Superoxide dismutase overexpression and cellular oxidative damage in diabetes. A commentary on "Overexpression of mitochondrial superoxide dismutase in mice protects the retina from diabetes-induced oxidative stress"

Free Radical Biology and Medicine

Volumn 41, Issue 8, 2006, Pages 1187-1190

  Jain, Sushil K ^a  

^a Louisiana State University School of Medicine Shreveport   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

SUPEROXIDE DISMUTASE;

ARTICLE; CELL METABOLISM; DIABETES MELLITUS; DISEASE ASSOCIATION; DISEASE COURSE; HUMAN; MORBIDITY; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN EXPRESSION; RETINOPATHY; RISK ASSESSMENT; RISK FACTOR; SIGNAL TRANSDUCTION; STATISTICAL SIGNIFICANCE;

EID: 33749075946     PISSN: 08915849     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.freeradbiomed.2006.07.017     Document Type: Note

References (41)

1. The Diabetes Control and Complications Trial Research Group. The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. N. Engl. J. Med. 329 (1993) 977-986
2. Lyons T.J., Jenkins A.J., Zheng D., Lackland D.T., McGee D., Garvey W.T., and Klein R.L. DCCT/EDIC Research Group. Diabetic retinopathy and serum lipoprotein subclasses in the DCCT/EDIC cohort. Invest. Ophthalmol. Visual Sci. 45 (2004) 910-918
3. 1c) to the risk of development and progression of retinopathy in the Diabetes Control and Complications Trial. Diabetes 44 (2005) 968-983
4. Giugliano D., Ceriollo A., and Paolisso G. Oxidative stress and diabetic vascular complications. Diabetes Care 19 (1996) 257-267
5. Brownlee M. Biochemistry and molecular cell biology of diabetic complications. Nature 414 (2001) 813-820
6. Kuroki T., Isshiki K., and King G.L. Oxidative stress: the lead or supporting actor in the pathogenesis of diabetic complications. J. Am. Soc. Nephrol. 14 (2003) S216-S220
7. Jain S.K., McVie R., Duett J., and Herbst J.J. Erythrocyte membrane lipid peroxidation and glycosylated hemoglobin in diabetes. Diabetes 38 (1989) 1539-1543
8. Dominguez C., Rutz E., Gussinye M., and Carrascosa A. Oxidative stress at onset and in early stages of type 1 diabetes in children and adolescents. Diabetes Care 21 (1998) 1736-1742
9. Santini S.A., Marra G., Giardina B., Cotroneo P., Mordente A., Martorana G.E., Manto A., and Ghirlanda G. Defective plasma antioxidant defences and enhanced susceptibility to lipid peroxidation in uncomplicated IDDM. Diabetes 46 (1997) 1853-1858
10. Laaksonen D.E., Atalay M., Niskanen L., Uusitupa M., Hanninen O., and Sen C.K. Increased resting and exercise-induced oxidative stress in young IDDM men. Diabetes Care 19 (1996) 569-574
11. Jain S.K. Hyperglycemia can cause membrane lipid peroxidation and osmotic fragility in human red blood cells. J. Biol. Chem. 264 (1989) 21340-21345
12. Rajeswari P., Natarajan R., Nadler J.L., and Kumar D. Glucose induces lipid peroxidation and inactivation of membrane associated iron transport enzymes in human erythrocytes in vivo and in vitro. J. Cell. Physiol. 149 (1991) 100-109
13. Jain S.K., Kannan K., and Lim G. Ketosis (acetoacetate) can generate oxygen radicals and cause increased lipid peroxidation and growth inhibition in human endothelial cells. Free Radical Biol. Med. 25 (1998) 1083-1088
14. Jain S.K., and McVie R. Hyperketonemia can increase lipid peroxidation and lower glutathione levels in human erythrocytes in vitro and in type 1 diabetic patients. Diabetes 48 (1999) 1850-1855
15. Jain S.K., McVie R., Jackson R., Levine S.N., and Lim G. Effect of hyperketonemia on lipid peroxidation levels of plasma in diabetic patients. Diabetes Care 22 (1999) 171-1175
16. Jain S.K., Kannan K., Lim G., Matthew-Greer J., McVie R., and Bocchini J.A. Elevated blood interleukin-6 levels in hyperketonemic type 1 diabetic patients and secretion by acetoacetate-treated cultured U937 monocytes. Diabetes Care 26 (2003) 2139-2143
17. Kitabchi A.E., Stentz F.B., and Umpierrez G.E. Diabetic ketoacidosis induces in vivo activation of human T-lymphocytes. Biochem. Biophys. Res. Commun. 315 (2004) 404-407
18. Abdelmegeed M.A., Kim S.K., Woodcroft K.J., and Novak R.F. Acetoacetate activation of extracellular signal-regulated kinase 1/2 and p38 mitogen-activated protein kinase in primary cultured rat hepatocytes: role of oxidative stress. J. Pharmacol. Exp. Ther. 310 (2004) 728-736
19. Jain S.K., McVie R., Jaramillo J.J., Palmer M., and Smith T. Effect of modest vitamin E supplementation on blood glycated hemoglobin and triglyceride levels and red cell indices in type-1 diabetic patients. J. Am. Coll. Nutr. 15 (1996) 458-461
20. Jain S.K., Krueger S.K., McVie R., Jaramillo J.J., Palmer M., and Smith T. Relationship of blood thromboxane-B2 with lipid peroxides and effect of vitamin E and placebo supplementation on TxB2 and lipid peroxide levels in type-1 diabetic patients. Diabetes Care 21 (1998) 1511-1516
21. Jain S.K., McVie R., and Smith T. Vitamin E supplementation restores glutathione and malondialdehyde to normal levels in red blood cells of type-1 diabetic children. Diabetes Care 23 (2000) 1389-1394
22. Fernandez-Robredo P., Moya D., Rodriquez J.A., and Garcia-Layana A. Vitamins C and E reduce retinal oxidative stress and nitric oxide metabolites and prevent ultrastructural alterations in porcine hypercholesterolemia. Invest. Ophthalmol. Visual Sci. 46 (2005) 1140-1146
23. Bursell S.E., Clermont A.C., Aiello L.P., Aiello L.M., Schlossman D.K., Feener E.P., Laffel L., and King G.L. High-dose vitamin E supplementation normalizes retinal blood flow and creatinine clearance in patients with type 1 diabetes. Diabetes Care 22 (1999) 1245-1251
24. Obrosova I.G., Minchenko A.G., Marinescu V., Fathallah L., Kennedy A., Stockert C.M., Frank R.N., and Stevens M.J. Antioxidants attenuate early up regulation of retinal vascular endothelial growth factor in streptozotocin-diabetic rats. Diabetologia 44 (2002) 1102-1110
25. Kowluru R.A., Tang J., and Kern T.S. Abnormalities of retinal metabolism in diabetes and experimental galactosemia: VII. Effect of long-term administration of antioxidants on the development of retinopathy. Diabetes 50 (2001) 1938-1942
26. Kowluru R.A., and Odenbach S. Effect of long-term administration of alpha lipoic acid on retinal capillary cell death and the development of retinopathy in diabetic rats. Diabetes 53 (2004) 3233-3238
27. Boveris A. Mitochondrial production of superoxide radical and hydrogen peroxide. Adv. Exp. Biol. Med. 78 (1977) 67-82
28. Stokes K.Y., Clanton E.C., Russell J.M., Ross C.R., and Granger D.N. NAD(P)H oxidase-derived superoxide mediates hypercholesterolemia-induced leukocyte-endothelial cell adhesion. Circ. Res. 88 (2001) 499-505
29. Singh U., Devaraj S.S., and Jialal I. Vitamin E, oxidative stress and inflammation. Annu. Rev. Nutr. 25 (2005) 151-174
30. Jain S.K. The neonatal erythrocyte and its oxidative susceptibility. Semin. Hematol. 26 (1989) 286-300
31. Beatty S., et al. The role of oxidative stress in the pathogenesis of age-related macular degeneration. Surv. Ophthalmol. 45 (2000) 115-134
32. Cingolani C., Rogers B., Lu L., Kachi S., Shen J., and Campochiaro P.A. Retinal degeneration from oxidative damage. Free Radical Biol. Med. 40 (2006) 660-669
33. Kowluru R.A. Diabetic retinopathy: mitochondrial dysfunction and retinal capillary cell death. Antioxid. Redox Signaling 7 (2005) 1581-1587
34. Kannan K., and Jain S.K. Oxidative stress and apoptosis. Pathophysiology 7 (2000) 153-163
35. Du Y., Miller C.M., and Kern T.S. Hyperglycemia increases mitochondrial superoxide in retina and retinal cells. Free Radical Biol. Med. 35 (2003) 1491-1499
36. Jain S.K. The accumulation of malonyldialdehyde, a product of fatty acid peroxidation, can disturb amino-phospholipid organization in the membrane bilayer of human erythrocytes. J. Biol. Chem. 259 (1984) 3391-3394
37. Jain S.K. In vivo externalization of phosphatidylserine and phosphatidylethanolamine in membrane bilayer and hypercoagulability by the lipid peroxidation of erythrocytes in rats. J. Clin. Invest. 76 (1985) 281-286
38. Kowluru, R. A.; Kowluru, V.; Xiong, Y.; Ho, Y. Overexpression of mitochondrial superoxide dismutase in mice protects the retina from diabetes-induced oxidative stress. Free Radical Biol. Med; 2006 (this issue). doi:10.1016/j.freeradbiomed.2006.01.012.
39. Niesman M.R., Johnson K.A., and Penn J.S. Therapeutic effect of liposomal superoxide dismutase in animal retinopathy of prematurity. Neurochem. Res. 22 (1997) 597-605
40. Matsubara A., Tamai K., Matsuda Y., Niwa Y., Morita H., Tomida K., Armstrong D., and Ogura Y. Protective effect of polyethylene glycol-superoxide dismutase on leukocyte dynamics in rat retinal microcirculation under lipid hydroperoxide-induced oxidative stress. Exp. Eye Res. 81 (2005) 193-199
41. Coppey L.J., Gellett J.S., Davidson E.P., Dunlap J.A., Lund D.D., Salvemini D., and Yorck M.A. Effect of M40403 treatment of diabetic rats on endoneurial blood flow, motor nerve conduction velocity and vascular function of epineurial arterioles of the sciatic nerve. Br. J. Pharmacol. 134 (2001) 21-29