Naoxintong Protects against Atherosclerosis through Lipid-lowering and Inhibiting Maturation of Dendritic Cells in LDL Receptor Knockout Mice fed a High-fat Diet

被引:15
作者
Zhao, Jingjing [1 ,3 ]
Zhu, Hong [1 ]
Wang, Shijun [1 ]
Ma, Xin [1 ,2 ]
Liu, Xiangwei [1 ]
Wang, Cong [1 ]
Zhao, Hangtian [1 ]
Fan, Shuxia [1 ]
Jin, Xueting [1 ]
Zhao, Buchang [4 ]
Zhao, Tao [4 ]
Jia, Lifu [4 ]
Wang, Keqiang [1 ]
Zou, Yunzeng [1 ,2 ]
Hu, Kai [1 ]
Sun, Aijun [1 ,2 ]
Ge, Junbo [1 ,2 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Shanghai Inst Cardiovasc Dis, Shanghai 200032, Peoples R China
[2] Fudan Univ, Inst Biomed Sci, Shanghai 200032, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Cardiol, Guangzhou 510000, Guangdong, Peoples R China
[4] Shandong Buchang PHARMACEUT CO LTD, Jinan 274000, Shandong, Peoples R China
关键词
Atherosclerosis; naoxintong; dendritic cell; LOW-DENSITY-LIPOPROTEIN; CORONARY-ARTERY-DISEASE; IMMUNE MATURATION; LESIONS; PROGRESSION; ACTIVATION; MECHANISMS; EXPRESSION; THERAPY; PPAR;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Naoxintong (NXT), a Chinese Materia Medica standardized product, extracted from 16 various kinds of Chinese traditional herbal medicines including Salvia miltiorrhiza, Angelica sinennsis, Astragali Radix, is clinically effective in treating atherosclerosis-related diseases. Here, we tested the hypothesis that the anti-atherosclerosis effects of NXT might be mediated by suppressing maturation of dendritic cells (DCs) in a mice model of atherosclerosis. LDLR-/- mice fed a high-fat diet were treated with placebo, NXT (0.7g/kg/d, oral diet) or simvastatin (100mg/kg/d, oral diet) for 8 weeks, respectively. NXT treatment significantly reduced plasma triglyceride (112 +/- 18 mg/dl vs. 192 +/- 68 mg/dl, P<0.05) and total cholesterol (944 +/- 158 mg/dl vs. 1387 +/- 208 mg/dl, P<0.05) compared to placebo treatment. Vascular lesions were significantly smaller and macrophage content and amount of DCs in plaques were significantly less in NXT and simvastatin groups than in placebo group (all P<0.05). In addition, expressions of splenic DC membrane molecules (CD40, CD86 and CD80) and the plasma level of IL-12p70 were significantly lower in NXT and simvastatin groups than in placebo group. In conclusion, NXT protects against atherosclerosis through lipid-lowering and inhibiting DCs maturation in this mice model of atherosclerosis.
引用
收藏
页码:5891 / 5896
页数:6
相关论文
共 33 条
[1]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[2]   Salvianolic acid B inhibits macrophage uptake of modified low density lipoprotein (mLDL) in a scavenger receptor CD36-dependent manner [J].
Bao, Yi ;
Wang, Li ;
Xu, Yanni ;
Yang, Yuan ;
Wang, Lifei ;
Si, Shuyi ;
Cho, Sunghee ;
Hong, Bin .
ATHEROSCLEROSIS, 2012, 223 (01) :152-159
[3]  
Bobryshev Y. V., 1999, Journal of Submicroscopic Cytology and Pathology, V31, P527
[4]  
Bobryshev YV, 1997, J SUBMICR CYTOL PATH, V29, P209
[5]   Dendritic cells in atherosclerosis: current status of the problem and clinical relevance [J].
Bobryshev, YV .
EUROPEAN HEART JOURNAL, 2005, 26 (17) :1700-1704
[6]   Detection of Chlamydophila pineumoniae in dendritic cells in atherosclerotic lesions [J].
Bobryshev, YV ;
Cao, WP ;
Phoon, MC ;
Tran, D ;
Chow, VTK ;
Lord, RSA ;
Lu, JH .
ATHEROSCLEROSIS, 2004, 173 (02) :185-195
[7]   S-100 POSITIVE CELLS IN HUMAN ARTERIAL INTIMA AND IN ATHEROSCLEROTIC LESIONS [J].
BOBRYSHEV, YV ;
LORD, RSA .
CARDIOVASCULAR RESEARCH, 1995, 29 (05) :689-696
[8]  
Ferrer IR, 2012, J IMMUNOL
[9]   Lipopolysaccharide-stimulated activation of murine DC2.4 cells is attenuated by n-butylidenephthalide through suppression of the NF-κB pathway [J].
Fu, Ru-Huei ;
Hran, Horng-Jyh ;
Chu, Ching-Liang ;
Huang, Chin-Mao ;
Liu, Shih-Ping ;
Wang, Yu-Chi ;
Lin, Ya-Hsien ;
Shyu, Woei-Cherng ;
Lin, Shinn-Zong .
BIOTECHNOLOGY LETTERS, 2011, 33 (05) :903-910
[10]   Advanced glycosylation end products might promote atherosclerosis through inducing the immune maturation of dendritic cells [J].
Ge, JB ;
Jia, QZ ;
Liang, C ;
Luo, YK ;
Huang, D ;
Sun, AJ ;
Wang, KQ ;
Zou, YZ ;
Chen, HZ .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (10) :2157-2163