Early life experience alters response of adult neurogenesis to stress

Requirement of hippocampal neurogenesis for the behavioral effects of antidepressants

Santarelli, L., Saxe, M., Gross, C., Surget, A., Battaglia, F., Dulawa, S., Weisstaub, N., Lee, J., Duman, R., Arancio, O., et al. (2003) · Science · doi:10.1126/science.1083328 · Cited by 4,321

The role of childhood trauma in the neurobiology of mood and anxiety disorders: preclinical and clinical studies

Heim, C., & Nemeroff, C. B. (2001) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01157-x · Cited by 2,791

Learning enhances adult neurogenesis in the hippocampal formation

Gould, E., Beylin, A., Tanapat, P., Reeves, A., & Shors, T. J. (1999) · Nature Neuroscience · doi:10.1038/6365 · Cited by 2,157

Hippocampal Volume Reduction in Major Depression

Bremner, J. D., Narayan, M., Anderson, E. R., Staib, L. H., Miller, H. L., & Charney, D. S. (2000) · American Journal of Psychiatry · doi:10.1176/ajp.157.1.115 · Cited by 1,670

Early, postnatal experience alters hypothalamic corticotropin-releasing factor (CRF) mRNA, median eminence CRF content and stress-induced release in adult rats

Plotsky, P. M., & Meaney, M. J. (1993) · Molecular Brain Research · doi:10.1016/0169-328x(93)90189-v · Cited by 1,638

Adult neurogenesis produces a large pool of new granule cells in the dentate gyrus

Cameron, H. A., & Mckay, R. D. G. (2001) · Journal of Comparative Neurology · doi:10.1002/cne.1040 · Cited by 1,585

Neurogenesis in the Dentate Gyrus of the Adult Tree Shrew Is Regulated by Psychosocial Stress and NMDA Receptor Activation

Gould, E., McEwen, B. S., Tanapat, P., Galea, L. A. M., & Fuchs, E. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-07-02492.1997 · Cited by 1,496

Proliferation of granule cell precursors in the dentate gyrus of adult monkeys is diminished by stress

Gould, E., Tanapat, P., McEwen, B. S., Flügge, G., & Fuchs, E. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.6.3168 · Cited by 1,395

Depression Duration But Not Age Predicts Hippocampal Volume Loss in Medically Healthy Women with Recurrent Major Depression

Sheline, Y. I., Sanghavi, M., Mintun, M. A., & Gado, M. H. (1999) · The Journal of Neuroscience · doi:10.1523/jneurosci.19-12-05034.1999 · Cited by 1,382 · cited 1×

Enhanced synaptic plasticity in newly generated granule cells of the adult hippocampus

Schmidt-Hieber, C., Jonas, P., & Bischofberger, J. (2004) · Nature · doi:10.1038/nature02553 · Cited by 1,292

Early life stress and hippocampal neurogenesis in the neonate: sexual dimorphism, long term consequences and possible mediators

Lajud, N., & Torner, L. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00003 · Cited by 76

Hitting a moving target: Basic mechanisms of recovery from acquired developmental brain injury

Giza, C. C., Kolb, B. E., Harris, N. G., Asarnow, R. F., & Prins, M. L. (2009) · Developmental Neurorehabilitation · doi:10.3109/17518420903087558 · Cited by 80

Major Depression: A Role for Hippocampal Neurogenesis?

Lee, M. M., Reif, A., & Schmitt, A. G. (2012) · Current topics in behavioral neurosciences · doi:10.1007/7854_2012_226 · Cited by 77

Neurogenesis in the aged and neurodegenerative brain

Shruster, A., Melamed, E., & Offen, D. (2010) · APOPTOSIS · doi:10.1007/s10495-010-0491-y · Cited by 77

Early micronutrient supplementation protects against early stress‐induced cognitive impairments

Naninck, E. F. G., Oosterink, J. E., Yam, K., Vries, L. P., Schierbeek, H., van Goudoever, J. B., Verkaik‐Schakel, R. N., Plantinga, J. A., Plösch, T., Lucassen, P. J., et al. (2016) · The FASEB Journal · doi:10.1096/fj.201600834r · Cited by 74

Early life trauma and directional brain connectivity within major depression

Grant, M. M., White, D. M., Hadley, J. A., Hutcheson, N. L., Shelton, R. C., Sreenivasan, K. R., & Deshpande, G. (2014) · Human Brain Mapping · doi:10.1002/hbm.22514 · Cited by 76

Social isolation disrupts hippocampal neurogenesis in young non-human primates

Cinini, S. M., Barnabe, G. F., Galvão-Coelho, N., de Medeiros, M. A., Perez-Mendes, P., Sousa, M. B. C., Covolan, L., & Mello, L. E. (2014) · Frontiers in Neuroscience · doi:10.3389/fnins.2014.00045 · Cited by 71

The long‐term impact of developmental stress. Evidence from later medieval and post‐medieval London (AD1117–1853)

Watts, R. (2015) · American Journal of Physical Anthropology · doi:10.1002/ajpa.22810 · Cited by 71

Antenatal Glucocorticoid Treatment Affects Hippocampal Development in Mice

Noorlander, C. W., Tijsseling, D., Hessel, E. V. S., de Vries, W. B., Derks, J. B., Visser, G. H. A., & Graan, P. N. E. D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0085671 · Cited by 77

Early life stress as an influence on limbic epilepsy: a hypothesis whose time has come?

Koe, A. S. (2009) · Frontiers in Behavioral Neuroscience · doi:10.3389/neuro.08.024.2009 · Cited by 74

Stress-Related Dysfunction of Adult Hippocampal Neurogenesis—An Attempt for Understanding Resilience?

Leschik, J., Lutz, B., & Gentile, A. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22147339 · Cited by 77

Encore: Behavioural animal models of stress, depression and mood disorders

Petković, A., & Chaudhury, D. (2022) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2022.931964 · Cited by 74

Early life stress accelerates age-induced effects on neurogenesis, depression, and metabolic risk

Ruiz, R., Roque, A., Pineda, E., Licona-Limón, P., Valdez-Alarcón, J. J., & Lajud, N. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2018.07.012 · Cited by 74

Early life stress delays hippocampal development and diminishes the adult stem cell pool in mice

Youssef, M., Atsak, P., Cardenas, J., Kosmidis, S., Leonardo, E. D., & Dranovsky, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-40868-0 · Cited by 75

Chronic stress in adulthood followed by intermittent stress impairs spatial memory and the survival of newborn hippocampal cells in aging animals: prevention by FGL, a peptide mimetic of neural cell adhesion molecule

Borcel, É., Pérez-Álvarez, L., Herrero, A. I., Brionne, T. C., Varea, E., Berezin, V., Bock, E., Sandi, C., & Venero, C. (2008) · Behavioural Pharmacology · doi:10.1097/fbp.0b013e3282f3fca9 · Cited by 68

The effects of brain serotonin deficiency on behavioural disinhibition and anxiety-like behaviour following mild early life stress

Sachs, B. D., Rodriguiz, R. M., Siesser, W. B., Kenan, A., Royer, E. L., Jacobsen, J. P. R., Wetsel, W. C., & Caron, M. G. (2013) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145713000321 · Cited by 71

Abnormal Fronto-striatal Connectivity in Children with Histories of Early Deprivation: A Diffusion Tensor Imaging Study

Behen, M. E., Muzik, O., Saporta, A. S. D., Wilson, B. J., Pai, D., Hua, J., & Chugani, H. T. (2009) · Brain Imaging and Behavior · doi:10.1007/s11682-009-9071-6 · Cited by 67

Paternal experience suppresses adult neurogenesis without altering hippocampal function in Peromyscus californicus

Glasper, E. R., Kozorovitskiy, Y., Pavlic, A., & Gould, E. (2011) · Journal of Comparative Neurology · doi:10.1002/cne.22628 · Cited by 66

Melatonin prevents glucocorticoid inhibition of cell proliferation and toxicity in hippocampal cells by reducing glucocorticoid receptor nuclear translocation

Quirós-González, I., Mayo, J. C., García‐Suárez, O., Hevia, D., Martı́n, V., Rodrı́guez, C., & Sainz, R. M. (2008) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2008.02.009 · Cited by 66

The timing of maternal separation affects morris water maze performance and long‐term potentiation in male rats

Cao, X., Huang, S., Cao, J.-J., Chen, T., Zhu, P., Zhu, R., Su, P., & Ruan, D. (2013) · Developmental Psychobiology · doi:10.1002/dev.21130 · Cited by 66

Status epilepticus during old age is not associated with enhanced hippocampal neurogenesis

Rao, M. S. R., Hattiangady, B., & Shetty, A. K. (2008) · Hippocampus · doi:10.1002/hipo.20449 · Cited by 64

Brain size variation in extremophile fish: local adaptation versus phenotypic plasticity

Eifert, C., Farnworth, M. S., Schulz‐Mirbach, T., Riesch, R., Bierbach, D., Klaus, S., Wurster, A., Tobler, M., Streit, B., Indy, J. R., et al. (2014) · Journal of Zoology · doi:10.1111/jzo.12190 · Cited by 62

Functional correlates for 5-HT(1A) receptors in maternally deprived rats displaying anxiety and depression-like behaviors.

Lambás-señas, L., Mnie-Filali, O., Certin, V., Faure, C., Lemoine, L., Zimmer, L., & Haddjeri, N. (2009) · Progress in Neuro-psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2008.11.017 · Cited by 70

Anxiolytic effects of rapid amygdala kindling, and the influence of early life experience in rats

Jones, N. C., Kumar, G., O'Brien, T. J., Morris, M. J., Rees, S. M., & Salzberg, M. R. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.04.023 · Cited by 61

Maternal insulin resistance multigenerationally impairs synaptic plasticity and memory via gametic mechanisms

Fusco, S., Spinelli, M., Cocco, S., Ripoli, C., Mastrodonato, A., Natale, F., Rinaudo, M., Livrizzi, G., & Grassi, C. (2019) · Nature Communications · doi:10.1038/s41467-019-12793-3 · Cited by 63

Adult Hippocampal Neurogenesis in Depression: Behavioral Implications and Regulation by the Stress System

Anacker, C. (2014) · Current topics in behavioral neurosciences · doi:10.1007/7854_2014_275 · Cited by 63

Psychological stressors as a model of maternal adversity: Diurnal modulation of corticosterone responses and changes in maternal behavior

Léonhardt, M., Matthews, S. G., Meaney, M. J., & Walker, C. (2006) · Hormones and Behavior · doi:10.1016/j.yhbeh.2006.08.008 · Cited by 61

Early-Life Blockade of 5-HT1A Receptors Alters Adult Anxiety Behavior and Benzodiazepine Sensitivity

Vinkers, C. H., Oosting, R. S., van Bogaert, M. J. V., Olivier, B., & Groenink, L. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.08.013 · Cited by 61

Glucocorticoid‐mediated mechanisms of hippocampal damage: Contribution of subgranular neurogenesis

Podgorny, O. V., & Gulyaeva, N. V. (2020) · Journal of Neurochemistry · doi:10.1111/jnc.15265 · Cited by 59

Effect of a multi-strain probiotic mixture consumption on anxiety and depression symptoms induced in adult mice by postnatal maternal separation

Santa, F. D., Strimpakos, G., Marchetti, N., Gargari, G., Torcinaro, A., Arioli, S., Mora, D., Petrella, C., & Vecchioli, S. F. (2024) · Microbiome · doi:10.1186/s40168-024-01752-w · Cited by 58

Adult neurogenesis in primate and rodent spinal cord: comparing a cervical dorsal rhizotomy with a dorsal column transection

Vessal, M., Aycock, A., Garton, M. T., Ciferri, M., & Darian‐Smith, C. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05871.x · Cited by 61

Offer and demand: proliferation and survival of neurons in the dentate gyrus

Lehmann, K., Butz, M., & Teuchert, G. (2005) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2005.04156.x · Cited by 58

Neurobiological correlates of social anxiety disorder: an update

Marazziti, D., Abelli, M., Baroni, S., Carpita, B., Ramacciotti, C., & Dell’Osso, L. (2014) · CNS Spectrums · doi:10.1017/s109285291400008x · Cited by 59

Chapter 3 Hormonal Influences on Seizures

Frye, C. (2008) · International review of neurobiology · doi:10.1016/s0074-7742(08)00003-2 · Cited by 35

Neonatal Maternal Separation Alters the Capacity of Adult Neural Precursor Cells to Differentiate into Neurons Via Methylation of Retinoic Acid Receptor Gene Promoter

Boku, S., Toda, H., Nakagawa, S., Kato, A., Inoue, T., Koyama, T., Hiroi, N., & Kusumi, I. (2015) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.07.008 · Cited by 56

Maternal Separation during Breastfeeding Induces Gender-Dependent Changes in Anxiety and the GABA-A Receptor Alpha-Subunit in Adult Wistar Rats

Rodríguez, D. A. L., & Dueñas, Z. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068010 · Cited by 59

Developmental exposure to SSRIs, in addition to maternal stress, has long-term sex-dependent effects on hippocampal plasticity

Rayen, I., Gemmel, M., Pauley, G., Steinbusch, H. W. M., & Pawluski, J. L. (2014) · Psychopharmacology · doi:10.1007/s00213-014-3758-0 · Cited by 57

Several stressors fail to reduce adult hippocampal neurogenesis

Hanson, N. D., Owens, M. J., Boss-Williams, K. A., Weiss, J. M., & Nemeroff, C. B. (2011) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.04.006 · Cited by 57

Regulation of adult neurogenesis in the hippocampus by stress, acetylcholine and dopamine

Srikumar, B. N., Veena, J., & Rao, B. S. (2011) · Journal of Natural Science Biology and Medicine · doi:10.4103/0976-9668.82312 · Cited by 59

Exercise and environment as an intervention for neonatal alcohol effects on hippocampal adult neurogenesis and learning

Hamilton, G. F., Jablonski, S. A., Schiffino, F. L., Cyr, S. A. S., Stanton, M. E., & Klintsova, A. Y. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.01.061 · Cited by 54

The shackles of misfortune: Social adversity assessment and representation in a chronic-disease epidemiological setting

Surtees, P. G., & Wainwright, N. W. J. (2006) · Social Science & Medicine · doi:10.1016/j.socscimed.2006.08.013 · Cited by 55

Predation threat exerts specific effects on rat maternal behaviour and anxiety-related behaviour of male and female offspring

Rahia Mashoodh, A., Sinal, C. J., & Perrot-Sinal, T. S. (2009) · Physiology & Behavior · doi:10.1016/j.physbeh.2009.01.001 · Cited by 57

Juvenile stress enhances anxiety and alters corticosteroid receptor expression in adulthood

Brydges, N. M., Jin, R. O., Seckl, J. R., Holmes, M. C., Drake, A. J., & Hall, J. (2013) · Brain and Behavior · doi:10.1002/brb3.182 · Cited by 53

Transcriptome analysis on maternal separation rats with depression-related manifestations ameliorated by electroacupuncture

Zheng, Y., He, J., Guo, L., Yao, L., Zheng, X., Yang, Z., Xia, Y., Wu, X., Su, Y., Xu, N., et al. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.00314 · Cited by 52

Effects of maternal separation on the neurobehavioral development of newborn Wistar rats

Farkas, J. I., Reglődi, D., Gaszner, B., Szogyi, D., Horváth, G., Lubics, A., Tamás, A., Frank, F., Besirevic, D., & Kiss, P. (2009) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2008.12.011 · Cited by 57

Interactions between Nitric Oxide and Corticosterone in the Regulation of Progenitor Cell Proliferation in the Dentate Gyrus of the Adult Rat

Pinnock, S. B., Balendra, R., Chan, M., Hunt, L. T., Turner‐Stokes, T., & Herbert, J. (2006) · Neuropsychopharmacology · doi:10.1038/sj.npp.1301245 · Cited by 52

Postnatal and Adult Neurogenesis in the Development of Human Disease

Danzer, S. C. (2007) · The Neuroscientist · doi:10.1177/1073858408317008 · Cited by 52

Evidence that neuropsychological deficits following early life adversity may underlie vulnerability to depression

Stuart, S. A., Hinchcliffe, J. K., & Robinson, E. S. J. (2019) · Neuropsychopharmacology · doi:10.1038/s41386-019-0388-6 · Cited by 54

Effects of pre-weaning exposure to a maze on stress responses in pigs at weaning and on subsequent performance in spatial and fear-related tests

Siegford, J. M., Rucker, G., & Zanella, A. J. (2007) · Applied Animal Behaviour Science · doi:10.1016/j.applanim.2007.03.022 · Cited by 52

The selective 5-HT6 receptor antagonists SB-271046 and SB-399885 potentiate NCAM PSA immunolabeling of dentate granule cells, but not neurogenesis, in the hippocampal formation of mature Wistar rats

Foley, A., Hirst, W. D., Gallagher, H. C., Barry, C. E., Hagan, J. J., Upton, N., Walsh, F. S., HUNTER, A., & REGAN, C. (2008) · Neuropharmacology · doi:10.1016/j.neuropharm.2008.03.012 · Cited by 52

Early and later life stress alter brain activity and sleep in rats

Mrdalj, J., Pallesen, S., Milde, A. M., Jellestad, F. K., Murison, R., Ursin, R., Bjorvatn, B., & Grønli, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0069923 · Cited by 51

How early maternal deprivation changes the brain and behavior?

Čater, M., & Majdič, G. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15238 · Cited by 51

Early Life Stress Differentially Modulates Distinct Forms of Brain Plasticity in Young and Adult Mice

Herpfer, I., Hezel, H., Reichardt, W., Clark, K., Geiger, J., Gross, C. M., Heyer, A., Neagu, V., Bhatia, H. S., Atas, H. C., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0046004 · Cited by 53

TheNPAS3gene—emerging evidence for a role in psychiatric illness

Pickard, B. S., Pieper, A. A., Porteous, D. J., Blackwood, D., & Muir, W. J. (2006) · Annals of Medicine · doi:10.1080/07853890600946500 · Cited by 51

Early-Life Forebrain Glucocorticoid Receptor Overexpression Increases Anxiety Behavior and Cocaine Sensitization

Wei, Q., Fentress, H. M., Hoversten, M. T., Zhang, L., Hebda‐Bauer, E. K., Watson, S. J., Seasholtz, A. F., & Akil, H. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.07.009 · Cited by 55

Maternal separation in rodents: a journey from gut to brain and nutritional perspectives

Rincel, M., & Darnaudéry, M. (2019) · Proceedings of The Nutrition Society · doi:10.1017/s0029665119000958 · Cited by 51

Memory impairments and hippocampal modifications in adult rats with neonatal isolation stress experience

Kosten, T. A., Karanian, D. A., Yeh, J., Haile, C. N., Kim, J. J., Kehoe, P., & Bahr, B. A. (2007) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2007.03.011 · Cited by 51

Effects of social isolation, re‐socialization and age on cognitive and aggressive behaviors of Kunming mice and BALB/c mice

An, D., Chen, W., Yu, D., Wang, S., Yu, W., Xu, H., Wang, D., Zhao, D. Y., Sun, Y., Wu, J., et al. (2016) · Animal Science Journal · doi:10.1111/asj.12688 · Cited by 49

Caregiver maltreatment causes altered neuronal DNA methylation in female rodents

Blaze, J., & Roth, T. L. (2017) · Development and Psychopathology · doi:10.1017/s0954579417000128 · Cited by 48

Plasticity of the Worker Bumblebee Brain in Relation to Age and Rearing Environment

Jones, B. M., Leonard, A. S., Papaj, D. R., & Gronenberg, W. (2013) · Brain Behavior and Evolution · doi:10.1159/000355845 · Cited by 48

Evaluating genetic markers and neurobiochemical analytes for fluoxetine response using a panel of mouse inbred strains

Benton, C. S., Miller, B. H., Skwerer, S., Suzuki, O., Schultz, L. E., Cameron, M. D., Marron, J. S., Pletcher, M. T., & Wiltshire, T. (2011) · Psychopharmacology · doi:10.1007/s00213-011-2574-z · Cited by 49

Investigating the Association Between Early Life Parental Care and Stress Responsivity in Adulthood

Engert, V., Buß, C., Khalili‐Mahani, N., Wadiwalla, M., Dedovic, K., & Pruessner, J. C. (2010) · Developmental Neuropsychology · doi:10.1080/87565641.2010.494752 · Cited by 53

Sexual experience restores age‐related decline in adult neurogenesis and hippocampal function

Glasper, E. R., & Gould, E. (2013) · Hippocampus · doi:10.1002/hipo.22090 · Cited by 52

Social regulation of adult neurogenesis: A comparative approach

Holmes, M. M. (2016) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2016.02.001 · Cited by 52

Neurobiological mechanisms underlying sex-related differences in stress-related disorders: Effects of neuroactive steroids on the hippocampus

Hillerer, K. M., Slattery, D. A., & Pletzer, B. A. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100796 · Cited by 49

Perinatal allopregnanolone influences prefrontal cortex structure, connectivity and behavior in adult rats

Grobin, A. C., Gizerian, S. S., Lieberman, J. A., & Morrow, A. L. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2005.12.026 · Cited by 49

Microstructural Abnormalities in Language and Limbic Pathways in Orphanage-Reared Children: A Diffusion Tensor Imaging Study

Kumar, A., Behen, M. E., Singsoonsud, P., Veenstra, A. L., Wolfe-Christensen, C., Helder, E., & Chugani, H. T. (2014) · Journal of Child Neurology · doi:10.1177/0883073812474098 · Cited by 46

A Comprehensive Overview of Stress, Resilience, and Neuroplasticity Mechanisms

Buenrostro-Jáuregui, M. H., Muñoz-Sánchez, S., Rojas-Hernández, J., Alonso-Orozco, A. I., Vega‐Flores, G., Tapia-de-Jesús, A., & Leal‐Galicia, P. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26073028 · Cited by 50

Maternal separation produces alterations of forebrain brain-derived neurotrophic factor expression in differently aged rats

Wang, Q., Shao, F., & Wang, W. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00049 · Cited by 48

Nectin-3 modulates the structural plasticity of dentate granule cells and long-term memory

Wang, X.-X., Li, J.-T., Xie, X.-M., Gu, Y., Si, T.-M., Schmidt, M. V., & Wang, X. (2017) · Translational Psychiatry · doi:10.1038/tp.2017.196 · Cited by 46

The effects of prenatal stress on the Purkinje cell neurogenesis

Ulupınar, E., Yücel, F., & Ortuğ, G. (2005) · Neurotoxicology and Teratology · doi:10.1016/j.ntt.2005.10.003 · Cited by 47

Stress-induced suppression of hippocampal neurogenesis in adult male rats is altered by prenatal ethanol exposure

Sliwowska, J. H., Barker, J. M., Barha, C. K., Lan, N., Weinberg, J., & Galea, L. A. M. (2010) · Stress · doi:10.3109/10253890903531582 · Cited by 46

Early life stress stimulates hippocampal reelin gene expression in a sex‐specific manner: Evidence for corticosterone‐mediated action

Gross, C. M., Flubacher, A., Tinnes, S., Heyer, A., Scheller, M., Herpfer, I., Berger, T., Frotscher, M., Lieb, K., & Haas, C. A. (2010) · Hippocampus · doi:10.1002/hipo.20907 · Cited by 47

A Baldwin interpretation of adult hippocampal neurogenesis: from functional relevance to physiopathology

Abrous, D. N., Koehl, M., & Lemoine, M. (2021) · Molecular Psychiatry · doi:10.1038/s41380-021-01172-4 · Cited by 51

Neonatal maternal separation and enhancement of the hypoxic ventilatory response in rat: the role of GABAergic modulation within the paraventricular nucleus of the hypothalamus

Genest, S., Balon, N., Laforest, S., Drolet, G., & Kinkead, R. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2007.135160 · Cited by 45

Associations between prenatal, childhood, and adolescent stress and variations in white-matter properties in young men

Jensen, S. K. G., Pangelinan, M., Björnholm, L., Klasnja, A., Leemans, A., Drakesmith, M., Evans, C. J., Barker, E. D., & Paus, T. (2018) · NeuroImage · doi:10.1016/j.neuroimage.2017.10.033 · Cited by 44

Repeated neonatal separation stress alters the composition of neurochemically characterized interneuron subpopulations in the rodent dentate gyrus and basolateral amygdala

Seidel, K., Helmeke, C., Poeggel, G., & Braun, K. (2008) · Developmental Neurobiology · doi:10.1002/dneu.20651 · Cited by 44

Regulation of adult hippocampal neurogenesis: relevance to depression

Vaidya, V. A., Fernandes, K. A., & Jha, S. (2007) · Expert Review of Neurotherapeutics · doi:10.1586/14737175.7.7.853 · Cited by 43

Maternal separation modulates short-term behavioral and physiological indices of the stress response

Litvin, Y., Tovote, P., Pentkowski, N. S., Zeyda, T., King, L. B., Vasconcellos, A., Dunlap, C., Spiess, J., Blanchard, D. C., & Blanchard, R. J. (2010) · Hormones and Behavior · doi:10.1016/j.yhbeh.2010.03.010 · Cited by 43

Memory development: implications for adults recalling childhood experiences in the courtroom

Howe, M. L. (2013) · Nature reviews. Neuroscience · doi:10.1038/nrn3627 · Cited by 43

Effects of early rearing conditions on cognitive performance in prepubescent male and female rats

Frankola, K. A., Flora, A. L., Torres, A. K., Grissom, E. M., Overstreet, S., & Dohanich, G. P. (2010) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2010.04.005 · Cited by 47

Dorsal Dentate Gyrus, a Key Regulator for Mood and Psychiatric Disorders

Sun, D., Mei, L., & Xiong, W. (2023) · Biological Psychiatry · doi:10.1016/j.biopsych.2023.01.005 · Cited by 47

Neonatal handling prevents anxiety-like symptoms in rats exposed to chronic mild stress: Behavioral and oxidative parameters

Boufleur, N., Antoniazzi, C. T. D. D., Pase, C. S., Benvegnú, D. M., Dias, V. T., Segat, H. J., Roversi, K., Roversi, K., Nora, M. D., Koakoskia, G., et al. (2012) · Stress · doi:10.3109/10253890.2012.723075 · Cited by 46

Early life adversity shapes social subordination and cell type–specific transcriptomic patterning in the ventral hippocampus

Kos, A., López, J. P., Bordes, J., Donno, C. D., Dine, J., Brivio, E., Karamihalev, S., Luecken, M. D., Almeida-Corrêa, S., Gasperoni, S., et al. (2023) · Science Advances · doi:10.1126/sciadv.adj3793 · Cited by 43

Antistress properties of antidepressant drugs and their clinical implications

Calabrese, F., Molteni, R., & Riva, M. A. (2011) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2011.05.007 · Cited by 42

Early handling effect on female rat spatial and non-spatial learning and memory

Plescia, F., Marino, R. A. M., Navarra, M., Gambino, G., Brancato, A., Sardo, P., & Cannizzaro, C. (2013) · Behavioural Processes · doi:10.1016/j.beproc.2013.10.011 · Cited by 42

A revival of Spiegel's campotomy: long term results of the stereotactic pallidothalamic tractotomy against the parkinsonian thalamocortical dysrhythmia

Aufenberg, C., Sarnthein, J., Morel, A., Rousson, V., Gallay, M. N., & Jeanmonod, D. (2005) · Thalamus & Related Systems · doi:10.1017/s147292880700012x · Cited by 40

Modulation of the suppressive effect of corticosterone on adult rat hippocampal cell proliferation by paroxetine

Qiu, G., Helmeste, D. M., Samaranayake, A. N., Lau, B. W.-M., Lee, T. M. C., Tang, S.-W., & So, K. (2007) · Neuroscience Bulletin · doi:10.1007/s12264-007-0019-9 · Cited by 42

Using cross-species comparisons and a neurobiological framework to understand early social deprivation effects on behavioral development

Brett, Z. H., Humphreys, K. L., Fleming, A. S., Kraemer, G. W., & Drury, S. S. (2015) · Development and Psychopathology · doi:10.1017/s0954579415000036 · Cited by 43

Probabilistic epigenesis: An alternative causal model for conduct disorders in children and adolescents

Cohen, D. (2009) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2009.07.011 · Cited by 44

The dentate gyrus in depression

Umschweif, G., Greengard, P., & Sagi, Y. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14640 · Cited by 40

Lifelong consequences of brain injuries during development: From risk to resilience

Weil, Z. M., & Karelina, K. (2019) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2019.100793 · Cited by 39

Glucocorticoid effects on the brain: from adaptive developmental plasticity to allostatic overload

Eachus, H., & Ryu, S. (2024) · Journal of Experimental Biology · doi:10.1242/jeb.246128 · Cited by 37

Possible Involvement of TLRs and Hemichannels in Stress-Induced CNS Dysfunction via Mastocytes, and Glia Activation

Aguirre, A., Maturana, C. J., Harcha, P. A., & Sáez, J. C. (2013) · Mediators of Inflammation · doi:10.1155/2013/893521 · Cited by 39

Abus, maltraitance et négligence : (1) épidémiologie et retentissements psychiques, somatiques et sociaux

Benarous, X., Consoli, A., Raffin, M., & Cohen, D. (2014) · Neuropsychiatrie de l Enfance et de l Adolescence · doi:10.1016/j.neurenf.2014.04.005 · Cited by 37

Stress early in life leads to cognitive impairments, reduced numbers of CA3 neurons and altered maternal behavior in adult female mice

Reshetnikov, V. V., Kovner, A. V., Lepeshko, A. A., Pavlov, K. S., Grinkevich, L. N., & Bondar, N. P. (2018) · Genes Brain & Behavior · doi:10.1111/gbb.12541 · Cited by 37

Ozone increases plasma kynurenine-tryptophan ratio and impacts hippocampal serotonin receptor and neurotrophic factor expression: Role of stress hormones

Rose, M., Filiatreault, A., Guénette, J., Williams, A., & Thomson, E. M. (2020) · Environmental Research · doi:10.1016/j.envres.2020.109483 · Cited by 39

Nutrient restriction during early life reduces cell proliferation in the hippocampus at adulthood but does not impair the neuronal differentiation process of the new generated cells

de Matos, R. J. B., Orozco-Solís, R., de Souza, S. L., Manhães‐de‐Castro, R., & Bolaños, F. J. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.08.071 · Cited by 37

Tobacco smoke diminishes neurogenesis and promotes gliogenesis in the dentate gyrus of adolescent rats

Bruijnzeel, A. W., Bauzo, R. M., Munikoti, V., Rodrick, G. B., Yamada, H., Fornal, C. A., Ormerod, B. K., & Jacobs, B. L. (2011) · Brain Research · doi:10.1016/j.brainres.2011.07.041 · Cited by 40

Consequences of different housing conditions on brain morphology in laying hens

Patzke, N., Ocklenburg, S., van der Staay, F. J., Güntürkün, O., & Manns, M. (2008) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2008.12.005 · Cited by 37

Periodic maternal separation decreases hippocampal neurogenesis without affecting basal corticosterone during the stress hyporesponsive period, but alters HPA axis and coping behavior in adulthood

Lajud, N., Roque, A., Cajero, M., Gutiérrez‐Ospina, G., & Torner, L. (2011) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2011.07.011 · Cited by 172

Stress in early life inhibits neurogenesis in adulthood

Karten, Y. J. G., Olariu, A., & Cameron, H. A. (2005) · Trends in Neurosciences · doi:10.1016/j.tins.2005.01.009 · Cited by 115

Early maternal deprivation decreases hippocampal neurogenesis in young female rats

Lucassen, P. J. (2009) · Frontiers in Behavioral Neuroscience · doi:10.3389/conf.neuro.09.2009.12.028

Severe Early Life Stress Hampers Spatial Learning and Neurogenesis, but Improves Hippocampal Synaptic Plasticity and Emotional Learning under High-Stress Conditions in Adulthood

Oomen, C. A., Soeters, H., Audureau, N., Vermunt, L., van Hasselt, F. N., Manders, E. M. M., Joëls, M., Lucassen, P. J., & Krugers, H. J. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.0247-10.2010 · Cited by 367

Maternal separation decreases adult hippocampal cell proliferation and impairs cognitive performance but has little effect on stress sensitivity and anxiety in adult Wistar rats

Hulshof, H. J., Novati, A., Sgoifo, A., Luiten, P. G. M., den Boer, J. A., & Meerlo, P. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2010.08.038 · Cited by 169