kinase (PERK). In conclusion, LCA alleviates abnormal gluconeogenesis and ER stress, thereby ameliorating the abnormal metabolism induced by T2DM.

licochalcone A  /  type 2 diabetes mellitus  /  gluconeogenesis  /  endoplasmic reticulum stress  /  metabolic disorder
Wen-pu XU, Jia-yu ZHANG, Dou-dou WANG, Wen-wen DING, Zi-yi CHEN, Yao XIAO, Ying LIU. Molecular mechanism underlying the effects of licochalcone A on abnormal gluconeogenesis and endoplasmic reticulum stress induced by type 2 diabetes mellitus[J]. Acta Pharmaceutica Sinica, 2024 , 59 (12) : 3291 -3303 . DOI: 10.16438/j.0513-4870.2024-0809
Year 2024 volume 59 Issue 12
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doi: 10.16438/j.0513-4870.2024-0809
  • Receive Date:2024-08-20
  • Online Date:2025-11-24
  • Published:2024-12-12
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  • Received:2024-08-20
  • Revised:2024-09-27
Affiliations
    1. School of Life Sciences, Beijing University of Chinese Medicine, Beijing 102488, China
    2. School of Chinese Pharmacy, 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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