Hostname: page-component-cd9895bd7-7cvxr Total loading time: 0 Render date: 2024-12-23T14:54:23.451Z Has data issue: false hasContentIssue false

Effects of birth weight, sex and neonatal glucocorticoid overexposure on glucose–insulin dynamics in young adult horses

Published online by Cambridge University Press:  20 December 2016

O. A. Valenzuela
Affiliation:
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK
J. K. Jellyman
Affiliation:
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK
V. L. Allen
Affiliation:
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK
N. B. Holdstock
Affiliation:
Department of Veterinary Medicine, University of Cambridge, Cambridge, UK
A. J. Forhead
Affiliation:
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK
A. L. Fowden*
Affiliation:
Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, UK
*
*Address for correspondence: A. L. Fowden, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge, CB2 3EG, UK. (Email [email protected])

Abstract

In several species, adult metabolic phenotype is influenced by the intrauterine environment, often in a sex-linked manner. In horses, there is also a window of susceptibility to programming immediately after birth but whether adult glucose–insulin dynamics are altered by neonatal conditions remains unknown. Thus, this study investigated the effects of birth weight, sex and neonatal glucocorticoid overexposure on glucose–insulin dynamics of young adult horses. For the first 5 days after birth, term foals were treated with saline as a control or ACTH to raise cortisol levels to those of stressed neonates. At 1 and 2 years of age, insulin secretion and sensitivity were measured by exogenous glucose administration and hyperinsulinaemic–euglycaemic clamp, respectively. Glucose-stimulated insulin secretion was less in males than females at both ages, although there were no sex-linked differences in glucose tolerance. Insulin sensitivity was greater in females than males at 1 year but not 2 years of age. Birth weight was inversely related to the area under the glucose curve and positively correlated to insulin sensitivity at 2 years but not 1 year of age. In contrast, neonatal glucocorticoid overexposure induced by adrenocorticotropic hormone (ACTH) treatment had no effect on whole body glucose tolerance, insulin secretion or insulin sensitivity at either age, although this treatment altered insulin receptor abundance in specific skeletal muscles of the 2-year-old horses. These findings show that glucose–insulin dynamics in young adult horses are sexually dimorphic and determined by a combination of genetic and environmental factors acting during early life.

Type
Original Article
Copyright
© Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2016 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1. Scheen, AJ, Van Cauter, E. The roles of time of day and sleep quality in modulating glucose regulation: clinical implications. Horm Res. 1998; 49, 191201.Google Scholar
2. Bulló, M, Cózar-Torrell, P, Salas-Salvadó, J. Dietary regulation of glucose metabolism in metabolic syndrome. Curr Vasc Pharmacol. 2013; 11, 928945.CrossRefGoogle ScholarPubMed
3. Ralston, SL. Insulin and glucose metabolism. Vet Clin North Am Equine Pract. 2002; 18, 295304.Google Scholar
4. Firshman, AM, Valberg, SJ. Factors affecting clinical assessment of insulin sensitivity in horses. Equine Vet J. 2007; 39, 567575.Google Scholar
5. McMillen, IC, Robinson, JS. Developmental origins of metabolic syndrome: prediction, plasticity and programming. Physiol Rev. 2005; 85, 571633.Google Scholar
6. Ong, TP, Ozanne, SE. Developmental programming of type 2 diabetes: early nutrition and epigenetic mechanisms. Curr Opin Clin Nutr Metab Care. 2015; 18, 354360.Google Scholar
7. Gonzalez-Bulnes, A, Astiz, S, Ovilo, C, et al. Developmental origins of health and disease in swine: implications for animal production and biomedical research. Theriogenology. 2016; 86, 110119.Google Scholar
8. Poore, KR, Fowden, AL. The effect of birth weight on glucose tolerance in pigs at 3 and 12 months of age. Diabetologia. 2002; 45, 12471254.Google Scholar
9. Hales, CN, Marker, DJ, Clark, PM, et al. Fetal and infant growth and impaired glucose tolerance at age 64. BMJ. 1991; 303, 10191022.CrossRefGoogle ScholarPubMed
10. Kind, KL, Clifton, PM, Grant, PA, et al. Effect of maternal feed restriction during pregnancy on glucose tolerance in the adult guinea pig. Am J Physiol Regul Integr Comp Physiol. 2003; 284, R140R152.Google Scholar
11. Lui, H, Schulz, CG, De Blasio, MJ, et al. Effect of placental restriction and neonatal exendin-4 treatment on postnatal growth, adult body composition and in vivo glucose metabolism in the sheep. Am J Physiol Endocrinol Metab. 2015; 309, E589E600.Google Scholar
12. Clarke, L, Firth, K, Heasman, L, et al. Influence of relative size at birth on growth and glucose homeostasis in twin lambs during juvenile life. Reprod Fertil Dev. 2000; 12, 6973.CrossRefGoogle ScholarPubMed
13. Jansson, T, Lambert, GW. Effect of intrauterine growth restriction on blood pressure, glucose tolerance and sympathetic nervous system activity in the rat at 3–4 months of age. J Hypertens. 1999; 17, 12391248.Google Scholar
14. Wang, J, Tang, H, Wang, H, et al. The structural alteration of gut microbiota in low-birth-weight mice undergoing accelerated postnatal growth. Sci Rep. 2016; 6, 27780.CrossRefGoogle ScholarPubMed
15. Coverdale, JA, Hammer, CJ, Walter, KW. Nutritional programming and the impact on mare and foal performance. J Anim Sci. 2015; 93, 32613267.Google Scholar
16. Fowden, AL, Jellyman, JK, Valenzuela, OA, Forhead, AJ. Nutritional programming of intrauterine development: a concept applicable to the horse? J Equine Vet Sci. 2013; 33, 295304.Google Scholar
17. George, LA, Staniar, WB, Trieber, KH, Harris, PA, Geor, RJ. Insulin sensitivity and glucose dynamics during pre-weaning foal development and in response to maternal dietary composition. Domest Anim Endocrinol. 2009; 37, 2329.Google Scholar
18. Ousey, JC, Fowden, AL, Wilsher, S, Allen, WR. The effects of maternal health and body condition on the endocrine responses of neonatal foals. Equine Vet J. 2008; 40, 673679.Google Scholar
19. Peugnet, P, Robies, M, Medoza, L, et al. Effects of moderate amounts of barley in late pregnancy on growth, glucose metabolism and osteoarticular status of pre-weaning horses. PLoS One. 2015; 10, e0122596.Google Scholar
20. Valenzuela, OA, Jellyman, JK, Allen, VL, Holdstock, NB, Fowden, AL. Effects of maternal dexamethasone treatment on pancreatic β cell function in the pregnant mare and postnatal foal. Equine Vet J. 2016; doi:10.111/evj.12560.Google Scholar
21. Jellyman, JK, Allen, VL, Holdstock, NB, Fowden, AL. Glucocorticoid over-exposure in neonatal life alters pancreatic β cell function in newborn foals. J Anim Sci. 2013; 91, 104110.Google Scholar
22. Jellyman, JK, Valenzuela, OA, Allen, VL, et al. Neonatal glucocorticoid overexposure programmes pituitary-adrenal function in ponies. Domest Anim Endocrinol. 2015; 50, 4549.Google Scholar
23. Jellyman, JK, Valenzuela, OA, Allen, VL, Holdstock, NB, Fowden, AL. Sex-associated differences in pancreatic β cell function in healthy pre-weaning foals. Equine Vet J. 2014; 46, 722728.Google Scholar
24. Carroll, CR, Huntingdon, PJ. Body condition scoring and weight estimation of horses. Equine Vet J. 1988; 20, 4145.Google Scholar
25. Hennecke, DR, Potter, GD, Kreider, JV, Yates, BF. Relationship between condition score, physical measurements and body fat percentage in mares. Equine Vet J. 1983; 16, 371372.Google Scholar
26. Panzini, SM, Villani, A, McGladdery, A, et al. Concentrations of 15-ketodihydro-PGF2alpha, cortisol and progesterone in the plasma of healthy and pathological foals. Theriogenology. 2009; 72, 10321040.Google Scholar
27. Silver, M, Ousey, JC, Dudan, FE, et al. Studies on equine prematurity2: postnatal adrenocortical activity in relation to plasma adenocorticotrophic hormone and catecholamine levels in term and premature foals. Equine Vet J. 1984; 16, 278286.CrossRefGoogle Scholar
28. Taylor, PM, White, KL, Fowden, AL, et al. Propofol anaesthesia for surgery in late gestation pony mares. Vet Anaes Anal. 2001; 28, 177187.CrossRefGoogle ScholarPubMed
29. deVries, M, Taylor, PM, Troughton, G, Fowden, AL, Sear, J. Real time monitoring of propofol blood concentration in ponies anaesthetized with propofol and ketamine. J Vet Pharmacol Ther. 2003; 36, 258266.Google Scholar
30. Borer-Weir, KE, Bailey, SR, Menzies-Gow, NJ, Harris, PA, Elliot, J. Evaluation of a commercially available radioimmunoassay and species specific ELISAs for measurement of high concentrations of insulin in equine serum. Am J Vet Res. 2012; 73, 15961602.CrossRefGoogle ScholarPubMed
31. Tinworth, KD, Wynn, PC, Boston, RC, et al. Evaluation of commercially available assays for the measurement of equine insulin. Domest Anim Endocrinol. 2011; 41, 8190.Google Scholar
32. Ozanne, SE, Nave, BT, Wang, CL, et al. Poor fetal nutrition causes long-term changes in expression of insulin signalling components in adipocytes. Am J Physiol. 1997; 273, E46E51.Google ScholarPubMed
33. Pratt, SE, Geor, RJ, McCutcheon, LG. Repeatability of 2 methods of assessment of insulin sensitivity and glucose dynamics in horses. J Vet Intern Med. 2005; 19, 883888.Google Scholar
34. Gatford, KL, De Blasio, MJ, Thavaneswaran, P, et al. Postnatal ontogeny of glucose homeostasis and insulin action in sheep. Am J Physiol Endocrinol Metab. 2004; 286, E1050E1059.Google Scholar
35. Chamson-Reig, A, Thyssen, SM, Hill, DJ, Arany, E. Exposure of the pregnant rat to low protein diet causes impaired glucose homeostasis in the young adult offspring by different mechanisms in males and females. Exp Biol Med (Maywood). 2009; 234, 14251436.Google Scholar
36. Brunton, PJ, Sullivan, KM, Kerrigan, D, et al. Sex-specific effects of prenatal stress on glucose homoeostasis and peripheral metabolism in rats. J Endocrinol. 2013; 217, 161173.Google Scholar
37. Hilawe, EH, Yatsuya, H, Kawaguchi, L, Aoyama, A. Difference by sex in the prevalence of diabetes mellitus, impaired fasting glycaemia and impaired glucose tolerance in sub-Saharan Africa: a systematic review and meta-analysis. Bull World Health Organ. 2013; 91, 671682.CrossRefGoogle ScholarPubMed
38. Han, R, Li, A, Li, L, Kitlinska, JB, Zukowska, Z. Material low-protein diet up-regulates the neuropeptide Y system in visceral fat and leads to abdominal obesity and glucose intolerance in a sex-and-time specific manner. FASEB J. 2012; 26, 35283536.Google Scholar
39. Owens, JA, Thavaneswaran, P, De Blasio, MJ, et al. Sex-specific effects of placental restriction on components of the metabolic syndrome in young adult sheep. Am J Physiol Endocrinol Metab. 2007; 292, E1879E1889.Google Scholar
40. McKnight, LL, Myrie, SB, Mackay, DS, Brunton, JA, Bertolo, RF. Glucose tolerance is affected by visceral adiposity and sex, but not birth weight, in Yucatan miniature pigs. Appl Physiol Nutr Metab. 2012; 37, 106114.Google Scholar
41. Reaven, EP, Curry, DL, Reaven, GM. Effect of age and sex on rat endocrine pancreas. Diabetes. 1987; 12, 13971400.Google Scholar
42. Galipeau, DM, Yao, L, McNeill, JH. Relationship among hyperinsulinemia, insulin resistance and hypertension is dependent on sex. Am J Physiol Heart Circ Physiol. 2002; 283, H562H567.Google Scholar
43. Ruhe, RC, Curry, DL, Herrmann, S, McDonald, RB. Age and gender effects on insulin secretion and glucose sensitivity of the endocrine pancreas. Am J Physiol. 1992; 262, R671R676.Google Scholar
44. Liu, H, Schultz, CG, De Blasio, MJ, et al. Effect of placental restriction and neonatal exendin-4 treatment on postnatal growth, adult body composition and in vivo glucose metabolism in sheep. Am J Physiol Endocrinol Metab. 2015; 309, E589E600.Google Scholar
45. Yki-Järvinen, H. Sex and insulin sensitivity. Metabolism. 1984; 33, 10111015.Google Scholar
46. Nagai, K, Yoshida, S, Konishi, H. Gender differences in the gene expression profiles of glucose transporter GLUT class I and SGLT in mouse tissues. Pharmazie. 2014; 69, 856859.Google Scholar
47. Langdown, ML, Holness, MJ, Sugden, MC. Early growth retardation induced excessive exposure to glucocorticoids in utero selectively increases cardiac GLUT1 protein expression and Akt/protein kinase B activity in adulthood. J Endocrinol. 2001; 169, 1122.Google Scholar
48. Jaquet, D, Vidal, H, Hankard, R, Czernichow, P, Levy-Marchal, C. Impaired regulation of glucose transporter 4 gene expression in insulin resistance associated with in utero undernutrition. J Clin Endocrinol Metab. 2001; 86, 32663271.Google Scholar
49. Zheng, S, Rollet, M, Pan, YX. Protein restriction during gestation alters histone modifications at the glucose transporter 4 (GLUT4) promoter region and induced GLUT4 expression in skeletal muscle of female rate offspring. J Nutr Biochem. 2012; 23, 10641071.Google Scholar
50. Rijnen, KE, van der Kolk, JH. Determination of reference range values indicative of glucose metabolism and insulin resistance by use of glucose clamp techniques in horses. Am J Vet Res. 2003; 64, 12601264.Google Scholar
51. Carter, RA, McCutcheon, LJ, George, LA, et al. Effects of diet-induced weight gain on insulin sensitivity and plasma hormone and lipid concentrations in horses. Am J Vet Res. 2009; 10, 12501258.Google Scholar
52. Powell, DM, Reddy, SE, Sessions, DR, Fitzgerald, BP. Effect of short-term exercise training on insulin sensitivity in obese and lean mares. Equine Vet J. 2002; 34, 8184.Google Scholar
53. Bamford, MJ, Potter, SJ, Harris, PA, Bailey, SR. Breed differences in insulin sensitivity and insulinemic responses to oral glucose in horses and ponies of moderate body condition score. Domest Anim Endocrinol. 2014; 47, 101107.CrossRefGoogle ScholarPubMed
54. Murphy, D, Reid, SWJ, Love, S. The effect of age and diet on the oral glucose tolerance test in ponies. Equine Vet J. 1997; 29, 467470.Google Scholar
55. Kelsey, MM, Zeitler, PS. Insulin resistance of puberty. Curr Diab Rep. 2016; 16, 64.Google Scholar
56. Guillaume, D, Salazar-Ortiz, J, Martin-Rosset, W. Effects of nutrition levels in mares’ ovarian activity and equines’ puberty. In Nutrition and Feeding of the Brood Mare (eds. Miraglia N, Martin-Rosset W), 2006; pp. 315339. Wageningen Academic Publishers: Wageningen, The Netherlands.Google Scholar
57. Poore, KR, Fowden, AL. Insulin sensitivity in juvenile and adult pigs of low and high birth weight. Diabetologia. 2004; 47, 340348.Google Scholar
58. Horton, DM, Saint, DA, Owens, JA, Kind, KL, Gatford, KL. Spontaneous intrauterine growth restriction due to increased litter size in the guinea pig programmes postnatal growth, appetite and adult body composition. J Dev Orig Health Dis. 2016; 7, 548562.Google Scholar
59. Peugnet, P, Wimel, L, Duchamp, G, et al. Enhanced or reduced fetal growth induced by embryo transfer into smaller or larger breeds alters post-natal growth and metabolism in pre-weaning horses. PLoS One. 2014; 9, e102044.Google Scholar
60. Nyirenda, MJ, Lindsay, RS, Kenyon, CJ, Burchell, A, Seckl, JR. Glucocorticoid exposure in late gestation permanently programs rat hepatic phosphoenolpyruvate carboxykinase and glucocorticoid receptor expression and causes glucose intolerance in adult offspring. J Clin Invest. 1998; 101, 21742181.Google Scholar
61. Jellyman, JK, Valenzuela, OA, Fowden, AL. Glucocorticoid programming of the hypothalamic-pituitary-adrenal axis and metabolic function: animal studies from mouse to horse. J Anim Sci. 2015; 93, 32453260.Google Scholar