Hostname: page-component-cd9895bd7-hc48f Total loading time: 0 Render date: 2024-12-23T13:13:19.851Z Has data issue: false hasContentIssue false

Offspring from maternal nutrient restriction in mice show variations in adult glucose metabolism similar to human fetal growth restriction

Published online by Cambridge University Press:  03 December 2018

B. N. Radford
Affiliation:
Department of Biochemistry, Schulich School of Medicine & Dentistry, Western University, London, ON, Canada Children’s Health Research Institute, London, ON, Canada
V. K. M. Han*
Affiliation:
Department of Biochemistry, Schulich School of Medicine & Dentistry, Western University, London, ON, Canada Children’s Health Research Institute, London, ON, Canada Department of Pediatrics, Schulich School of Medicine & Dentistry, Western University, London, ON, Canada
*
Address for correspondence: V.K.M. Han, MD, Children’s Health Research Institute, Victoria Hospital, 800 Commissioners Rd E, London, ON, Canada N6A 5W9. E-mail: [email protected]

Abstract

Fetal growth restriction (FGR) is a pregnancy condition in which fetal growth is suboptimal for gestation, and this population is at increased risk for type 2 diabetes as adults. In humans, maternal malnutrition and placental insufficiency are the most common causes of FGR, and both result in fetal undernutrition. We hypothesized that maternal nutrient restriction (MNR) in mice will cause FGR and alter glucose metabolism in adult offspring. Pregnant CD-1 mice were subjected to MNR (70% of average ad libitum) or control (ad libitum) from E6.5 to birth. Following birth, mice were fostered by mothers on ad libitum feeds. Weight, blood glucose, glucose tolerance and tissue-specific insulin sensitivity were assessed in male offspring. MNR resulted in reduced fetal sizes but caught up to controls by 3 days postnatal age. As adults, glucose intolerance was detected in 19% of male MNR offspring. At 6 months, liver size was reduced (P = 0.01), but pAkt-to-Akt ratios in response to insulin were increased 2.5-fold relative to controls (P = 0.004). These data suggest that MNR causes FGR and long-term glucose intolerance in a population of male offspring similar to human populations. This mouse model can be used to investigate the impacts of FGR on tissues of importance in glucose metabolism.

Type
Original Article
Copyright
© Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2018 

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

Han, VK, Seferovic, MD, Albion, CD, Gupta, MB. Intrauterine growth restriction: intervention strategies. In Neonatology (eds. Buonocore G, Bracci R, Weindling M), 2012; pp. 8993. Springer: Milano.CrossRefGoogle Scholar
Garite, TJ, Clark, R, Thorp, JA. Intrauterine growth restriction increases morbidity and mortality among premature neonates. Am J Obstet Gynecol. 2004; 191, 481487.CrossRefGoogle ScholarPubMed
Morrison, KM, Ramsingh, L, Gunn, E, et al. Cardiometabolic health in adults born premature with extremely low birth weight. Pediatrics. 2016; 138, e20160515.CrossRefGoogle ScholarPubMed
Würtz, P, Wang, Q, Niironen, M, et al. Metabolic signatures of birthweight in 18288 adolescents and adults. Int J Epidemiol. 2016; 45, 15391550.CrossRefGoogle Scholar
Hales, C, Barker, D. Type 2 (non-insulin-dependent) diabetes mellitus: the thrifty phenotype hypothesis. Diabetologia. 1992; 35, 595601.CrossRefGoogle ScholarPubMed
Oliveira, D, Cezar, J, Gomes, RM, et al. Protein restriction during the last third of pregnancy malprograms the neuroendocrine axes to induce metabolic syndrome in adult male rat offspring. Endocrinology. 2016; 157, 17991812.CrossRefGoogle ScholarPubMed
Xiao, D, Kou, H, Zhang, L, Guo, Y, Wang, H. Prenatal food restriction with postweaning high-fat diet alters glucose metabolic function in adult rat offspring. Arch Med Res. 2017; 48, 3545.CrossRefGoogle ScholarPubMed
Lee, S, You, Y-A, Kwon, EJ, et al. Maternal food restriction during pregnancy and lactation adversely affect hepatic growth and lipid metabolism in three-week-old rat offspring. Int J Mol Sci. 2016; 17, E2115.CrossRefGoogle ScholarPubMed
Nevin, CL, Formosa, E, Maki, Y, et al. Maternal nutrient restriction in guinea pigs as an animal model for studying growth restricted offspring with post-natal catch-up growth. Am J Physiol Regul Integr Comp Physiol. 2018; 314, R647R654.CrossRefGoogle Scholar
Wang, J, Cao, M, Zhuo, Y, et al. Catch-up growth following food restriction exacerbates adulthood glucose intolerance in pigs exposed to intrauterine undernutrition. Nutrition. 2016; 32, 12751284.CrossRefGoogle ScholarPubMed
Liu, Y, Ma, C, Li, H, et al. Effects of intrauterine growth restriction during late pregnancy on the cell apoptosis and related gene expression in ovine fetal liver. Theriogenology. 2017; 90, 204209.CrossRefGoogle ScholarPubMed
Vomhof-DeKrey, E, Darland, D, Ghribi, O, et al. Maternal low protein diet leads to placental angiogenic compensation via dysregulated M1/M2 macrophages and TNFα expression in Sprague-Dawley rats. J Reprod Immunol. 2016; 118, 917.CrossRefGoogle ScholarPubMed
Palha, AM, Pereira, SS, Costa, MM, et al. Differential GIP/GLP-1 intestinal cell distribution in diabetics’ yields distinctive rearrangements depending on Roux-en-Y biliopancreatic limb length. J Cell Biochem. 2018; 119, 75067514.CrossRefGoogle ScholarPubMed
Nauck, MA, Meier, JJ. Incretin hormones: their role in health and disease. Diabetes Obes. Metab. 2018; 20(Suppl 1), 521.CrossRefGoogle ScholarPubMed
Leighton, E, Sainsbury, CA, Jones, GC. A practical review of c-peptide testing in diabetes. Diabetes Ther. 2017; 8, 475487.CrossRefGoogle ScholarPubMed
Qatanani, M, Szwergold, NR, Greaves, DR, Ahima, RS, Lazar, MA. Macrophage-derived human resistin exacerbates adipose tissue inflammation and insulin resistance in mice. J Clin Invest. 2009; 119, 531539.CrossRefGoogle ScholarPubMed
Kaji, H. Adipose tissue-derived plasminogen activator inhibitor-1 function and regulation. Compr Physiol. 2016; 6, 18731896.CrossRefGoogle ScholarPubMed
Bewick, GA, Kent, A, Campbell, D, et al. Mice with hyperghrelinemia are hyperphagic and glucose intolerant and have reduced leptin sensitivity. Diabetes. 2009; 58, 840846.CrossRefGoogle ScholarPubMed
Kalra, SP, Ueno, N, Kalra, PS. Stimulation of appetite by ghrelin is regulated by leptin restraint: peripheral and central sites of action. J Nutr. 2005; 135, 13311335.CrossRefGoogle ScholarPubMed
Lecoutre, S, Marousez, L, Drougard, A, et al. Maternal undernutrition programs the apelinergic system of adipose tissue in adult male rat offspring. J Dev Orig Health Dis. 2017; 8, 37.CrossRefGoogle ScholarPubMed
Simchen, MJ, Weisz, B, Zilberberg, E, et al. Male disadvantage for neonatal complications of term infants, especially in small-for-gestational age neonates. J Matern Fetal Neonatal Med. 2014; 27, 839843.CrossRefGoogle ScholarPubMed
Delahaye, F, Wijetunga, NA, Heo, HJ, et al. Sexual dimorphism in epigenomic responses of stem cells to extreme fetal growth. Nat Commun. 2014; 5, 5187.CrossRefGoogle ScholarPubMed
Pae, M, Baek, Y, Lee, S, Wu, D. Loss of ovarian function in association with a high-fat diet promotes insulin resistance and disturbs adipose tissue immune homeostasis. J Nutr Biochem. 2018; 57, 93102.CrossRefGoogle ScholarPubMed
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. 2009; 234, 14251436.CrossRefGoogle Scholar
Nardozza, LMM, Araujo Júnior, E, Barbosa, MM, et al. Fetal growth restriction: current knowledge to the general Obs/Gyn. Arch Gynecol Obstet. 2012; 286, 113.CrossRefGoogle ScholarPubMed
Man, J, Hutchinson, JC, Ashworth, M, et al. Organ weights and ratios for postmortem identification of fetal growth restriction: utility and confounding factors. Ultrasound Obstet Gynecol Off J Int Soc. 2016; 48, 585590.CrossRefGoogle ScholarPubMed
Harris, RA, Alcott, CE, Sullivan, EL, et al. Genomic variants associated with resistance to high fat diet induced obesity in a primate model. Sci Rep. 2016; 6, 36123.CrossRefGoogle Scholar
Weingarten, A, Turchetti, L, Krohn, K, et al. Novel genes on rat chromosome 10 are linked to body fat mass, preadipocyte number and adipocyte size. Int J Obes. 2016; 40, 18321840.CrossRefGoogle ScholarPubMed
Chen, K, Jih, A, Osborn, O, et al. Distinct gene signatures predict insulin resistance in young mice with high fat diet-induced obesity. Physiol Genomics. 2018; 50, 144157.CrossRefGoogle ScholarPubMed
Zhu, W-F, Zhu, J-F, Liang, L, Shen, Z, Wang, Y-M. Maternal undernutrition leads to elevated hepatic triglycerides in male rat offspring due to increased expression of lipoprotein lipase. Mol Med Rep. 2016; 13, 44874493.CrossRefGoogle ScholarPubMed
Ma, J, Prince, AL, Bader, D, et al. High-fat maternal diet during pregnancy persistently alters the offspring microbiome in a primate model. Nat Commun. 2014; 5, 3889.CrossRefGoogle Scholar
Heo, HJ, Tozour, JN, Delahaye, F, et al. Advanced aging phenotype is revealed by epigenetic modifications in rat liver after in utero malnutrition. Aging Cell. 2016; 15, 964972.CrossRefGoogle ScholarPubMed
Camacho, LE, Chen, X, Hay, WW, Limesand, SW. Enhanced insulin secretion and insulin sensitivity in young lambs with placental insufficiency-induced intrauterine growth restriction. Am J Physiol Regul Integr Comp Physiol. 2017; 313, R101R109.CrossRefGoogle ScholarPubMed
Kim, S-H, Park, H-S, Hong, MJ, et al. Tongqiaohuoxue decoction ameliorates obesity-induced inflammation and the prothrombotic state by regulating adiponectin and plasminogen activator inhibitor-1. J Ethnopharmacol. 2016; 192, 201209.CrossRefGoogle ScholarPubMed
Veening, MA, Weissenbruch, V, Waal, MM, D de, AH. Glucose tolerance, insulin sensitivity, and insulin secretion in children born small for gestational age. J Clin Endocrinol Metab. 2002; 87, 46574661.CrossRefGoogle ScholarPubMed
de Souza, AP, Pedroso, AP, Watanabe, RLH, et al. Gender-specific effects of intrauterine growth restriction on the adipose tissue of adult rats: a proteomic approach. Proteome Sci. 2015; 13, 32.CrossRefGoogle ScholarPubMed
Soininen, S, Sidoroff, V, Lindi, V, et al. Body fat mass, lean body mass and associated biomarkers as determinants of bone mineral density in children 6–8years of age – The Physical Activity and Nutrition in Children (PANIC) study. Bone. 2018; 108, 106114.CrossRefGoogle ScholarPubMed
Xiao, X, Sun, Q, Kim, Y, et al. Exposure to permethrin promotes high fat diet-induced weight gain and insulin resistance in male C57BL/6J mice. Food Chem Toxicol. 2018; 111, 405416.CrossRefGoogle ScholarPubMed
Meakin, PJ, Jalicy, SM, Montagut, G, et al. Bace1-dependent amyloid processing regulates hypothalamic leptin sensitivity in obese mice. Sci Rep. 2018; 8, 55.CrossRefGoogle ScholarPubMed
Silveira, PP, Pokhvisneva, I, Gaudreau, H, et al. Fetal growth interacts with multilocus genetic score reflecting dopamine signaling capacity to predict spontaneous sugar intake in children. Appetite. 2018; 120, 596601.CrossRefGoogle ScholarPubMed
Lira, LA, Almeida, LCA, da Silva, AAM, et al. Perinatal undernutrition increases meal size and neuronal activation of the nucleus of the solitary tract in response to feeding stimulation in adult rats. Int J Dev Neurosci. 2014; 38, 2329.CrossRefGoogle ScholarPubMed
Supplementary material: File

Radford and Han supplementary material

Radford and Han supplementary material 1

Download Radford and Han supplementary material(File)
File 12.7 KB
Supplementary material: PDF

Radford and Han supplementary material

Radford and Han supplementary material 2

Download Radford and Han supplementary material(PDF)
PDF 63.9 KB
Supplementary material: Image

Radford and Han supplementary material

Radford and Han supplementary material 3

Download Radford and Han supplementary material(Image)
Image 491.5 KB
Supplementary material: Image

Radford and Han supplementary material

Radford and Han supplementary material 4

Download Radford and Han supplementary material(Image)
Image 380.4 KB
Supplementary material: Image

Radford and Han supplementary material

Radford and Han supplementary material 5

Download Radford and Han supplementary material(Image)
Image 24.4 MB