Resveratrol prevents the development of abdominal aortic aneurysm through attenuation of inflammation, oxidative stress, and neovascularization

被引:85
|
作者
Kaneko, Hidehiro [1 ]
Anzai, Toshihisa [1 ,2 ]
Morisawa, Maho [1 ]
Kohno, Takashi [1 ]
Nagai, Toshiyuki [1 ]
Anzai, Atsushi [1 ]
Takahashi, Toshiyuki [1 ]
Shimoda, Masayuki [3 ]
Sasaki, Aya [2 ]
Maekawa, Yuichiro [1 ]
Yoshimura, Koichi [4 ]
Aoki, Hiroki [5 ]
Tsubota, Kazuo [6 ]
Yoshikawa, Tsutomu [1 ]
Okada, Yasunori [3 ]
Ogawa, Satoshi [1 ,2 ]
Fukuda, Keiichi [1 ]
机构
[1] Keio Univ, Sch Med, Dept Med, Div Cardiol, Tokyo 160, Japan
[2] Int Univ Hlth & Welf, Ctr Cardiovasc, Mita Hosp, Minato Ku, Tokyo 1088329, Japan
[3] Keio Univ, Sch Med, Dept Pathol, Tokyo 160, Japan
[4] Yamaguchi Univ, Dept Mol Cardiovasc Biol, Sch Med, Yamaguchi, Japan
[5] Kurume Univ, Cardiovasc Dept, Sch Med, Fukuoka, Japan
[6] Keio Univ, Sch Med, Dept Ophthalmol, Tokyo 160, Japan
关键词
Abdominal aortic aneurysm; Extracellular matrix; Inflammation; Neoangiogenesis; Oxidative stress; FACTOR-KAPPA-B; TRANS-RESVERATROL; ANGIOTENSIN-II; INHIBITION; TRANSCRIPTION; ANGIOGENESIS; COMPOUND; ACID; WINE;
D O I
10.1016/j.atherosclerosis.2011.03.042
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: We sought to examine the effect of resveratrol (3,4',5-trihydroxy-trans-stilbene), a plant-derived polyphenolic compound, on the development of abdominal aortic aneurysm (AAA). Methods: AAA was induced in mice by periaortic application of CaCl2. NaCl (0.9%)-applied mice were used as a sham group. Mice were treated with intraperitoneal injection of PBS (Sham/CON, AAA/CON, n = 30 for each) or resveratrol (100 mg/kg/day) (AAA/RSVT, n = 30). Six weeks after the operation, aortic tissue was excised for further examinations. Results: Aortic diameter was enlarged in AAA/CON compared with Sham/CON. Resveratrol treatment reduced the aneurysm size and inflammatory cell infiltration in the aortic wall compared with AAA/CON. Elastica Van Gieson staining showed destruction of the wavy morphology of the elastic lamellae in AAA/CON, while it was preserved in AAA/RSVT. The increased mRNA expression of monocyte chemotactic protein-1, tumor necrosis factor-alpha, intercellular adhesion molecule-1, CD68, vascular endothelial growth factor-A, p47, glutathione peroxidase (GPX) 1 and GPX3 were attenuated by resveratrol treatment (all p < 0.05). Administration of resveratrol decreased protein expression of phospho-p65 in AAA. The increased 8-hydroxy-2'-deoxyguanosine-positive cell count and 4-hydroxy-2-nonenal-positive cell count in AAA were also reduced by resveratrol treatment. Zymographic activity of matrix metalloproteinase (MMP)-9 and MMP-2 was lower in AAA/RSVT compared with AAA/CON (both p < 0.05). Compared with AAA/CON, Mac-2(+) macrophages and CD31(+) vessels in the aortic wall were decreased in AAA/RSVT (both p < 0.05). Conclusion: Treatment with resveratrol in mice prevented the development of CaCl2-induced AAA, in association with reduced inflammation, oxidative stress, neoangiogenesis, and extracellular matrix disruption. These findings suggest therapeutic potential of resveratrol for AAA. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:350 / 357
页数:8
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