首页|茱萸丸通过PPARγ/NF-κB信号通路促进巨噬细胞M2型极化防治动脉粥样硬化

茱萸丸通过PPARγ/NF-κB信号通路促进巨噬细胞M2型极化防治动脉粥样硬化

扫码查看
旨在探讨茱萸丸对动脉粥样硬化(atherosclerosis,AS)的影响及可能作用机制。采用高脂饲料喂养诱导小鼠动脉粥样硬化模型,造模周期为 12 周。造模成功的 47 只ApoE-/-小鼠随机分成 5 组,即模型组 10 只,茱萸丸低、中、高剂量组各 9只,阿托伐他汀钙片组 10 只,C57BL/6J小鼠 10 只作为对照组。对照组与模型组予等体积无菌蒸馏水灌胃,茱萸丸低、中、高剂量组分别给予130。54、261。08、522。16 mg·kg-1·d-1 灌胃,阿托伐他汀钙片组10。40 mg·kg-1·d-1 灌胃,每日1 次,各组小鼠共灌胃 12 周。给药结束后,采用生化法检测总胆固醇(TC)、甘油三酯(TG)、高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇(LDL-C)水平;采用苏木素-伊红(HE)染色观测主动脉区域斑块分布;采用酶联免疫吸附测定法(ELISA)检测血清中M1 型促炎性因子[肿瘤坏死因子-α(TNF-α)、白细胞介素(IL)-6]水平和M2 型抗炎性因子(IL-13、IL-4)水平;免疫荧光检测诱导型一氧化氮合酶(iNOS)、精氨酸酶-1(Arg-1)蛋白表达水平;实时荧光定量聚合酶链式反应(real-time PCR)检测主动脉过氧化物酶体增殖物激活受体γ(PPARγ)、核因子-κB(NF-κB)、Arg-1和iNOS mRNA表达水平;Western blot检测小鼠主动脉中PPARγ、NF-κB 蛋白的表达水平。结果显示,与对照组比较,模型组小鼠血清中TC、TG、LDL-C升高,HDL-C降低;HE染色可见主动脉内膜大面积增厚;免疫荧光可见M1 型促炎性因子(TNF-α、IL-6)升高,M2 型抗炎性因子(IL-4、IL-13)降低;主动脉中PPARγ、Arg-1 mRNA与蛋白表达水平降低,iNOS、NF-κB mRNA与蛋白表达水平升高(P<0。01)。与模型组比较,茱萸丸低、中、高剂量组及阿托伐他汀钙片组TC、TG、LDL-C降低,HDL-C升高;HE染色可见随着茱萸丸浓度的增加,斑块富集区域逐渐缩小;免疫荧光可见M1 型促炎性因子(TNF-α、IL-6)降低,M2 型抗炎性因子(IL-4、IL-13)升高;主动脉中PPARγ、Arg-1 mRNA与蛋白表达水平升高,NF-κB、iNOS mRNA 与蛋白表达水平降低(P<0。05 或 P<0。01)。综上所述,茱萸丸可能通过调控PPARγ/NF-κB信号通路,抑制巨噬细胞M1 型极化,促进巨噬细胞M2 型极化,改善巨噬细胞炎症微环境,从而发挥抗动脉粥样硬化的作用。
Zhuyu Pills promote polarization of macrophages toward M2 phenotype to prevent atherosclerosis via PPARγ/NF-κB signaling pathway
This article aims to investigate the effect of Zhuyu Pills on atherosclerosis and decipher the underlying mechanism.The mouse model of atherosclerosis was induced by a high-fat diet,and the total modeling period was 12 weeks.A total of 47 ApoE-/-mice successfully modeled were randomized into 5 groups,including 10 in the model group,9 in each of low-,medium-,and high-dose(130.54,261.08 and 522.16 mg·kg-1·d-1,respectively)Zhuyu Pills groups,and 10 in the atorvastatin calcium(10.40 mg·kg-1·d-1)group.In addition,10 C57BL/6J mice were included as the normal group.The mice in the normal group and model group were administrated with an equal volume of sterile distilled water,and those in other groups with corresponding agents by gavage once a day for 12 weeks.At the end of drug intervention,the levels of total cholesterol(TC),triglyceride(TG),high-density lipoprotein cholesterol(HDL-C),and low-density lipoprotein cholesterol(LDL-C)were measured by the biochemical method.Hematoxylin-eosin(HE)staining was employed to observe the plaque distribution in the aortic region.The serum levels of pro-inflammatory cytokines tumor necrosis factor-α(TNF-α)and interleukin(IL)-6 in M1 macrophages and anti-inflammatory cytokines IL-13 and IL-4 in M2 macrophages were determined by enzyme-linked immunosorbent assay(ELISA).The expression levels of inducible nitric oxide synthase(iNOS)and arginase-1(Arg-1)were examined by immunofluorescence.Real-time fluorescence quantitative polymerase chain reaction(real-time PCR)was employed to measure the mRNA levels of peroxisome proliferator-activated receptor γ(PPARγ),nuclear factor-κB(NF-κB),Arg-1,and iNOS in the aorta.Western blot was employed to determine the protein levels of PPARγ and NF-κB in the aorta.The results showed that compared with the normal group,the modeling elevated the TC,TG,and LDL-C levels,lowered the HDL-C level,caused large area thickening of the aortic intima,elevated the TNF-α and IL-6 levels,lowered the IL-4 and IL-13 levels,down-regulated the mRNA and protein levels of PPARγ and Arg-1,and up-regulated the mRNA and protein levels of iNOS and NF-κB in the aorta(P<0.01).Compared with the model group,low-,medium-,and high-dose Zhuyu Pills and atorvastatin calcium lowered the TC,TG,and LDL-C levels,elevated the HDL-C level,reduced the plaque area in a concentration-dependent manner,lowered the TNF-α and IL-6 levels,elevated the IL-4 and IL-13 levels,up-regulated the mRNA and protein levels of PPARγ and Arg-1,and down-regulated the mRNA and protein levels of NF-κB and iNOS in the aorta(P<0.05 or P<0.01).In conclusion,Zhuyu Pills may play an anti-atherosclerosis role by regulating PPARγ/NF-κB signaling pathway,inhibiting the polarization of macrophages toward the M1 phenotype,promoting the polarization of macrophages toward the M2 phenotype,and improving the inflammatory microenvironment of macrophages.

Zhuyu PillsatherosclerosismacrophagespolarizationPPARγ/NF-κB signaling pathway

宋玮、张钟艺、王楷、邱海荣、张小波、沈涛

展开 >

成都中医药大学, 四川 成都 610075

湖北民族大学, 湖北 恩施 445000

茱萸丸 动脉粥样硬化 巨噬细胞 极化 PPARγ/NF-κB信号通路

国家自然科学基金四川省科技厅重点研发项目

819737432022YFS0381

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(1)
  • 19