The effect of alpha lipoic acid in a porcine in-stent restenosis model

초록

Background: The aim of this study was to investigate the effect of alpha lipoic acid (alpha-LA) on a porcine in-stent restenosis (ISR) model. Methods: In protocol 1, porcine vascular smooth muscle cells (PVSMC) were stimulated by granulocyte-colony stimulating factor (G-CSF) in the presence or absence of alpha-LA. MTT (3-[4,5-dimethylthiazole-2-yl] 2,5-diphenyl tetrazolium bromide) assay and western blotting were used to determine the cell growth inhibitory rate and anti-inflammatory effect associated with nuclear factor-kappa b (NF-kappa b) and extracellular signal-regulated kinase (ERK). In protocol 2, 28 days after balloon overdilation injuries, 24 bare metal stents were placed in coronary artery of 12 pigs. The pigs were randomly divided to receive control diet with or without alpha-LA (100 mg/kg). In protocol 3, 8 control stents and 8 alpha-LA coated stents were randomly implanted in 2 coronary arteries of 8 pigs and follow-up coronary angiogram and histopathologic assessment were performed 4 weeks after stenting. Results: Protocol 1. The proliferation of PVSMC was inhibited and protein expression of NF-kappa b and ERK were attenuated by alpha-LA pretreatment. Protocol 2. On histopathologic analysis, the neointimal area (4.0 +/- 1.0mm(2) VS. 1.5 +/- 0.7 mm(2), P < 0.001) and histopathologic area of stenosis (66.7 +/- 10.7% vs. 24.2 +/- 9.7%, p < 0.001) were reduced in the alpha-LA feeding group compared to controls. Protocol 3. On histopathologic analysis, the neointimal area (3.9 +/- 0.8 mm(2) vs. 1.0 +/- 0.4 mm(2), p < 0.001), and the histopathologic area of stenosis (67.1 +/- 8.8% vs. 17.4 +/- 10.0%, p < 0.001) were reduced in the (alpha-LA coated stent group compared to the control stent group. Conclusions: alpha-LA feeding and alpha-LA coated stents inhibit neointimal hyperplasia in porcine ISR, possibly through inhibiting the activation of NF-kappa b pathway and proliferation of PVSMC. (C) 2009 Japanese College of Cardiology. Published by Elsevier Ireland Ltd. All rights reserved.

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