Influence of maternal redox status on birth weight

Reproductive Toxicology

Volumn 31, Issue 1, 2011, Pages 35-40

  Osorio, Jesús Corría ^a,b   Cruz, Elio ^b   Milanés, María ^b   Ramírez, Yaila ^b,c   Sierra, Mercedes ^b   Cruz, Margarita ^d   Sanfiel, Loida ^b  

^a National Center of Medical Genetics   (Cuba)

^b Bayamo Medical School   (Cuba)

^c Carlos Manuel de Céspedes Hospital   (Cuba)

^d Epidemiology Center   (Cuba)

Author keywords

Antioxidant status; Birth weight; Oxidant status; Pregnant women

Indexed keywords

ALPHA TOCOPHEROL; ASCORBIC ACID; CAROTENOID; EXTRACELLULAR SUPEROXIDE DISMUTASE; GLUTATHIONE; MALONALDEHYDE; THIAMINE; TRACE ELEMENT;

ADULT; ARTICLE; BIRTH WEIGHT; CLINICAL ARTICLE; ENZYME ACTIVITY; FEMALE; FETUS DEVELOPMENT; GESTATIONAL AGE; HUMAN; LIPID PEROXIDATION; NORMAL HUMAN; NUTRIENT UPTAKE; OXIDATION REDUCTION STATE; OXIDATIVE STRESS; PREGNANCY OUTCOME; PROTEIN BLOOD LEVEL; PROTEIN PROTEIN INTERACTION; VITAMIN INTAKE;

ADULT; ANTIOXIDANTS; BIRTH WEIGHT; ERYTHROCYTES; FEMALE; FERRIC COMPOUNDS; GLUTATHIONE; HUMANS; MALONDIALDEHYDE; OXIDATION-REDUCTION; OXIDATIVE STRESS; PREGNANCY; PREGNANCY TRIMESTER, THIRD; SUPEROXIDE DISMUTASE;

EID: 79551597495     PISSN: 08906238     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.reprotox.2010.09.011     Document Type: Article

References (48)

1. Chamberlin R.W. Preventing low birth weight, child abuse, and school failure: the need for comprehensive, community-wide approaches. Pediatr Rev 1992, 13:64-71.
2. Colton T., Kayne H.L., Zhang Y., Heeren T. A metaanalysis of home uterine activity monitoring. Am J Obstet Gynecol 1995, 173:1499-1505.
3. Luo Z.C., Fraser W.D., Julien P., Deal C.L., Audibert F., Smith G.N., et al. Tracing the origins of " fetal origins" of adult diseases: Programming by oxidative stress?. Med Hypotheses 2006, 66:38-44.
4. Pacora P., Buzzio Y., Ingar W., Santibáñez A. El peso del recién nacido sano según edad gestacional en una población de Lima. An Fac Med 2005, 66(3):212-217.
5. Montoya-Restrepo N., Correa-Morales J. Curvas de Peso al Nacer. Rev Salud Pública 2007, 9(1):1-10.
6. Albaigés G. Frontera entre feto pequeño para edad gestacional y restricción de crecimiento intrauterino. Ginecol Obstet Clín 2004, 5(1):8-21.
7. Largo R.H., Wailli R., Duc G., Fanconi A., Prader A. Evaluation of perinatal growth. Helv Pedaitr Acta 1980, 35:419-436.
8. Gairdner D., Pearson J. A growth chart for premature and other infants. Arch Dis Child 1971, 46:783-787.
9. Malvehy J., Fontán F., Iglesias J. Relación entre el peso de nacimiento y la edad de gestación en una población de recién nacidos del Hospital Maternal Valle de Hebrón. An Esp Pediatr 1988, 28:497-502.
10. Niklasson A., Ericson A., Fryer J.G., Karlberg J., Lawrence C., Karlberg P. An update of the Swedish reference standars for weight, length and head circumference at birth for given gestational age. Acta Paediatr Scand 1991, 80:756-762.
11. Gupta P., Narang M., Banerjee B.D., Basu S. Oxidative stress in term small for gestational age neonates born to undernourished mothers: a case control study. BMC Pediatrics 2004, 4:14.
12. Min J., Park H., Park B., Kim Y.J., Park J., Lee H., et al. Paraoxonase gene polymorphism and vitamin levels during pregnancy: relationship with maternal oxidative stress and neonatal birth weights. Reprod Toxicol 2006, 22:418-424.
13. Young-Ju K., Yun-Chul H., Kwan-Hee L., Heon J.P., Eun A.E., Hye-Sung M., et al. Oxidative stress in pregnant women and birth weight reduction. Reprod Toxicol 2005, 19:487-492.
14. Karowicz-Bilinska A., Kedziora-Kornatowska K., Bartosz G. Indices of oxidative stress in pregnancy with fetal growth restriction. Free Radic Res 2007, 41(8):870-873.
15. Ochoa J.J., Contreras-Chova F., Muñoz S., Araujo-Nepomuceno E., Bonillo A., Molina-Carballo A., et al. Fluidity and oxidative stress in erythrocytes from very low birth weight infants during their first 7 days of life. Free Radic Res 2007, 41(9):1035-1040.
16. Zadrozna M., Gawlik M., Nowak B., Marcinek A., Mrowiec H., Walas S., et al. Antioxidants activities and concentration of selenium, zinc and copper in preterm and IUGR human placentae. J Trace Elem Med Biol 2009, 23(2):144-148.
17. Toy H., Camuzcuoglu H., Arioz D.T., Kurt S., Celik H., Aksoy N. Serum prolidase activity and oxidative stress markers in pregnancies with intrauterine growth restricted infants. J Obstet Gynaecol Res 2009, 35(December (6)):1047-1053.
18. Bosco C., Buffet C., Díaz E., Rodrigo R., Morales P., Barja P., et al. VEGF in the muscular layer of placental blood vessels: immuno-expression in preeclampsia and intrauterine growth restriction and its association with the antioxidant status. Cardiovasc Hematol Agents Med Chem 2010, 8(April (2)):87-95.
19. Saker M., Mokhtari N.S., Merzouk S.A., Merzouk H., Belarbi B., Narce M. Oxidant and antioxidant status in mothers and their newborns according to birth weight. Eur J Obstet Gynecol Reprod Biol 2008, 141:95-99.
20. FAO. CERES. Sistema automatizado para la evaluación del consumo de alimentos. FAO; 1997-2001.
21. Beutler E., Duron O., Nelly B. Improved methods for determination of blood glutathione. J Lab Clin Med 1963, 61:882-890.
22. Bahr P., Basulto Y. El Potencial Reductor Férrico (FRAP). Un ensayo para evaluar la capacidad antioxidante en suero. Rev Correo Científico Méd Holguín 2004, 8(4).
23. Yagi K. Assay for blood plasma or serum. Methods Enzymol 1984, 105:328-331.
24. Boehringer Mannheim. Biochemical Information. A revised biochemical reference sources Enzymes for routine, 1st ed. Germany: Boehringer Mannheim; 1987.
25. Schermelleh-Engel K., Moosbrugger H., Müller H. Evaluating the fit of Structural Equation Models: Tests of significance and descriptive goodness-of-fit measures. Methods Psychol Res 2003, 8(2):23-74. [Online].
26. Gicquel C., Le Bouc Y. Hormonal regulation of fetal growth. Horm Res 2006, 65(Suppl 3):28-33.
27. Murphy V.E., Smith R., Giles W.B., Clifton V.L. Endocrine regulation of human fetal growth: the role of mother, placenta, and fetus. Endocr Rev 2006, 27(2):141-169.
28. Setia S., Sridhar M. Changes in GH/IGF-1axis in intrauterine growth retardation: consequences of fetal programming. Horm Metab Res 2009, 41:791-798.
29. Delafontaine P., Ku L. Reactive oxygen species stimulate insulin-like growth factor I synthesis in vascular smooth muscle cells. Cardiovasc Res 1997, 33:216-222.
30. Roberts C.T., Owens J.A., Sferruzzi-Perri A.N. Distinct actions of insulin-like growth factors (IGFs) on placental development and fetal growth: lessons from mice and guinea pigs. Trophoblast Res 2008, 22:42-47. [Placenta 29, Supplement A].
31. Zhenyu Q., Krzysztof J.R., Tohru F., Neal L.W. Extracellular superoxide dismutase (ecSOD) in vascular biology: an update on exogenous gene transfer and endogenous regulators of ecSOD. Translational Res 2008, 151(2):68-78.
32. Fattman C.L., Schaefer L.M., Oury T.D. Extracellular superoxide dismutase in biology and medicine. Free Radic Biol Med 2003, 35(3):236-256.
33. Ottaviano F.G., Handy D.E., Loscalzo J.L. Redox regulation in the extracellular environment. Circ J 2008, 72:1-16.
34. Rosta K., Molvarec A., Enzsöly A., Nagy B., Rónai Z., Fekete A., et al. Association of extracellular superoxide dismutase (SOD3) Ala40Thr gene polymorphism with pre-eclampsia complicated by severe fetal growth restriction. Eur J Obstet Gynecol Reprod Biol 2009, 142(February (2)):134-138.
35. Tamai M., Furuta H., Kawashima H., Doi A., Hamanishi T., Shimomura H., et al. Extracellular superoxide dismutase gene polymorphism is associated with insulin resistance and the susceptibility to type 2 diabetes. Diabetes Res Clin Pract 2006, 71(February (2)):140-145.
36. Miao L., St.Clair D. Regulation of superoxide dismutase genes: implications in diseases. Free Radic Biol Med 2009, 47(August (4)):344-356.
37. Shane R.T., Paul K.W., Grant R.D. Redox control of endothelial function and dysfunction: molecular mechanisms and therapeutic opportunities. Antioxid Redox Signal 2008, 10(10):1713-1765.
38. Bakker S.J., Maaten J.C., Gans R.O. Thiamine supplementation to prevent induction of low birth weight by conventional therapy for gestacional diabetes mellitus. Med Hypotheses 2000, 55(1):88-90.
39. Fang Y.Z., Yang S.W.G. Free radicals, antioxidants and nutrition. Nutrition 2002, 18:872-879.
40. Ornoy A., Avgil Tsadok M., Yaffe P., Zangen W.S. The Cohen diabetic rat as a model for fetal growth restriction: vitamins C and E reduce fetal oxidative stress but do not restore normal growth. Reprod Toxicol 2009, 28:521-529.
41. Jones M.L., Mark P.J., Lewis J.L., Mori T.A., Keelan J.A., Waddell B.J Antioxidant defenses in the rat placenta in late gestation: increased labyrinthine expression of superoxide dismutases, glutathione peroxidase 3, and uncoupling protein 2. Biol Reprod 2010, 83(2):254-260.
42. Al-Gubory K., Fowler P., Garrel C. The roles of cellular reactive oxygen species, oxidative stress and antioxidants in pregnancy outcomes. Int J Biochem Cell Biol 2010, 42(10):1634-1650.
43. Biri A., Bozkurt N., Turp A., Kavutcu M., Himmetoglu O., Durak I. Role of oxidative stress in intrauterine growth restriction. Gynecol Obstet Invest 2007, 64(4):187-192.
44. Buonocore G., Perrone S. Biomarkers of oxidative stress in the fetus and newborn. Hematology 2006, 2:103-107.
45. Young A.J., Lowe G.M. Antioxidant and Prooxidant properties of carotenoids. Arch Biochem Biophys 2001, 385(1):20-27.
46. Wang Y., Walsh S.W. Antioxidant activities and mRNA expression of superoxide dismutase, catalase, and glutathione peroxidase in normal and preeclamptic placentae. J Soc Gynecol Invest 1996, 3:179-184.
47. Djuric Z., Ren J., Mekhovich O., Venkatranamoorthy R., Heilbrun L.K. Effects of high fruit-vegetable and/or low-fat intervention on plasma micronutrient levels. J Am Coll Nutr 2006, 25:178-187.
48. Polidori M.C., Carrillo J.C., Verde P.E., Sies H., Siegrist J., Stahl W. Plasma micronutrient status is improved after a 3-month dietary intervention with 5 daily portions of fruits and vegetables: implications for optimal antioxidant levels. Nutr J 2009, 8:10-13.