Nutritional Status of Pregnant Mothers Influence the Health in Adult Life of their Children

Authors

  • E.M. Echarte Instituto de Investigaciones Biológicas, Universidad Nacional de Mar del Plata, Argentina
  • Abalo Rocío Instituto de Investigaciones Biológicas, Universidad Nacional de Mar del Plata, Argentina
  • A.N. Chisari Instituto de Investigaciones Biológicas, Universidad Nacional de Mar del Plata, Argentina

DOI:

https://doi.org/10.6000/1929-5634.2015.04.01.3

Keywords:

Fetal programming, Low protein diet, Metabolic syndrome, Liver damage, oxidative stress.

Abstract

Pregnancy and fetal development are periods of rapid growth and cell differentiation when mother and offspring are vulnerable to changes. Adverse events during development can be linked to an increased risk in developing metabolic diseases. Growth restriction in utero is associated with the development of obesity, hypertension, and diabetes. In these processes, the liver plays a fundamental role.

The aim of this work was to evaluate the effects of a low protein diet in pregnant and lactating mothers on the antioxidant status of the offspring liver. To reproduce real conditions, we used an experimental rat model.

Both ROS and the protective antioxidant systems have to work in coordination to reach a state of redox homeostasis. Excess generation of ROS may result in cell death or different pathological processes. The study also highlights the complex nature of malnutrition injury in which ROS correlates with the hepatic injury in a cause-and-effect manner.

The male offspring with intrauterine growth restriction (IUGR) caused by the isocaloric low-protein diet (8%) showed decreased liver and body weight at birth. Hepatic cholesterol levels and serum transaminase increase, at weaning (24 day of age).

We observed excess generation of ROS, carbonyl group and lipoperoxidation with that may result in cell death or different pathological processes in the liver.

Conclusion: This study would suggests that liver injury due to accelerated release of toxic oxygen species and impaired antioxidant status may contribute to the high susceptibility to suffer metabolic diseases, that are related to diet in early life and that manifest in adulthood.

Author Biography

A.N. Chisari, Instituto de Investigaciones Biológicas, Universidad Nacional de Mar del Plata, Argentina

Instituto de Investigaciones Biológicas

References

Gagnon R. Placental insufficiency and its consequences. Eur J Obstet Gynecol Reprod Biol 2003; 110(Suppl 1): S99-S107. http://dx.doi.org/10.1016/S0301-2115(03)00179-9

Pryor J. The identification and long term effects of fetal growth restriction. Br J Obstet Gynaecol 1997; 104: 1116-1122. http://dx.doi.org/10.1111/j.1471-0528.1997.tb10933.x

Ravelli AC, van Der Meulen JH, Osmond C, Barker DJ, Bleker OP. Obesity at the age of 50 y in men and women exposed to famine prenatally. Am J Clin Nutr 1999; 70: 811-816.

Leon DA, Johansson M, Rasmussen F. Gestational age and growth rate of fetal mass are inversely associated with systolic blood pressure in young adults: an epidemiologic study of 165,136 Swedish men aged 18 years. Am J Epidemiol 2000; 152: 597-604. http://dx.doi.org/10.1093/aje/152.7.597

Gluckman PD, Hanson MA, Pinal C. The developmental origins of adult disease. Matern Child Nutr 2005; 1: 130-141. http://dx.doi.org/10.1111/j.1740-8709.2005.00020.x

Simmons R. Perinatal programming of obesity. Semin Perinatol 2008; 32: 371-374. http://dx.doi.org/10.1053/j.semperi.2008.08.004

McMillen IC, Robinson JS. Developmental origins of the metabolic syndrome: prediction, plasticity, and programming. Physiol Rev 2005; 85: 571-633. http://dx.doi.org/10.1152/physrev.00053.2003

Eriksson JG. Epidemiology, genes and the environment: lessons learned from the Helsinki Birth Cohort Study. J Intern Med 2007; 261: 418-425. http://dx.doi.org/10.1111/j.1365-2796.2007.01798.x

Eriksson JG. Early growth and coronary heart disease and type 2 diabetes: findings from the Helsinki Birth Cohort Study (HBCS). Am J Clin Nutr 2011; 94: 1799S-1802S. http://dx.doi.org/10.3945/ajcn.110.000638

Langley-Evans SC. Developmental programming of health and disease. Proc Nutr Soc 2006; 65: 97-105. http://dx.doi.org/10.1079/PNS2005478

Langley-Evans SC, Bellinger L, McMullen S. Animal models of programming: early life influences on appetite and feeding behaviour. Matern Child Nutr 2005; 1: 142-148. http://dx.doi.org/10.1111/j.1740-8709.2005.00015.x

Warner MJ, Ozanne SE. Mechanisms involved in the developmental programming of adulthood disease. Biochem J 2010; 427: 333-347. http://dx.doi.org/10.1042/BJ20091861

Faienza MF, Brunetti G, Ventura A, et al. Nonalcoholic fatty liver disease in prepubertal children born small for gestational age: influence of rapid weight catch-up growth. Horm Res Paediatr 2013; 79: 103-109. http://dx.doi.org/10.1159/000347217

VandeHaar MJ, Moats-Staats BM, Davenport ML, et al. Reduced serum concentrations of insulin-like growth factor-I (IGF-I) in protein-restricted growing rats are accompanied by reduced IGF-I mRNA levels in liver and skeletal muscle. J Endocrinol 1991; 130: 305-312. http://dx.doi.org/10.1677/joe.0.1300305

Thorn SR, Regnault TR, Brown LD, et al. Intrauterine growth restriction increases fetal hepatic gluconeogenic capacity and reduces messenger ribonucleic acid translation initiation and nutrient sensing in fetal liver and skeletal muscle. Endocrinology 2009; 150: 3021-3030. http://dx.doi.org/10.1210/en.2008-1789

Armitage JA, Taylor PD, Poston L. Experimental models of developmental programming: consequences of exposure to an energy rich diet during development. J Physiol 2005; 565: 3-8. http://dx.doi.org/10.1113/jphysiol.2004.079756

Ravelli AC, van der Meulen JH, Michels RP, Osmond C, Barker DJ, Hales CN, et al. Glucose tolerance in adults after prenatal exposure to famine. Lancet 1998; 351: 173-177. http://dx.doi.org/10.1016/S0140-6736(97)07244-9

Roseboom TJ, Vaan der Meulen JHP, Ravelli AC, Osmond C, Baarker DJP, Bleker OP. Effect of prenatal Dutch famine on adult disease in later life. Mol Cell Endocrinol 2001; 185: 93-98. http://dx.doi.org/10.1016/S0303-7207(01)00721-3

Garofano A, Czernichow P, Bréant B. Beta-cell mass and proliferation following late fetal and early postnatal malnutrition in the rat. Diabetologia 1998; 41: 1114-1120. http://dx.doi.org/10.1007/s001250051038

Chisari AN, Giovambattista A, Perello M, Spinedi E. Impact of maternal undernutrition on hypothalamo-pituitary-adrenal axis and adipocyte functions in male rat offspring. Endocrine 2001; 14: 375-382. http://dx.doi.org/10.1385/ENDO:14:3:375

Ozanne SE, Smith GD, Tikerpae J, Hales CN. Altered regulation of hepatic glucose output in the male offspring of protein-malnourished rat dams. Am J Physiol 1996; 270: E559-564.

Reusens B, Remacle C. Intergenerational effect of an adverse intrauterine environment on perturbation of glucose metabolism. Twin Res 2001; 4: 406-411. http://dx.doi.org/10.1375/1369052012597

Bavdekar A, Yajnik CS, Fall CH, Bapat S, Pandit AN, Deshpande V, et al. Insulin resistance syndrome in 8-year-old Indian children: small at birth, big at 8 years, or both? Diabetes 1999; 48: 2422-2429. http://dx.doi.org/10.2337/diabetes.48.12.2422

Kunz LH, King JC. Impact of maternal nutrition and metabolism on health of the offspring. Semin Fetal Neonatal Med 2007; 12: 71-77. http://dx.doi.org/10.1016/j.siny.2006.10.010

Zambrano E, Bautista CJ, Deás M, Martínez-Samayoa PM, González-Zamorano M, Ledesma H, et al. A low maternal protein diet during pregnancy and lactation has sex- and window of exposure-specific effects on offspring growth and food intake, glucose metabolism and serum leptin in the rat. J Physiol 2006; 571: 221-230. http://dx.doi.org/10.1113/jphysiol.2005.100313

Dahri S, Snoeck A, Reusens-Billen B, Remacle C, Hoet JJ. Islet function in offspring of mothers on low-protein diet during gestation. Diabetes 1991; 40: 115-120. http://dx.doi.org/10.2337/diab.40.2.S115

Petry CJ, Hales CN. Long-term effects on offspring of intrauterine exposure to deficits in nutrition. Hum Reprod Update 2000; 6: 578-586. http://dx.doi.org/10.1093/humupd/6.6.578

Kind KL, Clifton PM, Grant PA, Owens PC, Sohlstrom A, Roberts CT. Effect of maternal feed restriction during pregnancy on glucose tolerance in the adult guinea pig. Am J Physiol Regul Integr Comp Physiol 2003; 284: R140-R152. http://dx.doi.org/10.1152/ajpregu.00587.2001

D'Autreaux B, Toledano MB. ROS as signalling molecules: mechanisms that generate specificity in ROS homeostasis. Nat Rev Mol Cell Biol 2007; 8(10): 813-24. http://dx.doi.org/10.1038/nrm2256

Bedard K, Attar H, Bonnefont J, Jaquet V, Borel C, Plastre O, et al. Three common polymorphisms in the CYBA gene form a haplotype associated with decreased ROS generation. Hum Mutat 2009; 30(7): 1123-33. http://dx.doi.org/10.1002/humu.21029

Droge W. Free radicals in the physiological control of cell function. Physiol Rev 2002; 82(1): 47-95.

Becknneth B. and Ames Bruce N. The Free Radical Theory of Aging Matures. Physiol Rev 1998; 78(2).

Vina J, Borras C, Gambini J, Sastre J, Pallardo FV. Why females live longer than males? Importance of the upregulation of longevity-associated genes by oestrogenic compounds. FEBS Lett 2005; 579(12): 2541-5. http://dx.doi.org/10.1016/j.febslet.2005.03.090

Gabory A, Attig L, Junien C. Sexual dimorphism in environmental epigenetic programming. Mol Cell Endocrinol 2009; 304: 8-18. http://dx.doi.org/10.1016/j.mce.2009.02.015

Chisari AN, Sancho P, Caja L, Bertran E, Fabregat I. Lack of amino acids in mouse hepatocytes in culture induces the selection of preneoplastic cells. Cell Signal 2012; 24: 325-332. http://dx.doi.org/10.1016/j.cellsig.2011.09.018

Caballero VJ, Mendieta JR, Giudici AM, Crupkin AC, Barbeito CG, Ronchi VP, Chisari AN and Conde RD. Alternation between dietary protein depletion and normal feeding cause liver damage in mouse. J Physiol Biochem 2011. 67: 43-52. http://dx.doi.org/10.1007/s13105-010-0047-1

Barja G. Free radicals and aging. Trends Neurosci 2004; 27(10): 595-600.

Borrás C, Sastre J, García-Sala D, Lloret A, Pallardó FV, Viña J. Mitochondria from females exhibit higher antioxidant gene expression and lower oxidative damage than males. Free Radic Biol Med 2003; 34(5): 546-52.

Spinedi E, Gaillard RC, Chisari A.Sexual dimorphism of neuroendocrine-immune interactions. Front Horm Res 2002; 29: 91-107. http://dx.doi.org/10.1159/000061059

Chisari AN, Giovambattista A, Perelló M, Gaillard RC, Spinedi ES. Maternal undernutrition induces neuroendocrine immune dysfunction in male pups at weaning. Neuroimmunomodulation 2001; 9(1): 41-8. http://dx.doi.org/10.1159/000049006

Barker DJ, Eriksson JG, Forsen T, et al. Fetal origins of adult disease: strength of effects and biological basis. Int J Epidemiol 2002; 31: 1235-1239. http://dx.doi.org/10.1093/ije/31.6.1235

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Published

2015-04-14

How to Cite

Echarte, E., Rocío, A., & Chisari, A. (2015). Nutritional Status of Pregnant Mothers Influence the Health in Adult Life of their Children. Journal of Nutritional Therapeutics, 4(1), 12–19. https://doi.org/10.6000/1929-5634.2015.04.01.3

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