Protein expression in the brain of rat offspring in relation to prenatal caloric restriction

Journal of Maternal-Fetal and Neonatal Medicine

Volumn 29, Issue 16, 2016, Pages 2707-2714

  Aravidou, Eftychia ^a,e   Eleftheriades, Makarios ^a,b   Malamitsi Puchner, Ariadne ^c   Anagnostopoulos, Athanassios K ^d   Aravantinos, Leon ^a   Dontas, Ismene ^a   Aravidis, Christos ^a   Creatsas, Georgios ^a   Tsangaris, Georgios ^d   Chrousos, Georgios P ^a,d  

^a UNIVERSITY OF ATHENS MEDICAL SCHOOL   (Greece)

^b EmbryoCare   (Greece)

^c UNIVERSITY OF ATHENS   (Greece)

^d BIOMEDICAL RESEARCH FOUNDATION   (Greece)

^e UNIVERSITY OF ATHENS   (Greece)

Author keywords

Animal model; brain development; IUGR; proteomics

Indexed keywords

ALPHA ENOLASE; CALRETICULIN; COLLAPSIN RESPONSE MEDIATOR PROTEIN; ELONGATION FACTOR; FASCIN; HEAT SHOCK PROTEIN 70; HEAT SHOCK PROTEIN 90; ISOENZYME; PEROXIREDOXIN 2; PROTEIN 14 3 3; PYRUVATE KINASE; CHAPERONE; CYTOSKELETON PROTEIN; NERVE PROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BRAIN MATURATION; CALORIC RESTRICTION; CONTROLLED STUDY; DOWN REGULATION; ENERGY BALANCE; FEMALE; GROWTH REGULATION; INTRAUTERINE GROWTH RETARDATION; MALE; NERVE CELL PLASTICITY; NEWBORN; NONHUMAN; PRENATAL PERIOD; PRIORITY JOURNAL; PROGENY; PROTEIN DETERMINATION; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN ISOLATION; PROTEIN LOCALIZATION; PROTEOMICS; RAT; TWO DIMENSIONAL GEL ELECTROPHORESIS; UPREGULATION; ANIMAL; BRAIN; BRAIN CHEMISTRY; EMBRYOLOGY; ENERGY METABOLISM; FETOMATERNAL TRANSFUSION; GENE EXPRESSION; GENETICS; ISOLATION AND PURIFICATION; METABOLISM; OXIDATIVE STRESS; PREGNANCY; WISTAR RAT;

ANIMALS; BRAIN; BRAIN CHEMISTRY; CALORIC RESTRICTION; CYTOSKELETAL PROTEINS; ENERGY METABOLISM; FEMALE; FETAL GROWTH RETARDATION; GENE EXPRESSION; MALE; MATERNAL-FETAL EXCHANGE; MOLECULAR CHAPERONES; NERVE TISSUE PROTEINS; NEURONAL PLASTICITY; OXIDATIVE STRESS; PREGNANCY; PROTEOMICS; RATS; RATS, WISTAR;

EID: 84945552717     PISSN: 14767058     EISSN: 14764954     Source Type: Journal    
DOI: 10.3109/14767058.2015.1102222     Document Type: Article

References (40)

1. Wu G, Imhoff-Kunsch B, Girard AW. Biological mechanisms for nutritional regulation of maternal health and fetal development. Paediatr Perinat Epidemiol 2012; 26: 4-26
2. Hales CN, Barker DJ. The thrifty phenotype hypothesis. Br Med Bull 2001; 60: 5-20
3. Hanson MA, Gluckman PD. Developmental origins of health and disease: new insights. Basic Clin Pharmacol Toxicol 2008; 102: 90-3
4. Bryan SM, Hindmarsh P. Normal and abnormal fetal growth. Horm Res 2006; 65: 19-27
5. Warner MJ, Ozanne SE. Mechanisms involved in the developmental programming of adulthood disease. Biochem J 2010; 427: 333-47
6. Deshane J, Chaves L, Sarikonda KV, et al. Proteomics analysis of rat brain protein modulations by grape seed extract. J Agric Food Chem 2004; 52: 7872-83
7. Langley-Evans SC, Sculley DV. The association between birthweight and longevity in the rat is complex and modulated by maternal protein intake during fetal life. FEBS Lett 2006; 580: 4150-3
8. Schröder HJ. Models of fetal growth restriction. Eur J Obstet Gynecol Reprod Biol 2003; 110: S29-39
9. Aravidou E, Tsangaris G, Samara A, et al. Aberrant expression of collapsin response mediator proteins-1,-2 and-5 in the brain of intrauterine growth restricted rats. Int J Dev Neurosci 2013; 31: 53-60
10. Lillycrop KA, Slater-Jefferies JL, Hanson MA, et al. Induction of altered epigenetic regulation of the hepatic glucocorticoid receptor in the offspring of rats fed a protein-restricted diet during pregnancy suggests that reduced DNA methyltransferase-1 expression is involved in impaired DNA methylation and changes in histone modifications. Br J Nutr 2007; 97: 1064-73
11. Wallace JM, Luther JS, Milne JS, et al. Nutritional modulation of adolescent pregnancy outcome-A review. Placenta 2006; 27: S61-8
12. Fountoulakis M, Tsangaris GT, Maris A, Lubec G. The rat brain hippocampus proteome. J Chromatogr B Analyt Technol Biomed Life Sci 2005; 819: 115-29
13. Görg A, Weiss W, Dunn MJ. Current two-dimensional electrophoresis technology for proteomics. Proteomics 2004; 4: 3665-85
14. Stephanou A, Latchman DS. Transcriptional modulation of heat-shock protein gene expression. Biochem Res Int 2011; 2011: 238601
15. Schmechel DE, Brightman MW, Marangos PJ. Neurons switch from non-neuronal enolase to neuron-specific enolase during differentiation. Brain Res 1980; 190: 195-214
16. Berg D, Holzmann C, Riess O. 14-3-3 proteins in the nervous system. Nat Rev Neurosci 2003; 4: 752-62
17. Kim SH, Fountoulakis M, Cairns N, Lubec G. Protein levels of human peroxiredoxin subtypes in brains of patients with Alzheimer's disease and Down syndrome. J Neural Transm Suppl 2001; 61: 223-35
18. Quinn CC, Gray GE, Hockfield S A family of proteins implicated in axon guidance and outgrowth. J Neurobiol 1999; 41: 158-64
19. Neitzke U, Harder T, Schellong K, et al. Intrauterine growth restriction in a rodent model and developmental programming of the metabolic syndrome: a critical appraisal of the experimental evidence. Placenta 2008; 29: 246-54
20. Eleftheriades M, Pervanidou P, Vafaei H, et al. Metabolic profiles of adult Wistar rats in relation to prenatal and postnatal nutritional manipulation: the role of birthweight. Hormones (Athens) 2014; 13: 268-79
21. Bradford MM A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 1976; 72: 248-54
22. Berndt P, Hobohm U, Langen H. Reliable automatic protein identification from matrix-Assisted laser desorption/ionization mass spectrometric peptide fingerprints. Electrophoresis 1999; 20: 3521-6
23. Bateson P, Barker D, Clutton-Brock T, et al. Developmental plasticity and human health. Nature 2004; 430: 419-21
24. Pearl LH, Prodromou C. Structure and mechanism of the Hsp90 molecular chaperone machinery. Annu Rev Biochem 2006; 75: 271-94
25. Butterfield DA, Poon HF, St Clair D, et al. Redox proteomics identification of oxidatively modified hippocampal proteins in mild cognitive impairment: insights into the development of Alzheimer's disease. Neurobiol Dis 2006; 22: 223-32
26. Alexandre-Gouabau MC, Bailly E, Moyon TL, et al. Postnatal growth velocity modulates alterations of proteins involved in metabolism and neuronal plasticity in neonatal hypothalamus in rats born with intrauterine growth restriction. J NutrBiochem 2012; 23: 140-52
27. Foote M, Zhou Y. 14-3-3 proteins in neurological disorders. Int J Biochem Mol Biol 2012; 3: 152-64
28. Kjarland E, Keen TJ, Kleppe R. Does isoform diversity explain functional differences in the 14-3-3 protein family? Curr Pharm Biotechnol 2006; 7: 217-23
29. Immenschuh S, Baumgart-Vogt E. Peroxiredoxins, oxidative stress, and cell proliferation. Antioxid Redox Signal 2005; 7: 768-77
30. Boulos S, Meloni BP, Arthur PG, et al. Peroxiredoxin 2 overexpression protects cortical neuronal cultures from ischemic and oxidative injury but not glutamate excitotoxicity, whereas Cu/Zn superoxide dismutase 1 overexpression protects only against oxidative injury. J Neurosci Res 2007; 85: 3089-97
31. Hotta A, Inatome R, Yuasa-Kawada J, et al. Critical role of collapsin response mediator protein-Associated molecule CRAM for filopodia and growth cone development in neurons. Mol Biol Cell 2005; 16: 32-9
32. Mairesse J, Vercoutter-Edouart AS, Marrocco J, et al. Proteomic characterization in the hippocampus of prenatally stressed rats. J Proteomics 2012; 75: 1764-70
33. Opii WO, Joshi G, Head E, et al. Proteomic identification of brain proteins in the canine model of human aging following a long-Term treatment with antioxidants and a program of behavioral enrichment: relevance to Alzheimer's disease. Neurobiol Aging 2008; 29: 51-70
34. Scheetz AJ, Nairn AC, Constantine-Paton M. NMDA receptor-mediated control of protein synthesis at developing synapses. Nat Neurosci 2000; 3: 211-16
35. Arnaudeau S, Frieden M, Nakamura K, et al. Calreticulin differentially modulates calcium uptake and release in the endoplasmic reticulum and mitochondria. J Biol Chem 2002; 277: 46696-705
36. Núñez MT, Osorio A, Tapia V, et al. Iron-induced oxidative stress up-regulates calreticulin levels in intestinal epithelial (Caco-2) cells. J Cell Biochem 2001; 82: 660-5
37. Ilott NE, Schneider T, Mill J, et al. Long-Term effects of gestational nicotine exposure and food-restriction on gene expression in the striatum of adolescent rats. PLoS One 2014; 9: e88896
38. Akitake Y, Katsuragi S, Hosokawa M, et al. Moderate maternal food restriction in mice impairs physical growth, behavior, and neurodevelopment of offspring. Nutr Res 2015; 35: 76-87
39. Antonow-Schlorke I, Schwab M, Cox LA, et al. Vulnerability of the fetal primate brain to moderate reduction in maternal global nutrient availability. Proc Natl Acad Sci USA 2011; 108: 3011-16
40. Rodriguez JS, Bartlett TQ, Keenan KE, et al. Sex-dependent cognitive performance in baboon offspring following maternal caloric restriction in pregnancy and lactation. Reprod Sci 2012; 19: 493-504