The long range goal of my research program is to elucidate the pathogenesis of the late complications of diabetes. Several lines of evidence indicate that many, if not all, of the metabolic imbalances currently linked to early vascular and neural complications of diabetes either contribute to or are the consequence of glucose-induced metabolic hypoxia (""""""""hyperglycemic hypoxia""""""""), i.e., an increase in the ratio of NADH/NAD+ despite normal tissue p02. Previous studies have established that increased oxidation of sorbitol to fructose, which is coupled to reduction of NAD+ to NADH, is associated with an increased ratio of lactate/pyruvate (a reliable parameter of the cytosolic ratio of NADH/NAD+) and increased blood flow and vascular permeability. These redox changes and vascular dysfunction are similar to corresponding changes in ischemic/hypoxic myocardium and to redox and vascular changes associated with cyanide poisoning. Several lines of evidence support the hypothesis that these redox changes may initiate increased synthesis of nitric oxide (NO), a potent vasodilator, which could mediate the vascular dysfunction associated with all three of these conditions.
The specific aims of the experiments outlined in this proposal are to: (1) elucidate the role of increased NO production the pathogenesis of diabetic complications, (2) assess the effects of aminoguanidine, a newly discovered novel inhibitor of NO synthase, on metabolism of glucose via glycolysis and the sorbitol pathway, and (3) investigate the effects of elevated glucose levels and sorbitol pathway metabolism on NO synthesis from L-arginine. No synthase activity in cell free extracts and in tissues incubated in vitro will be monitored by the conversion of L- [guanidino14 C]-arginine to L-citrulline, measurement of cGMP levels, and measurement of NO2 (an oxidation product of NO). The potential significance of this research is that the insights it may provide regarding the pathogenesis of late complications of diabetes may contribute to the development of new approaches for the prevention and treatment of diabetic complications.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL039934-07
Application #
2219456
Study Section
Metabolism Study Section (MET)
Project Start
1988-03-01
Project End
1997-02-28
Budget Start
1994-03-01
Budget End
1995-02-28
Support Year
7
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Washington University
Department
Pathology
Type
Schools of Medicine
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
Ido, Yasuo; Nyengaard, Jens R; Chang, Kathy et al. (2010) Early neural and vascular dysfunctions in diabetic rats are largely sequelae of increased sorbitol oxidation. Antioxid Redox Signal 12:39-51
Shao, Baohai; Fu, Xiaoyun; McDonald, Thomas O et al. (2005) Acrolein impairs ATP binding cassette transporter A1-dependent cholesterol export from cells through site-specific modification of apolipoprotein A-I. J Biol Chem 280:36386-96
Pennathur, Subramaniam; Ido, Yasuo; Heller, Jozsef I et al. (2005) Reactive carbonyls and polyunsaturated fatty acids produce a hydroxyl radical-like species: a potential pathway for oxidative damage of retinal proteins in diabetes. J Biol Chem 280:22706-14
Ido, Yasuo; Chang, Katherine; Williamson, Joseph R (2004) NADH augments blood flow in physiologically activated retina and visual cortex. Proc Natl Acad Sci U S A 101:653-8
Nyengaard, Jens R; Ido, Yassuo; Kilo, Charles et al. (2004) Interactions between hyperglycemia and hypoxia: implications for diabetic retinopathy. Diabetes 53:2931-8
Ido, Y; Chang, K C; Lejeune, W S et al. (2001) Vascular dysfunction induced by AGE is mediated by VEGF via mechanisms involving reactive oxygen species, guanylate cyclase, and protein kinase C. Microcirculation 8:251-63
Schmidt, R E; Dorsey, D A; Beaudet, L N et al. (2001) Inhibition of sorbitol dehydrogenase exacerbates autonomic neuropathy in rats with streptozotocin-induced diabetes. J Neuropathol Exp Neurol 60:1153-69
Tilton, R G; Chang, K C; LeJeune, W S et al. (1999) Role for nitric oxide in the hyperpermeability and hemodynamic changes induced by intravenous VEGF. Invest Ophthalmol Vis Sci 40:689-96
Stephan, C C; Chang, K C; LeJeune, W et al. (1998) Role for heparin-binding growth factors in glucose-induced vascular dysfunction. Diabetes 47:1771-8
Ido, Y; Vindigni, A; Chang, K et al. (1997) Prevention of vascular and neural dysfunction in diabetic rats by C-peptide. Science 277:563-6

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