Objective: A direct correlation between blood glucose levels and the microvascular complications of diabetes is well established. However, the effects of hyperglycaemia on the vasa vasorum, a microvascular network which surrounds and supplies the walls of large arteries, is not known. The objective of this study is to investigate the effects of hyperglycaemia on the vasa vasorum and to examine correlations between these effects and the development of atherosclerosis in a mouse model. Methods: The micro- and macrovascular effects of hyperglycaemia were examined in streptozotocin-injected apolipoprotein-E deficient (ApoE(-/-))mice. Retina and aortic sinus were isolated from hyperglycaemic mice and normoglycaemic controls at 5-20 weeks of age. Retinal and vasa vasorum microvessel densities were quantified and correlated to atherosclerotic lesion development. The expression levels of pro-angiogenic factors including vascular endothelial growth factor (VEGF) and VEGF receptor 2 were examined. Results: In normoglycaemic ApoE(-/-) mice atherogenesis is associated with vasa vasorum expansion, which likely corresponds to the increasing blood supply demands of the thickening artery wall. In hyperglycaemic ApoE(-/-) mice there is no significant neovascularization of the vasa vasorum, despite the fact that lesions are significantly larger. This defect may result from a localized deficiency in VEGF. Conclusions: These findings are the first evidence that hyperglycaemia alters the structure of the vasa vasorum. Such microvascular changes directly correlate, and may contribute to, the development and progression of atherosclerosis in hyperglycaemic ApoE-deficient mice. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
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Kumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, JapanKumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, Japan
Murakami-Nishida, Saiko
Matsumura, Takeshi
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Kumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, JapanKumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, Japan
Matsumura, Takeshi
Senokuchi, Takafumi
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Kumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, JapanKumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, Japan
Senokuchi, Takafumi
Ishii, Norio
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Kumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, JapanKumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, Japan
Ishii, Norio
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Kinoshita, Hiroyuki
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Yamada, Sarie
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Morita, Yutaro
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Nishida, Shuhei
Motoshima, Hiroyuki
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Kumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, JapanKumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, Japan
Motoshima, Hiroyuki
Kondo, Tatsuya
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Kumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, JapanKumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, Japan
Kondo, Tatsuya
Komohara, Yoshihiro
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Kumamoto Univ, Fac Life Sci, Dept Cell Pathol, Kumamoto, JapanKumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, Japan
Komohara, Yoshihiro
Araki, Eiichi
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Kumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, Japan
Kumamoto Univ, Fac Life Sci, Ctr Metab Regulat Hlth Aging CMHA, Kumamoto, JapanKumamoto Univ, Fac Life Sci, Dept Metab Med, 1-1-1 Honjo, Kumamoto 8605886, Japan