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
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