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首页|期刊导航|针刺研究|电针调控PI3K/AKT/FoxO1信号通路改善2型糖尿病大鼠肝脏糖异生的机制研究

电针调控PI3K/AKT/FoxO1信号通路改善2型糖尿病大鼠肝脏糖异生的机制研究

阚文静 袁爱红 宋蝴蝶 叶敏 杨骏

针刺研究2026,Vol.51Issue(9):1189-1197,9.
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针刺研究2026,Vol.51Issue(9):1189-1197,9.DOI:10.13702/j.1000-0607.20260219

电针调控PI3K/AKT/FoxO1信号通路改善2型糖尿病大鼠肝脏糖异生的机制研究

Mechanism of electroacupuncture regulating PI3K/AKT/FoxO1 signaling pathway to improve hepatic gluconeogenesis in type 2 diabetic rats

阚文静 1袁爱红 2宋蝴蝶 1叶敏 3杨骏2

作者信息

  • 1. 安徽中医药大学第一临床医学院,合肥 230000
  • 2. 安徽中医药大学第一附属医院,合肥 230000||新安医学教育部重点实验室,合肥 230000||经脉脏腑相关安徽省重点实验室,合肥 230000
  • 3. 安徽中医药大学第一附属医院,合肥 230000
  • 折叠

摘要

Abstract

Objective To investigate the regulatory effects of electroacupuncture(EA)intervention on the phosphatidylinositol 3-kinase(PI3K)/protein kinase B(AKT)/forkhead box transcription factor O1(FoxO1)signaling pathway and gluconeogenic function in liver tissue of type 2 diabetes mellitus(T2DM)model rats,so as to elucidate the possible mechanisms underlying EA improvement of blood glucose levels.Methods Male SD rats were fed with a high-fat diet combined with intraperitoneal injection of streptozotocin to establish T2DM model.The rats were randomly divided into model,EA,and EA+LY294002 groups,with 10 rats in each group;another 10 age-matched SD rats were selected as the control group.Rats in the EA group received EA intervention at"Zusanli"(ST36)and"Neiting"(ST44)as well as acupuncture at"Weiwanxiashu"(EX-B3),once daily for 15 min each time,6 times a week,for 4 consecutive weeks.The EA+LY294002 group received intraperitoneal injection of the PI3K inhibitor LY294002(10 mg/kg)in addition to the EA treatment once daily,with the same intervention period with the EA group.Random blood glucose was measured using a glucometer;body weight was measured with an electronic balance;HE staining was used to observe pathological changes in liver tissue;real-time quantitative PCR was used to detect the mRNA expression levels of PI3K,AKT,FoxO1,phosphoenolpyruvate carboxykinase(PEPCK),and glucose-6-phosphatase(G6Pase);Western blot was used to detect the protein expression levels of PI3K,p-PI3K,AKT,p-AKT,FoxO1,PEPCK,and G6Pase.Results After treatment,compared with the control group,the model group showed significantly elevated random blood glucose levels(P<0.01),decreased body weight(P<0.01),severe liver tissue damage with enlarged hepatocytes and numerous fatty vacuoles,decreased mRNA expression levels of PI3K and AKT and reduced p-PI3K/PI3K and p-AKT/AKT protein expression ratios(P<0.01,P<0.05),and increased mRNA and protein expression levels of FoxO1,PEPCK,and G6Pase(P<0.01)in liver tissue.Compared with the model group,the EA group showed significantly decreased random blood glucose(P<0.01),increased body weight(P<0.01),improved liver pathological injury with reduced hepatocyte size and attenuated steatosis,significantly increased mRNA expression levels of PI3K and AKT and elevated p-PI3K/PI3K and p-AKT/AKT protein expression ratios(P<0.01),and decreased mRNA and protein expression levels of FoxO1,PEPCK,and G6Pase(P<0.01)in liver tissue.Compared with the EA group,the EA+LY294002 group showed elevated random blood glucose(P<0.01),decreased body weight(P<0.05),aggravated liver tissue injury,decreased mRNA expression levels of PI3K and AKT and reduced p-AKT/AKT protein expression ratio(P<0.01,P<0.05),and increased mRNA and protein expression levels of FoxO1,PEPCK,and G6Pase(P<0.01,P<0.05)in liver tissue.Conclusion EA at EX-B3,ST36,and ST44 can significantly reduce blood glucose levels,increase body weight,and improve liver injury in T2DM rats.The underlying mechanism may involve activation of the hepatic PI3K/AKT/FoxO1 signaling pathway,which suppresses the expression of the downstream gluconeogenic key enzymes PEPCK and G6Pase,thereby reducing hepatic glucose output.

关键词

2型糖尿病/电针/PI3K/AKT/FoxO1信号通路/糖异生/肝糖输出

Key words

Type 2 diabetes mellitus/Electroacupuncture/PI3K/AKT/FoxO1 signaling pathway/Gluconeogenesis/Hepatic glucose output

引用本文复制引用

阚文静,袁爱红,宋蝴蝶,叶敏,杨骏..电针调控PI3K/AKT/FoxO1信号通路改善2型糖尿病大鼠肝脏糖异生的机制研究[J].针刺研究,2026,51(9):1189-1197,9.

基金项目

国家自然科学基金项目(No.82575227) (No.82575227)

第五批全国中医临床优秀人才研修项目(No.国中医药人教函[2022]1号) (No.国中医药人教函[2022]1号)

第九批省"特支计划"卫生创新人才项目(No.皖组办字[2023]35号) (No.皖组办字[2023]35号)

杨骏全国名中医传承工作室项目(No.皖中医药发展秘[2022]19号) (No.皖中医药发展秘[2022]19号)

袁爱红安徽省名中医工作室项目(No.皖中医药发展秘[2023]23号) (No.皖中医药发展秘[2023]23号)

安徽高校自然科学重大研究项目(No.2024AH040148) (No.2024AH040148)

针刺研究

1000-0607

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