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Maternal undernutrition around the time of conception and embryo number each impact on the abundance of key regulators of cardiac growth and metabolism in the fetal sheep heart

Published online by Cambridge University Press:  05 August 2013

S. Lie
Affiliation:
Sansom Institute for Health Research, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, Australia
S. M. Sim
Affiliation:
Sansom Institute for Health Research, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, Australia
I. C. McMillen
Affiliation:
Sansom Institute for Health Research, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, Australia
O. Williams-Wyss
Affiliation:
Sansom Institute for Health Research, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, Australia Discipline of Physiology, School of Medical Sciences, University of Adelaide, Adelaide, SA, Australia
S. M. MacLaughlin
Affiliation:
Sansom Institute for Health Research, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, Australia
D. O. Kleemann
Affiliation:
South Australian Research and Development Institute, Turretfield Research Centre, Rosedale, SA, Australia
S. K. Walker
Affiliation:
South Australian Research and Development Institute, Turretfield Research Centre, Rosedale, SA, Australia
C. T. Roberts
Affiliation:
Discipline of Obstetrics and Gynaecology, University of Adelaide, Adelaide, SA, Australia
J. L. Morrison*
Affiliation:
Sansom Institute for Health Research, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, SA, Australia
*
*Address for correspondence: A/Prof. J. L. Morrison, Heart Foundation South Australian Cardiovascular Health Network Fellow, Early Origins of Adult Health Research Group, School of Pharmacy and Medical Sciences, Sansom Institute for Health Research, University of South Australia, GPO Box 2471, Adelaide, SA 5001, Australia. (Email Janna.Morrison@unisa.edu.au)

Abstract

Poor maternal nutrition before and during pregnancy is associated with an increased risk of cardiovascular disease in later life. To determine the impact of maternal undernutrition during the periconceptional (PCUN: −45 days to 6 days) and preimplantation (PIUN: 0–6 days) periods on cardiac growth and metabolism, we have quantified the mRNA and protein abundance of key regulators of cardiac growth and metabolism in the left ventricle of the sheep fetus in late gestation. The cardiac protein abundance of AMP-activated protein kinase (AMPK), phospho-acetyl CoA carboxykinase (ACC) and pyruvate dehydrogenase kinase-4 (PDK-4) were decreased, whereas ACC was increased in singletons in the PCUN and PIUN groups. In twins, however, cardiac ACC was decreased in the PCUN and PIUN groups, and carnitine palmitoyltransferase-1 (CPT-1) was increased in the PIUN group. In singletons, the cardiac abundance of insulin receptor β (IRβ) was decreased in the PCUN group, and phosphoinositide-dependent protein kinase-1 (PDPK-1) was decreased in the PCUN and PIUN groups. In twins, however, the cardiac abundance of IRβ and phospho-Akt substrate 160kDa (pAS160) were increased in the PIUN group. The cardiac abundance of insulin-like growth factor-2 receptor (IGF-2R), protein kinase C alpha (PKCα) and mammalian target of rapamycin (mTOR) were decreased in PCUN and PIUN singletons and extracellular-signal-regulated kinase (ERK) was also decreased in the PIUN singletons. In contrast, in twins, cardiac abundance of IGF-2R and PKCα were increased in the PCUN and PIUN groups, phospho-ribosomal protein S6 (pRPS6) was increased in the PCUN group, and ERK and eukaryotic initiation factor 4E (eIF4E) were also increased in the PIUN fetuses. In conclusion, maternal undernutrition limited to around the time of conception is sufficient to alter the abundance of key factors regulating cardiac growth and metabolism and this may increase the propensity for cardiovascular diseases in later life.

Type
Original Article
Copyright
Copyright © Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2013 

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References

1.Edwards, LJ, McMillen, IC. Periconceptional nutrition programs development of the cardiovascular system in the fetal sheep. Am J Physiol Regul Integr Comp Physiol. 2002; 283, R669R679.Google Scholar
2.Kwong, WY, Wild, AE, Roberts, P, Willis, AC, Fleming, TP. Maternal undernutrition during the preimplantation period of rat development causes blastocyst abnormalities and programming of postnatal hypertension. Development. 2000; 127, 41954202.CrossRefGoogle ScholarPubMed
3.Gardner, DS, Pearce, S, Dandrea, J, et al. Peri-implantation undernutrition programs blunted angiotensin II evoked baroreflex responses in young adult sheep. Hypertension. 2004; 43, 12901296.CrossRefGoogle ScholarPubMed
4.MacLaughlin, SM, Walker, SK, Kleemann, DO, et al. Impact of periconceptional undernutrition on adrenal growth and adrenal insulin-like growth factor and steroidogenic enzyme expression in the sheep fetus during early pregnancy. Endocrinology. 2007; 148, 19111920.CrossRefGoogle ScholarPubMed
5.Roseboom, T, de Rooij, S, Painter, R. The Dutch famine and its long-term consequences for adult health. Earl Hum Dev. 2006; 82, 485491.CrossRefGoogle ScholarPubMed
6.Watkins, AJ, Wilkins, A, Cunningham, C, et al. Low protein diet fed exclusively during mouse oocyte maturation leads to behavioural and cardiovascular abnormalities in offspring. J Physiol. 2008; 586, 22312244.CrossRefGoogle ScholarPubMed
7.Roseboom, TJ, van der Meulen, JH, Ravelli, AC, et al. Effects of prenatal exposure to the Dutch famine on adult disease in later life: an overview. Twin Res. 2001; 4, 293298.CrossRefGoogle Scholar
8.Roseboom, TJ, van der Meulen, JHP, Osmond, C, et al. Coronary heart disease after prenatal exposure to the Dutch famine, 1944–45. Heart. 2000; 84, 595598.CrossRefGoogle Scholar
9.Roseboom, TJ, van der Meulen, JHP, Osmond, C, et al. Plasma lipid profiles in adults after prenatal exposure to the Dutch famine. Am J Clin Nutr. 2000; 72, 11011106.Google Scholar
10.Painter, RC, de Rooij, SR, Bossuyt, PM, et al. Early onset of coronary artery disease after prenatal exposure to the Dutch famine. Am J Clin Nutr. 2006; 84, 322327.CrossRefGoogle Scholar
11.Levy, D, Garrison, RJ, Savage, DD, Kannel, WB, Castelli, WP. Prognostic implications of echocardiographically determined left ventricular mass in the Framingham Heart Study. N Engl J Med. 1990; 322, 15611566.CrossRefGoogle ScholarPubMed
12.Mandavia, CH, Aroor, AR, DeMarco, VG, Sowers, JR. Molecular and metabolic mechanisms of cardiac dysfunction in diabetes. Life Sci. 2012; 92, 601608.Google Scholar
13.Brooks, G, Poolman, RA, Li, J-M. Arresting developments in the cardiac myocyte cell cycle: role of cyclin-dependent kinase inhibitors. Cardiovasc Res. 1998; 39, 301311.Google Scholar
14.Cohick, WS, Clemmons, DR. The insulin-like growth factors. Annu Rev Physiol. 1993; 55, 131153.CrossRefGoogle ScholarPubMed
15.Sherr, CJ. G1 phase progression: cycling on cue. Cell. 1994; 79, 551555.Google Scholar
16.Sundgren, NC, Giraud, GD, Schultz, JM, et al. Extracellular signal-regulated kinase and phosphoinositol-3 kinase mediate IGF-1 induced proliferation of fetal sheep cardiomyocytes. Am J Physiol Regul Integr Comp Physiol. 2003; 285, R1481R1489.CrossRefGoogle ScholarPubMed
17.Kornfeld, S. Structure and function of the mannose 6-phosphate/insulin like growth factor II receptors. Annu Rev Biochem. 1992; 61, 307330.Google Scholar
18.Chu, CH, Tzang, BS, Chen, LM, et al. IGF-II/mannose-6-phosphate receptor signaling induced cell hypertrophy and atrial natriuretic peptide/BNP expression via Galphaq interaction and protein kinase C-alpha/CaMKII activation in H9c2 cardiomyoblast cells. J Endocrinol. 2008; 197, 381390.Google Scholar
19.Wang, KCW, Brooks, DA, Thornburg, KL, Morrison, JL. Activation of IGF-2R stimulates cardiomyocyte hypertrophy in the late gestation sheep fetus. J Physiol. 2012; 590, 54255437.CrossRefGoogle ScholarPubMed
20.Dietz, R, Haass, M, Kübler, W. Atrial natriuretic factor. Its possible role in hypertension and congestive heart failure. Am J Hypertens. 1989; 2, 29S33S.Google Scholar
21.Nishikimi, T, Maeda, N, Matsuoka, H. The role of natriuretic peptides in cardioprotection. Cardiovasc Res. 2006; 69, 318328.CrossRefGoogle ScholarPubMed
22.Pause, A, Belsham, GJ, Gingras, A-C, et al. Insulin-dependent stimulation of protein synthesis by phosphorylation of a regulator of 5′-cap function. Nature. 1994; 371, 762767.Google Scholar
23.Gingras, AC, Kennedy, SG, O'Leary, MA, Sonenberg, N, Hay, N. 4E-BP1, a repressor of mRNA translation, is phosphorylated and inactivated by the Akt(PKB) signaling pathway. Genes Dev. 1998; 12, 502513.Google Scholar
24.Kang, S, Chemaly, ER, Hajjar, RJ, Lebeche, D. Resistin promotes cardiac hypertrophy via the AMP-activated protein kinase/mammalian target of rapamycin (AMPK/mTOR) and c-Jun N-terminal kinase/insulin receptor substrate 1 (JNK/IRS1) pathways. J Biol Chem. 2011; 286, 1846518473.CrossRefGoogle ScholarPubMed
25.Brown, EJ, Beal, PA, Keith, CT, et al. Control of P70 S6 kinase by kinase-activity of FRAP in-vivo. Nature. 1995; 377, 441446.CrossRefGoogle ScholarPubMed
26.Kawasome, H, Papst, P, Webb, S, et al. Targeted disruption of p70s6k defines its role in protein synthesis and rapamycin sensitivity. Proc Natl Acad Sci U S A. 1998; 95, 50335038.Google Scholar
27.Dong, F, Ford, SP, Fang, CX, et al. Maternal nutrient restriction during early to mid gestation up-regulates cardiac insulin-like growth factor (IGF) receptors associated with enlarged ventricular size in fetal sheep. Growth Horm IGF Res. 2005; 15, 291299.CrossRefGoogle ScholarPubMed
28.Bertram, C, Khan, O, Ohri, S, et al. Transgenerational effects of prenatal nutrient restriction on cardiovascular and hypothalamic–pituitary–adrenal function. J Physiol. 2008; 586, 22172229.Google Scholar
29.Lopaschuk, GD, Jaswal, JS. Energy metabolic phenotype of the cardiomyocyte during development, differentiation, and postnatal maturation. J Cardiovasc Pharmacol. 2010; 56, 130140.Google Scholar
30.Hay, WWJ. Placental transport of nutrients to the fetus. Horm Res. 1994; 42, 215222.Google ScholarPubMed
31.Taniguchi, CM, Emanuelli, B, Kahn, CR. Critical nodes in signalling pathways: insights into insulin action. Nat Rev Mol Cell Biol. 2006; 7, 8596.Google Scholar
32.Pineiro, R, Iglesias, MJ, Gallego, R, et al. Adiponectin is synthesized and secreted by human and murine cardiomyocytes. FEBS Lett. 2005; 579, 51635169.Google Scholar
33.Yamauchi, T, Kamon, J, Ito, Y, et al. Cloning of adiponectin receptors that mediate antidiabetic metabolic effects. Nature. 2003; 423, 762769.Google Scholar
34.Park, SH, Gammon, SR, Knippers, JD, et al. Phosphorylation-activity relationships of AMPK and acetyl-CoA carboxylase in muscle. J Appl Physiol. 2002; 92, 24752482.Google Scholar
35.Lopaschuk, GD, Gamble, J. The 1993 Merck Frosst Award. Acetyl-CoA carboxylase: an important regulator of fatty acid oxidation in the heart. Can J Physiol Pharmacol. 1994; 72, 11011109.CrossRefGoogle ScholarPubMed
36.McGarry, JD. The mitochondrial carnitine palmitoyltransferase system: its broadening role in fuel homoeostasis and new insights into its molecular features. Biochem Soc Trans. 1995; 23, 321324.Google Scholar
37.Kadowaki, T, Yamauchi, T. Adiponectin and adiponectin receptors. Endocr Rev. 2005; 26, 439451.Google Scholar
38.Wu, P, Sato, J, Zhao, Y, et al. Starvation and diabetes increase the amount of pyruvate dehydrogenase kinase isoenzyme 4 in rat heart. Biochem J. 1998; 329, 197201.Google Scholar
39.Sugden, MC, Holness, MJ. Mechanisms underlying regulation of the expression and activities of the mammalian pyruvate dehydrogenase kinases. Arch Physiol Biochem. 2006; 112, 139149.Google Scholar
40.Burrell, JH, Boyn, AM, Kumarasamy, V, et al. Growth and maturation of cardiac myocytes in fetal sheep in the second half of gestation. Anat Rec A Discov Mol Cell Evol Biol. 2003; 274A, 952961.CrossRefGoogle Scholar
41.Jonker, SS, Zhang, L, Louey, S, et al. Myocyte enlargement, differentiation, and proliferation kinetics in the fetal sheep heart. J Appl Physiol. 2007; 102, 11301142.Google Scholar
42.Watkins, AJ, Lucas, ES, Wilkins, A, Cagampang, FRA, Fleming, TP. Maternal periconceptional and gestational low protein diet affects mouse offspring growth, cardiovascular and adipose phenotype at 1 year of age. PLoS One. 2011; 6, e28745.CrossRefGoogle ScholarPubMed
43.Roseboom, TJ, Painter, RC, van Abeelen, AFM, Veenendaal, MVE, de Rooij, SR. Hungry in the womb: what are the consequences? Lessons from the Dutch famine. Maturitas. 2011; 70, 141145.Google Scholar
44.Rutter, MK, Parise, H, Benjamin, EJ, et al. Impact of glucose intolerance and insulin resistance on cardiac structure and function. Circulation. 2003; 107, 448454.Google Scholar
45.Mora, A, Sakamoto, K, McManus, EJ, Alessi, DR. Role of the PDK1–PKB–GSK3 pathway in regulating glycogen synthase and glucose uptake in the heart. FEBS Lett. 2005; 579, 36323638.Google Scholar
46.Stride, N, Larsen, S, Treebak, JT, et al. 5′-AMP activated protein kinase is involved in the regulation of myocardial β-oxidative capacity in mice. Front Physiol. 2012; 3, article 33.Google Scholar
47.Turdi, S, Kandadi, MR, Zhao, J, et al. Deficiency in AMP-activated protein kinase exaggerates high fat diet-induced cardiac hypertrophy and contractile dysfunction. J Mol Cell Cardiol. 2011; 50, 712722.CrossRefGoogle ScholarPubMed
48.Meurs, K, Lahmers, S, Keene, B, et al. A splice site mutation in a gene encoding for PDK4, a mitochondrial protein, is associated with the development of dilated cardiomyopathy in the Doberman pinscher. Hum Genet. 2012; 131, 13191325.CrossRefGoogle Scholar
49.Lopes, R, Solter, PF, Sisson, DD, Oyama, MA, Prosek, R. Characterization of canine mitochondrial protein expression in natural and induced forms of idiopathic dilated cardiomyopathy. Am J Vet Res. 2006; 67, 963970.CrossRefGoogle ScholarPubMed
50.Samovski, D, Su, X, Xu, Y, Abumrad, NA, Stahl, PD. Insulin and AMPK regulate FA translocase/CD36 plasma membrane recruitment in cardiomyocytes via Rab GAP AS160 and Rab8a Rab GTPase. J Lipid Res. 2012; 53, 709717.CrossRefGoogle ScholarPubMed
51.Ginion, A, Auquier, J, Benton, CR, et al. Inhibition of the mTOR/p70S6 K pathway is not involved in the insulin-sensitizing effect of AMPK on cardiac glucose uptake. Am J Physiol Heart Circ Physiol. 2011; 301, H469H477.Google Scholar
52.Waterland, RA, Michels, KB. Epigenetic epidemiology of the developmental origins hypothesis. Annu Rev Nutr. 2007; 27, 363388.Google Scholar
53.Guay, C, Roggli, E, Nesca, V, Jacovetti, C, Regazzi, R. Diabetes mellitus, a microRNA-related disease? Transl Res. 2011; 157, 253264.CrossRefGoogle ScholarPubMed
54.Rottiers, V, Najafi-Shoushtari, SH, Kristo, F, et al. MicroRNAs in metabolism and metabolic diseases. Cold Spring Harb Symp Quant Biol. 2011; 76, 225233.Google Scholar
55.Bartel, DP. MicroRNAs: genomics, biogenesis, mechanism, and function. Cell. 2004; 116, 281297.Google Scholar