Probucol and cilostazol exert a combinatorial anti-atherogenic effect in cholesterol-fed rabbits

被引:23
作者
Chen, Yulong [1 ,2 ]
Zhao, Sihai [1 ,2 ]
Huang, Bingqiao [1 ,2 ]
Wang, Yanli [1 ,2 ]
Li, Yafeng [1 ,2 ]
Waqar, Ahmed Bilal [3 ]
Liu, Ruihan [1 ,2 ]
Bai, Liang [1 ,2 ]
Fan, Jianglin [1 ,2 ]
Liu, Enqi [1 ,2 ]
机构
[1] Xi An Jiao Tong Univ, Cardiovasc Res Ctr, Res Inst Atherosclerot Dis, Xian 710061, Shaanxi, Peoples R China
[2] Xi An Jiao Tong Univ, Sch Med, Lab Anim Ctr, Xian 710061, Shaanxi, Peoples R China
[3] Univ Yamanashi, Interdisciplinary Grad Sch Med & Engn, Dept Mol Pathol, Yamanashi 4093898, Japan
基金
中国国家自然科学基金;
关键词
Probucol; Cilostazol; Atherosclerosis; S-nitrosylation; Rabbits; HUMAN ENDOTHELIAL-CELLS; LOW-DENSITY LIPOPROTEINS; PROTEIN S-NITROSYLATION; NITRIC-OXIDE SYNTHASE; OXIDATIVE STRESS; CONCURRENT TREATMENT; DOWN-REGULATION; ATHEROSCLEROSIS; ACTIVATION; EXPRESSION;
D O I
10.1016/j.thromres.2013.09.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Probucol (PB) and cilostazol (CZ) both exhibit anti-atherogenic effects. However, their combinatorial effects are unclear. This study was designed to investigate their combinatorial anti-atherogenic effect in cholesterol-fed rabbits. Materials and Methods: Rabbits were fed a cholesterol diet with PB or CZ alone or both PB and CZ for 16 weeks. The plasma levels of total cholesterol, LDL-cholesterol, HDL-cholesterol, C-reactive protein, superoxide dismutase, malondialdehyde, and nitric oxide (NO) were measured. The aortic atherosclerotic lesions were grossly and microscopically evaluated. Additionally, in vitro experimentswere conducted using human umbilical vein endothelial cells. Results and Conclusion: We found that the PB group and the PB + CZ group exhibited a reduction in the lesion areas (70% in the PB + CZ group, 56% in the PB group) compared with the vehicle group. However, although PB alone and PB + CZ led to a reduction in the lesion size, the histological analysis revealed that only PB + CZ significantly decreased the macrophage accumulation and smooth muscle cell proliferation in the lesions compared with the vehicle group. The plasma levels of total cholesterol in the PB + CZ group were decreased compared with the vehicle group, Moreover, PB + CZ exerted obvious anti-oxidant and anti-inflammatory effects. Interestingly, the PB + CZ treatment led to amarked increase in the levels of plasmaNO. The in vitro experiments showed that the combinatorial treatment up-regulated the levels of NO and protein S-nitrosylation in endothelial cells treated with oxidized LDL. In summary, these results suggest that PB and CZ exert combinatorial antiatherogenic effects. (C) 2013 The Authors. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:565 / 571
页数:7
相关论文
共 43 条
[1]   Endothelial dysfunction - A marker of atherosclerotic risk [J].
Bonetti, PO ;
Lerman, LO ;
Lerman, A .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2003, 23 (02) :168-175
[2]  
Bonomini F, 2008, HISTOL HISTOPATHOL, V23, P381, DOI 10.14670/HH-23.381
[3]   17β-Estradiol induces protein S-nitrosylation in the endothelium [J].
Chakrabarti, Subhadeep ;
Lekontseva, Olga ;
Peters, Amber ;
Davidge, Sandra T. .
CARDIOVASCULAR RESEARCH, 2010, 85 (04) :796-805
[4]   Reduction of oxidative stress and atherosclerosis in hyperlipidemic rabbits by Dioscorea rhizome [J].
Chang, WC ;
Yu, YM ;
Wu, CH ;
Tseng, YH ;
Wu, KY .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 2005, 83 (05) :423-430
[5]   Detection of protein S-nitrosylation with the biotin-switch technique [J].
Forrester, Michael T. ;
Foster, Matthew W. ;
Benhar, Moran ;
Stamler, Jonathan S. .
FREE RADICAL BIOLOGY AND MEDICINE, 2009, 46 (02) :119-126
[6]   Effect of probucol treatment on gene expression of VCAM-1, MCP-1, and M-CSF in the aortic wall of LDL receptor-deficient rabbits during early atherogenesis [J].
Fruebis, J ;
Gonzalez, V ;
Silvestre, M ;
Palinski, W .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1997, 17 (07) :1289-1302
[7]   Antioxidant effects of statins via S-nitrosylation and activation of thioredoxin in endothelial cells -: A novel vasculoprotective function of statins [J].
Haendeler, J ;
Hoffmann, J ;
Zeiher, AM ;
Dimmeler, S .
CIRCULATION, 2004, 110 (07) :856-861
[8]   Activation of endothelial nitric oxide synthase by cilostazol via a cAMP/protein kinase A- and phosphatidylinositol 3-kinase/Akt-dependent mechanism [J].
Hashimoto, Ayako ;
Miyakoda, Goro ;
Hirose, Yoshimi ;
Mori, Toyoki .
ATHEROSCLEROSIS, 2006, 189 (02) :350-357
[9]   RETRACTED: Cilostazol inhibits cytokine-induced nuclear factor-κB activation via AMP-activated protein kinase activation in vascular endothelial cells (Retracted article. See vol. 92, pg. 181, 2011) [J].
Hattori, Yoshiyuki ;
Suzuki, Kunihiro ;
Tomizawa, Atsuko ;
Hirama, Noriko ;
Okayasu, Toshie ;
Hattori, Sachiko ;
Satoh, Hiroko ;
Akimoto, Kazumi ;
Kasai, Kikuo .
CARDIOVASCULAR RESEARCH, 2009, 81 (01) :133-139
[10]   Probucol enhances the expression of human hepatic scavenger receptor class B type I, possibly through a species-specific mechanism [J].
Hirano, K ;
Ikegami, C ;
Tsujii, K ;
Zhang, ZY ;
Matsuura, F ;
Nakagawa-Toyama, Y ;
Koseki, M ;
Masuda, D ;
Maruyama, T ;
Shimomura, I ;
Ueda, Y ;
Yamashita, S .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (11) :2422-2427