Endothelium-specific insulin resistance leads to accelerated atherosclerosis in areas with disturbed flow patterns: A role for reactive oxygen species

被引:44
|
作者
Gage, Matthew C. [1 ]
Yuldasheva, Nadira Y. [1 ]
Viswambharan, Hema [1 ]
Sukumar, Piruthivi [1 ]
Cubbon, Richard M. [1 ]
Galloway, Stacey [1 ]
Imrie, Helen [1 ]
Skromna, Anna [1 ]
Smith, Jessica [1 ]
Jackson, Christopher L. [2 ]
Kearney, Mark T. [1 ]
Wheatcroft, Stephen B. [1 ]
机构
[1] Univ Leeds, Leeds Multidisciplinary Cardiovasc Res Ctr, Div Cardiovasc & Diabet Res, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Bristol, Bristol Heart Inst, Bristol BS8 1TH, Avon, England
基金
欧洲研究理事会; 英国医学研究理事会;
关键词
Atherosclerosis; Nitric oxide; Insulin resistance; Oxidative stress; Endothelium; NITRIC-OXIDE PRODUCTION; VASCULAR SUPEROXIDE; DYSFUNCTION; PROTECTS; SENSITIVITY; DEFICIENCY; MECHANISMS; SYNTHASE; RECEPTOR; DISEASE;
D O I
10.1016/j.atherosclerosis.2013.06.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: Systemic insulin resistance is associated with a portfolio of risk factors for atherosclerosis development. We sought to determine whether insulin resistance specifically at the level of the endothelium promotes atherosclerosis and to examine the potential involvement of reactive oxygen species. Methods: We cross-bred mice expressing a dominant negative mutant human insulin receptor specifically in the endothelium (ESMIRO) with ApoE(-/-) mice to examine the effect of endothelium-specific insulin resistance on atherosclerosis. Results: ApoE(-/-) /ESMIRO mice had similar blood pressure, plasma lipids and whole-body glucose tolerance, but blunted endothelial insulin signalling, in comparison to ApoE(-/-) mice. Atherosclerosis was significantly increased in ApoE(-/-) /ESMIRO mice at the aortic sinus (226 +/- 16 versus 149 +/- 24 x 10(3) mm(2), P = 0.01) and lesser curvature of the aortic arch (12.4 +/- 1.2% versus 9.4 +/- 0.9%, P = 0.035). Relaxation to acetylcholine was blunted in aorta from ApoE(-/-) /ESMIRO mice (E-max 65 +/- 41% versus 103 + 6%, P = 0.02) and was restored by the superoxide dismutase mimetic MnTMPyP (E-max 112 +/- 15% versus 65 +/- 41%, P = 0.048). Basal generation of superoxide was increased 1.55 fold (P = 0.01) in endothelial cells from ApoE(-/-) /ESMIRO mice and was inhibited by the NADPH oxidase inhibitor gp91ds-tat (-12 +/- 0.04%, P - 0.04), the NO synthase inhibitor L-NMMA (-8 +/- 0.02%, P - 0.001) and the mitochondrial specific inhibitor rotenone (-23 +/- 0.04%, P = 0.006). Conclusions: Insulin resistance specifically at the level of the endothelium leads to acceleration of atherosclerosis in areas with disturbed flow patterns such as the aortic sinus and the lesser curvature of the aorta. We have identified a potential role for increased generation of reactive oxygen species from multiple enzymatic sources in promoting atherosclerosis in this setting. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:131 / 139
页数:9
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