首页|二陈汤通过抑制mTORC1/SREBP1/CAV1通路改善高脂饮食小鼠肝脏线粒体功能的作用研究

二陈汤通过抑制mTORC1/SREBP1/CAV1通路改善高脂饮食小鼠肝脏线粒体功能的作用研究

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研究二陈汤对高脂饮食小鼠肝脏线粒体功能的影响及可能的作用机制.将60只C57BL/6J小鼠随机分为正常组、高脂组、二陈汤组、mTORC1激活剂(MHY)组、二陈汤+MHY组、多烯磷脂酰胆碱(PPC)组,每组10只.正常组给予普通饲料,其余各组给予高脂饲料,喂养20周.第17周,二陈汤组和二陈汤+MHY组小鼠每日灌胃二陈汤(8.7 g·kg-1),PPC组小鼠灌胃PPC(0.18 g·kg-1),其余组小鼠灌胃生理盐水(0.01 mL·g-1),持续4周.第19周,MHY组和二陈汤+MHY组小鼠隔日腹腔注射MHY(5 mg·kg-1),持续2周.观察小鼠一般情况,检测小鼠血清中甘油三酯(TG)、总胆固醇(TC)含量,HE染色和油红O染色观察肝组织形态变化,化学发光法检测三磷酸腺苷(ATP)含量,荧光探针(JC-1)法检测线粒体膜电位,免疫印迹法检测雷帕霉素靶蛋白复合物1(mTORC1)、核糖体蛋白S6激酶(S6K)、固醇调节元件结合蛋白1(SREBP1)、小窝蛋白1(CAV1)的表达.结果显示,与正常组比较,高脂组小鼠体质量和腹围显著增加(P<0.01);TG、TC含量均显著升高(P<0.01);肝小叶界限不清,细胞肿大变圆、排列不规则,有明显脂滴沉积,并伴有炎症细胞浸润;肝脏ATP含量和线粒体膜电位显著降低(P<0.01);p-mTOR、p-S6K、n-SREBP1蛋白表达显著增加(P<0.01),CAV1蛋白表达显著减少(P<0.01).与高脂组比较,二陈汤组和PPC组小鼠体质量显著降低(P<0.05),TG含量显著降低(P<0.05),肝细胞形态、脂质沉积及炎症细胞浸润均改善,ATP含量和线粒体膜电位显著升高(P<0.05或P<0.01);二陈汤组小鼠p-mTOR、p-S6K、n-SREBP1表达显著减少(P<0.01),CAV1表达显著增加(P<0.01);而MHY组小鼠以上指标没有得到改善.与MHY组比较,二陈汤+MHY组小鼠体质量和TG含量显著降低(P<0.05),肝细胞形态、脂质沉积及炎症细胞浸润得到改善,肝脏ATP含量和线粒体膜电位显著升高(P<0.05 或 P<0.01),p-mTOR、p-S6K、n-SREBP1 表达显著降低(P<0.01),CAV1 表达显著升高(P<0.01).综上表明,二陈汤可通过调节mTORC1/SREBP1/CAV1通路改善线粒体功能,可能是其化痰调脂的部分内在机制.
Effect of Erchen Decoction on liver mitochondrial function by inhibiting mTORC1/SREBP1/CAV1 pathway in mice with high-fat diet
This study aims to investigate the effect of Erchen Decoction(ECD)on liver mitochondrial function in mice with a high-fat diet and its possible mechanism.A total of sixty C57BL/6J mice were randomly divided into a normal group,high-fat group,ECD group,mTORCl activator(MHY)group,ECD+MHY group,and polyene phosphatidyl choline(PPC)group,with 10 rats in each group.The normal group was given a normal diet,and the other groups were fed a high-fat diet for 20 weeks.At the 17th week,the ECD group and ECD+MHY group were given ECD(8.7 g·kg-1)daily,and the PPC group was given PPC(0.18 g·kg-1)daily,while the remaining groups were given normal saline(0.01 mL·g-1)daily for four weeks.In the 19th week,the MHY group and ECD+MHY group were injected intraperitoneally with MHY(5 mg·kg-1)every other day for two weeks.During the experiment,the general conditions of the mice were observed.The contents of triglyceride(TG)and total cholesterol(TC)in serum were measured.Morphological changes in liver tissue were examined through HE and oil red O staining.The content of adenosine triphosphate(ATP)was determined using chemiluminescence,and mitochondrial membrane potential was assessed using a fluorescence probe(JC-1).Western blot was performed to detect the expression of rapamycin target protein complex 1(mTORl),ribosomal protein S6 kinase Bl(S6K),sterol regulatory element binding protein 1(SREBP1),and caveolin 1(CAV1).Results revealed that compared with the normal group,the mice in the high-fat group exhibited significant increases in body weight and abdominal circumference(P<0.01).Additionally,there were significant increases in TG and TC levels(P<0.01).HE and oil red O staining showed that the boundaries of hepatic lobules were unclear;hepatocytes were enlarged,round,and irregularly arranged,with obvious lipid droplet deposition and inflammatory cell infiltration.The liver ATP content and mitochondrial membrane potential decreased significantly(P<0.01).The expression of p-mTOR,p-S6K,and n-SREBP1 increased significantly(P<0.01),while the expression of CAV1 decreased significantly(P<0.01).Compared with the high-fat group,the body weight and TG content of mice in the ECD group and PPC group decreased significantly(P<0.05).Improvements were observed in hepatocyte morphology,lipid deposition,and inflammatory cell infiltration.Furthermore,there were significant increases in ATP content and mitochondrial membrane potential(P<0.05 or P<0.01).The expression of p-mTOR,p-S6K,and n-SREBP1 decreased significantly in the ECD group(P<0.01),while CAV1 expression increased significantly(P<0.01).However,the indices mentioned above did not show improvement in the MHY group.When the ECD+MHY group was compared with the MHY group,there were significant reductions in body weight and TG contents(P<0.05).The morphological changes of hepatocytes,lipid deposition,and inflammatory cell infiltration were recovered.Moreover,there were significant increases in liver ATP content and mitochondrial membrane potential(P<0.05 or P<0.05).The expression of p-mTOR,p-S6K,and n-SREBP1 decreased significantly(P<0.01),while CAV1 expression increased significantly(P<0.01).In conclusion,ECD can improve mitochondrial function by regulating the mTORC1/SREBP1/CAV1 pathway.This mechanism may be involved in the resolution of phlegm syndrome and the regulation of lipid metabolism.

Erchen Decoctionphlegm syndromelipid metabolismmitochondrial functionmTORC1/SREBP1/CAV1

丁珊珊、庄妍、廖颖、康洁、张凌媛、沈建英、廖凌虹

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福建中医药大学,福建福州 350122

二陈汤 痰证 脂质代谢 线粒体功能 mTORC1/SREBP1/CAV1

福建省自然科学基金面上项目国家自然科学基金

2020J0174081873234

2024

中国中药杂志
中国药学会

中国中药杂志

CSTPCD北大核心
影响因子:1.718
ISSN:1001-5302
年,卷(期):2024.49(3)
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