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电针"丰隆""足三里"对非酒精性脂肪肝大鼠SIRT1/FOXO1信号通路的影响

胡馨月 张宁 罗亚 祖芳 张华雨 甄文桧 肖莎莎 吴杰 饶佳佳 杨孝芳

针刺研究2025,Vol.50Issue(2):150-158,9.
针刺研究2025,Vol.50Issue(2):150-158,9.DOI:10.13702/j.1000-0607.20240849

电针"丰隆""足三里"对非酒精性脂肪肝大鼠SIRT1/FOXO1信号通路的影响

Effects of electroacupuncture at"Fenglong"(ST40)and"Zusanli"(ST36)on the SIRT1/FOXO1 signaling pathway in non-alcoholic fatty liver disease model rats

胡馨月 1张宁 2罗亚 1祖芳 1张华雨 1甄文桧 1肖莎莎 1吴杰 1饶佳佳 1杨孝芳1

作者信息

  • 1. 贵州中医药大学针灸推拿学院,贵阳 550025
  • 2. 贵州中医药大学针灸推拿学院,贵阳 550025||贵州中医药大学第一附属医院,贵阳 550001
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摘要

Abstract

Objective To investigate the effects of electroacupuncture(EA)on liver function,lipid metabolism,hepatic histopathology,and the expression of molecules in the SIRT1/FOXO1 signaling pathway in rats with non-alcoholic fatty liver disease(NAFLD),as well as to explore its potential underlying mechanisms.Methods A total of 13 SD rats were assigned to the blank group and fed a standard diet.An NAFLD model was established in 43 SD rats through a 12-week high-fat diet.Three rats from each group were randomly selected to confirm successful model establishment.After confirmation,rats in the modeling group were randomly divided into four groups:model group,EA group,EA+inhibitor group,and agonist group,with 10 rats in each group.The blank and model groups underwent immobilization three times per week for four weeks.The agonist group received intraperitoneal injections of the SIRT1 agonist resveratrol(200 mg/kg)three times per week for four weeks.The EA group received EA at"Fenglong"(ST40)and"Zusanli"(ST36)acupoints for 30 minutes,three times per week for four weeks.The EA+inhibitor group was administered the SIRT1 inhibitor EX527(5 mg/kg)intraperitoneally,with the remaining treatment identical to that of the EA group.After the interventions,contents of serum high-density lipoprotein cholesterol(HDL-C),low-density lipoprotein cholesterol(LDL-C),total cholesterol(TC),triglycerides(TG),as well as activities of alanine aminotransferase(ALT)and aspartate aminotransferase(AST)were measured by using colorimetric method.Liver histopathology was assessed using hematoxylin-eosin(HE)and Oil Red O staining.The protein and mRNA expressions of SIRT1,FOXO1,and ABCA1 in liver tissue,as well as the protein expression of acetylated FOXO1(AC-FOXO1),were detected using Western blot and PCR.Results Compared with the blank group,the model group exhibited significantly decreased serum HDL-C contents(P<0.05),along with increased contents of LDL-C,TC,TG,and activities of ALT and AST(P<0.01,P<0.05);histological analysis revealed disorganization of hepatocytes and pronounced fat vacuolization,additionally,the expressions of hepatic SIRT1,FOXO1,and ABCA1 proteins and mRNA were reduced(P<0.05,P<0.01),whereas AC-FOXO1 protein expression was elevated(P<0.05).Compared with the model group,the EA and agonist groups demonstrated increased serum HDL-C contents(P<0.05),along with decreased contents of LDL-C,TC,TG,and ALT and AST activities(P<0.01,P<0.05);histological results showed improved hepatocyte morphology and reduced steatosis,along with elevated expression of SIRT1,FOXO1,and ABCA1 proteins and mRNA(P<0.05,P<0.01)and decreased AC-FOXO1 protein expression(P<0.05).Compared with the EA group,the EA+inhibitor group had significantly lower serum HDL-C contents(P<0.05),and higher contents of LDL-C,TC,TG,and activities of ALT and AST(P<0.01,P<0.05);histological analysis revealed more fat vacuoles and pronounced lipid droplet deposition,alongside decreased hepatic SIRT1,FOXO1,and ABCA1 protein and mRNA expressions(P<0.05,P<0.01),and elevated AC-FOXO1 protein expression(P<0.05).Conclusion EA may alleviate liver injury in NAFLD rats by activating the SIRT1/FOXO1 signaling pathway to promote cholesterol efflux.

关键词

非酒精性脂肪肝/电针/沉默信息调节因子1/叉头框蛋白O1

Key words

Non-alcoholic fatty liver disease/Electroacupuncture/Silent information regulator 1/Forkhead box protein O1

引用本文复制引用

胡馨月,张宁,罗亚,祖芳,张华雨,甄文桧,肖莎莎,吴杰,饶佳佳,杨孝芳..电针"丰隆""足三里"对非酒精性脂肪肝大鼠SIRT1/FOXO1信号通路的影响[J].针刺研究,2025,50(2):150-158,9.

基金项目

国家自然科学基金项目(No.82160937、82360978) (No.82160937、82360978)

贵州省科技计划项目(No.黔科合基础-ZK[2022]一般499) (No.黔科合基础-ZK[2022]一般499)

针刺研究

OA北大核心

1000-0607

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