» Articles » PMID: 19152178

Impaired Coronary Microvascular Dilation Correlates with Enhanced Vascular Smooth Muscle MLC Phosphorylation in Diabetes

Overview
Date 2009 Jan 20
PMID 19152178
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: Impaired endothelium-independent vasodilation is a known consequence of types 1 and 2 diabetes, and the mechanism of impaired vasodilation is not well understood. The following study investigated the effects of types 1 and 2 diabetes in endothelial-independent vasodilation associated with coronary vascular smooth muscle (VSM) relaxation and contractile signaling mechanisms.

Materials And Methods: Type 1 diabetes was induced in Yucatan miniswine via alloxan injection and treated with or without insulin (DM and IDM). Nondiabetic swine served as controls (ND). Expression and/or phosphorylation of determinants of VSM relaxation and contraction signaling were examined in coronary arteries and microvessels. Coronary microvessel relaxation was assessed by using sodium nitroprusside (SNP). In addition, SNP-induced vasodilation and myosin light-chain (MLC) phosphorylation was determined in coronary microvessels isolated from ND and type 2 diabetic human atrial appendage.

Results: Diabetic impairment in SNP-induced relaxation was completely normalized by insulin. Soluble guanylate cyclase (sGC) VSM expression decreased in both DM and IDM groups and did not correlate with vasorelaxation. Phosphorylation of MLC and myosin phosphatase increased in the DM group and MLC phosphorylation strongly correlated with impaired VSM relaxation (r=0.670, P<0.01). Coronary microvessels from type 2 diabetic human patients exhibited similarly impaired vasodilation and enhanced VSM MLC phosphorylation.

Conclusions: Impaired vasodilation in type 1 diabetes correlates with enhanced VSM MLC phosphorylation. In addition, enhanced VSM MLC phosphorylation is associated with impaired vasodilation in type 2 diabetes in humans.

Citing Articles

Mechanisms and clinical implications of endothelium-dependent vasomotor dysfunction in coronary microvasculature.

Sabe S, Feng J, Sellke F, Abid M Am J Physiol Heart Circ Physiol. 2022; 322(5):H819-H841.

PMID: 35333122 PMC: 9018047. DOI: 10.1152/ajpheart.00603.2021.


Myocardial Blood Flow Control by Oxygen Sensing Vascular Kvβ Proteins.

Ohanyan V, Raph S, Dwenger M, Hu X, Pucci T, Mack G Circ Res. 2021; 128(6):738-751.

PMID: 33499656 PMC: 8486354. DOI: 10.1161/CIRCRESAHA.120.317715.


The Altered Signaling on EFS-Induced Colon Contractility in Diabetic Rats.

Thein W, Po W, Kim D, Sohn U Biomol Ther (Seoul). 2020; 28(4):328-336.

PMID: 32126734 PMC: 7327146. DOI: 10.4062/biomolther.2019.181.


Comparison of cerebral and cutaneous microvascular dysfunction with the development of type 1 diabetes.

Feng W, Liu S, Zhang C, Xia Q, Yu T, Zhu D Theranostics. 2019; 9(20):5854-5868.

PMID: 31534524 PMC: 6735377. DOI: 10.7150/thno.33738.


Ethanol promotes arteriogenesis and restores perfusion to chronically ischemic myocardium.

Lassaletta A, Elmadhun N, Liu Y, Feng J, Burgess T, Karlson N Circulation. 2013; 128(11 Suppl 1):S136-43.

PMID: 24030397 PMC: 3983870. DOI: 10.1161/CIRCULATIONAHA.112.000207.


References
1.
Lee J, Ragolia L . AKT phosphorylation is essential for insulin-induced relaxation of rat vascular smooth muscle cells. Am J Physiol Cell Physiol. 2006; 291(6):C1355-65. PMC: 1636679. DOI: 10.1152/ajpcell.00125.2006. View

2.
Amano M, Ito M, Kimura K, Fukata Y, Chihara K, Nakano T . Phosphorylation and activation of myosin by Rho-associated kinase (Rho-kinase). J Biol Chem. 1996; 271(34):20246-9. DOI: 10.1074/jbc.271.34.20246. View

3.
Kimura K, Ito M, Amano M, Chihara K, Fukata Y, Nakafuku M . Regulation of myosin phosphatase by Rho and Rho-associated kinase (Rho-kinase). Science. 1996; 273(5272):245-8. DOI: 10.1126/science.273.5272.245. View

4.
Munzel T, Daiber A, Ullrich V, Mulsch A . Vascular consequences of endothelial nitric oxide synthase uncoupling for the activity and expression of the soluble guanylyl cyclase and the cGMP-dependent protein kinase. Arterioscler Thromb Vasc Biol. 2005; 25(8):1551-7. DOI: 10.1161/01.ATV.0000168896.64927.bb. View

5.
Browner N, Dey N, Bloch K, Lincoln T . Regulation of cGMP-dependent protein kinase expression by soluble guanylyl cyclase in vascular smooth muscle cells. J Biol Chem. 2004; 279(45):46631-6. DOI: 10.1074/jbc.M408518200. View