Swings in blood glucose levels accelerate atherogenesis in apolipoprotein E-deficient mice

被引:86
作者
Mita, Tomoya
Otsuka, Aiko
Azuma, Kosuke
Uchida, Toyoyoshi
Ogihara, Takeshi
Fujitani, Yoshio
Hirose, Takahisa
Mitsumata, Masako
Kawamori, Ryuzo
Watada, Hirotaka
机构
[1] Juntendo Univ, Sch Med, Dept Med Metab & Endocrinol, Bunkyo Ku, Tokyo 1138421, Japan
[2] Nihon Univ, Sch Med, Dept Pathol, Tokyo 1738610, Japan
关键词
monocyte adhesion; glucose fluctuation; postprandial hyperglycemia; cardiovascular disease; endothelial cell;
D O I
10.1016/j.bbrc.2007.04.118
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of this study was to investigate the effect of fluctuations in blood glucose levels on atherogenesis. Apolipoprotein (apo) E-deficient mice fed maltose twice daily were used as a model of repetitive postprandial glucose spikes. We investigated the number of macrophages adherent to the endothelium and the area of fibrotic arteriosclerotic lesions, with and without administration of miglitol.. an a-glucosidase inhibitor. Macrophage adhesion to endothelial cells in thoracic aorta was quantitated by the en face method for optimal observation of endothelial surface after immunohistochemical staining for Mae-2. The area of arteriosclerotic lesions was measured in elastica van Giesson-stained proximal aorta. The number of adherent macrophages increased at I week after commencement of maltose feeding and the size of arteriosclerotic lesion increased at 5 weeks after such feeding. These increases were prevented by simultaneous use of miglitol. Our data demonstrated that glucose fluctuations accelerate atherogenesis. This was independent of changes in serum cholesterol level in vivo. Reduction of glucose fluctuation by alpha-glucosidase inhibitor efficiently controlled the progression of atherosclerosis. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:679 / 685
页数:7
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