Early life factors and type 2 diabetes mellitus

Journal of Diabetes Research

Volumn 2013, Issue , 2013, Pages

  Jiang, Xinli ^a   Ma, Huijie ^a   Wang, Yan ^a   Liu, Yan ^a  

^a HEBEI MEDICAL UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ANIMAL; DIET; FEMALE; HUMAN; MATERNAL NUTRITION; NEWBORN; NON INSULIN DEPENDENT DIABETES MELLITUS; PHYSIOLOGY; PREGNANCY; PRENATAL EXPOSURE; REVIEW; RISK FACTOR;

ADULT; ANIMALS; DIABETES MELLITUS, TYPE 2; DIET; FEMALE; HUMANS; INFANT, NEWBORN; MATERNAL NUTRITIONAL PHYSIOLOGICAL PHENOMENA; PREGNANCY; PRENATAL EXPOSURE DELAYED EFFECTS; RISK FACTORS;

EID: 84893735472     PISSN: 23146745     EISSN: 23146753     Source Type: Journal    
DOI: 10.1155/2013/485082     Document Type: Article

References (128)

1. Mathers J. C., Early nutrition: impact on epigenetics. Forum of Nutrition 2007 60 42 48 2-s2.0-34547968390 10.1159/0000107066
2. Portrait F., Teeuwiszen E., Deeg D., Early life undernutrition and chronic diseases at older ages: the effects of the Dutch famine on cardiovascular diseases and diabetes. Social Science and Medicine 2011 73 5 711 718 2-s2.0-80051885978 10.1016/j.socscimed.2011.04.005
3. Yajnik C. S., Early life origins of insulin resistance and type 2 diabetes in india and other Asian countries. Journal of Nutrition 2004 134 1 205 210 2-s2.0-0348230971 (Pubitemid 38057450)
4. Orozco-Solís R., Matos R. J. B., Guzmán-Quevedo O., de Souza S. L., Bihouée A., Houlgatte R., de Castro R. M., Bolaños-Jiménez F., Nutritional programming in the rat is linked to long-lasting changes in nutrient sensing and energy homeostasis in the hypothalamus. PLoS ONE 2010 5 10 2-s2.0-78149440714 10.1371/journal.pone.0013537 e13537
5. Tarry-Adkins J. L., Chen J., Jones R. H., Smith N. H., Ozanne S. E., Poor maternal nutrition leads to alterations in oxidative stress, antioxidant defense capacity, and markers of fibrosis in rat islets: potential underlying mechanisms for development of the diabetic phenotype in later life. FASEB Journal 2010 24 8 2762 2771 2-s2.0-77955794377 10.1096/fj.10-156075
6. Sandovici I., Smith N. H., Nitert M. D., Ackers-Johnson M., Uribe-Lewis S., Ito Y., Jones R. H., Marquez V. E., Cairns W., Tadayyon M., O'Neill L. P., Murrell A., Ling C., Constância M., Ozanne S. E., Maternal diet and aging alter the epigenetic control of a promoter-enhancer interaction at the Hnf4a gene in rat pancreatic islets. Proceedings of the National Academy of Sciences of the United States of America 2011 108 13 5449 5454 2-s2.0-79955096234 10.1073/pnas.1019007108
7. Theys N., Ahn M., Bouckenooghe T., Reusens B., Remacle C., Maternal malnutrition programs pancreatic islet mitochondrial dysfunction in the adult offspring. Journal of Nutritional Biochemistry 2011 22 10 985 994 2-s2.0-80053120348 10.1016/j.jnutbio.2010.08.015
8. Rodriguez-Trejo A., Ortiz-Lopez M. G., Zambrano E., Granados-Silvestre M. L., Mendez C., Blondeau B., Bréant B., Nathanielsz P. W., Menjivar M., Developmental programming of neonatal pancreatic β -cells by a maternal low-protein diet in rats involves a switch from proliferation to differentiation. The American Journal of Physiology-Endocrinology and Metabolism 2012 302 11 E1431 E1439 10.1152/ajpendo.00619.2011
9. Maurer A. D., Reimer R. A., Maternal consumption of high-prebiotic fibre or -protein diets during pregnancy and lactation differentially influences satiety hormones and expression of genes involved in glucose and lipid metabolism in offspring in rats. The British Journal of Nutrition 2011 105 3 329 338 2-s2.0-79951677393 10.1017/S0007114510003533
10. Sadashiv, Tiwari S., Paul B. N., Kumar S., Chandra A., Dhananjai S., Negi M. P., Resistin gene expression in visceral adipose tissue of postmenopausal women and its association with insulin resistance. Women's Health 2012 8 5 521 528 10.2217/whe.12.46
11. Matsubara T., Mita A., Minami K., Hosooka T., Kitazawa S., Takahashi K., Tamori Y., Yokoi N., Watanabe M., Matsuo E., Nishimura O., Seino S., PGRN is a key adipokine mediating high fat diet-induced insulin resistance and obesity through IL-6 in adipose tissue. Cell Metabolism 2012 15 1 38 50 2-s2.0-84855430348 10.1016/j.cmet.2011.12.002
12. Lee K. M., Yang S. J., Kim Y. D., Choi Y. D., Nam J. H., Choi C. S., Choi H. S., Park C. S., Disruption of the cereblon gene enhances hepatic AMPK activity and prevents high-fat diet-induced obesity and insulin resistance in mice. Diabetes 2013 62 6 1855 1864 10.2337/db12-1030
13. Black M. H., Watanabe R. M., Trigo E., Takayanagi M., Lawrence J. M., Buchanan T. A., Xiang A. H., High-fat diet is associated with obesity-mediated insulin resistance and β -cell dysfunction in Mexican Americans. Journal of Nutrition 2013 143 4 479 485 10.3945/jn.112.170449
14. Masuyama H., Hiramatsu Y., Effects of a high-fat diet exposure in utero on the metabolic syndrome-like phenomenon in mouse offspring through epigenetic changes in adipocytokine gene expression. Endocrinology 2012 153 6 2823 2830
15. Liang C., Oest M. E., Prater M. R., Intrauterine exposure to high saturated fat diet elevates risk of adult-onset chronic diseases in C57BL/6 mice. Birth Defects Research B 2009 86 5 377 384 2-s2.0-70350707630 10.1002/bdrb.20206
16. Rajia S., Chen H., Morris M. J., Maternal overnutrition impacts offspring adiposity and brain appetite markers-modulation by postweaning diet. Journal of Neuroendocrinology 2010 22 8 905 914 2-s2.0-77954713690 10.1111/j.1365-2826. 2010.02005.x
17. Briancon N., McNay D. E., Maratos-Flier E., Flier J. S., Combined neural inactivation of suppressor of cytokine signaling-3 and protein-tyrosine phosphatase-1B reveals additive, synergistic, and factor-specific roles in the regulation of body energy balance. Diabetes 2010 59 12 3074 3084 2-s2.0-78650071301 10.2337/db10-0481
18. Ashino N. G., Saito K. N., Souza F. D., Nakutz F. S., Roman E. A., Velloso L. A., Torsoni A. S., Torsoni M. A., Maternal high-fat feeding through pregnancy and lactation predisposes mouse offspring to molecular insulin resistance and fatty liver. Journal of Nutritional Biochemistry 2012 23 4 341 348 2-s2.0-84858289329 10.1016/j.jnutbio.2010.12.011
19. Yang K. F., Shen X. H., Cai W., Prenatal and early postnatal exposure to high-saturated-fat diet represses Wnt signaling and myogenic genes in offspring rats. Experimental Biology and Medicine 2012 237 8 912 918 10.1258/ebm.2012. 011395
20. Abiola M., Favier M., Christodoulou-Vafeiadou E., Pichard A., Martelly I., Guillet-Deniau I., Activation of Wnt/ β -catenin signaling increases insulin sensitivity through a reciprocal regulation of Wnt10b and SREBP-1c in skeletal muscle cells. PLoS ONE 2009 4 12 e8509 2-s2.0-77949493593
21. Thompson A. K., Minihane A.-M., Williams C. M., Trans fatty acids, insulin resistance and diabetes. European Journal of Clinical Nutrition 2011 65 5 553 564 2-s2.0-79955657300 10.1038/ejcn.2010.240
22. Micha R., Mozaffarian D., Trans fatty acids: effects on metabolic syndrome, heart disease and diabetes. Nature Reviews Endocrinology 2009 5 6 335 344 2-s2.0-68949086659 10.1038/nrendo.2009.79
23. Dorfman S. E., Laurent D., Gounarides J. S., Li X., Mullarkey T. L., Rocheford E. C., Sari-Sarraf F., Hirsch E. A., Hughes T. E., Commerford S. R., Metabolic implications of dietary trans-fatty acids. Obesity 2009 17 6 1200 1207 2-s2.0-67650478372 10.1038/oby.2008.662
24. Kavanagh K., Sajadian S., Jenkins K. A., Wilson M. D., Carr J. J., Wagner J. D., Rudel L. L., Neonatal and fetal exposure to trans-fatty acids retards early growth and adiposity while adversely affecting glucose in mice. Nutrition Research 2010 30 6 418 426 2-s2.0-77954916996 10.1016/j.nutres.2010.06.006
25. Bayol S. A., Simbi B. H., Fowkes R. C., Stickland N. C., A maternal "junk food" diet in pregnancy and lactation promotes nonalcoholic fatty liver disease in rat offspring. Endocrinology 2010 151 4 1451 1461 2-s2.0-77950284708 10.1210/en.2009-1192
26. Ramirez T., Tong M., Chen W. C., Nguyen Q. G., Wands J. R., de la Monte S. M., Chronic alcohol-induced hepatic insulin resistance and endoplasmic reticulum stress ameliorated by peroxisome-proliferator activated receptor-delta agonist treatment. Journal of Gastroenterology and Hepatology 2013 28 1 179 187 10.1111/j.1440-1746.2012.07256.x
27. Yue F., Zhang X., Zhang H., Jiang X., Gao L., Zhao J., Association of alcohol consumption with the impaired β -cell function independent of body mass index among Chinese men. Endocrine Journal 2012 59 5 425 433 10.1507/endocrj.EJ12-0003
28. Chen L., Nyomba B. L. G., Effects of prenatal alcohol exposure on glucose tolerance in the rat offspring. Metabolism 2003 52 4 454 462 2-s2.0-0038751824 10.1053/meta.2003.50073 (Pubitemid 36773268)
29. Chen L., Zhang T., Nyomba B. L. G., Insulin resistance of gluconeogenic pathways in neonatal rats after prenatal ethanol exposure. The American Journal of Physiology-Regulatory Integrative and Comparative Physiology 2004 286 3 R554 R559 2-s2.0-1342267441 (Pubitemid 38252621)
30. Chen L., Yao X. H., Nyomba B. L. G., In vivo insulin signaling through PI3-kinase is impaired in skeletal muscle of adult rat offspring exposed to ethanol in utero. Journal of Applied Physiology 2005 99 2 528 534 2-s2.0-23044432133 10.1152/japplphysiol.01098.2004 (Pubitemid 41061145)
31. Yao X. H., Chen L., Nyomba B. L. G., Adult rats prenatally exposed to ethanol have increased gluconeogenesis and impaired insulin response of hepatic gluconeogenic genes. Journal of Applied Physiology 2006 100 2 642 648 2-s2.0-33646351086 10.1152/japplphysiol.01115.2005 (Pubitemid 43671620)
32. Yao X. H., Nyomba B. L. G., Hepatic insulin resistance induced by prenatal alcohol exposure is associated with reduced PTEN and TRB3 acetylation in adult rat offspring. The American Journal of Physiology-Regulatory Integrative and Comparative Physiology 2008 294 6 R1797 R1806 2-s2.0-47549092773 10.1152/ajpregu.00804.2007
33. Yao X. H., Nyomba B. L. G., Abnormal glucose homeostasis in adult female rat offspring after intrauterine ethanol exposure. The American Journal of Physiology-Regulatory Integrative and Comparative Physiology 2007 292 5 R1926 R1933 2-s2.0-34248155673 10.1152/ajpregu.00822.2006 (Pubitemid 46708548)
34. Beguinot F., Tribbles homologue 3 (TRIB3) and the insulin-resistance genes in type 2 diabetes. Diabetologia 2010 53 9 1831 1834 2-s2.0-77955552917 10.1007/s00125-010-1824-7
35. Gupta A., Dey C. S., PTEN, a widely known negative regulator of insulin/PI3K signaling, positively regulates neuronal insulin resistance. Molecular Biology of the Cell 2012 23 19 3882 3898 10.1091/mbc.E12-05-0337
36. Nammi S., Dembele K., Nyomba B. L. G., Increased 11 β -hydroxysteroid dehydrogenase type-1 and hexose-6-phosphate dehydrogenase in liver and adipose tissue of rat offspring exposed to alcohol in utero. The American Journal of Physiology-Regulatory Integrative and Comparative Physiology 2007 292 3 R1101 R1109 2-s2.0-33847762288 10.1152/ajpregu.00255.2006 (Pubitemid 46377073)
37. Groff T., Bisphenol A: invisible pollution. Current Opinion in Pediatrics 2010 22 4 524 529 2-s2.0-77955229220 10.1097/MOP.0b013e32833b03f8
38. Alonso-Magdalena P., Morimoto S., Ripoll C., Fuentes E., Nadal A., The estrogenic effect of bisphenol a disrupts pancreatic β -cell function in vivo and induces insulin resistance. Environmental Health Perspectives 2006 114 1 106 112 2-s2.0-30344444488 10.1289/ehp.8451 (Pubitemid 43056876)
39. Nadal A., Alonso-Magdalena P., Soriano S., Quesada I., Ropero A. B., The pancreatic β -cell as a target of estrogens and xenoestrogens: implications for blood glucose homeostasis and diabetes. Molecular and Cellular Endocrinology 2009 304 1-2 63 68 2-s2.0-67349253060 10.1016/j.mce.2009.02.016
40. Alonso-Magdalena P., Ropero A. B., Soriano S., Quesada I., Nadal A., Bisphenol-A: a new diabetogenic factor? Hormones 2010 9 2 118 126 2-s2.0-77953181779
41. Makaji E., Raha S., Wade M. G., Holloway A. C., Effect of environmental contaminants on β cell function. International Journal of Toxicology 2011 30 4 410 418 2-s2.0-84555217997
42. Lang I. A., Galloway T. S., Scarlett A., Henley W. E., Depledge M., Wallace R. B., Melzer D., Association of Urinary Bisphenol A concentration with medical disorders and laboratory abnormalities in adults. The Journal of the American Medical Association 2008 300 11 1303 1310 2-s2.0-51949106158 10.1001/jama.300.11.1303
43. Wei J., Lin Y., Li Y., Ying C., Chen J., Song L., Zhou Z., Lv Z., Xia W., Chen X., Xu S., Perinatal exposure to bisphenol A at reference dose predisposes offspring to metabolic syndrome in adult rats on a high-fat diet. Endocrinology 2011 152 8 3049 3061 2-s2.0-79960731559 10.1210/en.2011-0045
44. Alonso-Magdalena P., Vieira E., Soriano S., Menes L., Burks D., Quesada I., Nadal A., Bisphenol a exposure during pregnancy disrupts glucose homeostasis in mothers and adult male offspring. Environmental Health Perspectives 2010 118 9 1243 1250 2-s2.0-77956808565 10.1289/ehp.1001993
45. Ryan K. K., Haller A. M., Sorrell J. E., Woods S. C., Jandacek R. J., Seeley R. J., Perinatal exposure to bisphenol-A and the development of metabolic syndrome in CD-1 mice. Endocrinology 2010 151 6 2603 2612 2-s2.0-77954530270 10.1210/en.2009-1218
46. Cao L., Mao C., Li S., Zhang Y., Lv J., Jiang S., Xu Z., Hepatic insulin signaling changes: possible mechanism in prenatal hypoxia-increased susceptibility of fatty liver in adulthood. Endocrinology 2012 153 10 4955 4965 10.1210/en.2012-1349
47. Camm E. J., Martin-Gronert M. S., Wright N. L., Hansell J. A., Ozanne S. E., Giussani D. A., Prenatal hypoxia independent of undernutrition promotes molecular markers of insulin resistance in adult offspring. FASEB Journal 2011 25 1 420 427 2-s2.0-79251581849 10.1096/fj.10-158188
48. Chang S. A., Smoking and type 2 diabetes mellitus. Diabetes and Metabolism Journal 2012 36 6 399 403 10.4093/dmj.2012.36.6.399
49. Bergman B. C., Perreault L., Hunerdosse D., Kerege A., Playdon M., Samek A. M., Eckel R. H., Novel a, nd reversible mechanisms of smoking-induced insulin resistance in humans. Diabetes 2012 61 12 3156 3166 10.2337/db12-0418
50. Thiering E., Brüske I., Kratzsch J., Thiery J., Sausenthaler S., Meisinger C., Koletzko S., Bauer C., Schaaf B., von Berg A., Berdel D., Lehmann I., Herbarth O., Krämer U., Wichmann H.-., Heinrich J., Prenatal and postnatal tobacco smoke exposure and development of insulin resistance in 10 year old children. International Journal of Hygiene and Environmental Health 2011 214 5 361 368 2-s2.0-80051791734 10.1016/j.ijheh.2011.04.004
51. Bruin J. E., Kellenberger L. D., Gerstein H. C., Morrison K. M., Holloway A. C., Fetal and neonatal nicotine exposure and postnatal glucose homeostasis: identifying critical windows of exposure. Journal of Endocrinology 2007 194 1 171 178 2-s2.0-34547403058 10.1677/JOE-07-0050 (Pubitemid 47162896)
52. Holloway A. C., Cuu D. Q., Morrison K. M., Gerstein H. C., Tarnopolsky M. A., Transgenerational effects of fetal and neonatal exposure to nicotine. Endocrine 2007 31 3 254 259 2-s2.0-35348881464 10.1007/s12020-007-0043-6 (Pubitemid 47574977)
53. Somm E., Schwitzgebel V. M., Vauthay D. M., Camm E. J., Chen C. Y., Giacobino J., Sizonenko S. V., Aubert M. L., Hüppi P. S., Prenatal nicotine exposure alters early pancreatic islet and adipose tissue development with consequences on the control of body weight and glucose metabolism later in life. Endocrinology 2008 149 12 6289 6299 2-s2.0-57349197879 10.1210/en.2008-0361
54. Chen H., Saad S., Sandow S. L., Bertrand P. P., Cigarette smoking and brain regulation of energy homeostasis. Frontiers in Pharmacology 2012 3 article 147
55. Coe C. L., Lubach G. R., Shirtcliff E. A., Maternal stress during pregnancy predisposes for iron deficiency in infant monkeys impacting innate immunity. Pediatric Research 2007 61 5, part 1 520 524 2-s2.0-34247528878 10.1203/pdr.0b013e318045be53 (Pubitemid 46650001)
56. Lesage J., Del-Favero F., Leonhardt M., Louvart H., Maccari S., Vieau D., Darnaudery M., Prenatal stress induces intrauterine growth restriction and programmes glucose intolerance and feeding behaviour disturbances in the aged rat. Journal of Endocrinology 2004 181 2 291 296 2-s2.0-2942530662 10.1677/joe.0.1810291 (Pubitemid 38744678)
57. Li J., Olsen J., Vestergaard M., Obel C., Kristensen J. K., Virk J., Prenatal exposure to bereavement and type-2 diabetes: a Danish longitudinal population based study. PLoS ONE 2012 7 8 e43508
58. Entringer S., Wüst S., Kumsta R., Layes I. M., Nelson E. L., Hellhammer D. H., Wadhwa P. D., Prenatal psychosocial stress exposure is associated with insulin resistance in young adults. The American Journal of Obstetrics and Gynecology 2008 199 5 498.e1 498.e7 2-s2.0-53349140184 10.1016/j.ajog.2008.03.006
59. Entringer S., Epel E. S., Kumsta R., Lin J., Hellhammer D. H., Blackburn E. H., Wüst S., Wadhwa P. D., Stress exposure in intrauterine life is associated with shorter telomere length in young adulthood. Proceedings of the National Academy of Sciences of the United States of America 2011 108 33 E513 E518 2-s2.0-80051988894 10.1073/pnas.1107759108
60. Salpea K. D., Talmud P. J., Cooper J. A., Maubaret C. G., Stephens J. W., Abelak K., Humphries S. E., Association of telomere length with type 2 diabetes, oxidative stress and UCP2 gene variation. Atherosclerosis 2010 209 1 42 50 2-s2.0-77049106292 10.1016/j.atherosclerosis.2009.09.070
61. Buxton J. L., Walters R. G., Visvikis-Siest S., Meyre D., Froguel P., Blakemore A. I. F., Childhood obesity is associated with shorter leukocyte telomere length. Journal of Clinical Endocrinology and Metabolism 2011 96 5 1500 1505 2-s2.0-79955674904 10.1210/jc.2010-2924
62. Fernandez-Twinn D. S., Blackmore H. L., Siggens L., Giussani D. A., Cross C. M., Foo R., Ozanne S. E., The programming of cardiac hypertrophy in the offspring by maternal obesity is associated with hyperinsulinemia, AKT, ERK, and mTOR activation. Endocrinology 2012 153 12 5961 5971 10.1210/en.2012-1508
63. O'Reilly J. R., Reynolds R. M., The risk of maternal obesity to the long-term health of the offspring. Clinical Endocrinology 2013 78 1 9 16 10.1111/cen.12055
64. Obregon M., Maternal obesity results in offspring prone to metabolic syndrome. Endocrinology 2010 151 8 3475 3476 2-s2.0-77954904040 10.1210/en.2010-0611
65. Boney C. M., Verma A., Tucker R., Vohr B. R., Metabolic syndrome in childhood: association with birth weight, maternal obesity, and gestational diabetes mellitus. Pediatrics 2005 115 3 e290 e296 2-s2.0-20344382306 10.1542/peds.2004-1808 (Pubitemid 43373011)
66. Shankar K., Kang P., Harrell A., Zhong Y., Marecki J. C., Ronis M. J. J., Badger T. M., Maternal overweight programs insulin and adiponectin signaling in the offspring. Endocrinology 2010 151 6 2577 2589 2-s2.0-77954487878 10.1210/en.2010-0017
67. Zhang L., Long N. M., Hein S. M., Ma Y., Nathanielsz P. W., Ford S. P., Maternal obesity in ewes results in reduced fetal pancreatic β -cell numbers in late gestation and decreased circulating insulin concentration at term. Domestic Animal Endocrinology 2011 40 1 30 39 2-s2.0-78649451421 10.1016/j.domaniend.2010.08.004
68. Ford S. P., Zhang L., Zhu M., Miller M. M., Smith D. T., Hess B. W., Moss G. E., Nathanielsz P. W., Nijland M. J., Maternal obesity accelerates fetal pancreatic β -cell but not α -cell development in sheep: prenatal consequences. The American Journal of Physiology-Regulatory Integrative and Comparative Physiology 2009 297 3 R835 R843 2-s2.0-69249110098 10.1152/ajpregu.00072.2009
69. Oben J. A., Mouralidarane A., Samuelsson A., Matthews P. J., Morgan M. L., Mckee C., Soeda J., Fernandez-Twinn D. S., Martin-Gronert M. S., Ozanne S. E., Sigala B., Novelli M., Poston L., Taylor P. D., Maternal obesity during pregnancy and lactation programs the development of offspring non-alcoholic fatty liver disease in mice. Journal of Hepatology 2010 52 6 913 920 2-s2.0-77952420159 10.1016/j.jhep.2009.12.042
70. Borengasser S. J., Lau F., Kang P., Blackburn M. L., Ronis M. J. J., Badger T. M., Shankar K., Maternal obesity during gestation impairs fatty acid oxidation and mitochondrial SIRT3 expression in rat offspring at weaning. PLoS ONE 2011 6 8 2-s2.0-80052050501 10.1371/journal.pone.0024068 e24068
71. Boerschmann H., Pflüger M., Henneberger L., Ziegler A., Hummel S., Prevalence and predictors of overweight and insulin resistance in offspring of mothers with gestational diabetes mellitus. Diabetes Care 2010 33 8 1845 1849 2-s2.0-77958187116 10.2337/dc10-0139
72. Bush N. C., Chandler-Laney P. C., Rouse D. J., Granger W. M., Oster R. A., Gower B. A., Higher maternal gestational glucose concentration is associated with lower offspring insulin sensitivity and altered β -cell function. Journal of Clinical Endocrinology and Metabolism 2011 96 5 E803 E809 2-s2.0-79955661840 10.1210/jc.2010-2902
73. Song Y., Li J., Zhao Y., Zhang Q., Liu Z., Li J., Chen X., Yang Z., Yu C., Xiao X., Severe maternal hyperglycemia exacerbates the development of insulin resistance and fatty liver in the offspring on high fat diet. Experimental Diabetes Research 2012 2012 8 254976 10.1155/2012/254976
74. Ma J. M., Zeng C. J., Zhang L., Shou C., Yang H. X., Increased hepatic peroxisome proliferator-activated receptor coactivator-1 α expression precedes the development of insulin resistance in offspring of rats from severe hyperglycemic mothers. Chinese Medical Journal 2012 125 7 1224 1229 2-s2.0-84859942983 10.3760/cma.j.issn.0366-6999.2012.07.007
75. Natali A., Muscelli E., Mari A., Balkau B., Walker M., Tura A., Anderwald C., Golay A., Ferrannini E., Insulin sensitivity and β -cell function in the offspring of type 2 diabetic patients: impact of line of inheritance. Journal of Clinical Endocrinology and Metabolism 2010 95 10 4703 4711 2-s2.0-77957820339 10.1210/jc.2009-2721
76. King A. J., Olivier N. B., Mohankumar P. S., Lee J. S., Padmanabhan V., Fink G. D., Hypertension caused by prenatal testosterone excess in female sheep. The American Journal of Physiology-Endocrinology and Metabolism 2007 292 6 E1837 E1841 2-s2.0-34447580063 10.1152/ajpendo.00668.2006 (Pubitemid 47084721)
77. Recabarren S. E., Padmanabhan V., Codner E., Lobos A., Durán C., Vidal M., Foster D. L., Sir-Petermann T., Postnatal developmental consequences of altered insulin sensitivity in female sheep treated prenatally with testosterone. The American Journal of Physiology-Endocrinology and Metabolism 2005 289 5 E801 E806 2-s2.0-27144489633 10.1152/ajpendo.00107.2005 (Pubitemid 41504379)
78. Padmanabhan V., Veiga-Lopez A., Abbott D. H., Recabarren S. E., Herkimer C., Developmental programming: impact of prenatal testosterone excess and postnatal weight gain on insulin sensitivity index and transfer of traits to offspring of overweight females. Endocrinology 2010 151 2 595 605 2-s2.0-74949096775 10.1210/en.2009-1015
79. Nada S. E., Thompson R. C., Padmanabhan V., Developmental programming: differential effects of prenatal testosterone excess on insulin target tissues. Endocrinology 2010 151 11 5165 5173 2-s2.0-78049490908 10.1210/en.2010-0666
80. Roland A. V., Nunemaker C. S., Keller S. R., Moenter S. M., Prenatal androgen exposure programs metabolic dysfunction in female mice. Journal of Endocrinology 2010 207 2 213 223 2-s2.0-78049388028 10.1677/JOE-10-0217
81. Amalfi S., Velez L. M., Heber M. F., Vighi S., Ferreira S. R., Orozco A. V., Pignataro O., Motta A. B., Prenatal hyperandrogenization induces metabolic and endocrine alterations which depend on the levels of testosterone exposure. PLoS ONE 2012 7 5 e37658 10.1371/journal.pone.0037658
82. Sun M., Maliqueo M., Benrick A., Johansson J., Shao R., Hou L., Jansson T., Wu X., Stener-Victorin E., Maternal androgen excess reduces placental and fetal weights, increases placental steroidogenesis, and leads to long-term health effects in their female offspring. The American Journal of Physiology-Endocrinology and Metabolism 2012 303 11 E1373 E1385 10.1152/ajpendo.00421.2012
83. Bruns C. M., Baum S. T., Colman R. J., Eisner J. R., Kemnitz J. W., Weindruch R., Abbott D. H., Insulin resistance and impaired insulin secretion in prenatally androgenized male rhesus monkeys. Journal of Clinical Endocrinology and Metabolism 2004 89 12 6218 6223 2-s2.0-10344240900 10.1210/jc.2004-0918 (Pubitemid 39628436)
84. Hogg K., Wood C., McNeilly A. S., Duncan W. C., The in utero programming effect of increased maternal androgens and a direct fetal intervention on liver and metabolic function in adult sheep. PLoS ONE 2011 6 9 2-s2.0-80052830410 10.1371/journal.pone.0024877 e24877
85. Nyirenda M. J., Dean S., Lyons V., Chapman K. E., Seckl J. R., Prenatal programming of hepatocyte nuclear factor 4 α in the rat: a key mechanism in the "foetal origins of hyperglycaemia"? Diabetologia 2006 49 6 1412 1420 2-s2.0-33646530739 10.1007/s00125-006-0188-5
86. Nyirenda M. J., Lindsay R. S., Kenyon C. J., Burchell A., Seckl J. R., Glucocorticoid exposure in late gestation permanently programs rat hepatic phosphoenolpyruvate carboxykinase and glucocorticoid receptor expression and causes glucose intolerance in adult offspring. Journal of Clinical Investigation 1998 101 10 2174 2181 2-s2.0-0032524014 (Pubitemid 28244101)
87. Franko K. L., Giussani D. A., Forhead A. J., Fowden A. L., Effects of dexamethasone on the glucogenic capacity of fetal, pregnant, and non-pregnant adult sheep. Journal of Endocrinology 2007 192 1 67 73 2-s2.0-33947381879 10.1677/joe.1.07063 (Pubitemid 46444396)
88. Nyirenda M. J., Carter R., Tang J. I., de Vries A., Schlumbohm C., Hillier S. G., Streit F., Oellerich M., Armstrong V. W., Fuchs E., Seckl J. R., Prenatal programming of metabolic syndrome in the common marmoset is associated with increased expression of 11 β -hydroxysteroid dehydrogenase type 1. Diabetes 2009 58 12 2873 2879 2-s2.0-73249138413 10.2337/db09-0873
89. Li G., Hernandez-Ono A., Crooke R. M., Graham M. J., Ginsberg H. N., Antisense reduction of 11 β -hydroxysteroid dehydrogenase type 1 enhances energy expenditure and insulin sensitivity independent of food intake in C57BL/6J mice on a Western-type diet. Metabolism 2012 61 6 823 835 2-s2.0-84455162035 10.1016/j.metabol.2011.11.008
90. Xu D., Liang G., Yan Y. E., He W. W., Liu Y. S., Chen L. B., Magdalou J., Wang H., Nicotine-induced over-exposure to maternal glucocorticoid and activated glucocorticoid metabolism causes hypothalamic-pituitary-adrenal axis-associated neuroendocrine metabolic alterations in fetal rats. Toxicology Letters 2012 209 3 282 290 2-s2.0-84856324058 10.1016/j.toxlet.2012.01.006
91. Valtat B., Dupuis C., Zenaty D., Singh-Estivalet A., Tronche F., Bréant B., Blondeau B., Genetic evidence of the programming of β cell mass and function by glucocorticoids in mice. Diabetologia 2011 54 2 350 359 2-s2.0-78951488762 10.1007/s00125-010-1898-2
92. Liang G., Chen M., Pan X. L., Zheng J., Wang H., Ethanol-induced inhibition of fetal hypothalamic-pituitary-adrenal axis due to prenatal overexposure to maternal glucocorticoid in mice. Experimental and Toxicologic Pathology 2011 63 7-8 607 611 2-s2.0-80053237831 10.1016/j.etp.2010.04.015
93. Bruce K. D., Hanson M. A., The developmental origins, mechanisms, and implications of metabolic syndrome. Journal of Nutrition 2010 140 3 648 652 2-s2.0-77249117213 10.3945/jn.109.111179
94. Fernandez-Twinn D. S., Ozanne S. E., Mechanisms by which poor early growth programs type-2 diabetes, obesity and the metabolic syndrome. Physiology and Behavior 2006 88 3 234 243 2-s2.0-33745215673 10.1016/j.physbeh.2006.05.039
95. Martin-Gronert M. S., Ozanne S. E., Mechanisms linking suboptimal early nutrition and increased risk of type 2 diabetes and obesity. Journal of Nutrition 2010 140 3 662 666 2-s2.0-77249087654 10.3945/jn.109.111237
96. Deng H. Z., Deng H., Su Z., Li Y. H., Ma H. M., Chen H. S., Du M. L., Insulin resistance and adiponectin levels are associated with height catch-up growth in pre-pubertal Chinese individuals born small for gestational age. Nutrition and Metabolism 2012 9 1, article 107 10.1186/1743-7075-9-107
97. Crowther N. J., Cameron N., Trusler J., Toman M., Norris S. A., Gray I. P., Influence of catch-up growth on glucose tolerance and β -cell function in 7-year-old children: results from the birth to twenty study. Pediatrics 2008 121 6 e1715 e1722 2-s2.0-48949103061 10.1542/peds.2007-3147
98. Ong K. K., Petry C. J., Emmett P. M., Saradhu M. S., Kiess W., Hales C. N., Ness A. R., Dunger D. B., Insulin sensitivity and secretion in normal children related to size at birth, postnatal growth, and plasma insulin-like growth factor-I levels. Diabetologia 2004 47 6 1064 1070 2-s2.0-3142754168 (Pubitemid 38918166)
99. Cettour-Rose P., Samec S., Russell A. P., Summermatter S., Mainieri D., Carrillo-Theander C., Montani J., Seydoux J., Rohner-Jeanrenaud F., Dulloo A. G., Redistribution of glucose from skeletal muscle to adipose tissue during catch-up fat: a link between catch-up growth and later metabolic syndrome. Diabetes 2005 54 3 751 756 2-s2.0-20044364157 10.2337/diabetes.54.3.751 (Pubitemid 40322078)
100. Dulloo A. G., Thrifty energy metabolism in catch-up growth trajectories to insulin and leptin resistance. Best Practice and Research in Clinical Endocrinology and Metabolism 2008 22 1 155 171 2-s2.0-38949142226 10.1016/j.beem.2007.08.001 (Pubitemid 351218276)
101. Dulloo A. G., Jacquet J., Seydoux J., Montani J.-., The thrifty "catch-up fat" phenotype: its impact on insulin sensitivity during growth trajectories to obesity and metabolic syndrome. International Journal of Obesity 2006 30 supplement 4 S23 S35 2-s2.0-33751536127 10.1038/sj.ijo.0803516 (Pubitemid 44837546)
102. Lima N. S., de Moura E. G., Passos M. C. F., Neto J. F. N., Reis A. M., de Oliveira E., Lisboa P. C., Early weaning causes undernutrition for a short period and programmes some metabolic syndrome components and leptin resistance in adult rat offspring. The British Journal of Nutrition 2011 105 9 1405 1413 2-s2.0-79956033907 10.1017/S0007114510005064
103. Pentinat T., Ramon-Krauel M., Cebria J., Diaz R., Jimenez-Chillaron J. C., Transgenerational inheritance of glucose intolerance in a mouse model of neonatal overnutrition. Endocrinology 2010 151 12 5617 5623 2-s2.0-78649832440 10.1210/en.2010-0684
104. Davidowa H., Plagemann A., Insulin resistance of hypothalamic arcuate neurons in neonatally overfed rats. NeuroReport 2007 18 5 521 524 2-s2.0-34247552309 10.1097/WNR.0b013e32805dfb93 (Pubitemid 46668046)
105. Plagemann A., Roepke K., Harder T., Brunn M., Harder A., Wittrock-Staar M., Ziska T., Schellong K., Rodekamp E., Melchior K., Dudenhausen J. W., Epigenetic malprogramming of the insulin receptor promoter due to developmental overfeeding. Journal of Perinatal Medicine 2010 38 4 393 400 2-s2.0-77954601343 10.1515/JPM.2010.051
106. Conceicao E. P., Franco J. G., Oliveira E., Resende A. C., Amaral T. A., Peixoto-Silva N., Passos M. C., Moura E. G., Lisboa P. C., Oxidative stress programming in a rat model of postnatal early overnutrition-role of insulin resistance. Journal of Nutritional Biochemistry 2013 24 1 81 87 10.1016/j.jnutbio.2012.02.010
107. Kaufman D., Banerji M. A., Shorman I., Smith E. L. P., Coplan J. D., Rosenblum L. A., Kral J. G., Early-life stress and the development of obesity and insulin resistance in juvenile bonnet macaques. Diabetes 2007 56 5 1382 1386 2-s2.0-34248229213 10.2337/db06-1409 (Pubitemid 46715631)
108. Gorski J. N., Dunn-Meynell A. A., Hartman T. G., Levin B. E., Postnatal environment overrides genetic and prenatal factors influencing offspring obesity and insulin resistance. The American Journal of Physiology-Regulatory Integrative and Comparative Physiology 2006 291 3 R768 R778 2-s2.0-33748450150 10.1152/ajpregu.00138.2006 (Pubitemid 44352361)
109. de Oliveira E., Moura E. G., Santos-Silva A. P., Pinheiro C. R., Lima N. S., Neto J. F. N., Nunes-Freitas A. L., Abreu-Villaça Y., Passos M. C. F., Lisboa P. C., Neonatal nicotine exposure causes insulin and leptin resistance and inhibits hypothalamic leptin signaling in adult rat offspring. Journal of Endocrinology 2010 206 1 55 63 2-s2.0-77953816890 10.1677/JOE-10-0104
110. Loizzo S., Campana G., Vella S., Fortuna A., Galietta G., Guarino I., Costa L., Capasso A., Renzi P., Frajese G. V., Franconi F., Loizzo A., Spampinato S., Post-natal stress-induced endocrine and metabolic alterations in mice at adulthood involve different pro-opiomelanocortin-derived peptides. Peptides 2010 31 11 2123 2129 2-s2.0-77957844265 10.1016/j.peptides.2010.08.001
111. Loizzo A., Loizzo S., Galietta G., Caiola S., Spampinato S., Campana G., Seghieri G., Ghirlanda G., Franconi F., Overweight and metabolic and hormonal parameter disruption are induced in adult male mice by manipulations during lactation period. Pediatric Research 2006 59 1 111 115 2-s2.0-33644829469 10.1203/01.pdr.0000190575.12965.ce
112. Baxi D. B., Singh P. K., Vachhrajani K. D., Ramachandran A. V., Plasticity changes in adult metabolic homeostasis and tissue oxidative stress: neonatal programming by corticosterone and melatonin as deprogrammer. Journal of Maternal-Fetal and Neonatal Medicine 2012 25 6 831 844 10.3109/14767058.2011. 599456
113. Alexanderson C., Eriksson E., Stener-Victorin E., Lönn M., Holmáng A., Early postnatal oestradiol exposure causes insulin resistance and signs of inflammation in circulation and skeletal muscle. Journal of Endocrinology 2009 201 1 49 58 2-s2.0-67651009611 10.1677/JOE-08-0534
114. Nilsson C., Niklasson M., Eriksson E., Björntorp P., Holmäng A., Imprinting of female offspring with testosterone results in insulin resistance and changes in body fat distribution at adult age in rats. Journal of Clinical Investigation 1998 101 1 74 78 2-s2.0-0031985351 (Pubitemid 28058905)
115. Kuznetsova E. G., Amstislavskaya T. G., Bulygina V. V., Il'nitskaya S. I., Tibeikina M. A., Skrinskaya Y. A., Effects of administration of sodium glutamate during the neonatal period on behavior and blood corticosterone levels in male mice. Neuroscience and Behavioral Physiology 2007 37 8 827 833 2-s2.0-35048817365 10.1007/s11055-007-0088-2 (Pubitemid 47555143)
116. Rácz B., Tamás A., Kiss P., Tóth G., Gasz B., Borsiczky B., Ferencz A., Gallyas F. Jr., Roth E., Reglodi D., Involvement of ERK and CREB signaling pathways in the protective effect of PACAP in monosodium glutamate-induced retinal lesion. Annals of the New York Academy of Sciences 2006 1070 507 511 2-s2.0-33746467019 10.1196/annals.1317.070 (Pubitemid 44126694)
117. Chaparro-Huerta V., Rivera-Cervantes M. C., Flores-Soto M. E., Gómez-Pinedo U., Beas-Zárate C., Proinflammatory cytokines and apoptosis following glutamate-induced excitotoxicity mediated by p38 MAPK in the hippocampus of neonatal rats. Journal of Neuroimmunology 2005 165 1-2 53 62 2-s2.0-22144488038 10.1016/j.jneuroim.2005.04.025 (Pubitemid 40984623)
118. Hirata A. E., Andrade I. S., Vaskevicius P., Dolnikoff M. S., Monosodium glutamate (MSG)-obese rats develop glucose intolerance and insulin resistance to peripheral glucose uptake. Brazilian Journal of Medical and Biological Research 1997 30 5 671 674 2-s2.0-0031134821 (Pubitemid 127521185)
119. Roman-Ramos R., Almanza-Perez J. C., Garcia-Macedo R., Blancas-Flores G., Fortis-Barrera A., Jasso E. I., Garcia-Lorenzana M., Campos-Sepulveda A. E., Cruz M., Alarcon-Aguilar F. J., Monosodium glutamate neonatal intoxication associated with obesity in adult stage is characterized by chronic inflammation and increased mRNA expression of peroxisome proliferator-activated receptors in mice. Basic and Clinical Pharmacology and Toxicology 2011 108 6 406 413 2-s2.0-79955951104 10.1111/j.1742-7843.2011.00671.x
120. Sasaki Y., Suzuki W., Shimada T., Iizuka S., Nakamura S., Nagata M., Fujimoto M., Tsuneyama K., Hokao R., Miyamoto K., Aburada M., Dose dependent development of diabetes mellitus and non-alcoholic steatohepatitis in monosodium glutamate-induced obese mice. Life Sciences 2009 85 13-14 490 498 2-s2.0-70349164862 10.1016/j.lfs.2009.07.017
121. Andreazzi A. E., Scomparin D. X., Mesquita F. P., Balbo S. L., Gravena C., de Oliveira J. C., Rinaldi W., Garcia R. M. G., Grassiolli S., Mathias P. C. F., Swimming exercise at weaning improves glycemic control and inhibits the onset of monosodium L-glutamate-obesity in mice. Journal of Endocrinology 2009 201 3 351 359 2-s2.0-67849089031 10.1677/JOE-08-0312
122. Sasaki Y., Shimada T., Iizuka S., Suzuki W., Makihara H., Teraoka R., Tsuneyama K., Hokao R., Aburada M., Effects of bezafibrate in nonalcoholic steatohepatitis model mice with monosodium glutamate-induced metabolic syndrome. European Journal of Pharmacology 2011 662 1-3 1 8 2-s2.0-79957591055 10.1016/j.ejphar.2011.04.051
123. Maty S. C., Lynch J. W., Raghunathan T. E., Kaplan G. A., Childhood socioeconomic position, gender, adult body mass index, and incidence of type 2 diabetes mellitus over 34 years in the Alameda county study. The American Journal of Public Health 2008 98 8 1486 1494 2-s2.0-48749087112 10.2105/AJPH.2007.123653
124. Tamayo T., Christian H., Rathmann W., Impact of early psychosocial factors (childhood socioeconomic factors and adversities) on future risk of type 2 diabetes, metabolic disturbances and obesity: a systematic review. BMC Public Health 2010 10, article 525 2-s2.0-77956462081 10.1186/1471-2458-10-525
125. van Abeelen A. F., Elias S. G., Bossuyt P. M., Grobbee D. E., van der Schouw Y. T., Roseboom T. J., Uiterwaal C. S., Famine exposure in the young and the risk of type 2 diabetes in adulthood. Diabetes 2012 61 9 2255 2260 10.2337/db11-1559
126. Biro F. M., Wien M., Childhood obesity and adult morbidities. The American Journal of Clinical Nutrition 2010 91 5 1499S 1505S 2-s2.0-77951948444 10.3945/ajcn.2010.28701B
127. Franks P. W., Hanson R. L., Knowler W. C., Sievers M. L., Bennett P. H., Looker H. C., Childhood obesity, other cardiovascular risk factors, and premature death. The New England Journal of Medicine 2010 362 6 485 493 2-s2.0-76649086071 10.1056/NEJMoa0904130
128. Caceres M., Teran C. G., Rodriguez S., Medina M., Prevalence of insulin resistance and its association with metabolic syndrome criteria among Bolivian children and adolescents with obesity. BMC Pediatrics 2008 8, article 31 2-s2.0-51049101907 10.1186/1471-2431-8-31