Hippocampal apoptosis involved in learning deficits in the offspring exposed to maternal high sucrose diets

Journal of Nutritional Biochemistry

Volumn 25, Issue 9, 2014, Pages 985-990

  Kuang, Hanzhe ^a   Sun, Miao ^a   Lv, Juanxiu ^a   Li, Jiayue ^a   Wu, Chonglong ^a   Chen, Ningjing ^a   Bo, Le ^a   Wei, Xiaoguang ^a   Gu, Xiuxia ^a   Liu, Zhen ^a   Mao, Caiping ^a   Xu, Zhice ^a,b  

^a THE FIRST AFFILIATED HOSPITAL OF SOOCHOW UNIVERSITY   (China)

^b LOMA LINDA UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Apoptosis; High sucrose; Hippocampus; Offspring; Spatial cognition

Indexed keywords

CASPASE 3; N METHYL DEXTRO ASPARTIC ACID RECEPTOR; PHOSPHATIDYLINOSITOL 3 KINASE; PROTEIN KINASE B; SOMATOMEDIN C; SUCROSE; GLUCOSE BLOOD LEVEL;

ANIMAL EXPERIMENT; ANIMAL MODEL; APOPTOSIS; ARTICLE; BRAIN METABOLISM; BRAIN WEIGHT; COGNITIVE DEFECT; CONTROLLED STUDY; FEMALE; GLUCOSE BLOOD LEVEL; HIPPOCAMPAL CA2 REGION; HIPPOCAMPAL CA3 REGION; LATENT PERIOD; LEARNING DISORDER; MORRIS WATER MAZE TEST; NERVE CELL; NONHUMAN; PRENATAL DEVELOPMENT; PROGENY; PROTEIN EXPRESSION; RAT; SPATIAL MEMORY; ANIMAL; DRUG EFFECTS; HIPPOCAMPUS; METABOLISM; ORGAN SIZE; PATHOLOGY; PREGNANCY; PRENATAL EXPOSURE; SPRAGUE DAWLEY RAT;

ANIMALS; APOPTOSIS; BLOOD GLUCOSE; FEMALE; HIPPOCAMPUS; LEARNING DISORDERS; ORGAN SIZE; PREGNANCY; PRENATAL EXPOSURE DELAYED EFFECTS; RATS; RATS, SPRAGUE-DAWLEY; SPATIAL MEMORY; SUCROSE;

EID: 84905278287     PISSN: 09552863     EISSN: 18734847     Source Type: Journal    
DOI: 10.1016/j.jnutbio.2014.04.012     Document Type: Article

References (37)

1. Barker D.J. The fetal origins of diseases of old age. Eur J Clin Nutr 1992, 46(3):S3-S9.
2. Lv J., Mao C., Zhu L., Zhang H., Pengpeng H., Xu F., et al. The effect of prenatal nicotine on expression of nicotine receptor subunits in the fetal brain. Neurotoxicology 2008, 29:722-726.
3. Eriksson U.J. Congenital anomalies in diabetic pregnancy. Seminars in Fetal and Neonatal Medicine; 2009 2009, 85-93. Elsevier.
4. Pogoda J.M., Preston-Martin S., Howe G., Lubin F., Mueller B.A., Holly E.A., et al. An international case-control study of maternal diet during pregnancy and childhood brain tumor risk: a histology-specific analysis by food group. Ann Epidemiol 2009, 19(3):148-160.
5. Chang T.I., Horal M., Jain S.K., Wang F., Patel R., Loeken M. Oxidant regulation of gene expression and neural tube development: insights gained from diabetic pregnancy on molecular causes of neural tube defects. Diabetologia 2003, 46(4):538-545.
6. Hendricks K.A., Nuno O.M., Suarez L., Larsen R. Effects of hyperinsulinemia and obesity on risk of neural tube defects among Mexican Americans. Epidemiology 2001, 12:630-635.
7. Shaw G.M., Quach T., Nelson V., Carmichael S.L., Schaffer D.M., Selvin S., et al. Neural tube defects associated with maternal periconceptional dietary intake of simple sugars and glycemic index. Am J Clin Nutr 2003, 78(5):972-978.
8. Rizzo T., Metzger B.E., Burns W.J., Burns K. Correlations between antepartum maternal metabolism and intelligence of offspring. N Engl J Med 1991, 325:911-916.
9. Lever C., Wills T., Cacucci F., Burgess N., O'Keefe J. Long-term plasticity in hippocampal place-cell representation of environmental geometry. Nature 2002, 416:90-94.
10. Ye P., D'Ercole A.J. Insulin like growth factor actions during development of neural stem cells and progenitors in the central nervous system. J Neurosci Res 2006, 83(1):1-6.
11. D'Ercole A.J., Ye P., Calikoglu A.S., Gutierrez-Ospina G. The role of the insulin-like growth factors in the central nervous system. Mol Neurobiol 1996, 13(3):227-255.
12. Duarte A.I., Moreira P.I., Oliveira C.R. Insulin in central nervous system: more than just a peripheral hormone. J Aging Res 2012, 2012:384017.
13. Vestling M., Wiehager B., Tanii H., Cowburn R.F. Akt activity in presenilin 1 wild-type and mutation transfected human SH-SY5Y neuroblastoma cells after serum deprivation and high glucose stress. J Neurosci Res 2001, 66(3):448-456.
14. Leinninger G.M., Backus C., Uhler M.D., Lentz S.I., Feldman E.L. Phosphatidylinositol 3-kinase and Akt effectors mediate insulin-like growth factor-I neuroprotection in dorsal root ganglia neurons. FASEB J 2004, 18(13):1544-1546.
15. Barber A.J., Nakamura M., Wolpert E.B., Reiter C.E., Seigel G.M., Antonetti D.A., et al. Insulin rescues retinal neurons from apoptosis by a phosphatidylinositol 3-kinase/Akt-mediated mechanism that reduces the activation of caspase-3. J Biol Chem 2001, 276(35):32814-32821.
16. Dastidar S.G., Landrieu P.M.Z., D'Mello S.R. FoxG1 promotes the survival of postmitotic neurons. J Neurosci 2011, 31(2):402-413.
17. Tagami M., Yamagata K., Nara Y., Fujino H., Kubota A., Numano F., et al. Insulin-like growth factors prevent apoptosis in cortical neurons isolated from stroke-prone spontaneously hypertensive rats. Lab Investig 1997, 76(5):603-612.
18. Morris R. Developments of a water-maze procedure for studying spatial learning in the rat. J Neurosci Methods 1984, 11(1):47-60.
19. Paxinos G., Watson C. The rat brain in stereotaxic coordinates: hard cover edition 2006, Academic press.
20. De La Puente A., Goya L., Ramos S., Martin M., Alvarez C., Escriva F., et al. Effects of experimental diabetes on renal IGF/IGFBP system during neonatal period in the rat. Am J Physiol Renal Physiol 2000, 279(6):F1067-F1076.
21. Marsh K., Barclay A., Colagiuri S., Brand-Miller J. Glycemic index and glycemic load of carbohydrates in the diabetes diet. Curr Diab Rep 2011, 11(2):120-127.
22. Li Y., Dai Q., Jackson J.C., Zhang J. Overweight is associated with decreased cognitive functioning among school-age children and adolescents. Obesity 2008, 16(8):1809-1815.
23. Armitage J.A., Khan I.Y., Taylor P.D., Nathanielsz P.W., Poston L. Developmental programming of the metabolic syndrome by maternal nutritional imbalance: how strong is the evidence from experimental models in mammals?. J Physiol 2004, 561(2):355-377.
24. Leib S.L., Heimgartner C., Bifrare Y.D., Loeffler J.M., Täuber M.G. Dexamethasone aggravates hippocampal apoptosis and learning deficiency in pneumococcal meningitis in infant rats. Pediatr Res 2003, 54(3):353-357.
25. Magliozzi R., Howell O.W., Reeves C., Roncaroli F., Nicholas R., Serafini B., et al. A Gradient of neuronal loss and meningeal inflammation in multiple sclerosis. Ann Neurol 2010, 68(4):477-493.
26. Nakazawa K., Quirk M.C., Chitwood R.A., Watanabe M., Yeckel M.F., Sun L.D., et al. Requirement for hippocampal CA3 NMDA receptors in associative memory recall. Science 2002, 297(5579):211-218.
27. Lee I., Kesner R.P. Differential contributions of dorsal hippocampal subregions to memory acquisition and retrieval in contextual fear conditioning. Hippocampus 2004, 14(3):301-310.
28. Clark R.S.B., Kochanek P.M., Chen M., Watkins S.C., Marion D.W., Chen J., et al. Increases in Bcl-2 and cleavage of caspase-1 and caspase-3 in human brain after head injury. FASEB J 1999, 13(8):813-821.
29. Enari M., Sakahira H., Yokoyama H., Okawa K., Iwamatsu A., Nagata S. A caspase-activated DNase that degrades DNA during apoptosis, and its inhibitor ICAD. Nature 1998, 391(6662):43-50.
30. Li Z.G., Zhang W., Grunberger G., Sima A.A. Hippocampal neuronal apoptosis in type 1 diabetes. Brain Res 2002, 946(2):221-231.
31. Swanton E., Savory P., Cosulich S., Clarke P., Woodman P. Bcl-2 regulates a caspase-3/caspase-2 apoptotic cascade in cytosolic extracts. Oncogene 1999, 18(10):1781-1787.
32. Ishii D.N. Implication of insulin-like growth factors in the pathogenesis of diabetic neuropathy. Brain Res Rev 1995, 20(1):47-67.
33. Steen E., Terry B.M., Rivera E.J., Cannon J.L., Neely T.R., Tavares R., et al. Impaired insulin and insulin-like growth factor expression and signaling mechanisms in Alzheimer's disease-is this type 3 diabetes?. J Alzheimers Dis 2005, 7(1):63-80.
34. Traynelis S.F., Wollmuth L.P., McBain C.J., Menniti F.S., Vance K.M., Ogden K.K., et al. Glutamate receptor ion channels: structure, regulation, and function. Pharmacol Rev 2010, 62(3):405-496.
35. Gupta K., Hardingham G.E., Chandran S. NMDA receptor-dependent glutamate excitotoxicity in human embryonic stem cell-derived neurons. Neurosci Lett 2013, 543:95-100.
36. Arsenijevic Y., Weiss S., Schneider B., Aebischer P. Insulin-like growth factor-I is necessary for neural stem cell proliferation and demonstrates distinct actions of epidermal growth factor and fibroblast growth factor-2. J Neurosci 2001, 21(18):7194-7202.
37. Lee K.H., Calikoglu A.S., Ye P., D'Ercole A.J. Insulin-like growth factor-I (IGF-I) ameliorates and IGF binding protein-1 (IGFBP-1) exacerbates the effects of undernutrition on brain growth during early postnatal life: studies in IGF-I and IGFBP-1 transgenic mice. Pediatr Res 1999, 45(3):331-336.