Neutralization of interleukin-18 inhibits neointimal formation in a rat model of vascular injury

被引:61
作者
Maffia, Pasquale
Grassia, Gianluca
Di Meglio, Paola
Carnuccio, Rosa
Berrino, Liberato
Garside, Paul
Ianaro, Angela
Ialenti, Armando
机构
[1] Univ Naples Federico II, Dept Expt Pharmacol, I-80131 Naples, Italy
[2] Univ Glasgow, Div Immunol Infect & Inflammat, Glasgow, Lanark, Scotland
[3] Univ Glasgow, Div Cardiovasc & Med Sci, Glasgow, Lanark, Scotland
[4] Univ Naples 2, Excellence Res Ctr Cardiovasc Dis, Naples, Italy
[5] Univ Naples 2, Dept Expt Med, Naples, Italy
[6] Univ Strathclyde, Ctr Biophoton, Strathclyde Inst Biomed Sci, Glasgow, Lanark, Scotland
关键词
angioplasty; balloon; carotid arteries; interleukins;
D O I
10.1161/CIRCULATIONAHA.105.602714
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background - Studies in humans and animal models suggest that interleukin-18 (IL-18) plays a crucial role in vascular pathologies. IL-18 is a predictor of cardiovascular death in angina and is involved in atherotic plaque destabilization. Higher IL-18 plasma levels also are associated with restenosis after coronary artery angioplasty performed in patients with acute myocardial infarction. We investigated the effective role of IL-18 in neointimal formation in a balloon-induced rat model of vascular injury. Methods and Results - Endothelial denudation of the left carotid artery was performed by use of a balloon embolectomy catheter. Increased expression of IL-18 and IL-18R alpha/beta mRNA was detectable in carotid arteries from days 2 to 14 after angioplasty. The active form of IL-18 was highly expressed in injured arteries. Strong immunoreactivity for IL-18 was detected in the medial smooth muscle cells at days 2 and 7 after balloon injury and in proliferating/migrating smooth muscle cells in neointima at day 14. Moreover, serum concentrations of IL-18 were significantly higher among rats subjected to vascular injury. Treatment with neutralizing rabbit anti-rat IL-18 immunoglobulin G significantly reduced neointimal formation (by 27%; P < 0.01), reduced the number of proliferating cells, and inhibited interferon-gamma, IL-6, and IL-8 mRNA expression and nuclear factor-kappa B activation in injured arteries. In addition, in vitro data show that IL-18 affects smooth muscle cell proliferation. Conclusions - These results identify a critical role for IL-18 in neointimal formation in a rat model of vascular injury and suggest a potential role for IL-18 neutralization in the reduction of neointimal development.
引用
收藏
页码:430 / 437
页数:8
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