Paeonol suppresses oxidized low-density lipoprotein induced endothelial cell apoptosis via activation of LOX-1/p38MAPK/NF-κB pathway

被引:96
作者
Bao, Mei-hua [1 ,2 ]
Zhang, Yi-wen [1 ]
Zhou, Hong-hao [1 ]
机构
[1] Cent South Univ, Inst Clin Pharmacol, Changsha 410078, Hunan, Peoples R China
[2] Changsha Med Univ, Dept Pharm, Changsha, Hunan, Peoples R China
关键词
Paeonol; Endothelial cells; Atherosclerosis; Apoptosis; Lectin-like low-density lipoprotein receptor-1; NF-KAPPA-B; PROTEIN-KINASE; P38; LDL; RECEPTOR; MAPK; ATHEROSCLEROSIS; PHOSPHORYLATION; STIMULATION; DYSFUNCTION;
D O I
10.1016/j.jep.2013.01.019
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Paeonol is an active compound isolated from traditional Chinese medicine, and has been shown to have anti-atherosclerosis, anti-inflammatory, antioxidant effects. The present investigation was undertaken to determine the suppression effects of paeonol on oxidized low-density lipoprotein (ox-LDL) induced endothelial cell line HUVEC apoptosis and to uncover some of the underlying mechanisms of these effects. Cell viability and lactate dehydrogenase (LDH) were measured to evaluate the cell injuries. Apoptosis was evaluated by Hoechst 33342 staining and flow cytometry. Intracellular reactive oxygen species (ROS) generation was detected by 2',7'-dichlorofluorescein diacetate (DCFH-DA). Real-time PCR was used to confirm the expression of LOX-1 mRNA. Western blotting was used to evaluate the protein expression of LOX-1 and Bcl-2, as well as caspase-3 cleavage, p38-mitogen-activated protein kinase (p38MAPK) phosphorylation. NF-kappa B nuclear translocation was detected by Western blotting and immunofluorescence. Caspase-3 activity was measured using a colorimetric protease assay kit. The results showed that ox-LDL significantly decreased cell viability and increased the LDH release, as well as the apoptotic rate (P < 0.01). Pre-treatment of paeonol resulted in remarkable increase of cell viability, decrease of LDH release and cell apoptosis in a concentration-dependent manner. Besides, ox-LDL caused the up-regulation of LOX-1, the down-regulation of Bcl-2, the phosphorylation of p38MAPK, the translocation of NF-kappa B and the activation of caspase-3. Paeonol pre-treatment reversed these effects introduced by ox-LDL. Moreover, paeonol also showed its inhibition effects on ox-LDL induced ROS overproduction. These results indicate the preventive effects of paeonol on ox-LDL induced endothelial cell apoptosis. The effects might, at least partly, be obtained via inhibition of LOX-1-ROS- p38MAPK-NF-kappa B signaling pathway. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:543 / 551
页数:9
相关论文
共 50 条
[1]   p38-MAPK signals survival by phosphorylation of caspase-8 and caspase-3 in human neutrophils [J].
Alvarado-Kristensson, M ;
Melander, F ;
Leandersson, K ;
Rönnstrand, L ;
Wernstedt, C ;
Andersson, T .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (04) :449-458
[2]   Isorhamnetin prevent endothelial cell injuries from oxidized LDL via activation of p38MAPK [J].
Bao, Meihua ;
Lou, Yijia .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2006, 547 (1-3) :22-30
[3]   Endothelial dysfunction in cardiovascular diseases - The role of oxidant stress [J].
Cai, H ;
Harrison, DG .
CIRCULATION RESEARCH, 2000, 87 (10) :840-844
[4]   Apoptosis and angiogenesis are induced in the unstable coronary atherosclerotic plaque [J].
Chen, F ;
Eriksson, P ;
Kimura, T ;
Herzfeld, I ;
Valen, G .
CORONARY ARTERY DISEASE, 2005, 16 (03) :191-197
[5]   CTGF enhances the motility of breast cancer cells via an integrin-αvβ3-ERK1/2-dependent S100A4-upregulated pathway [J].
Chen, Pai-Sheng ;
Wang, Ming-Yang ;
Wu, Shin-Ni ;
Su, Jen-Liang ;
Hong, Chih-Chen ;
Chuang, Shuang-En ;
Chen, Min-Wei ;
Hua, Kuo-Tai ;
Wu, Yu-Ling ;
Cha, Shih-Ting ;
Babu, Munisamy Suresh ;
Chen, Chiung-Nien ;
Lee, Po-Huang ;
Chang, King-Jen ;
Kuo, Min-Liang .
JOURNAL OF CELL SCIENCE, 2007, 120 (12) :2053-2065
[6]   Comparative study of p38 MAPK signal transduction pathway of peripheral blood mononuclear cells from patients with coal-combustion-type fluorosis with and without high hair selenium levels [J].
Chen, Qun ;
Wang, Zhilun ;
Xiong, Yongmin ;
Zou, Xiuzhen ;
Liu, Zhengwen .
INTERNATIONAL JOURNAL OF HYGIENE AND ENVIRONMENTAL HEALTH, 2010, 213 (05) :381-386
[7]   Ikarisoside A inhibits inducible nitric oxide synthase in lipopolysaccharide-stimulated RAW 264.7 cells via p38 kinase and nuclear factor-κB signaling pathways [J].
Choi, Hwa Jung ;
Eun, Jae-Soon ;
Park, Young-Ran ;
Kim, Dae Keun ;
Li, Rihua ;
Moon, Woo Sung ;
Park, Jeong Mi ;
Kim, Hyung Sup ;
Cho, Nam-Pyo ;
Cho, Sung-Dae ;
Soh, Yunjo .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2008, 601 (1-3) :171-178
[8]   Flow, NO, and atherogenesis [J].
Cooke, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (03) :768-770
[9]  
Dai Min, 2006, Zhongguo Yaolixue Tongbao, V22, P587
[10]   Oxidation-sensitive mechanisms, vascular apoptosis and atherosclerosis [J].
de Nigris, F ;
Lerman, A ;
Ignarro, LJ ;
Williams-Ignarro, S ;
Sica, V ;
Baker, AH ;
Lerman, LO ;
Geng, YJ ;
Napoli, C .
TRENDS IN MOLECULAR MEDICINE, 2003, 9 (08) :351-359