Marimastat inhibits neointimal thickening in a model of human arterial intimal hyperplasia

Objective: matrix metalloproteases (MMPs) produced by vascular smooth-muscl e cells (VSMCs) degrade extracellular matrix and facilitate the migration o f these cells. This is a fundamental process in arterial intimal hyperplasi a. This study investigated whether Marimastat (a selective but non-specific MMP inhibitor) can prevent intimal hyperplasia in cultured human internal mammary artery (IMA). Materials and methods: segments of IMA from 8 patients were prepared and cu ltured for 14 days in serum-supplemented medium (control) or in medium supp lemented with Marimastat at 2 concentrations (treatment groups). The tissue was fixed, sectioned, stained and neointimal thicknesses measured by compu ter-aided image analysis. Further sections were cultured in the same manner and prepared for gel enzymography to quantify the production of MMPs. Results: neointimal thickness was significantly reduced by Marimastat in a dose-dependent manner when compared to controls (p = 0.008 Wilcoxon). Gel e nzymography demonstrated a reduction in levels of MMP2 and MMP9. This was m ost significant for the active forms of the enzymes (p = 0.03). Conclusions: our results suggest that there is a potential therapeutic role for specific inhibition of the gelatinases in the prevention of human arte rial restenosis.