Article ID Journal Published Year Pages File Type
5948460 Atherosclerosis 2012 7 Pages PDF
Abstract

ObjectivesTo study the effects of reduced lipoic acid gene expression on diabetic atherosclerosis in apolipoprotein E null mice (Apoe−/−).Methods and resultsHeterozygous lipoic acid synthase gene knockout mice (Lias+/−) crossed with Apoe−/− mice were used to evaluate the diabetic effect induced by streptozotocin on atherosclerosis in the aortic sinus of the heart. While diabetes markedly increased atherosclerotic plaque size in Apoe−/− mice, a small but significant effect of reduced expression of lipoic acid gene was observed in diabetic Lias+/−Apoe−/− mice. In the aortic lesion area, the Lias+/−Apoe−/− mice exhibited significantly increased macrophage accumulation and cellular apoptosis than diabetic Lias+/+Apoe−/− littermates. Plasma glucose, cholesterol, and interleukin-6 were also higher. These abnormalities were accompanied with increased oxidative stress including a decreased ratio of reduced glutathione/oxidized glutathione in erythrocytes, increased systemic lipid peroxidation, and increased Gpx1 and MCP1 gene expression in the aorta.ConclusionsDecreased endogenous lipoic acid gene expression plays a role in development of diabetic atherosclerosis. These findings extend our understanding of the role of antioxidant in diabetic atherosclerosis.

► We evaluate effects of reduced lipoic acid synthase gene expression on diabetic atherosclerosis. ► Apolipoprotein E null mice were crossed with Lias antioxidant model and then induced to diabetes. ► Reduced endogenous lipoic acid capacity plays a role in development of diabetic atherosclerosis. ► These findings extend our understanding of the role of antioxidant in diabetic atherosclerosis.

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