Hippocampal mechanisms in impaired spatial learning and memory in male offspring of rats fed a low-protein isocaloric diet in pregnancy and/or lactation

The Rat Brain in Stereotaxic Coordinates

Paxinos, G., & Watson, C. (1983) · Elsevier eBooks · doi:10.1016/c2009-0-63235-9 · Cited by 28,585 · see citing works

Long-Term Potentiation and Memory

Lynch, M. A. (2004) · Physiological Reviews · doi:10.1152/physrev.00014.2003 · Cited by 2,001 · see citing works

Hippocampal sharp wave-ripple: A cognitive biomarker for episodic memory and planning

Buzsáki, G. (2015) · Hippocampus · doi:10.1002/hipo.22488 · Cited by 1,759 · see citing works

The Nature of the Arrestin·Receptor Complex Determines the Ultimate Fate of the Internalized Receptor

Pan, L., Gurevich, E. V., & Gurevich, V. V. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m209532200 · Cited by 1,758 · see citing works

Early Developmental Conditioning of Later Health and Disease: Physiology or Pathophysiology?

Hanson, M. A., & Gluckman, P. D. (2014) · Physiological Reviews · doi:10.1152/physrev.00029.2013 · Cited by 1,188 · see citing works

Balancing Structure and Function at Hippocampal Dendritic Spines

Bourne, J. N., & Harris, K. M. (2008) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.31.060407.125646 · Cited by 916 · see citing works

An increase in dendritic spine density on hippocampal CA1 pyramidal cells following spatial learning in adult rats suggests the formation of new synapses.

Moser, M., Trommald, M., & Andersen, P. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.26.12673 · Cited by 615 · see citing works

Development of the mossy fibers of the dentate gyrus: I. A light and electron microscopic study of the mossy fibers and their expansions

Amaral, D. G., & Dent, J. A. (1981) · The Journal of Comparative Neurology · doi:10.1002/cne.901950106 · Cited by 606 · see citing works

Hippocampus as comparator: Role of the two input and two output systems of the hippocampus in selection and registration of information

Vinogradova, O. S. (2001) · Hippocampus · doi:10.1002/hipo.1073 · Cited by 550 · see citing works

Early programming of the hypothalamo–pituitary–adrenal axis

MATTHEWS, S. (2002) · Trends in Endocrinology and Metabolism · doi:10.1016/s1043-2760(02)00690-2 · Cited by 513 · see citing works

Overview on the structure, composition, function, development, and plasticity of hippocampal dendritic spines

Sorra, K. E., & Harris, K. M. (2000) · Hippocampus · doi:10.1002/1098-1063(2000)10:5 · Cited by 456 · see citing works

Nutrition in early life and the programming of adult disease: a review.

Langley-Evans, S. (2015) · Journal of human nutrition and dietetics (Print) · doi:10.1111/jhn.12212 · Cited by 438 · see citing works

A low maternal protein diet during pregnancy and lactation has sex‐ and window of exposure‐specific effects on offspring growth and food intake, glucose metabolism and serum leptin in the rat

Zambrano, E., Bautista, C. J., Deás, M., Martínez‐Samayoa, P. M., González-Zamorano, M., Ledesma, H. V., Morales, J., Larrea, F., & Nathanielsz, P. W. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.100313 · Cited by 411 · see citing works

Gonadal Hormones Affect Spine Synaptic Density in the CA1 Hippocampal Subfield of Male Rats

Léránth, C., Petneházy, Ö., & MacLusky, N. J. (2003) · Journal of Neuroscience · doi:10.1523/jneurosci.23-05-01588.2003 · Cited by 407 · see citing works

Sex differences in transgenerational alterations of growth and metabolism in progeny (F2) of female offspring (F1) of rats fed a low protein diet during pregnancy and lactation

Zambrano, E., Martínez‐Samayoa, P. M., Bautista, C. J., Deás, M., Guillén-Pineda, L. E., Rodríguez-González, G. L., Guzmán, C., Larrea, F., & Nathanielsz, P. W. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.086462 · Cited by 325 · see citing works

Maternal protein restriction leads to hyperinsulinemia and reduced insulin-signaling protein expression in 21-mo-old female rat offspring

Fernandez‐Twinn, D. S., Wayman, A., Ekizoglou, S., Martin, M. S., Hales, C. N., & Ozanne, S. E. (2004) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00206.2004 · Cited by 256 · see citing works

Fetal programming of hypothalamic–pituitary–adrenal (HPA) axis function and behavior by synthetic glucocorticoids

Kapoor, A., Sophie Petropoulos, A., & Matthews, S. G. (2007) · Brain Research Reviews · doi:10.1016/j.brainresrev.2007.06.013 · Cited by 249 · see citing works

A maternal low protein diet during pregnancy and lactation in the rat impairs male reproductive development

Zambrano, E., Rodríguez-González, G. L., Guzmán, C., Garcı́a-Becerra, R., Boeck, L., Dı́az, L., Menjívar, M., Larrea, F., & Nathanielsz, P. W. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.078543 · Cited by 218 · see citing works

Androgens Increase Spine Synapse Density in the CA1 Hippocampal Subfield of Ovariectomized Female Rats

Léránth, C., Hajszán, T., & MacLusky, N. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.4516-03.2004 · Cited by 206 · see citing works

Endocrine and metabolic programming during intrauterine development

Fowden, A. L., Giussani, D. A., & Forhead, A. J. (2005) · Early Human Development · doi:10.1016/j.earlhumdev.2005.06.007 · Cited by 196 · see citing works

Fetal programming of adult Leydig cell function by androgenic effects on stem/progenitor cells

Kilcoyne, K. R., Smith, L. B., Atanassova, N. N., Macpherson, S., McKinnell, C., van den Driesche, S., Jobling, M. S., Chambers, T. J. G., Gendt, K. D., Verhoeven, G., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1320735111 · Cited by 186 · see citing works

Exposure to undernutrition in fetal life determines fat distribution, locomotor activity and food intake in ageing rats

Bellinger, L., Sculley, D. V., & Langley-Evans, S. C. (2006) · International Journal of Obesity · doi:10.1038/sj.ijo.0803205 · Cited by 183 · see citing works

Developmental programming of cardiovascular disease by prenatal hypoxia

Giussani, D. A., & Davidge, S. T. (2013) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s204017441300010x · Cited by 182 · see citing works

Spatial long-term memory is related to mossy fiber synaptogenesis

Ramı́rez-Amaya, V., Balderas, I., Sandoval, J., Escobar, M. L., & Bermúdez-Rattoni, F. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-18-07340.2001 · Cited by 177 · see citing works

Dentate gyrus-selective colchicine lesion and disruption of performance in spatial tasks: Difficulties in ?place strategy? because of a lack of flexibility in the use of environmental cues?

Xavier, G. F., Oliveira-Filho, F. J. B., & Santos, A. M. G. (1999) · Hippocampus · doi:10.1002/(sici)1098-1063(1999)9:6 · Cited by 175 · see citing works

Exercise in obese female rats has beneficial effects on maternal and male and female offspring metabolism

Vega-García, C. C., Reyes‐Castro, L. A., Bautista, C. J., Larrea, F., Nathanielsz, P. W., & Zambrano, E. (2013) · International Journal of Obesity · doi:10.1038/ijo.2013.150 · Cited by 158 · see citing works

DNA Methylation Signatures of Early Childhood Malnutrition Associated With Impairments in Attention and Cognition

Peter, C. J., Fischer, L. K., Kundaković, M., Garg, P., Jakovcevski, M., Dincer, A., Amaral, A. C. S., Ginns, E. I., Galdzicka, M. M., Bryce, C. P., et al. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.03.2100 · Cited by 156 · see citing works

Protein restriction during gestation and/or lactation causes adverse transgenerational effects on biometry and glucose metabolism in F1 and F2 progenies of rats

Pinheiro, A. R., Salvucci, I. D. M., Aguila, M. B., & Mandarim-de-Lacerda, C. A. (2008) · Clinical Science · doi:10.1042/cs20070302 · Cited by 153 · see citing works

Cholinergic modulation of excitatory synaptic transmission in the CA3 area of the hippocampus

Vogt, K. E., & Regehr, W. G. (2001) · The Journal of Neuroscience · doi:10.1523/jneurosci.21-01-00075.2001 · Cited by 149 · see citing works

Postnatal volumetric development of the prefrontal cortex in the rat

van Eden, C. G., & Uylings, H. B. M. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902410303 · Cited by 135 · see citing works

Removing zinc from synaptic vesicles does not impair spatial learning, memory, or sensorimotor functions in the mouse

Cole, T. B., Martyanova, A., & Palmiter, R. D. (2001) · Brain Research · doi:10.1016/s0006-8993(00)03220-0 · Cited by 135 · see citing works

Prenatal protein malnutrition and working memory performance in adult rats

Tonkiss, J., & Galler, J. R. (1990) · Behavioural Brain Research · doi:10.1016/0166-4328(90)90002-v · Cited by 132 · see citing works

Effect of prenatal protein malnutrition on numbers of neurons in the principal cell layers of the adult rat hippocampal formation

Lister, J. P., Blatt, G. J., DeBassio, W. A., Kemper, T. L., Tonkiss, J., Galler, J. R., & Rosene, D. L. (2005) · Hippocampus · doi:10.1002/hipo.20065 · Cited by 128 · see citing works

Fetal programming of sexual development and reproductive function

Zambrano, E., Guzmán, C., Rodríguez-González, G. L., Durand-Carbajal, M., & Nathanielsz, P. W. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.09.008 · Cited by 128 · see citing works

Resveratrol partially prevents oxidative stress and metabolic dysfunction in pregnant rats fed a low protein diet and their offspring

Vega-García, C. C., Reyes‐Castro, L. A., Rodríguez-González, G. L., Bautista, C. J., Vázquez‐Martínez, M., Larrea, F., Chamorro‐Cevallos, G. A., Nathanielsz, P. W., & Zambrano, E. (2015) · The Journal of Physiology · doi:10.1113/jp271543 · Cited by 123 · see citing works

Apoptosis Plays a Distinct Role in the Loss of Precursor Lymphocytes during Zinc Deficiency in Mice

King, L. E., Osati-Ashtiani, F., & Fraker, P. J. (2002) · Journal of Nutrition · doi:10.1093/jn/132.5.974 · Cited by 120 · see citing works

HPA axis programming by maternal undernutrition in the male rat offspring

Vieau, D., Sebaai, N., Léonhardt, M., Dutriez-Casteloot, I., Molendi‐Coste, O., Laborie, C., Breton, C., DELOOF, S., & Lésage, J. (2007) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2007.03.014 · Cited by 117 · see citing works

Early maternal undernutrition programs increased feed intake, altered glucose metabolism and insulin secretion, and liver function in aged female offspring

George, L. A., Zhang, L., Tuersunjiang, N., Ma, Y., Long, N., Uthlaut, A. B., Smith, D. T., Nathanielsz, P. W., & Ford, S. P. (2012) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00241.2011 · Cited by 111 · see citing works

Selective immunolesions of hippocampal cholinergic input fail to impair spatial working memory

McMahan, R. W., Sobel, T. J., & Baxter, M. G. (1997) · Hippocampus · doi:10.1002/(sici)1098-1063(1997)7:2 · Cited by 109 · see citing works

The effects of prenatal stress on learning in adult offspring is dependent on the timing of the stressor

Kapoor, A., Kostaki, A., Janus, C., & Matthews, S. G. (2008) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.08.018 · Cited by 109 · see citing works

Mechanisms by which maternal obesity programs offspring for obesity: evidence from animal studies

Zambrano, E., & Nathanielsz, P. W. (2013) · Nutrition Reviews · doi:10.1111/nure.12068 · Cited by 109 · see citing works

Malnutrition and Reactivity to Drugs Acting in the Central Nervous System

Almeida, S. S., Tonkiss, J., & Galler, J. R. (1996) · Neuroscience & Biobehavioral Reviews · doi:10.1016/0149-7634(95)00054-2 · Cited by 104 · see citing works

Maternal obesity and the developmental programming of hypertension: a role for leptin

Taylor, P. D., Samuelsson, A., & Poston, L. (2014) · Acta Physiologica · doi:10.1111/apha.12223 · Cited by 103 · see citing works

Different types of nutritional deficiencies affect different domains of spatial memory function checked in a radial arm maze

Ranade, S. C., Rose, A., Rao, M. S. R., Gallego, J., Gressèns, P., & Mani, S. (2008) · Neuroscience · doi:10.1016/j.neuroscience.2008.01.002 · Cited by 101 · see citing works

Effects of prenatal protein deprivation on postnatal development of granule cells in the fascia dentata

Díaz-Cintra, S. Y., Cintra, L., Galván, A., Aguilar, A., Kemper, T. L., & Morgane, P. J. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903100306 · Cited by 98 · see citing works

Ultrastructural synaptic correlates of spatial learning in rat hippocampus

Rusakov, D. A., Davies, H. A., Harrison, E., Diana, G., Richter‐Levin, G., Bliss, T. V. P., & Stewart, M. G. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00125-5 · Cited by 98 · see citing works

Developmental programming of hypothalamic neuronal circuits: impact on energy balance control

Ramamoorthy, T. G., Begum, G., Harno, E., & White, A. E. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00126 · Cited by 96 · see citing works

Differential regulation of BDNF, synaptic plasticity and sprouting in the hippocampal mossy fiber pathway of male and female rats

Scharfman, H. E., & MacLusky, N. J. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.04.029 · Cited by 93 · see citing works

Milk consumption is a risk factor for prostate cancer in Western countries: evidence from cohort studies.

Qin, L., Xu, J., Wang, P., Tong, J., & Hoshi, K. (2007) · PubMed · Cited by 91 · see citing works

The development of the dentate area and the hippocampal mossy fiber projection of the rat

Gaarskjaer, F. B. (1985) · The Journal of Comparative Neurology · doi:10.1002/cne.902410204 · Cited by 88 · see citing works

Maternal obesity and overnutrition increase oxidative stress in male rat offspring reproductive system and decrease fertility

Rodríguez-González, G. L., Vega-García, C. C., Boeck, L., Vázquez, M., Bautista, C. J., Reyes‐Castro, L. A., Saldaña, O., Lovera, D., Nathanielsz, P. W., & Zambrano, E. (2014) · International Journal of Obesity · doi:10.1038/ijo.2014.209 · Cited by 83 · see citing works

Prenatal protein malnutrition affects synaptic potentiation in the dentate gyrus of rats in adulthood

Austin, K. B., Bronzino, J. D., & Morgane, P. J. (1986) · Developmental Brain Research · doi:10.1016/0165-3806(86)90102-1 · Cited by 82 · see citing works

Stress-induced changes in extracellular dopamine and serotonin in the medial prefrontal cortex and dorsal hippocampus of prenatally malnourished rats

Mokler, D. J., Torres, O. I., Galler, J. R., & Morgane, P. J. (2007) · Brain Research · doi:10.1016/j.brainres.2007.02.031 · Cited by 82 · see citing works

Corticosterone infused into the dorsal striatum selectively enhances memory consolidation of cued water-maze trainingPreprint

Quirarte, G. L., de la Teja, I. S. L., Casillas, M., Serafín, N., Prado-Alcalá, R. A., & Roozendaal, B. (2009) · Learning & Memory · doi:10.1101/lm.1493609 · Cited by 76 · see citing works

Effects of prtein undernutrition on the dentate gyrus in rats of three] age groups

Cintra, L., Díaz-Cintra, S. Y., Galván, A., Kemper, T. L., & Morgane, P. J. (1990) · Brain Research · doi:10.1016/0006-8993(90)91769-d · Cited by 74 · see citing works

Interventions to prevent adverse fetal programming due to maternal obesity during pregnancy

Nathanielsz, P. W., Ford, S. P., Long, N., Vega-García, C. C., Reyes‐Castro, L. A., & Zambrano, E. (2013) · Nutrition Reviews · doi:10.1111/nure.12062 · Cited by 74 · see citing works

Maternal protein restriction in the rat during pregnancy and/or lactation alters cognitive and anxiety behaviors of female offspring

Reyes‐Castro, L. A., Rodriguez, J. S., Charco, R., Bautista, C. J., Larrea, F., Nathanielsz, P. W., & Zambrano, E. (2011) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2011.10.002 · Cited by 73 · see citing works

Possible roles for glucocorticoids and apoptosis in the suppression of lymphopoiesis during zinc deficiency: a review.

Fraker, P. J., Osati-Ashtiani, F., Wagner, M. A., & King, L. E. (1995) · Journal of the American College of Nutrition · doi:10.1080/07315724.1995.10718467 · Cited by 73 · see citing works

Perinatal Maternal Food Restriction Induces Alterations in Hypothalamo-Pituitary-Adrenal Axis Activity and in Plasma Corticosterone-Binding Globulin Capacity of Weaning Rat Pups

Léonhardt, M., Lésage, J., Dufourny, L., Dickès-Coopman, A., Montel, V., & Dupouy, J. (2002) · Neuroendocrinology · doi:10.1159/000048220 · Cited by 73 · see citing works

Long‐evans and sprague‐dawley rats differ in their spatial navigation performance during ontogeny and at maturity

Tonkiss, J., Shultz, P., & Galler, J. R. (1992) · Developmental Psychobiology · doi:10.1002/dev.420250804 · Cited by 71 · see citing works

Increase of mushroom spine density in CA1 apical dendrites produced by water maze training is prevented by ovariectomy

Campos, V., Prado-Alcalá, R. A., León-Jacinto, U., Aguilar-Vázquez, A. R., Quirarte, G. L., Ramı́rez-Amaya, V., & Díaz-Cintra, S. Y. (2010) · Brain Research · doi:10.1016/j.brainres.2010.10.105 · Cited by 70 · see citing works

Effect of Prenatal Protein Deprivation on Postnatal Granule Cell Generation in the Hippocampal Dentate Gyrus

DeBassio, W. A., Kemper, T. L., Tonkiss, J., & Galler, J. R. (1996) · Brain Research Bulletin · doi:10.1016/s0361-9230(96)00214-6 · Cited by 69 · see citing works

Programming of hypothalamic neuropeptide gene expression in rats by maternal dietary protein content during pregnancy and lactation

Cripps, R. L., Martin‐Gronert, M. S., Archer, Z. A., Hales, C. N., Mercer, J. G., & Ozanne, S. E. (2009) · Clinical Science · doi:10.1042/cs20080393 · Cited by 66 · see citing works

Moderate maternal food restriction in mice impairs physical growth, behavior, and neurodevelopment of offspring

Akitake, Y., Katsuragi, S., Hosokawa, M., 三島, 健., Ikeda, T., Miyazato, M., & Hosoda, H. (2014) · Nutrition Research · doi:10.1016/j.nutres.2014.10.014 · Cited by 60 · see citing works

Androgen Effects on Hippocampal CA1 Spine Synapse Numbers Are Retained in Tfm Male Rats with Defective Androgen Receptors

MacLusky, N. J., Hajszán, T., Johansen, J. A., Jordan, C. L., & Leranth, C. (2006) · Endocrinology · doi:10.1210/en.2005-0673 · Cited by 60 · see citing works

Structure and molecular organization of dendritic spines.

Tashiro, A., & Yuste, R. (2003) · PubMed · doi:10.14670/hh-18.617 · Cited by 60 · see citing works

Effect of protein malnutrition on CA3 hippocampal pyramidal cells in rats of three ages

García-Ruiz, M., Díaz-Cintra, S. Y., Cintra, L., & Corkidi, G. (1993) · Brain Research · doi:10.1016/0006-8993(93)91060-6 · Cited by 59 · see citing works

Perinatal Food Deprivation Induces Marked Alterations of the Hypothalamo-Pituitary-Adrenal Axis in 8-Month-Old Male Rats both under Basal Conditions and after a Dehydration Period

Sebaai, N., Lésage, J., Breton, C., Vieau, D., & DELOOF, S. (2004) · Neuroendocrinology · doi:10.1159/000078098 · Cited by 57 · see citing works

An analysis of spatial navigation in prenatally protein malnourished rats

Tonkiss, J., Shultz, P. L., & Galler, J. R. (1994) · Physiology & Behavior · doi:10.1016/0031-9384(94)90126-0 · Cited by 56 · see citing works

Zinc transporter‐1: a novel NMDA receptor‐binding protein at the postsynaptic density

Mellone, M., Pelucchi, S., Alberti, L. D., Genazzani, A. A., Luca, M. D., & Gardoni, F. (2014) · Journal of Neurochemistry · doi:10.1111/jnc.12968 · Cited by 55 · see citing works

Estimating the number of granule cells in the dentate gyrus with the disector

West, M. J., Coleman, P. D., & Flood, D. G. (1988) · Brain Research · doi:10.1016/0006-8993(88)91114-6 · Cited by 53 · see citing works

Effects of maternal mild zinc deficiency and zinc supplementation in offspring on spatial memory and hippocampal neuronal ultrastructural changes

Yu, X., Yu, X., Jin, L., et al. (2013) · Nutrition · doi:10.1016/j.nut.2012.09.002 · Cited by 51 · see citing works

The effects of protein deprivation on the nucleus raphe dorsalis: A morphometric golgi study in rats of three age groups

́az-Cintra, S. D., Cintra, L., Kemper, T. L., Resnick, O., & Morgane, P. J. (1981) · Brain Research · doi:10.1016/0006-8993(81)90775-7 · Cited by 51 · see citing works

Adult exercise effects on oxidative stress and reproductive programming in male offspring of obese rats

Santos, M., Rodríguez-González, G. L., Ibáñez, C. A., Vega-García, C. C., Nathanielsz, P. W., & Zambrano, E. (2014) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00398.2014 · Cited by 50 · see citing works

Early Life Exposure to Undernutrition Induces ER Stress, Apoptosis, and Reduced Vascularization in Ovaries of Adult Rat Offspring1

Chan, K. A., Bernal, A. B., Vickers, M. H., Gohir, W., Petrik, J., & Sloboda, D. M. (2015) · Biology of Reproduction · doi:10.1095/biolreprod.114.124149 · Cited by 46 · see citing works

Accelerated aging of reproductive capacity in male rat offspring of protein-restricted mothers is associated with increased testicular and sperm oxidative stress

Rodríguez-González, G. L., Reyes‐Castro, L. A., Vega-García, C. C., Boeck, L., Ibáñez, C. A., Nathanielsz, P. W., Larrea, F., & Zambrano, E. (2014) · AGE · doi:10.1007/s11357-014-9721-5 · Cited by 45 · see citing works

Effects of postnatal protein malnutrition on learning and memory procedures

Valadares, C. T., Fukuda, M. T. H., Françolin-Silva, A. L., Hernandes, A. S., & Almeida, S. S. (2010) · Nutritional Neuroscience · doi:10.1179/147683010x12611460764769 · Cited by 45 · see citing works

The dendritic trees of neurons from the hippocampal formation of protein-deprived adult rats. A quantitative Golgi study

Andrade, J. P., Castanheira-Vale, A. J., Paz-Dias, P. G., Madeira, M. D., & Paula-Barbosa, M. M. (1996) · Experimental Brain Research · doi:10.1007/bf00229626 · Cited by 44 · see citing works

Correlations between Hypothalamus-Pituitary-Adrenal Axis Parameters Depend on Age and Learning Capacity

Meijer, O. C., Topic, B., Steenbergen, P. J., Jocham, G., Huston, J. P., & Oitzl, M. S. (2004) · Endocrinology · doi:10.1210/en.2004-0416 · Cited by 44 · see citing works

Pre-and/or postnatal protein restriction developmentally programs affect and risk assessment behaviors in adult male rats

Reyes-Castro, L. A., Rodriguez, J. S., Rodríguez-González, G. L., Chavira, R., Bautista, C. J., McDonald, T. J., Nathanielsz, P. W., & Zambrano, E. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.06.008 · Cited by 44 · see citing works

Effects of chronic maternal stress on hypothalamo–pituitary–adrenal (HPA) function and behavior: No reversal by environmental enrichment

Emack, J., & Matthews, S. G. (2011) · Hormones and Behavior · doi:10.1016/j.yhbeh.2011.08.008 · Cited by 43 · see citing works

Prenatal malnutrition effect on pyramidal and granule cell generation in the hippocampal formation

DeBassio, W. A., Kemper, T. L., Galler, J. R., & Tonkiss, J. (1994) · Brain Research Bulletin · doi:10.1016/0361-9230(94)90216-x · Cited by 43 · see citing works

Effects of malnutrition and environment on the acquisition and extinction of avoidance behavior in rats

Oliveira, L. M. D., & Almeida, S. S. (1985) · Physiology & Behavior · doi:10.1016/0031-9384(85)90092-7 · Cited by 42 · see citing works

Pre‐ and/or postnatal protein restriction in rats impairs learning and motivation in male offspring

Reyes‐Castro, L. A., Rodriguez, J. S., Rodríguez-González, G. L., Wimmer, R. D., McDonald, T. J., Larrea, F., Nathanielsz, P. W., & Zambrano, E. (2010) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2010.11.002 · Cited by 39 · see citing works

Perinatal food restriction impaired spatial learning and memory behavior and decreased the density of nitric oxide synthase neurons in the hippocampus of adult male rat offspring

Zhang, Y., Li, N., & Yang, Z. R. (2010) · Toxicology Letters · doi:10.1016/j.toxlet.2010.01.002 · Cited by 39 · see citing works

Effects of different malnutrition techniques on the behavior of rats tested in the elevated T-maze

Hernandes, A. D. S., Françolin-Silva, A. L., Valadares, C. T., Fukuda, M. T. H., & Almeida, S. S. (2005) · Behavioural Brain Research · doi:10.1016/j.bbr.2005.03.008 · Cited by 38 · see citing works

Corticosterone rapidly increases thorns of CA3 neurons via synaptic/extranuclear glucocorticoid receptor in rat hippocampus

Yoshiya, M., Komatsuzaki, Y., Hojo, Y., Ikeda, M., Mukai, H., Hatanaka, Y., Murakami, G., Kawata, M., Kimoto, T., & Kawato, S. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00191 · Cited by 38 · see citing works

Anxiolytic-like effects of short-term postnatal protein malnutrition in the elevated plus-maze test

FRANCOLINSILVA, A., DASILVAHERNANDES, A., FUKUDA, M., et al. (2006) · Behavioural Brain Research · doi:10.1016/j.bbr.2006.06.042 · Cited by 38 · see citing works

The effects of perinatal protein malnutrition on spatial learning and memory behaviour and brain-derived neurotrophic factor concentration in the brain tissue in young rats.

Wang, L., & Xu, R. (2007) · PubMed · Cited by 38 · see citing works

Mild prenatal protein malnutrition increases α2C‐adrenoceptor density in the cerebral cortex during postnatal life and impairs neocortical long‐term potentiation and visuo‐spatial performance in rats

Soto‐Moyano, R., Valladares, L., Sierralta, W. D., Pérez, H., Mondaca, M., Fernández, V., Burgos, H., & Hernández, A. (2005) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2005.03094.x · Cited by 36 · see citing works

Prenatal protein malnutrition decreases mossy fibers-CA3 thorny excrescences asymmetrical synapses in adult rats

Granados-Rojas, L., Larriva-Sahd, J. A., Cintra, L., Gutiérrez‐Ospina, G., Rondán-Zarate, A., & Díaz-Cintra, S. Y. (2002) · Brain Research · doi:10.1016/s0006-8993(02)02314-4 · Cited by 35 · see citing works

Modulation of 5-HT release in the hippocampus of 30-day-old rats exposed in utero to protein malnutrition

Mokler, D. J., Galler, J. R., & Morgane, P. J. (2003) · Developmental Brain Research · doi:10.1016/s0165-3806(03)00093-2 · Cited by 34 · see citing works

Effect of Prenatal Protein Malnutrition on Long-Term Potentiation and BDNF Protein Expression in the Rat Entorhinal Cortex after Neocortical and Hippocampal Tetanization

Hernández, A., Burgos, H., Mondaca, M., Barra, R., Núñez, H., Pérez, H., Soto‐Moyano, R., Sierralta, W. D., Fernández, V., Olivares, R., et al. (2008) · Neural Plasticity · doi:10.1155/2008/646919 · Cited by 33 · see citing works

Long-term low-protein diet reduces the number of hippocampal mossy fiber synapses

Andrade, J. P., Cadete‐Leite, A., Madeira, M. D., et al. (1991) · Experimental Neurology · doi:10.1016/0014-4886(91)90121-r · Cited by 33 · see citing works

Elevated glucocorticoids during ovine pregnancy increase appetite and produce glucose dysregulation and adiposity in their granddaughters in response to ad libitum feeding at 1 year of age

Long, N. M., Smith, D. T., Ford, S. P., & Nathanielsz, P. W. (2013) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2013.05.051 · Cited by 32 · see citing works

Prenatal Malnutrition Leads to Deficits in Attentional Set Shifting and Decreases Metabolic Activity in Prefrontal Subregions that Control Executive Function

McGaughy, J. A., Amaral, A. C. S., Rushmore, J., Mokler, D. J., Morgane, P. J., Rosene, D. L., & Galler, J. R. (2014) · Developmental Neuroscience · doi:10.1159/000366057 · Cited by 30 · see citing works

Maternal protein restriction during pregnancy and lactation alters central leptin signalling, increases food intake, and decreases bone mass in 1 year old rat offspring

Qasem, R. J., Li, J., Tang, H. M., Pontiggia, L., & D’mello, A. P. (2016) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/1440-1681.12545 · Cited by 30 · see citing works

Extinction procedure induces pruning of dendritic spines in CA1 hippocampal field depending on strength of training in rats

Garín-Aguilar, M. E., Díaz-Cintra, S. Y., Quirarte, G. L., Aguilar-Vázquez, A. R., Medina, A. C., & Prado-Alcalá, R. A. (2012) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2012.00012 · Cited by 28 · see citing works

Effects of early protein malnutrition and scopolamine on learning and memory in the Morris water maze

Fukuda, M. T. H., Françolin-Silva, A. L., Hernandes, A. S., et al. (2007) · Nutritional Neuroscience · doi:10.1080/10284150701723818 · Cited by 25 · see citing works

The Mossy Fiber System of the Hippocampal Formation is Decreased by Chronic and Postnatal but not by Prenatal Protein Malnutrition in Rats

Granados-Rojas, L., Aguilar, A., & Díaz-Cintra, S. Y. (2004) · Nutritional Neuroscience · doi:10.1080/10284150400017306 · Cited by 25 · see citing works

Maternal protein restriction in pregnancy and/or lactation affects seminiferous tubule organization in male rat offspring

Rodríguez-González, G. L., Vigueras‐Villaseñor, R. M., Millán, S., et al. (2012) · Journal of Developmental Origins of Health and Disease · doi:10.1017/s2040174412000360 · Cited by 23 · see citing works

Maternal nutrient restriction during pregnancy impairs an endothelium-derived hyperpolarizing factor-like pathway in sheep fetal coronary arteries

Shukla, P., Ghatta, S., Dubey, N., Lemley, C. O., Johnson, M. L., Modgil, A., Vonnahme, K. A., Caton, J. S. S., Reynolds, L. P., Sun, C., et al. (2014) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00595.2013 · Cited by 22 · see citing works

Fetal baboon sex-specific outcomes in adipocyte differentiation at 0.9 gestation in response to moderate maternal nutrient reduction

Tchoukalova, Y. D., Krishnapuram, R., White, U. A., Burk, D., Fang, X., Nijland, M. J., & Nathanielsz, P. W. (2014) · International Journal of Obesity · doi:10.1038/ijo.2013.106 · Cited by 19 · see citing works

Gestational protein restriction induces CA3 dendritic atrophy in dorsal hippocampal neurons but does not alter learning and memory performance in adult offspring

Lopes, A., Torres, D., Rodrigues, A. J., Cerqueira, J., Pêgo, J. M., Sousa, N., Gontijo, J. A. R., & Boer, P. A. (2012) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2012.12.003 · Cited by 19 · see citing works

Impact of Maternal Undernutrition on Hypothalamo-Pituitary-Adrenal Axis and Adipocyte Functions in Male Rat Offspring

Chisari, A. N., Giovambattista, A., Perelló, M., & Spinedi, E. (2001) · Endocrine · doi:10.1385/endo:14:3:375 · Cited by 19 · see citing works

Effects of maternal nutrient restriction, intrauterine growth restriction, and glucocorticoid exposure on phosphoenolpyruvate carboxykinase‐1 expression in fetal baboon hepatocytes in vitro

Li, C., Shu, Z., Lee, S., et al. (2013) · Journal of Medical Primatology · doi:10.1111/jmp.12048 · Cited by 18 · see citing works

Significance of Zn2+ signaling in cognition: Insight from synaptic Zn2+ dyshomeostasis

Takeda, A. (2014) · Journal of Trace Elements in Medicine and Biology · doi:10.1016/j.jtemb.2014.06.021 · Cited by 17 · see citing works

Effects of undernutrition on glutamatergic parameters in the cerebral cortex of young rats

Rotta, L. N., Leszczinski, D. N., Brusque, A. M., et al. (2008) · Physiology & Behavior · doi:10.1016/j.physbeh.2008.03.018 · Cited by 14 · see citing works

Mice undernourished before, but not after, weaning perform better in motor coordination and spatial learning tasks than well-fed controls

Partadiredja, G., & Bedi, K. S. (2011) · Nutritional Neuroscience · doi:10.1179/147683011x13009738172486 · Cited by 13 · see citing works

Perinatal undernutrition attenuates field excitatory postsynaptic potentials and influences dendritic spine density and morphology in hippocampus of male rat offspring

Zhang, Y., Wei, J., & Yang, Z. R. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.03.061 · Cited by 12 · see citing works

Effects of postnatal malnutrition and senescence on learning, long-term memory, and extinction in the rat

Martínez, Y., Díaz-Cintra, S. Y., León-Jacinto, U., Aguilar-Vázquez, A. R., Medina, A. C., Quirarte, G. L., & Prado-Alcalá, R. A. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.04.016 · Cited by 10 · see citing works

Plasticidad sináptica estructural en el hipocampo inducida por la experiencia espacial y sus implicaciones en el procesamiento de información

Carasatorre, M., Ramı́rez-Amaya, V., & Díaz-Cintra, S. Y. (2013) · Neurología · doi:10.1016/j.nrl.2012.12.005 · Cited by 9 · see citing works

Effects of chronic malnourishment and aging on the ultrastructure of pyramidal cells of the dorsal hippocampus

Castro-Chavira, S. A., Aguilar-Vázquez, A. R., Martínez-Chávez, Y., Palma, L., Padilla‐Gómez, E., & Díaz-Cintra, S. Y. (2015) · Nutritional Neuroscience · doi:10.1179/1476830515y.0000000009 · Cited by 9 · see citing works

Structural synaptic plasticity in the hippocampus induced by spatial experience and its implications in information processing

Carasatorre, M., Ramı́rez-Amaya, V., & Díaz-Cintra, S. Y. (2016) · Neurología (English Edition) · doi:10.1016/j.nrleng.2012.12.006 · Cited by 8 · see citing works

Effect of 17ß-estradiol on zinc content of hippocampal mossy fibers in ovariectomized adult rats

Padilla‐Gómez, E., Campos, V., Montes, S., Dı́az-Ruiz, A., Quirarte, G. L., Rı́os, C., & Díaz-Cintra, S. Y. (2012) · BioMetals · doi:10.1007/s10534-012-9575-1 · Cited by 2 · see citing works

Beneficial Effects of Spirulina Consumption on Brain Health

Trotta, T., Porro, C., Cianciulli, A., & Panaro, M. A. (2022) · Nutrients · doi:10.3390/nu14030676 · Cited by 98 · see citing works

Amelioration of neurobehavioral and cognitive abilities of F1 progeny following dietary supplementation with Spirulina to protein malnourished mothers

Sinha, S., Patro, N., & Patro, I. K. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2019.08.181 · Cited by 39 · see citing works

Maternal Spirulina supplementation during pregnancy and lactation partially prevents oxidative stress, glial activation and neuronal damage in protein malnourished F1 progeny

Sinha, S., Patro, N., Tiwari, P. K., & Patro, I. K. (2020) · Neurochemistry International · doi:10.1016/j.neuint.2020.104877 · Cited by 28 · see citing works

Effect of the Age of Pregnant Females on Brain Development in the Offspring

Ryzhavskii, B. Y., Sapozhnikov, Y. A., Учакина, Р. В., et al. (2004) · Bulletin of Experimental Biology and Medicine · doi:10.1023/b:bebm.0000048385.61529.af · Cited by 3 · see citing works

Metabolic syndrome in Korean adolescents and young adult offspring and their parents.

Lee, K. (2017) · PubMed · doi:10.6133/apjcn.082016.02 · Cited by 7 · see citing works

Effects of perinatal exposure to bisphenol A on the behavior of offspring in F344 rats

Negishi, T., Kawasaki, K., Takatori, A., Ishii, Y., Kyuwa, S., Kuroda, Y., & Yoshikawa, Y. (2003) · Environmental Toxicology and Pharmacology · doi:10.1016/s1382-6689(03)00044-9 · Cited by 57 · see citing works

The relationship between maternal phenotype and offspring quality: Do older mothers really produce the best offspring?

Marshall, D. J., Heppell, S. S., Munch, S. B., et al. (2010) · Ecology · doi:10.1890/09-0156.1 · Cited by 155 · see citing works

Are increased concentrations of maternal corticosterone adaptive to offspring? A test using a placentotrophic lizard

Cadby, C., Jones, S., & Wapstra, E. (2009) · Functional Ecology · doi:10.1111/j.1365-2435.2009.01637.x · Cited by 24 · see citing works