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Multigenerational impact of maternal overnutrition/obesity in the sheep on the neonatal leptin surge in granddaughters

Abstract

Background/objectives:

We have reported that maternal overnutrition/obesity (OB) in sheep resulting from feeding 150% of National Research Council (NRC) requirements throughout gestation leads to maternal hyperglycemia and hyperinsulinemia. Further, newborn lambs born to OB vs control-fed (CON, 100% of NRC) ewes exhibited greater adiposity, increased blood cortisol, insulin and glucose and the elimination of the postnatal leptin spike seen in lambs born to CON ewes. This early postnatal leptin peak is necessary for the development of hypothalamic circuits, which program appetite in later life. This study evaluated the multigenerational impact of OB on insulin:glucose dynamics of mature female F1 offspring fed only to requirements throughout gestation and on their lambs (F2 generation).

Design and methods:

Adult F1 female offspring born to OB (n=10) or CON (n=7) ewes were utilized. All F1 ewes were subjected to a glucose tolerance test at midgestation and late gestation. Jugular blood was obtained from F2 lambs at birth (day 1) through postnatal day 11, and plasma glucose, insulin, cortisol and leptin concentrations were determined. Dual-energy X-ray absorptiometry was utilized to determine bone mineral density, bone mineral content, lean tissue mass and fat tissue mass.

Results:

Fasted blood glucose and insulin concentrations were greater (P<0.05) in OBF1 than CONF1 ewes at midgestation and late gestation. Further, after glucose infusion, both glucose and insulin concentrations remained higher in OBF1 ewes (P<0.05) than CONF1 ewes, demonstrating greater insulin resistance. Blood concentrations of glucose, insulin and cortisol and adiposity were higher (P<0.01) in OBF2 lambs than CONF2 lambs at birth. Importantly, OBF2 lambs failed to exhibit the early postnatal leptin peak exhibited by CONF2 lambs.

Conclusions:

These data suggest that these OBF2 lambs are predisposed to exhibit the same metabolic alterations as their mothers, suggesting a multigenerational programming effect.

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References

  1. Catalano PM, Hauguel-De Mouzon S . Is it time to revisit the Pedersen hypothesis in the face of the obesity epidemic? Am J Obstet Gynecol 2011; 204: 479–487.

    Article  Google Scholar 

  2. Ogden CL, Carroll MD, Kit BK, Flegal KM . Prevalence of obesity in the United States, 2009-2010. NCHS Data Brief 2012; 82: 1–7.

    Google Scholar 

  3. Cnop M, Landchild MJ, Vidal J, Havel PJ, Knowles NG, Carr DR et al. The concurrent accumulation of intra-abdominal and subcutaneous fat explains the association between insulin resistance and plasma leptin concentrations: distinct metabolic effects of two fat compartments. Diabetes 2002; 51: 1005–1015.

    Article  CAS  Google Scholar 

  4. Boney CM, Verma A, Tucker R, Vohr BR . Metabolic syndrome in childhood: association with birth weight, maternal obesity, and gestational diabetes mellitus. Pediatrics 2005; 115: e290–e296.

    Article  Google Scholar 

  5. Mingrone G, Manco M, Mora ME, Guidone C, Iaconelli A, Gniuli D et al. Influence of maternal obesity on insulin sensitivity and secretion in offspring. Diabetes Care 2008; 31: 1872–1876.

    Article  Google Scholar 

  6. Delahave F, Breton C, Risold PY, Enache M, Dutriez-Casteloot I, Laborie C et al. Maternal perinatal undernutrition drastically reduces postnatal leptin surge and affects the development of arcuate nucleus proopiomelanocortin neurons in neonatal male rat pups. Endocrinology 2008; 149: 470–475.

    Article  Google Scholar 

  7. Long NM, Ford SP, Nathanielsz PW . Maternal obesity eliminates the neonatal lamb plasma leptin peak. J Physiol 2011; 589: 1455–1462.

    Article  CAS  Google Scholar 

  8. Bouret SG . Leptin, nutrition, and the programming of hypothalamic feeding circuits. Nestle Nutr Workshop Ser Pediatr Program 2010; 65: 25–35.

    Article  Google Scholar 

  9. Elmquist JK, Ahima RS, Elias CF, Flier JS, Saper CB . Leptin activates distinct projections from the dorsomedial and ventromedial hypothalamic nuclei. Proc Natl Acad Sci USA 1998; 95: 741–746.

    Article  CAS  Google Scholar 

  10. Bouret SG, Draper SJ, Simerly RB . Trophic action of leptin on hypothalamic neurons that regulate feeding. Science 2004; 304: 108–110.

    Article  CAS  Google Scholar 

  11. Steppan CM, Swick AG . A role for leptin in brain development. Biochem Biophys Res Commun 1999; 256: 600–602.

    Article  CAS  Google Scholar 

  12. Long NM, George LA, Uthlaut AB, Smith DT, Nijland MJ, Nathanielsz PW et al. Maternal obesity and increased nutrient intake before and during gestation in the ewe results in altered growth, adiposity, and glucose tolerance in adult offspring. J Anim Sci 2010; 88: 3546–3553.

    Article  CAS  Google Scholar 

  13. Morton GJ, Schwartz MW . Leptin and the central nervous system control of glucose metabolism. Physiol Rev 2011; 91: 389–411.

    Article  CAS  Google Scholar 

  14. Kamohara S, Burcelin R, Halaas JL, Friedman JM, Charron MJ . Acute stimulation of glucose metabolism in mice by leptin treatment. Nature 1997; 389: 374–377.

    Article  CAS  Google Scholar 

  15. Barker DJ . The origins of the developmental origins theory. J Intern Med 2007; 261: 412–417.

    Article  CAS  Google Scholar 

  16. Gluckman PD, Hanson MA, Cooper C, Thornburg KL . Effect of in utero and early-life conditions on adult health and disease. N Engl J Med 2008; 359: 61–73.

    Article  CAS  Google Scholar 

  17. Hanson MA, Gluckman PD . Developmental origins of health and disease: moving from biological concepts to interventions and policy. Int J Gynaecol Obstet 2011; 115 (Suppl 1): S3–S5.

    Article  Google Scholar 

  18. Heerwagen MJ, Miller MR, Barbour LA, Friedman JE . Maternal obesity and fetal metabolic programming: a fertile epigenetic soil. Am J Physiol Integr Comp Physiol 2010; 299: R711–R722.

    Article  CAS  Google Scholar 

  19. Skinner MK . What is an epigenetic transgenerational phenotype? F3 or F2. Reprod Toxicol 2008; 25: 2–6.

    Article  CAS  Google Scholar 

  20. Dunn GA, Bale TL . Maternal high-fat diet promotes body length increases and insulin insensitivity in second-generation mice. Endocrinology 2009; 150: 4999–5009.

    Article  CAS  Google Scholar 

  21. Srinivasan M, Mitrani P, Sadhanandan G, Dodds C, Shbeir-Eldika S, Thamotharan S et al. A high-carbohydrate diet in the immediate postnatal life of rats induces adaptations predisposing to adult-onset obesity. J Endocrinol 2008; 197: 565–574.

    Article  CAS  Google Scholar 

  22. Zambrano E, Martınez-Samayoa P, Bautista C, Deas M, Guillen L, Rodrıguez-Gonzalez G et al. Sex differences in transgenerational alterations of growth and metabolism in progeny (f2) of female offspring (f1) of rats fed a low protein diet during pregnancy and lactation. J Physiol 2005; 566: 225–236.

    Article  CAS  Google Scholar 

  23. Benyshek D, Johnston C, Martin J . Glucose metabolism is altered in the adequately-nourished grand-offspring (f3 generation) of rats malnourished during gestation and perinatal life. Diabetologia 2006; 49: 1117–1119.

    Article  CAS  Google Scholar 

  24. Jimenez-Chillaron JC, Isganaitis E, Charalambous M, Gesta S, Pentinat-Pelegrin T, Faucette RR et al. Intergenerational transmission of glucose intolerance and obesity by in utero undernutrition in mice. Diabetes 2009; 58: 460–468.

    Article  CAS  Google Scholar 

  25. Harrison M, Langley-Evans SC . Intergenerational programming of impaired nephrogenesis and hypertension in rats following maternal protein restriction during pregnancy. Br J Nutr 2009; 101: 1020–1030.

    Article  CAS  Google Scholar 

  26. Painter R, Osmond C, Gluckman P, Hanson M, Phillips D, Roseboom T . Transgenerational effects of prenatal exposure to the Dutch famine on neonatal adiposity and health in later life. BJOG 2008; 115: 1243–1249.

    Article  CAS  Google Scholar 

  27. Lumey L, Stein AD, Kahn HS, Romijn J . Lipid profiles in middle-aged men and women after famine exposure during gestation: the Dutch hunger winter families study. Am J Clin Nutr 2009; 89: 1737–1743.

    Article  CAS  Google Scholar 

  28. George LA, Uthlaut AB, Long NM, Zhang L, Ma Y, Smith DT et al. Different levels of overnutrition and weight gain during pregnancy have differential effects on fetal growth and organ development. Reprod Biol Endocrinol 2010; 8: 75.

    Article  Google Scholar 

  29. Muhlhausler BS, Adam CL, Findlay PA, Duffield JA, McMillen IC . Increased maternal nutrition alters development of the appetite-regulating network in the brain. FASEB J 2006; 20: 1257–1259.

    Article  CAS  Google Scholar 

  30. National Research Council. (eds). Nutrient Requirements of Sheep, 6th edn. National Academy Press: Washington, DC, USA, 1985.

  31. Sanson DW, West TR, Tatman WR, Riley ML, Judkins MB, Moss GE . Relationship of body composition of mature ewes with condition score and body weight. J Anim Sci 1993; 71: 1112–1116.

    Article  CAS  Google Scholar 

  32. Ford SP, Zhang L, Zhu M, Miller MM, Smith DT, Hess BW et al. Maternal obesity accelerates fetal pancreatic beta-cell but not alpha-cell development in sheep: prenatal consequences. Am J Physiol Regul Integr Comp Physiol 2009; 297: R835–R843.

    Article  CAS  Google Scholar 

  33. Mercier J, Pomar C, Marcoux M, Goulet F, Theriault M, Castonguay FW . The use of dual-energy X-ray absorptiometry to estimate the dissected composition of lamb carcasses. Meat Sci 2006; 73: 249–257.

    Article  CAS  Google Scholar 

  34. Pearce KL, Ferguson M, Gardner G, Smith N, Greef J, Pethick DW . Dual X-ray absorptiometry predicts carcass composition from live sheep and chemical composition of live and dead sheep. Meat Sci 2009; 81: 285–293.

    Article  CAS  Google Scholar 

  35. Ford SP, Hess BW, Schwope MM, Nijland MJ, Gilbert JS, Vonnahme KA et al. Maternal undernutrition during early to mid-gestation in the ewe results in altered growth, adiposity, and glucose tolerance in male offspring. J Anim Sci 2007; 85: 1285–1294.

    Article  CAS  Google Scholar 

  36. Dong F, Ford SP, Nijland MJ, Nathanielsz PW, Ren J . Influence of maternal undernutrition and overfeeding on cardiac ciliary neurotrophic factor receptor and ventricular size in fetal sheep. J Nutr Biochem 2008; 19: 409–414.

    Article  CAS  Google Scholar 

  37. Ahren B, Pacini G . Importance of quantifying insulin secretion in relation to insulin sensitivity to accurately assess beta cell function in clinical studies. Eur J Endocrinol 2004; 150: 97–104.

    Article  CAS  Google Scholar 

  38. Aerts L, van Assche FA . Animal evidence for the transgenerational development of diabetes mellitus. Int J Biochem Cell Biol 2006; 38: 894–903.

    Article  CAS  Google Scholar 

  39. Dhawan S, Georgia S, Bhushan A . Formation and regeneration of the endocrine pancreas. Curr Opin Cell Biol 2007; 19: 634–645.

    Article  CAS  Google Scholar 

  40. Ruager-Martin R, Hyde MJ, Modi N . Maternal obesity and infant outcomes. Early Hum Dev 2010; 86: 715–722.

    Article  Google Scholar 

  41. Hay Jr WW . Placental-fetal glucose exchange and fetal glucose metabolism. Trans Am Clin Climatol Assoc 2006; 117: 321–339 discussion 339-340.

    PubMed  PubMed Central  Google Scholar 

  42. Caluwaerts S, Lambin S, van Bree R, Peeters H, Vergote I, Verhaeghe J . Diet-induced obesity in gravid rats engenders early hyperadiposity in the offspring. Metabolism 2007; 56: 1431–1438.

    Article  CAS  Google Scholar 

  43. Bunnell A, Estes BT, Guilak F, Gimble JM . Differentiation of adipose stem cells. Methods Mol Biol 2008; 456: 155–171.

    Article  Google Scholar 

  44. Randle PJ, Garland PB, Hales CN, Newsholme EA . The glucose fatty-acid cycle. Its role in insulin sensitivity and the metabolic disturbances of diabetes mellitus. Lancet 1963; 1: 785–789.

    Article  CAS  Google Scholar 

  45. Hannan MT, Felson DT, Anderson JJ . Bone mineral density in elderly men and women: results from the Framingham osteoporosis study. J Bone Miner Res 1992; 7: 547–553.

    Article  CAS  Google Scholar 

  46. Koo WW, Walters J, Bush AJ, Chesney RW, Carlson SE . Dual-energy X-ray absorptiometry studies of bone mineral status in newborn infants. J Bone Miner Res 1996; 11: 997–102.

    Article  CAS  Google Scholar 

  47. Clark EM, Ness AR, Tobias JH . Gender differences in the ratio between humerus width and length are established prior to puberty. Osteoporos Int 2007; 18: 463–470.

    Article  CAS  Google Scholar 

  48. Harrington TA, Thomas EL, Frost G, Modi N, Bell JD . Distribution of adipose tissue in the newborn. Pediatr Res 2004; 55: 437–441.

    Article  Google Scholar 

  49. McCance RA, Widdowson EM . Fat. Pediatr Res 1977; 11: 1081–1083.

    Article  CAS  Google Scholar 

  50. Spray CM, Widdowson EM . The effect of growth and development on the composition of mammals. Br J Nutr 1950; 4: 332–353.

    Article  CAS  Google Scholar 

  51. Stini WA . Body composition and nutrient reserves in evolutionary perspective. World Rev Nutr Diet 1981; 37: 55–83.

    Article  CAS  Google Scholar 

  52. Park KS, Rhee BD, Lee KU, Kim SY, Lee HK, Koh CS et al. Intra-abdominal fat is associated with decreased insulin sensitivity in healthy young men. Metabolism 1991; 40: 600–603.

    Article  CAS  Google Scholar 

  53. Rendell M, Hulthen UL, Tornquist C, Groop L, Mattiasson I . Relationship between abdominal fat compartments and glucose and lipid metabolism in early postmenopausal women. J Clin Endocrinol Metab 2001; 86: 744–749.

    CAS  PubMed  Google Scholar 

  54. Despres JP, Nadeau A, Tremblay A, Ferland M, Moorjani S, Lupien PJ et al. Role of deep abdominal fat in the association between regional adipose tissue distribution and glucose tolerance in obese women. Diabetes 1989; 38: 304–309.

    Article  CAS  Google Scholar 

  55. Fujioka S, Matsuzawa Y, Tokunaga K, Tarui S . Contribution of intra-abdominal fat accumulation to the impairment of glucose and lipid metabolism in human obesity. Metabolism 1987; 36: 54–59.

    Article  CAS  Google Scholar 

  56. Kissebah AH, Vydelingum N, Murray R, Evans DJ, Hartz AJ, Kalkhoff RK et al. Relation of body fat distribution to metabolic complications of obesity. J Clin Endocrinol Metab 1982; 54: 254–260.

    Article  CAS  Google Scholar 

  57. Vague J . The degree of masculine differentiation of obesities: a factor determining predisposition to diabetes, atherosclerosis, gout, and uric calculous disease. Am J Clin Nutr 1956; 4: 20–34.

    Article  CAS  Google Scholar 

  58. Bouret SG, Bates SH, Chen S, Myers Jr MG, Simerly RB . Distinct roles for specific leptin receptor signals in the development of hypothalamic feeding circuits. J Neurosci 2012; 32: 1244–125.

    Article  CAS  Google Scholar 

  59. Fowden Al, Forhead AJ . The role of hormones in intrauterine development. In: Barker DJP (ed). Fetal Origins of Cardiovascular and Like Disease. Marcel Decker: New York, NY, USA, 2000. pp 199–228.

    Google Scholar 

  60. Long NM, Smith DT, Ford SP, Nathanielsz PW . Elevated glucocorticoids during ovine pregnancy increase appetite and produce glucose dysregulation and adiposity in their granddaughters in response to ad libitum feeding at 1 year of age. Am J Obstet Gynecol 2013; 209 (353): e1–e9.

    Google Scholar 

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Acknowledgements

We thank the students of the Center for the Study of Fetal Programming for their assistance in animal care and data collection on the farm. We also thank Adam Uthlaut and Robert Cordery-Cotter for animal care and management. This work was supported by the National Institutes of Health (NIH) INBRE no. P20 RR016474.

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Correspondence to S P Ford.

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Shasa, D., Odhiambo, J., Long, N. et al. Multigenerational impact of maternal overnutrition/obesity in the sheep on the neonatal leptin surge in granddaughters. Int J Obes 39, 695–701 (2015). https://doi.org/10.1038/ijo.2014.190

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  • DOI: https://doi.org/10.1038/ijo.2014.190

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