In vivo Effect of Insulin to Decrease Matrix Metalloproteinase-2 and-9 Activity after Arterial Injury

被引:11
作者
Guo, June [1 ]
Dhaliwall, Jiwanjeet K. [1 ]
Chan, Kalam K. [1 ]
Ghanim, Husam [6 ]
Al Koudsi, Nael [1 ]
Lam, Loretta [1 ]
Madadi, Golnaz [1 ]
Dandona, Paresh [6 ]
Giacca, Adria [1 ,2 ,4 ,5 ]
Bendeck, Michelle P. [2 ,3 ]
机构
[1] Univ Toronto, Dept Physiol, Toronto, ON M5S 1A8, Canada
[2] Univ Toronto, Dept Med, Toronto, ON M5S 1A8, Canada
[3] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON M5S 1A8, Canada
[4] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A8, Canada
[5] Univ Toronto, Banting & Best Diabet Ctr, Toronto, ON M5S 1A8, Canada
[6] SUNY Buffalo, Div Endocrinol Diabet & Metab, Buffalo, NY 14260 USA
关键词
Arterial injury; Hyperinsulinemia; Insulin; Matrix metalloproteinases; Metabolic syndrome; Tissue inhibitors of matrix metalloproteinases; MUSCLE-CELL-MIGRATION; NITRIC-OXIDE SYNTHASE; NF-KAPPA-B; NEOINTIMA FORMATION; INHIBITION; MATRIX-METALLOPROTEINASE-9; TRANSCRIPTION; EXPRESSION; HYPERPLASIA; DEFICIENCY;
D O I
10.1159/000351611
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
In vitro, insulin has both growth-promoting and vasculoprotective effects. In vivo, the effect of insulin is mainly protective. Insulin treatment (3 U/day) decreases smooth muscle cell (SMC) migration and neointimal growth after carotid angioplasty in normal rats maintained at normoglycemia by oral glucose. SMC migration requires limited proteolysis of the extracellular matrix, which is mediated by matrix metalloproteinases (MMPs). In this study, we investigated the effects of normoglycennic hyperinsulinemia on MMP activity after balloon angioplasty. Rats were divided into three groups: (1) control implants and tap water; (2) control implants and oral glucose, and (3) insulin implants (3 U/day) and oral glucose. Results: Gelatin zynnography revealed that insulin reduced the gelatinolytic activity of pro-MMP-2 by 46%(p <0.05), MMP-2 by 44% (p <0.05) and MMP-9 by 51% (p < 0.05) compared to controls after arterial injury. Insulin also reduced mRNA levels of MMP-2 (p <0.05) and MMP-9 (p <0.05) and protein levels of MMP-2 (p <0.05). In contrast, there were no significant changes in membrane-type 1 MMP protein and tissue inhibitors of MMP activity after insulin treatment. Thus, these results suggest a mechanism by which insulin inhibits SMC migration and supports a vasculoprotective role for insulin in vivo. copyright (C) 2013 S. Karger AG, Basel
引用
收藏
页码:279 / 288
页数:10
相关论文
共 47 条
[1]   Harmonizing the Metabolic Syndrome A Joint Interim Statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity [J].
Alberti, K. G. M. M. ;
Eckel, Robert H. ;
Grundy, Scott M. ;
Zimmet, Paul Z. ;
Cleeman, James I. ;
Donato, Karen A. ;
Fruchart, Jean-Charles ;
James, W. Philip T. ;
Loria, Catherine M. ;
Smith, Sidney C., Jr. .
CIRCULATION, 2009, 120 (16) :1640-1645
[2]   Insulin inhibits NFκB and MCP-1 expression in human aortic endothelial cells [J].
Aljada, A ;
Ghanim, H ;
Saadeh, R ;
Dandona, P .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (01) :450-453
[3]   Regulation of mitogen-activated protein kinase phosphatase-1 induction by insulin in vascular smooth muscle cells - Evaluation of the role of the nitric oxide signaling pathway and potential defects in hypertension [J].
Begum, N ;
Ragolia, L ;
Rienzie, J ;
McCarthy, M ;
Duddy, N .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (39) :25164-25170
[4]   Inhibition of matrix metalloproteinase activity inhibits smooth muscle cell migration but not neointimal thickening after arterial injury [J].
Bendeck, MP ;
Irvin, C ;
Reidy, MA .
CIRCULATION RESEARCH, 1996, 78 (01) :38-43
[5]   SMOOTH-MUSCLE CELL-MIGRATION AND MATRIX METALLOPROTEINASE EXPRESSION AFTER ARTERIAL INJURY IN THE RAT [J].
BENDECK, MP ;
ZEMPO, N ;
CLOWES, AW ;
GALARDY, RE ;
REIDY, MA .
CIRCULATION RESEARCH, 1994, 75 (03) :539-545
[6]   The β3 integrin antagonist m7E3 reduces matrix metalloproteinase activity and smooth muscle cell migration [J].
Bendeck, MP ;
Nakada, MT .
JOURNAL OF VASCULAR RESEARCH, 2001, 38 (06) :590-599
[7]   A functional activating protein 1 (AP-1) site regulates matrix metalloproteinase 2 (MMP-2) transcription by cardiac cells through interactions with JunB-Fra1 and JunB-FosB heterodimers [J].
Bergman, MR ;
Cheng, S ;
Honbo, N ;
Piacentini, L ;
Karliner, JS ;
Lovett, DH .
BIOCHEMICAL JOURNAL, 2003, 369 (03) :485-496
[8]   Inhibition of transcription factor NF-κB reduces matrix metalloproteinase-1,-3 and-9 production by vascular smooth muscle cells [J].
Bond, M ;
Chase, AJ ;
Baker, AH ;
Newby, AC .
CARDIOVASCULAR RESEARCH, 2001, 50 (03) :556-565
[9]   Resveratrol inhibits neointimal formation after arterial injury through an endothelial nitric oxide synthase-dependent mechanism [J].
Breen, Danna M. ;
Dolinsky, Vernon W. ;
Zhang, Hangjun ;
Ghanim, Husam ;
Guo, June ;
Mroziewicz, Margaret ;
Tsiani, Evangelia L. ;
Bendeck, Michelle P. ;
Dandona, Paresh ;
Dyck, Jason R. B. ;
Heximer, Scott P. ;
Giacca, Adria .
ATHEROSCLEROSIS, 2012, 222 (02) :375-381
[10]   Insulin Inhibits and Oral Sucrose Increases Neointimal Growth after Arterial Injury in Rats [J].
Breen, Danna M. ;
Dhaliwall, Jiwanjeet K. ;
Chan, Kalam K. ;
Guo, June ;
Lam, Loretta ;
Bendeck, Michelle P. ;
Giacca, Adria .
JOURNAL OF VASCULAR RESEARCH, 2010, 47 (05) :412-422