Common phenotypes and the developmental origins of disease

Current Opinion in Clinical Nutrition and Metabolic Care

Volumn 16, Issue 4, 2013, Pages 398-404

  McMullen, Sarah ^a   Swali, Angie ^a  

^a UNIVERSITY OF NOTTINGHAM   (United Kingdom)

Author keywords

Epigenetics; Metabolism; Microarray; Nutrition; Proteomics

Indexed keywords

DEVELOPMENTAL STAGE; DISEASE COURSE; GENE CONTROL; GENE EXPRESSION; MATERNAL NUTRITION; NONHUMAN; NUTRIENT SUPPLY; PERINATAL PERIOD; PHENOTYPE; PROGENY; REVIEW;

CELL CYCLE; DIET; EPIGENESIS, GENETIC; FEMALE; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HUMANS; MATERNAL NUTRITIONAL PHYSIOLOGICAL PHENOMENA; METABOLIC DISEASES; PHENOTYPE; PREGNANCY;

ANIMALIA;

EID: 84880324732     PISSN: 13631950     EISSN: 14736519     Source Type: Journal    
DOI: 10.1097/MCO.0b013e328361f879     Document Type: Review

References (39)

1. Godfrey KM, Gluckman PD, Hanson MA. Developmental origins of metabolic disease:life course and intergenerational perspectives. Trends Endocrinol Metab 2010; 21:199-205.
2. McMullen S, Mostyn A. Animal models for the study of the developmental origins of health and disease. Proc Nutr Soc 2009; 68:306-320.
3. McMullen S, Langley-Evans SC, Gambling L, et al. A common cause for a common phenotype:the gatekeeper hypothesis in fetal programming. Med Hypotheses 2012; 78:88-94.
4. Swali A, McMullen S, Hayes H, et al. Cell cycle regulation and cytoskeletal remodelling are critical processes in the nutritional programming of embryonic development. Plos One 2011; 6:e23189.
5. Swali A, McMullen S, Hayes H, et al. Processes underlying the nutritional programming of embryonic development by iron deficiency in the rat. Plos One 2012; 7:e48133.
6. Altmann S, Murani E, Metges CC, et al. Effect of gestational protein deficiency and excess on hepatic expression of genes related to cell cycle and proliferation in offspring from late gestation to finishing phase in pig. Molec Biol Rep 2012; 39:7095-7104.
7. Oster M, Murani E, Metges CC, et al. A high protein diet during pregnancy affects hepatic gene expression of energy sensing pathways along ontogenesis in a porcine model. PLoS One 2011; 6:e21691.
8. Oster M, Murani E, Metges CC, et al. A low protein diet during pregnancy provokes a lasting shift of hepatic expression of genes related to cell cycle throughout ontogenesis in a porcine model. BMC Genomics 2012; 16:93.
9. Oster M, Murani E, Metges CC, et al. A Gestational high protein diet affects the abundance of muscle transcripts related to cell cycle regulation throughout development in porcine progeny. Plos One 2012; 7:e34519. 10.
10. Silva-Junior GO, Aguila MB, Mandarim-de-Lacerda CA. Insights into coronary artery development in model of maternal protein restriction in mice. Anat Rec (Hoboken) 2011; 294:1757-1764.
11. Yamada M, Wolfe D, Han G, et al. Early onset of fatty liver in growthrestricted rat fetuses and newborns. Congenital Anomalies 2011; 51:167-173.
12. Picone O, Laigre P, Fortun-Lamothe L, et al. Hyperlipidic hypercholesterolemic diet in prepubertal rabbits affects gene expression in the embryo, restricts fetal growth and increases offspring susceptibility to obesity. Theriogenology 2011; 75:287-299.
13. Luzzo KM, Wang Q, Purcell SH, et al. High fat diet induced developmental defects in the mouse:oocyte meiotic aneuploidy and fetal growth retardation/ brain defects. Plos One 2012; 7:e49217.
14. Dominguez-Salas P, Cox SE, Prentice AM, et al. Maternal nutritional status, C-1 metabolism and offspring DNA methylation:A review of current evidence in human subjects. Proc Nutr Soc 2012; 71:154-165.
15. Yang K-f, Cai W, Xu J-l, Shi W. Maternal high-fat diet programs Wnt genes through histone modification in the liver of neonatal rats. J Molec Endocrinol 2012; 49:107-114.
16. Kelsall CJ, Hoile SP, Irvine NA, et al. Vascular dysfunction induced in offspring by maternal dietary fat involves altered arterial polyunsaturated fatty acid biosynthesis. Plos One 2012; 7:e34492.
17. Cong R, Jia Y, Li R, et al. Maternal low-protein diet causes epigenetic deregulation of HMGCR and CYP7 alpha 1 in the liver of weaning piglets. J Nutr Biochem 2012; 23:1647-1654.
18. Jia Y, Cong R, Li R, et al. Maternal low-protein diet induces gender-dependent changes in epigenetic regulation of the glucose-6-phosphatase gene in newborn piglet liver. J Nutr 2012; 142:1659-1665.
19. Zheng S, Rollet M, Pan Y-X, et al. Protein restriction during gestation alters histone modifications at the glucose transporter 4 (GLUT4) promoter region and induces GLUT4 expression in skeletal muscle of female rat offspring. J Nutr Biochem 2012; 23:1064-1071.
20. Begum G, Stevens A, Smith EB, et al. Epigenetic changes in fetal hypothalamic energy regulating pathways are associated with maternal undernutrition and twinning. FASEB J 2012; 26:1694-1703.
21. Ivanova E, Chen J-H, Segonds-Pichon A, et al. DNA methylation at differentially methylated regions of imprinted genes is resistant to developmental programming by maternal nutrition. Epigenetics 2012; 7:1200-1210.
22. Han R, Li A, Li L, et al. Maternal 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; 26:3528-3536.
23. Tarry-Adkins JL, Martin-GronertMS, Fernandez-Twinn DS, et al. Poor maternal nutrition followed by accelerated postnatal growth leads to alterations in DNA damage and repair, oxidative and nitrosative stress, and oxidative defense capacity in rat heart. FASEB J 2013; 27:379-390.
24. Blackmore HL, Piekarz AV, Fernandez-Twinn DS, et al. Poor maternal nutrition programmes a pro-atherosclerotic phenotype in ApoE(-/-) mice. Clin Sci 2012; 123:251-257.
25. Yates Z, Tarling EJ, Langley-Evans SC, Salter AM. Maternal undernutrition programmes atherosclerosis in the ApoE-3-Leiden mouse. Br J Nutr 2009; 101:1185-1194.
26. Sathishkumar K, Elkins R, Yallampalli U, Yallampalli C. Protein restriction during pregnancy induces hypertension in adult female rat offspring -influence of oestradiol. Br J Nutr 2012; 107:665-673. This study is novel in that it used postnatal gondectomy to investigate the protective role of female sex which is observed in several programming models, demonstrating that oestrogen contributes to the sexual dimporphism observed.
27. Oliver MH, Bloomfield FH, Jaquiery AL, et al. Periconceptional undernutrition suppresses cortisol response to arginine vasopressin and corticotropinreleasing hormone challenge in adult sheep offspring. J Develop Origins Health D 2012; 3:52-58.
28. George LA, Zhang L, Tuersunjiang N, et al. Early maternal undernutrition programs increased feed intake, altered glucose metabolism and insulin secretion, and liver function in aged female offspring. Am J Physiol Regul Integr Comp Physiol 2012; 302:R797-804.
29. Theys N, Ahn M-T, Bouckenooghe T, et al. Maternal malnutrition programs pancreatic islet mitochondrial dysfunction in the adult offspring. J Nutr Biochem 2011; 22:985-994.
30. Ponzio BF, Catelli Carvalho MH, Fortes ZB, Franco MdC. Implications of maternal nutrient restriction in transgenerational programming of hypertension and endothelial dysfunction across F1-F3 offspring. Life Sci 2012; 90:571-577.
31. 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.
32. Fernandez-Twinn DS, Blackmore HL, Siggens L. The programming of cardiac hypertrophy in the offspring by maternal obesity is associated with hyperinsulinemia, AKT, ERK, and mTOR activation. Endocrinology 2012; 153:5961-5971.
33. Ashino NG, Saito KN, Souza FD, et al. Maternal high-fat feeding through pregnancy and lactation predisposes mouse offspring to molecular insulin resistance and fatty liver. J Nutr Biochem 2012; 23:341-348.
34. Laura Burgueno A, Cabrerizo R, Gonzales Mansilla N, et al. Maternal high-fat intake during pregnancy programs metabolic-syndrome-related phenotypes through liver mitochondrial DNA copy number and transcriptional activity of liver PPARGC1A. J Nutr Biochem 2013; 24:6-13.
35. Whitaker KW, Totoki K, Reyes TM. Metabolic adaptations to early life protein restriction differ by offspring sex and postweaning diet in the mouse. Nutr Metab Cardiovasc Dis 2012; 22:1067-1074.
36. Akyol A,McMullen S, Langley-Evans SC. Glucose intolerance associated with early-life exposure to maternal cafeteria feeding is dependent upon postweaning diet. Br J Nutr 2012; 107:964-978.
37. Simar D, Chen H, Lambert K, et al. Interaction between maternal obesity and postnatal over-nutrition on skeletal muscle metabolism. Nutr Metab Cardiovasc Dis 2012; 22:269-276.
38. Bourque SL, Komolova M, McCabe K, et al. Perinatal iron deficiency combined with a high-fat diet causes obesity and cardiovascular dysregulation. Endocrinology 2012; 153:1174-1182.
39. Sun B, Purcell RH, Terrillion CE, et al. Maternal high-fat diet during gestation or suckling differentially affects offspring leptin sensitivity and obesity. Diabetes 2012; 61:2833-2841.