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逐瘀丸通过PPARγ/NF-κB信号通路促进巨噬细胞向M2表型极化以预防动脉粥样硬化

[Zhuyu Pills promote polarization of macrophages toward M2 phenotype to prevent atherosclerosis via PPARγ/NF-κB signaling pathway].

作者信息

Song Wei, Zhang Zhong-Yi, Wang Kai, Qiu Hai-Rong, Zhang Xiao-Bo, Shen Tao

机构信息

Chengdu University of Traditional Chinese Medicine Chengdu 610075, China.

Hubei Minzu University Enshi 445000, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2024 Jan;49(1):243-250. doi: 10.19540/j.cnki.cjcmm.20230823.501.

Abstract

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.

摘要

本文旨在研究逐瘀丸对动脉粥样硬化的影响并阐明其潜在机制。采用高脂饮食诱导小鼠动脉粥样硬化模型,总建模周期为12周。将47只成功建模的ApoE⁻/⁻小鼠随机分为5组,包括模型组10只、低、中、高剂量逐瘀丸组(分别为130.54、261.08和522.16 mg·kg⁻¹·d⁻¹)各9只、阿托伐他汀钙组(10.40 mg·kg⁻¹·d⁻¹)10只。另外,纳入10只C57BL/6J小鼠作为正常组。正常组和模型组小鼠灌胃等体积无菌蒸馏水,其他组小鼠每天灌胃相应药物,共12周。药物干预结束后,采用生化方法检测总胆固醇(TC)、甘油三酯(TG)、高密度脂蛋白胆固醇(HDL-C)和低密度脂蛋白胆固醇(LDL-C)水平。采用苏木精-伊红(HE)染色观察主动脉区域斑块分布。采用酶联免疫吸附测定(ELISA)法检测M1巨噬细胞中促炎细胞因子肿瘤坏死因子-α(TNF-α)和白细胞介素(IL)-6以及M2巨噬细胞中抗炎细胞因子IL-13和IL-4的血清水平。采用免疫荧光法检测诱导型一氧化氮合酶(iNOS)和精氨酸酶-1(Arg-1)的表达水平。采用实时荧光定量聚合酶链反应(实时PCR)检测主动脉中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的mRNA水平。采用蛋白质印迹法检测主动脉中PPARγ和NF-κB的蛋白水平。结果显示,与正常组相比,建模后小鼠TC、TG和LDL-C水平升高,HDL-C水平降低,主动脉内膜大面积增厚,TNF-α和IL-6水平升高,IL-4和IL-13水平降低,主动脉中PPARγ和Arg-1的mRNA和蛋白水平下调,iNOS和NF-κB的mRNA和蛋白水平上调(P<0.01)。与模型组相比,低、中、高剂量逐瘀丸和阿托伐他汀钙均可降低TC、TG和LDL-C水平,升高HDL-C水平,以浓度依赖方式减少斑块面积,降低TNF-α和IL-6水平,升高IL-4和IL-13水平,上调主动脉中PPARγ和Arg-1的mRNA和蛋白水平,下调NF-κB和iNOS的mRNA和蛋白水平(P<0.05或P<0.01)。综上所述,逐瘀丸可能通过调节PPARγ/NF-κB信号通路,抑制巨噬细胞向M1表型极化,促进巨噬细胞向M2表型极化,改善巨噬细胞炎症微环境,发挥抗动脉粥样硬化作用。

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