Oxidative stress programming in a rat model of postnatal early overnutrition - role of insulin resistance

Journal of Nutritional Biochemistry

Volumn 24, Issue 1, 2013, Pages 81-87

  Conceição, Ellen P S ^a   Franco, Juliana G ^a   Oliveira, Elaine ^a   Resende, Angela C ^a   Amaral, Taline A S ^a   Peixoto Silva, Nayara ^a   Passos, Magna C F ^a   Moura, Egberto G ^a   Lisboa, Patrícia C ^a  

^a STATE UNIVERSITY OF RIO DE JANEIRO   (Brazil)

Author keywords

Insulin signaling; Reactive oxygen species; Small litter

Indexed keywords

CATALASE; FAT DROPLET; GLUTATHIONE PEROXIDASE; INSULIN; MALONALDEHYDE; PHOSPHATIDYLINOSITOL 3 KINASE; SUPEROXIDE DISMUTASE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BIOAVAILABILITY; BODY WEIGHT; CONTROLLED STUDY; ENZYME ACTIVITY; FEMALE; FOOD INTAKE; HYPERPHAGIA; INFLAMMATORY CELL; INSULIN RESISTANCE; INTRAABDOMINAL FAT; LIVER HISTOLOGY; LIVER INJURY; MALE; NEWBORN; NONHUMAN; OVERNUTRITION; OXIDATIVE STRESS; PERINATAL PERIOD; RAT;

ANIMALS; ANIMALS, NEWBORN; BODY WEIGHT; CATALASE; EATING; FEMALE; GLUTATHIONE PEROXIDASE; INSULIN; INSULIN RESISTANCE; INTRA-ABDOMINAL FAT; LITTER SIZE; LIVER; NITRITES; OVERNUTRITION; OXIDATIVE STRESS; PROTO-ONCOGENE PROTEINS C-AKT; RATS; RATS, WISTAR; SUPEROXIDE DISMUTASE;

ANIMALIA; RATTUS;

EID: 84870455641     PISSN: 09552863     EISSN: 18734847     Source Type: Journal    
DOI: 10.1016/j.jnutbio.2012.02.010     Document Type: Article

References (55)

1. de Onis M., Blössner M., Borghi E. Global prevalence and trends of overweight and obesity among preschool children. Am J Clin Nutr 2010, 92:1257-1264.
2. Lucas A. Role of nutritional programming in determining adult morbidity. Arch Dis Child 1994, 71:288-290.
3. Barker D.J. The developmental origins of adult disease. J Am Coll Nutr 2004, 23:588-595.
4. de Moura E.G., Lisboa P.C., Passos M.C. Neonatal programming of neuroimmunomodulation - role of adipocytokines and neuropeptides. Neuroimmunomodulation 2008, 15:176-188.
5. Dörner G., Hagen N., Witthuhn W. Early postnatal overfeeding as an etiopathogenetic factor in adult obesity. Acta Biol Med Ger 1976, 35:799-803.
6. Rodrigues A.L., de Moura E.G., Passos M.C., Dutra S.C., Lisboa P.C. Postnatal early overnutrition changes the leptin signaling pathway in the hypothalamic-pituitary-thyroid axis of young and adult rats. J Physiol 2009, 587:2647-2661.
7. Rodrigues A.L., de Moura E.G., Passos M.C., Trevenzoli I.H., da Conceição E.P., Bonono I.T., et al. Postnatal early overfeeding induces hypothalamic higher SOCS3 expression and lower STAT3 activity in adult rats. J Nutr Biochem 2011, 22:109-117.
8. Risnes K.R., Vatten L.J., Baker J.L., Jameson K., Sovio U., Kajantie E., et al. Birthweight and mortality in adulthood: a systematic review and meta-analysis. Int J Epidemiol 2011, 10.1093/ije/dyq267.
9. Plagemann A., Roepke K., Harder T., Brunn M., Harder A., Wittrock-Staar M., et al. Epigenetic malprogramming of the insulin receptor promoter due to developmental overfeeding. J Perinat Med 2010, 38:393-400.
10. You S., Gotz F., Rohde W., Dorner G. Early postnatal overfeeding and diabetes susceptibility. Exp Clin Endocrinol 1990, 96:301-306.
11. Plagemann A., Heidrich I., Götz F., Rohde W., Dörner G. Obesity and enhanced diabetes and cardiovascular risk in adult rats due to early postnatal overfeeding. Exp Clin Endocrinol 1992, 99:154-158.
12. Boullu-Ciocca S., Dutour A., Guillaume V., Achard V., Oliver C., Grino M. Postnatal diet-induced obesity in rats upregulates systemic and adipose tissue glucocorticoid metabolism during development and in adulthood: its relationship with the metabolic syndrome. Diabetes 2005, 54:197-203.
13. Davidowa H., Plagemann A. Hypothalamic neurons of postnatally overfed, overweight rats respond differentially to corticotropin-releasing hormones. Neurosci Lett 2004, 371:64-68.
14. Rodrigues A.L., De Souza E.P., da Silva S.V., Rodrigues D.S., Nascimento A.B., Barja-Fidalgo C., et al. Low expression of insulin signaling molecules impairs glucose uptake in adipocytes after early overnutrition. J Endocrinol 2007, 195:485-494.
15. Chang Y.C., Chuang L.M. The role of oxidative stress in the pathogenesis of type 2 diabetes: from molecular mechanism to clinical implication. Am J Transl Res. 2010, 2:316-331.
16. Archuleta T.L., Lemieux A.M., Saengsirisuwan V., Teachey M.K., Lindborg K.A., Kim J.S., et al. Oxidant stress-induced loss of IRS-1 and IRS-2 proteins in rat skeletal muscle: role of p38 MAPK. Free Radic Biol Med 2009, 47:1486-1493.
17. Marques R.G., Morales M.M., Petroianu A. Brazilian law for scientific use of animals. Acta Cir Bras 2009, 24:69-74.
18. Drummond G.B. Reporting ethical matters in The Journal of Physiology: standards and advice. J Physiol 2009, 587:713-719.
19. Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976, 72:248-254.
20. Bannister J.V., Calabrese L. Assays for superoxide dismutase. Methods Biochem Anal 1987, 32:279-312.
21. Aebi H. Catalase in vitro. Methods Enzymol. 1984, 105:121-126.
22. Flohé L., Günzler W.A. Assays of glutathione peroxidase. Methods Enzymol 1984, 105:114-121.
23. Valença S.S., Pimenta W.A., Rueff-Barroso C.R., Ferreira T.S., Resende A.C., Moura R.S., et al. Involvement of nitric oxide in acute lung inflammation induced by cigarette smoke in the mouse. Nitric Oxide. 2009, 20:175-181.
24. Franco J.G., de Moura E.G., Koury J.C., Trotta P.A., Cordeiro A., Souza L.L., et al. S, Pazos-Moura CC, Lisboa PC, Passos MC. Resveratrol reduces lipid peroxidation and increases sirtuin 1 expression in adult animals programmed by neonatal protein restriction. J Endocrinol 2010, 207:319-328.
25. de Oliveira P.R., da Costa C.A., de Bem G.F. Marins de Cavalho LC, de Sousa MA, de Lemos Neto M, da Cunha Sousa PJ, de Moura RS, Resende AC. Effects of an extract obtained from fruits of Euterpe Oleracea Mart in the components of metabolic syndrome induced in C57BL/6J mice fed a high-fat diet. J Cardiovasc Pharmacol 2010, 56:619-626.
26. Levine R.L., Garland D., Oliver C.N., Amici A., Climent I., Lenz A.G., et al. Determination of carbonyl content in oxidatively modified proteins. Methods Enzymol 1990, 186:464-478.
27. Velkoska E., Cole T.J., Morris M.J. Early dietary intervention: long-term effects on blood pressure, brain neuropeptide Y, and adiposity markers. Am J Physiol Endocrinol Metab 2005, 288:1236-1243.
28. Davidowa H., Plagemann A. Insulin resistance of hypothalamic arcuate neurons in neonatally overfed rats. Neuroreport 2007, 18:521-524.
29. Rudich A., Kanety H., Bashan N. Adipose stress-sensing kinases: linking obesity to malfunction. Trends Endocrinol Metab 2007, 18:291-299.
30. Paravicini T.M., Touyz R.M. NADPH oxidases, reactive oxygen species, and hypertension: clinical implications and therapeutic possibilities. Diabetes Care 2008, 31:170-180.
31. Rector R.S., Thyfault J.P., Uptergrove G.M., Morris E.M., Naples S.P., Borengasser S.J., et al. Mitochondrial dysfunction precedes insulin resistance and hepatic steatosis and contributes to the natural history of non-alcoholic fatty liver disease in an obese rodent model. J Hepatol 2010, 52:727-736.
32. Goldstein S., Merényi G. The chemistry of peroxynitrite: implications for biological activity. Methods Enzymol 2008, 436:49-61.
33. Kohen R., Nyska A. Oxidation of biological systems: oxidative stress phenomena, antioxidants, redox reactions, and methods for their quantification. Toxicol Pathol 2002, 30:620-650.
34. Gryglewski R.J., Palmer R.M., Moncada S. Superoxide anion is involved in the breakdown of endothelium-derived vascular relaxing factor. Nature 1986, 320:454-456.
35. Tabit C.E., Chung W.B., Hamburg N.M., Vita J.A. Endothelial dysfunction in diabetes mellitus: molecular mechanisms and clinical implications. Rev Endocr Metab Disord 2010, 11:61-74.
36. Hirosumi J., Tuncman G., Chang L., Görgün C.Z., Uysal K.T., Maeda K., et al. A central role for JNK in obesity and insulin resistance. Nature 2002, 420:333-336.
37. Martins M.R., Vieira A.K.G., de Souza E.P.G., Moura A.S. Early overnutrition impaired insulin signaling in the heart of adult Swiss mice. J Endocrinol 2008, 198:591-598.
38. Cunha A.C., Pereira R.O., Pereira M.J. Soares Vde M, Martins MR, Teixeira MT, Souza EP, Moura AS. Long-term effects of overfeeding during lactation on insulin secretion - the role of GLUT-2. J Nutr Biochem 2009, 20:435-442.
39. Kmiec Z. Aging and peptide control of food intake. Curr Protein Pept Sci 2011, 12(4):271-279.
40. Rossi A.P., Watson N.L., Newman A.B., Harris T.B., Kritchevsky S.B., Bauer D.C., et al. Effects of body composition and adipose tissue distribution on respiratory function in elderly men and women: the health, aging, and body composition study. J Gerontol A Biol Sci Med Sci 2011, 66(7):801-808.
41. Garg A. Regional adiposity and insulin resistance. J Clin Endocrinol Metab 2004, 89:4206-4210.
42. Savage D.B., Petersen K.F., Shulman G.I. Disordered lipid metabolism and the pathogenesis of insulin resistance. Physiol Rev 2007, 87:507-520.
43. Meshkani R., Adeli K. Hepatic insulin resistance, metabolic syndrome and cardiovascular disease. Clin Biochem 2009, 42:1331-1346.
44. Fan J.G., Farrell G.C. VAT fat is bad for the liver, SAT fat is not!. J Gastroenterol Hepatol 2008, 23:829-832.
45. Popa C., Riel P.L.C.M., Meer W.M., Stalenhoef A.F.H. The role of TNF-α in chronic inflammatory conditions, intermediary metabolism, and cardiovascular risk. J Lipid Res 2007, 48:751-762.
46. Nonogaki K., Fuller G.M., Fuentes N.L., Moser A.H., Staprans I., Grunfeld C., et al. Interleukin-6 stimulates hepatic triglyceride secretion in rats. Endocrinology 1995, 136:2143-2149.
47. Kroder G., Bossenmaier B., Kellerer M., Capp E., Stoyanov B., Mühlhöfer A., et al. Tumor necrosis factor-alpha- and hyperglycemia-induced insulin resistance. Evidence for different mechanisms and different effects on insulin signalling. J Clin Invest 1996, 97:1471-1477.
48. Mooney R.A., Senn J., Cameron S., Inamdar N., Boivin L.M., Shang Y., et al. Suppressors of cytokine signalling-1 and 6 associate with and inhibit the insulin receptor. A potential mechanism for cytokine-mediated insulin resistance. J Biol Chem 2001, 276:25889-25893.
49. Kathirvel E., Morgan K., French S.W., Morgan T.R. Overexpression of liver-specific cytochrome P4502E1 impairs hepatic insulin signaling in a transgenic mouse model of nonalcoholic fatty liver disease. Eur J Gastroenterol Hepatol 2009, 21:973-983.
50. Rolo A.P., Teodoro J.S., Palmeira C.M. Role of oxidative stress in the pathogenesis of nonalcoholic steatohepatitis. Free Radic Biol Med 2011, [Epub ahead of print].
51. Wong M.C., Portmann B., Sherwood R., Niemela O., Koivisto H., Parkkila S., et al. The cytoprotective effect of a-tocopherol and daidzein against d-galactosamine induced oxidative damage in the rat liver. Metabolism Clinical and Experimental. 2007, 56:865-875.
52. Pooranaperundevi M., Sumiyabanu M.S., Viswanathan P., Sundarapandiyan R., Anuradha C.V. Insulin resistance induced by a high-fructose diet potentiates thioacetamide hepatotoxicity. Singapore Med J 2010, 51(5):389-398.
53. Huo H.Z., Wang B., Liang Y.K., Bao Y.Y., Gu Y. Hepatoprotective and antioxidant effects of licorice extract against CCl4-induced oxidative damage in rats. Int J Mol Sci 2011, 12:6529-6543.
54. Jiang M., Zhang Y., Liu M., Lan M.S., Fei J., Fan W., et al. Hypermethylation of hepatic glucokinase and L-type pyruvate kinase promoters in high-fat diet-induced obese rats. Endocrinology 2011, 152(4):1284-1289.
55. Sookoian S., Rosselli M.S., Gemma C., Burgueño A.L., Fernández Gianotti T., Castaño G.O., et al. Epigenetic regulation of insulin resistance in nonalcoholic fatty liver disease: impact of liver methylation of the peroxisome proliferator-activated receptor γ coactivator 1α promoter. Hepatology 2010, 52(6):1992-2000.