Exercise training enhanced myocardial endothelial nitric oxide synthase (eNOS) function in diabetic Goto-Kakizaki (GK) rats
Open Access
- 19 November 2008
- journal article
- Published by Springer Nature in Cardiovascular Diabetology
- Vol. 7 (1) , 34
Abstract
Background: Different mechanisms of diabetic-induced NO dysfunction have been proposed and central to most of them are significant changes in eNOS function as the rate-limiting step in NO bioavailability. eNOS exists in both monomeric and dimeric conformations, with the dimeric form catalyzing the synthesis of nitric oxide, while the monomeric form catalyzes the synthesis of superoxide (O2 -). Diabetic-induced shifts to decrease the dimer:monomer ratio is thought to contribute to the degradation of nitric oxide (NO) bioavailability. Exercise has long been useful in the management of diabetes. Although exercise-induced increases expression of eNOS has been reported, it is unclear if exercise may alter the functional coupling of eNOS. Methods: To investigate this question, Goto-Kakizaki rats (a model of type II diabetes) were randomly assigned to a 9-week running program (train) or sedentary (sed) groups. Results: Exercise training significantly (p < .05) increased plantaris muscle cytochrome oxidase, significantly improved glycosylated hemoglobin (sed: 7.33 ± 0.56%; train: 6.1 ± 0.18%), ad improved insulin sensitivity. Exercise increased both total eNOS expression and the dimer:monomer ratio in the left ventricle LV (sed: 11.7 ± 3.2%; train: 41.4 ± 4.7%). Functional analysis of eNOS indicated that exercise induced significant increases in nitric oxide (+28%) production and concomitant decreases in eNOS-dependent superoxide (-12%) production. This effect was observed in the absence of tetrahydrobiopterin (BH4), but not in the presence of exogenous BH4. Exercise training also significantly decreased NADPH-dependent O2 - activity. Conclusion: Exercise-induced increased eNOS dimerization resulted in an increased coupling of the enzyme to facilitate production of NO at the expense of ROS generation. This shift that could serve to decrease diabetic-related oxidative stress, which should serve to lessen diabetic-related complications.Keywords
This publication has 68 references indexed in Scilit:
- Apocynin Is Not an Inhibitor of Vascular NADPH Oxidases but an AntioxidantHypertension, 2008
- A negative feedback mechanism involving nitric oxide and nuclear factor kappa-B modulates endothelial nitric oxide synthase transcriptionJournal of Molecular and Cellular Cardiology, 2005
- The effect of high glucose on NO and O2− through endothelial GTPCH1 and NADPH oxidaseLife Sciences, 2004
- Plasma aldosterone concentration in the patient with diabetes mellitus Rapid CommunicationKidney International, 2004
- Increased Superoxide Production in Coronary Arteries in HyperhomocysteinemiaArteriosclerosis, Thrombosis, and Vascular Biology, 2003
- Lack of Nitric Oxide Mediation of Flow-Dependent Arteriolar Dilation in Type I Diabetes Is Restored by SepiapterinJournal of Vascular Research, 2003
- Impaired glucose tolerance and insulinopenia in the GK‐rat causes peripheral neuropathyDiabetes/Metabolism Research and Reviews, 2002
- Subcellular Targeting and Agonist-induced Site-specific Phosphorylation of Endothelial Nitric-oxide SynthaseJournal of Biological Chemistry, 2002
- Acylation Targets Endothelial Nitric-oxide Synthase to Plasmalemmal CaveolaeJournal of Biological Chemistry, 1996
- Diabetic control and the renin-angiotensin system, catecholamines, and blood pressure.Hypertension, 1985