Korean Circ J.  2006 Jul;36(7):495-502. 10.4070/kcj.2006.36.7.495.

The Effect of Oral Administration of Alpha Lipoic Acid and Alpha Lipoic Acid Coated Stent in Porcine In-Stent Restenosis Model

Affiliations
  • 1Department of Internal Medicine, Cheju National University, Jeju, Korea.
  • 2The Heart Center of Chonnam National University Hospital, Gwangju, Chonnam National University Research Institute of Medical Science, Gwangju, Korea. myungho@chollian.net
  • 3Chemical Engineering of Chonnam National University, Gwangju, Korea.

Abstract

BACKGROUND AND OBJECTIVES: Alpha lipoic acid (ALA) is beneficial for improving endothelial dysfunction and preventing atherosclerosis-related diseases. We evaluated the affect of ALA on stent restenosis in a porcine model.
MATERIALS AND METHODS
The First experiment: Balloon overdilation injuries were performed in two coronary arteries in 12 pigs. Four weeks after the balloon overdilation injury, 24 bare metal stents were placed for 24 injured coronary arteries. We randomized into two groups (12 stents per group; control group: aspirin and clopidogrel only, ALA group: aspirin and clopidogrel plus 100 mg/kg ALA during 4 weeks). The Second experiment: Stents were randomly implanted in 2 coronary arteries in 8 pigs. Group I was the control stent group (n=8), and group II was the ALA coated stent group (n=8). Follow-up coronary angiogram and histopathologic assessment were performed at 4 weeks after stenting in both experiments.
RESULTS
The First experiment On histopathologic analysis, the injury score and internal elastic lamina area did not differ significantly between the two groups. The neointimal area was 7.3+/-0.9 mm2 in the control group and 2.2+/-1.1 mm2 in the ALA group (p<0.001), and the histopathologic area of stenosis was 75.9+/-8.5% in the control group and 23.5+/-10.5% in the ALA group (p<0.001). The Second experiment: The injury score and internal elastic lamina area were not significantly different between the two groups. The neointimal area was 7.4+/-1.1 mm2 in the control group and 1.4+/-0.8 mm2 in the ALA group (p<0.001), and the histopathologic area of stenosis was 77.6+/-10.9% in the control group and 15.6+/-7.6% in the ALA group (p<0.001).
CONCLUSION
Both a high dose of oral ALA and ALA coated stents inhibited neointimal hyperplasia in this porcine coronary artery stent restenosis model.

Keyword

Coronary disease; Restenosis; Stents; Anti-oxidants

MeSH Terms

Administration, Oral*
Aspirin
Constriction, Pathologic
Coronary Disease
Coronary Vessels
Follow-Up Studies
Hyperplasia
Stents*
Swine
Thioctic Acid*
Aspirin
Thioctic Acid
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