全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
Health  2014 

Long-Term Impact of Maternal Protein Malnutrition on Learning and Memory Abilities and DNA Methylating Profiles of the Nervous System in Offspring Rats

DOI: 10.4236/health.2014.615239, PP. 2047-2065

Keywords: Maternal Protein Malnutrition, Morris Water Maze, Methylation, Grin2b, NMDA Receptors

Full-Text   Cite this paper   Add to My Lib

Abstract:

Objective: To determine the mechanisms by which protein deficiency during pregnancy can lead to long-term alterations in learning and memory abilities of the offspring in rats. Study design: Fourty-two pregnant rats were fed control (n = 23) or low protein (n = 19) diets ad libitum until parturition. On the 8th week of post-natal life which represented early adulthood, eighty-four offsprings (control group: n = 52, LP group: n = 32) were determined their learning & memory ability by using the Morris water maze test. Six offprings’ brain tissue (control group: n = 3, LP group: n = 3) was also analysed for DNA methylating profiles, the GO and KEGG pathways, methylation status and twelve for protein expression (control group: n = 6, LP group: n = 6). Results: The offsprings of the protein-deficient-diet fed rats learnt faster initially then lagged behind those of the control rats, especially in female rats (p = 0.035). There were a series of genes methylated in the CpG island and pormoter area. Quantitative Mass Array data showed methylation differences in Grin2b and Grin2b_3CpG 3, 4, & 5 might be the target sites as shown by dual-luciferase assay. A decreased level of protein expression of NMDAR2B was observed. Conclusion: Differential methylation status in Grin2b and changes in expression of NMDAR2B may partially explain the long-term impact of maternal protein deficiency on the cognitive and learning capabilities of offsprings.

References

[1]  Barker, D.J. and Osmond, C. (1988) Low Birth Weight and Hypertension. BMJ, 297, 134-135.
http://dx.doi.org/10.1136/bmj.297.6641.134-b
[2]  Barker, D.J., Osmond, C., Golding, J., Kuh, D. and Wadsworth, M.E. (1989) Growth in Utero, Blood Pressure in Childhood and Adult Life, and Mortality from Cardiovascular Disease. BMJ, 298, 564-567.
http://dx.doi.org/10.1136/bmj.298.6673.564
[3]  Beltrand, J. and Levy-Marchal, C. (2008) Pathophysiology of Insulin Resistance in Subjects Born Small for Gestational Age. Best Practice Research Clinical Endocrinology Metabolism, 22, 503-515.
http://dx.doi.org/10.1016/j.beem.2008.01.015
[4]  Gardner, J.M., Walker, S.P., Powell, C.A. and Grantham-McGregor, S. (2003) A Randomized Controlled Trial of a Home-Visiting Intervention on Cognition and Behavior in Term Low Birth Weight Infants. Journal of Pediatrics, 143, 634-639.
http://dx.doi.org/10.1067/S0022-3476(03)00455-4
[5]  Sommerfelt, K., Andersson, H.W., Sonnander, K., Ahlsten, G., Ellertsen, B., Markestad, T., Jacobsen, G., Hoffman, H.J. and Bakketeig, L. (2000) Cognitive Development of Term Small for Gestational Age Children at Five Years of Age. Archives of Disease in Childhood, 83, 25-30.
http://dx.doi.org/10.1136/adc.83.1.25
[6]  Desai, M., Crowther, N.J., Lucas, A. and Hales, C.N. (1996) Organ-Selective Growth in the Offspring of Protein-Restricted Mothers. British Journal of Nutrition, 76, 591-603.
http://dx.doi.org/10.1079/BJN19960065
[7]  Petrik, J., Reusens, B., Arany, E., Remacle, C., Coelho, C., Hoet, J.J. and Hill, D.J. (1999) A Low Protein Diet Alters the Balance of Islet Cell Replication and Apoptosis in the Fetal and Neonatal Rat and Is Associated with a Reduced Pancreatic Expression of Insulin-Like Growth Factor-II. Endocrinology, 140, 4861-4873.
[8]  Garofano, A., Czernichow, P. and Breant, B. (1997) In Utero Undernutrition Impairs Rat Beta-Cell Development. Diabetologia, 40, 1231-1234.
http://dx.doi.org/10.1007/s001250050812
[9]  Alexander, B.T. (2003) Placental Insufficiency Leads to Development of Hypertension in Growth-Restricted Offspring. Hypertension, 41, 457-462.
http://dx.doi.org/10.1161/01.HYP.0000053448.95913.3D
[10]  Grantham-McGregor, S.M., Lira, P.I., Ashworth, A., Morris, S.S. and Assuncao, A.M. (1998) The Development of Low Birth Weight Term Infants and the Effects of the Environment in Northeast Brazil. Journal of Pediatrics, 132, 661-666.
http://dx.doi.org/10.1016/S0022-3476(98)70357-9
[11]  Vieau, D., Sebaai, N., Leonhardt, M., Dutriez-Casteloot, I., Molendi-Coste, O., Laborie, C., Breton, C., Deloof, S. and Lesage, J. (2007) HPA Axis Programming by Maternal Undernutrition in the Male Rat Offspring. Psychoneuroendocrinology, 32, S16-S20.
http://dx.doi.org/10.1016/j.psyneuen.2007.03.014
[12]  Dean, W., Lucifero, D. and Santos, F. (2005) DNA Methylation in Mammalian Development and Disease. Birth Defects Research Part C: Embryo Today: Reviews, 75, 98-111.
http://dx.doi.org/10.1002/bdrc.20037
[13]  Walter, J. and Paulsen, M. (2003) Imprinting and Disease. Seminars in Cell & Developmental Biology, 14, 101-110.
http://dx.doi.org/10.1016/S1084-9521(02)00142-8
[14]  Wilson, V.L. and Jones, P.A. (1983) DNA Methylation Decreases in Aging but Not in Immortal Cells. Science, 220, 1055-1057.
http://dx.doi.org/10.1126/science.6844925
[15]  Hornsby, P.J., Yang, L. and Gunter, L.E. (1992) Demethylation of Satellite I DNA during Senescence of Bovine Adrenocortical Cells in Culture. Mutation Research/DNAging, 275, 13-19.
http://dx.doi.org/10.1016/0921-8734(92)90004-9
[16]  Ehrlich, M. (2003) Expression of Various Genes Is Controlled by DNA Methylation during Mammalian Development. Journal of Cellular Biochemistry, 88, 899-910.
http://dx.doi.org/10.1002/jcb.10464
[17]  Futscher, B.W., Oshiro, M.M., Wozniak, R.J., Holtan, N., Hanigan, C.L., Duan, H. and Domann, F.E. (2002) Role for DNA Methylation in the Control of Cell Type-Specific Maspin Expression. Nature Genetics, 31, 175-179.
http://dx.doi.org/10.1038/ng886
[18]  Nakagawa, H., Nuovo G.J., Zervos, E.E., Martin Jr., E.W., Salovaara, R., Aaltonen, L.A. and de la Chapelle, A. (2001) Age-Related Hypermethylation of the 5’ Region of MLH1 in Normal Colonic Mucosa Is Associated with Microsatellite-Unstable Colorectal Cancer Development. Cancer Research, 61, 6991-6995.
[19]  Chen, Y., Sharma, R.P., Costa, R.H., Costa, E. and Grayson, D.R. (2002) On the Epigenetic Regulation of the Human Reelin Promoter. Nucleic Acids Research, 30, 2930-2939.
http://dx.doi.org/10.1093/nar/gkf401
[20]  Morris, R.G., Garrud, P., Rawlins, J.N. and O’Keefe, J. (1982) Place Navigation Impaired in Rats with Hippocampal Lesions. Nature, 297, 681-683.
http://dx.doi.org/10.1038/297681a0
[21]  D’Hooge, R. and De Deyn, P.P. (2001) Applications of the Morris Water Maze in the Study of Learning and Memory. Brain Research Reviews, 36, 60-90.
http://dx.doi.org/10.1016/S0165-0173(01)00067-4
[22]  Zilberman, D. (2007) The Human Promoter Methylome. Nature Genetics, 39, 442-443.
http://dx.doi.org/10.1038/ng0407-442
[23]  Nelson, E.D., Kavalali, E.T. and Monteggia, L.M. (2008) Activity-Dependent Suppression of Miniature Neurotransmission through the Regulation of DNA Methylation. The Journal of Neuroscience, 28, 395-406.
http://dx.doi.org/10.1523/JNEUROSCI.3796-07.2008
[24]  Elgersma, Y. and Silva, A.J. (1999) Molecular Mechanisms of Synaptic Plasticity and Memory. Current Opinion in Neurobiology, 9, 209-213.
http://dx.doi.org/10.1016/S0959-4388(99)80029-4
[25]  Bliss, T.V. and Collingridge, G.L. (1993) A Synaptic Model of Memory: Long-Term Potentiation in the Hippocampus. Nature, 361, 31-39.
http://dx.doi.org/10.1038/361031a0
[26]  de Quervain, D.J, Roozendaal, B. and McGaugh, J.L. (1998) Stress and Glucocorticoids Impair Retrieval of Long-Term Spatial Memory. Nature, 394, 787-790.
http://dx.doi.org/10.1038/29542
[27]  Díaz-Cintra, S., González-Maciel, A., Morales, M.A., Aguilar, A., Cintra, L. and Prado-Alcalá, R.A. (2007) Protein Malnutrition Differentially Alters the Number of Glutamic Acid Decarboxylase-67 Interneurons in Dentate Gyrus and CA1-3 Subfields of the Dorsal Hippocampus. Experimental Neurology, 208, 47-53.
http://dx.doi.org/10.1016/j.expneurol.2007.07.003
[28]  Bonatto, F., Polydoro, M., Andrades, M.E., da Frota Jr., M.L., Dal-Pizzol, F., Rotta, L.N., et al. (2005) Effect of Protein Malnutrition on Redox State of the Hippocampus of Rat. Brain Research, 1042, 17-22.
http://dx.doi.org/10.1016/j.brainres.2005.02.002
[29]  Ranade, S.C., Rose, A., Rao, M., Gallego, J., Gressens, P. and Mani, S. (2008) Different Types of Nutritional Deficiencies Affect Different Domains of Spatial Memory Function Checked in a Radial Arm Maze. Neuroscience & Bio-behavioral Reviews, 152, 859-866.
[30]  Reul, J.M., Hesketh, S.A., Collins, A. and Mecinas, M.G. (2009) Epigenetic Mechanisms in the Dentate Gyrus Act as a Molecular Switch in Hippocampus-Associated Memory Formation. Epigenetics, 4, 434-439.
http://dx.doi.org/10.4161/epi.4.7.9806
[31]  Levenson, J.M. and Sweatt, J.D. (2006) Epigenetic Mechanisms: A Common Theme in Vertebrate and Invertebrate Memory Formation. Cellular and Molecular Life Sciences CMLS, 63, 1009-1016.
http://dx.doi.org/10.1007/s00018-006-6026-6
[32]  Levenson, J.M., Roth, T.L., Lubin, F.D., Miller, C.A., Huang, I.C., Desai, P., Malone, L.M. and Sweatt, J.D. (2006) Evidence That DNA (Cytosine-5) Methyltransferase Regulates Synaptic Plasticity in the Hippocampus. The Journal of Biological Chemistry, 281, 15763-15773.
http://dx.doi.org/10.1074/jbc.M511767200
[33]  Bailey, C.H., Kandel, E.R. and Si, K. (2004) The Persistence of Long-Term Memory: A Molecular Approach to Self-Sustaining Changes in Learning-Induced Synaptic Growth. Neuron, 44, 49-57.
http://dx.doi.org/10.1016/j.neuron.2004.09.017
[34]  Dai, W., Cheng, H.L., Huang, R.Q., Zhuang, Z. and Shi, J.X. (2009) Quantitative Detection of the Expression of Mitochondrial Cytochrome c Oxidase Subunits mRNA in the Cerebral Cortex after Experimental Traumatic Brain Injury. Brain Research, 1251, 287-295.
http://dx.doi.org/10.1016/j.brainres.2008.11.034
[35]  Kumar, A., Zou, L., Yuan, X., Long, Y. and Yang, K. (2002) N-methyl-D-aspartate Receptors: Transient Loss of NR1/ NR2A/NR2B Subunits after Traumatic Brain Injury in a Rodent Model. Journal of Neuroscience Research, 67, 781-786.
http://dx.doi.org/10.1002/jnr.10181
[36]  Fontán-Lozano, A., Sáez-Cassanelli, J.L., Inda, M.C., de los Santos-Arteaga, M., Sierra-Domínguez, S.A., López-Lluch, G., Delgado-Garcia, J.M. and Carrión, A.M. (2007) Caloric Restriction Increases Learning Consolidation and Facilitates Synaptic Plasticity through Mechanisms Dependent on NR2B Subunits of the NMDA Receptor. The Journal of Neuroscience, 27, 10185-10195.
http://dx.doi.org/10.1523/JNEUROSCI.2757-07.2007
[37]  Tsien, J.Z., Huerta, P.T. and Tonegawa, S. (1996) The Essential Role of Hippocampal CA1 NMDA Receptor-Dependent Synaptic Plasticity in Spatial Memory. Cell, 87, 1327-1338.
http://dx.doi.org/10.1016/S0092-8674(00)81827-9
[38]  Schlotz, W. and Phillips, D.I.W. (2009) Fetal Origins of Mental Health: Evidence and Mechanisms. Brain, Behavior and Immunity, 23, 905-916.
http://dx.doi.org/10.1016/j.bbi.2009.02.001
[39]  Leitner, Y., Heldman, D., Harel, S. and Pick, C.G. (2005) Deficits in Spatial Orientation of Children with Intrauterine Growth Retardation. Brain Research Bulletin, 67, 13-18.
http://dx.doi.org/10.1016/j.brainresbull.2005.04.017
[40]  Pryor, J., Silva, P. and Brooke, M. (1995) Growth, Development and Behavior in Adolescents Born Small-for-Gestational-Age. Journal of Paediatrics and Child Health, 31, 403-407.
http://dx.doi.org/10.1111/j.1440-1754.1995.tb00847.x

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133