Neutralization of Interleukin-18 Inhibits Neointimal Formation in a Rat Model of Vascular Injury

Author:

Maffia Pasquale1,Grassia Gianluca1,Di Meglio Paola1,Carnuccio Rosa1,Berrino Liberato1,Garside Paul1,Ianaro Angela1,Ialenti Armando1

Affiliation:

1. From the Department of Experimental Pharmacology, University of Naples Federico II, Naples, Italy (P.M., G.G., P.D.M., R.C., A.I., A.I.); Division of Immunology, Infection and Inflammation and Division of Cardiovascular and Medical Sciences, University of Glasgow, Glasgow, UK (P.M.); Excellence Research Center for Cardiovascular Diseases and Department of Experimental Medicine, Second University of Naples, Naples, Italy (L.B.); and Centre for Biophotonics, Strathclyde Institute for Biomedical...

Abstract

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-18Rα/β 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-γ, IL-6, and IL-8 mRNA expression and nuclear factor-κB 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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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