Regional differences in dendritic spine density confer resilience to chronic social defeat stress

The Mouse Brain in Stereotaxic Coordinates

Paxinos, G. (2001) · Cited by 12,859 · see citing works

mouse brain in stereotaxic coordinates

Franklin, K. B. J., & Paxinos, G. (1997) · Cited by 3,258 · see citing works

The mesolimbic dopamine reward circuit in depression

Nestler, E. J., & Carlezon, W. A. (2006) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.09.018 · Cited by 2,059 · see citing works

Animal models of neuropsychiatric disorders

Nestler, E. J., & Hyman, S. E. (2010) · Nature Neuroscience · doi:10.1038/nn.2647 · Cited by 2,023 · see citing works

Psychobiology and molecular genetics of resilience

Feder, A., Nestler, E. J., & Charney, D. S. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2649 · Cited by 1,272 · see citing works

Neurobiology of resilience

Russo, S. J., Murrough, J. W., Han, M.-H., Charney, D. S., & Nestler, E. J. (2012) · Nature Neuroscience · doi:10.1038/nn.3234 · Cited by 1,206 · see citing works

Glutamate N-methyl-D-aspartate Receptor Antagonists Rapidly Reverse Behavioral and Synaptic Deficits Caused by Chronic Stress Exposure

Li, N., Liu, R.-J., Dwyer, J. M., Banasr, M., Lee, B., Son, H., Li, X.-Y., Aghajanian, G., & Duman, R. S. (2011) · Biological Psychiatry · doi:10.1016/j.biopsych.2010.12.015 · Cited by 1,082 · see citing works

Repeated Stress Induces Dendritic Spine Loss in the Rat Medial Prefrontal Cortex

Radley, J. J., Rocher, A. B., Miller, M., Janssen, W. G. M., Liston, C., Hof, P. R., McEwen, B. S., & Morrison, J. H. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhi104 · Cited by 820 · see citing works

R-ketamine: a rapid-onset and sustained antidepressant without psychotomimetic side effects

Yang, C., Shirayama, Y., Zhang, J.-C., Ren, Q., Yao, W., Ma, M., Dong, C., & Hashimoto, K. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.136 · Cited by 605 · see citing works

Brain-derived Neurotrophic Factor (BDNF)-TrkB Signaling in Inflammation-related Depression and Potential Therapeutic Targets

Zhang, J.-C., Yao, W., & Hashimoto, K. (2016) · Current Neuropharmacology · doi:10.2174/1570159x14666160119094646 · Cited by 538 · see citing works

Resilience to Chronic Stress Is Mediated by Hippocampal Brain-Derived Neurotrophic Factor

Taliaz, D., Loya, A., Gersner, R., Haramati, S., Chen, A., & Zangen, A. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.5725-10.2011 · Cited by 311 · see citing works

Antidepressant Effects of TrkB Ligands on Depression-Like Behavior and Dendritic Changes in Mice After Inflammation

Zhang, J.-C., Wu, J., Fujita, Y., Yao, W., Ren, Q., Yang, C., Li, S.-X., Shirayama, Y., & Hashimoto, K. (2015) · International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyu077 · Cited by 289 · see citing works

Spine synapse remodeling in the pathophysiology and treatment of depression

Duman, C. H., & Duman, R. S. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.01.022 · Cited by 257 · see citing works

Bifidobacterium in the gut microbiota confer resilience to chronic social defeat stress in mice

Yang, C., Fujita, Y., Ren, Q., Ma, M., Dong, C., & Hashimoto, K. (2017) · Scientific Reports · doi:10.1038/srep45942 · Cited by 202 · see citing works

Comparison of ketamine, 7,8-dihydroxyflavone, and ANA-12 antidepressant effects in the social defeat stress model of depression

Zhang, J.-C., Yao, W., Dong, C., Yang, C., Ren, Q., Ma, M., Han, M., & Hashimoto, K. (2015) · Psychopharmacology · doi:10.1007/s00213-015-4062-3 · Cited by 183 · see citing works

Gene deficiency and pharmacological inhibition of soluble epoxide hydrolase confers resilience to repeated social defeat stress

Ren, Q., Ma, M., Ishima, T., Morisseau, C. H. P., Yang, J., Wagner, K. M., Zhang, J.-C., Yang, C., Yao, W., Dong, C., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1601532113 · Cited by 161 · see citing works

Brain-derived neurotrophic factor and hypothalamic-pituitary-adrenal axis adaptation processes in a depressive-like state induced by chronic restraint stress

Naert, G., IXART, G., Maurice, T., Tapia‐Arancibia, L., & Givalois, L. (2010) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2010.08.006 · Cited by 154 · see citing works

Role of Keap1-Nrf2 signaling in depression and dietary intake of glucoraphanin confers stress resilience in mice

Yao, W., Zhang, J.-C., Ishima, T., Dong, C., Yang, C., Ren, Q., Ma, M., Han, M., Wu, J., Suganuma, H., et al. (2016) · Scientific Reports · doi:10.1038/srep30659 · Cited by 154 · see citing works

Alterations in brain-derived neurotrophic factor (BDNF) and its precursor proBDNF in the brain regions of a learned helplessness rat model and the antidepressant effects of a TrkB agonist and antagonist

Shirayama, Y., Yang, C., Zhang, J.-C., Ren, Q., Yao, W., & Hashimoto, K. (2015) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2015.09.002 · Cited by 137 · see citing works

Rapid and Sustained Antidepressant Action of the mGlu2/3 Receptor Antagonist MGS0039 in the Social Defeat Stress Model: Comparison with Ketamine

Dong, C., Zhang, J.-C., Yao, W., Ren, Q., Ma, M., Yang, C., Chaki, S., & Hashimoto, K. (2016) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyw089 · Cited by 116 · see citing works

Prophylactic effects of sulforaphane on depression-like behavior and dendritic changes in mice after inflammation

Zhang, J., Yao, W., Dong, C., Yang, C., Ren, Q., Ma, M., Han, M., Wu, J., Ushida, Y., Suganuma, H., et al. (2016) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2016.10.004 · Cited by 113 · see citing works

Glutamate Signaling in Synaptogenesis and NMDA Receptors as Potential Therapeutic Targets for Psychiatric Disorders

Ohgi, Y., Futamura, T., & Hashimoto, K. (2015) · Current Molecular Medicine · doi:10.2174/1566524015666150330143008 · Cited by 107 · see citing works

BDNF–TrkB signaling in the nucleus accumbens shell of mice has key role in methamphetamine withdrawal symptoms

Ren, Q., Ma, M., Yang, C., Zhang, J.-C., Yao, W., & Hashimoto, K. (2015) · Translational Psychiatry · doi:10.1038/tp.2015.157 · Cited by 99 · see citing works

Regional differences in the expression of brain-derived neurotrophic factor (BDNF) pro-peptide, proBDNF and preproBDNF in the brain confer stress resilience

Yang, B., Yang, C., Ren, Q., Zhang, J.-C., Chen, Q., Shirayama, Y., & Hashimoto, K. (2016) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-016-0693-6 · Cited by 69 · see citing works

Adjunctive treatment of brexpiprazole with fluoxetine shows a rapid antidepressant effect in social defeat stress model: Role of BDNF-TrkB signaling

Ma, M., Ren, Q., Yang, C., Zhang, J.-C., Yao, W., Dong, C., Ohgi, Y., Futamura, T., & Hashimoto, K. (2016) · Scientific Reports · doi:10.1038/srep39209 · Cited by 58 · see citing works

Glutamate N-methyl-D-aspartate Receptor Antagonists Rapidly Reverse Behavioral and Synaptic Deficits Caused by Chronic Stress Exposure

리, 난., 이보영, 류, 롱., 아흐자니안, 죠., 샤오유엔, 리., 바나스, 모., 드와이더, 제., & 듀먼, 로. (2011) · Cited by 2 · see citing works

The molecular and cellular mechanisms of depression: a focus on reward circuitry

Fox, M. E., & Lobo, M. K. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0415-3 · Cited by 232 · see citing works

Stress-induced plasticity and functioning of ventral tegmental dopamine neurons

Douma, E. H., & de Kloet, E. R. (2019) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2019.10.015 · Cited by 226 · see citing works

Microglial ERK-NRBP1-CREB-BDNF Signaling in Sustained Antidepressant Actions of (R)-Ketamine

Yao, W., Cao, Q., Luo, S., He, L., Yang, C., Chen, J., Qi, Q., Hashimoto, K., & Zhang, J.-C. (2022) · Molecular Psychiatry · doi:10.1038/s41380-021-01377-7 · Cited by 216 · see citing works

Psychedelics and Other Psychoplastogens for Treating Mental Illness.

Vargas, M. V., Meyer, R., Avanes, A. A., Rus, M., & Olson, D. E. (2021) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.727117 · Cited by 166 · see citing works

Brexanolone, a neurosteroid antidepressant, vindicates the GABAergic deficit hypothesis of depression and may foster resilience

Lüscher, B., & Möhler, H. (2019) · F1000Research · doi:10.12688/f1000research.18758.1 · Cited by 105 · see citing works

Resilience Is Associated With Larger Dentate Gyrus, While Suicide Decedents With Major Depressive Disorder Have Fewer Granule Neurons

Boldrini, M., Galfalvy, H., Dwork, A. J., Rosoklija, G. B., Trencevska-Ivanovska, I., Pavlovski, G., Hen, R., Arango, V., & Mann, J. J. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2018.12.022 · Cited by 116 · see citing works

Running from Stress: Neurobiological Mechanisms of Exercise-Induced Stress Resilience

Nowacka-Chmielewska, M. M., Grabowska, K., Grabowski, M., Meybohm, P., Burek, M., & Małecki, A. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113348 · Cited by 117 · see citing works

Rodent models of social stress and neuronal plasticity: Relevance to depressive-like disorders

Patel, D., Kas, M. J., Chattarji, S., & Buwalda, B. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.111900 · Cited by 105 · see citing works

Microglia Polarization and Endoplasmic Reticulum Stress in Chronic Social Defeat Stress Induced Depression Mouse

Tang, J., Yu, W., Chen, S., Gao, Z., & Xiao, B. (2018) · Neurochemical Research · doi:10.1007/s11064-018-2504-0 · Cited by 101 · see citing works

Maturational Changes in Prefrontal and Amygdala Circuits in Adolescence: Implications for Understanding Fear Inhibition during a Vulnerable Period of Development

Zimmermann, K. S., Richardson, R., & Baker, K. (2019) · Brain Sciences · doi:10.3390/brainsci9030065 · Cited by 101 · see citing works

Abnormal composition of gut microbiota is associated with resilience versus susceptibility to inescapable electric stress

Zhang, K., Fujita, Y., Chang, L., Qu, Y., Pu, Y., Wang, S., Shirayama, Y., & Hashimoto, K. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0571-x · Cited by 98 · see citing works

Functional Contribution of the Medial Prefrontal Circuitry in Major Depressive Disorder and Stress-Induced Depressive-Like Behaviors

Bittar, T. P., & Labonté, B. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.699592 · Cited by 87 · see citing works

Dendritic Spines: Mediators of Cognitive Resilience in Aging and Alzheimer’s Disease

Walker, C. K., & Herskowitz, J. H. (2021) · The Neuroscientist · doi:10.1177/1073858420945964 · Cited by 86 · see citing works

Chronic Stress Induces Sex-Specific Functional and Morphological Alterations in Corticoaccumbal and Corticotegmental Pathways

Bittar, T. P., Pelaez, M. C., Silva, J. C. H., Quessy, F., Lavigne, A.-A., Morency, D., Blanchette, L.-J., Arsenault, E., Chérasse, Y., Seigneur, J., et al. (2021) · Biological Psychiatry · doi:10.1016/j.biopsych.2021.02.014 · Cited by 64 · see citing works

Alterations and adaptation of ventral tegmental area dopaminergic neurons in animal models of depression

Kaufling, J. (2019) · Cell and Tissue Research · doi:10.1007/s00441-019-03007-9 · Cited by 60 · see citing works

(R)-Ketamine Rapidly Ameliorates the Decreased Spine Density in the Medial Prefrontal Cortex and Hippocampus of Susceptible Mice After Chronic Social Defeat Stress

Zhang, J., Qu, Y., Chang, L., Pu, Y., & Hashimoto, K. (2019) · International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyz048 · Cited by 55 · see citing works

The hippocampus in stress susceptibility and resilience: Reviewing molecular and functional markers

Larosa, A., & Wong, T. P. (2022) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2022.110601 · Cited by 47 · see citing works

Prophylactic Ketamine Treatment Promotes Resilience to Chronic Stress and Accelerates Recovery: Correlation with Changes in Synaptic Plasticity in the CA3 Subregion of the Hippocampus

Krzystyniak, A., Bączyńska, E., Magnowska, M., Antoniuk, S., Roszkowska, M., Zaręba-Kozioł, M., Das, N., Basu, S., Pikuła, M., & Włodarczyk, J. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20071726 · Cited by 46 · see citing works

Stress-induced alterations of mesocortical and mesolimbic dopaminergic pathways

Quessy, F., Bittar, T., Blanchette, L. J., Lévesque, M., & Labonté, B. (2021) · Scientific Reports · doi:10.1038/s41598-021-90521-y · Cited by 42 · see citing works

Rapid antidepressant-like effect of non-hallucinogenic psychedelic analog lisuride, but not hallucinogenic psychedelic DOI, in lipopolysaccharide-treated mice

Qu, Y., Chang, L., Ma, L., Wan, X., & Hashimoto, K. (2022) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2022.173500 · Cited by 41 · see citing works

Social defeat stress in adult mice causes alterations in gene expression, alternative splicing, and the epigenetic landscape of H3K4me3 in the prefrontal cortex: An impact of early-life stress

Reshetnikov, V. V., Kisaretova, P. E., Ershov, N., Merkulova, T. I., & Bondar, N. P. (2020) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2020.110068 · Cited by 40 · see citing works

Deficient Autophagy in Microglia Aggravates Repeated Social Defeat Stress-Induced Social Avoidance

Sakai, M., Yu, Z., Hirayama, R., Nakasato, M., Kikuchi, Y., Ono, C., Komatsu, H., Nakanishi, M., Yoshii, H., Stellwagen, D., et al. (2022) · Neural Plasticity · doi:10.1155/2022/7503553 · Cited by 37 · see citing works

Chronic social defeat stress differentially regulates the expression ofBDNFtranscripts and epigenetic modifying enzymes in susceptible and resilient mice

Mallei, A., Ieraci, A., & Popoli, M. (2018) · The World Journal of Biological Psychiatry · doi:10.1080/15622975.2018.1500029 · Cited by 35 · see citing works

The dentate gyrus in depression

Umschweif, G., Greengard, P., & Sagi, Y. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14640 · Cited by 38 · see citing works

NPAS4 in the medial prefrontal cortex mediates chronic social defeat stress-induced anhedonia-like behavior and reductions in excitatory synapses

Hughes, B. W., Siemsen, B. M., Tsvetkov, E., Berto, S., Kumar, J., Cornbrooks, R. G., Akiki, R. M., Cho, J. Y., Carter, J. S., Snyder, K. K., et al. (2023) · eLife · doi:10.7554/elife.75631 · Cited by 34 · see citing works

PGC-1α–FNDC5–BDNF signaling pathway in skeletal muscle confers resilience to stress in mice subjected to chronic social defeat

Zhan, G., Huang, N., Li, S., Hua, D., Zhang, J., Fang, X., Yang, N., Luo, A., & Yang, C. (2018) · Psychopharmacology · doi:10.1007/s00213-018-5041-2 · Cited by 32 · see citing works

Klotho Regulated by Estrogen Plays a Key Role in Sex Differences in Stress Resilience in Rats

Tan, Z.-N., Li, Y., Guan, Y., Iqbal, J., Wang, C., Yan, R., & Ma, X. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24021206 · Cited by 32 · see citing works

Influence of gut microbiota on resilience and its possible mechanisms

Wang, J., Zhou, T., Liu, F., Huang, Y., Xiao, Z., Qian, Y., & Zhou, W. (2023) · International Journal of Biological Sciences · doi:10.7150/ijbs.82362 · Cited by 30 · see citing works

Deletion of serine racemase confers D-serine –dependent resilience to chronic social defeat stress

Dong, C., Zhang, J., Ren, Q., Ma, M., Qu, Y., Zhang, K., Yao, W., Ishima, T., Mori, H., & Hashimoto, K. (2018) · Neurochemistry International · doi:10.1016/j.neuint.2018.03.008 · Cited by 26 · see citing works

Structure and function differences in the prelimbic cortex to basolateral amygdala circuit mediate trait vulnerability in a novel model of acute social defeat stress in male mice

Grossman, Y. S., Fillinger, C., Manganaro, A., Voren, G., Waldman, R. N., Zou, T., Janssen, W. G. M., Kenny, P. J., & Dumitriu, D. (2021) · Neuropsychopharmacology · doi:10.1038/s41386-021-01229-6 · Cited by 24 · see citing works

Repeated intermittent administration of (R)-ketamine during juvenile and adolescent stages prevents schizophrenia-relevant phenotypes in adult offspring after maternal immune activation: a role of TrkB signaling

Tan, Y., Fujita, Y., Pu, Y., Chang, L., Qu, Y., Wang, X., & Hashimoto, K. (2022) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-021-01365-6 · Cited by 22 · see citing works

Cognitive and Emotional Symptoms Induced by Chronic Stress Are Regulated by EGR1 in a Subpopulation of Hippocampal Pyramidal Neurons

Sancho‐Balsells, A., Borràs‐Pernas, S., Brito, V., Alberch, J., Girault, J., & Giralt, A. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24043833 · Cited by 20 · see citing works

Circuit- and laminar-specific regulation of medial prefrontal neurons by chronic stress

Liu, W.-Z., Wang, C.-Y., Wang, Y., Cai, M.-T., Zhong, W.-X., Liu, T., Wang, Z.-H., Pan, H.-Q., Zhang, W.-H., & Pan, B.-X. (2023) · Cell & Bioscience · doi:10.1186/s13578-023-01050-2 · Cited by 21 · see citing works

Spatial transcriptomic analysis of the mouse brain following chronic social defeat stress

Wang, T., Song, Z., Zhao, X., Wu, Y., Wu, L., Haghparast, A., & Wu, H. (2023) · Exploration · doi:10.1002/exp.20220133 · Cited by 20 · see citing works

mGlu2/3 receptor in the prelimbic cortex is implicated in stress resilience and vulnerability in mice

Jing, X.-Y., Wang, Y., Zou, H.-W., Li, Z.-L., Liu, Y.-J., & Li, L. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.174231 · Cited by 18 · see citing works

Sortilin deletion in the prefrontal cortex and hippocampus ameliorates depressive-like behaviors in mice via regulating ASM/ceramide signaling

Chen, S.-J., Gao, C., Lv, Q., Zhao, M.-Q., Qin, X., & Liao, H. (2021) · Acta Pharmacologica Sinica · doi:10.1038/s41401-021-00823-0 · Cited by 18 · see citing works

Corticostriatal contributions to dysregulated motivated behaviors in stress, depression, and substance use disorders

Siemsen, B. M., Franco, D., & Lobo, M. K. (2022) · Neuroscience Research · doi:10.1016/j.neures.2022.12.014 · Cited by 12 · see citing works

The effects of Kctd12, an auxiliary subunit of GABAB receptor in dentate gyrus on behavioral response to chronic social defeat stress in mice

Deng, S., Hu, Z., Mao, L., Gao, B., Yang, Q., Wang, F., & Chen, J. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.105355 · Cited by 12 · see citing works

Comparison of Golgi-Cox and Intracellular Loading of Lucifer Yellow for Dendritic Spine Density and Morphology Analysis in the Mouse Brain

Walker, C. K., Greathouse, K. M., Liu, E., Muhammad, H. M., Boros, B. D., Freeman, C. D., Seo, J. V., & Herskowitz, J. H. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.06.029 · Cited by 11 · see citing works

Aberrant ventral dentate gyrus structure and function in trauma susceptible mice

Dirven, B. C. J., van der Geugten, D., Temporão, C., van Bodegom, M., Madder, L., van Agen, L., Homberg, J. R., Kozicz, T., & Henckens, M. J. A. G. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-02264-7 · Cited by 11 · see citing works

Hippocampal HDAC5-mediated histone acetylation underlies stress susceptibility in mice exposed to chronic social defeat stress

Li, N., Liu, T., Wang, Y.-Y., Xu, T., Shi, H., Chang, L., & Zhu, L. (2024) · Neuroscience · doi:10.1016/j.neuroscience.2024.08.010 · Cited by 11 · see citing works

Chronic Social Defeat Stress Gives Rise to Social Avoidance Through Fear Learning

Lee, J., Aubry, A., Hanif, S., Grunfeld, I. S., Likhtik, E., & Burghardt, N. S. (2024) · Behavioural Brain Research · doi:10.1016/j.bbr.2024.115245 · Cited by 9 · see citing works

The P2X7 receptor in depression: Novel insights and therapeutic implications

Zhong, Y.-T., Pi, C., Zuo, Y., Yan, W., Li, W., Jiang, Y., Lei, T., Zheng, W., Jiang, J., Yang, Y., et al. (2025) · Neurobiology of Disease · doi:10.1016/j.nbd.2025.107011 · Cited by 9 · see citing works

Behavioral flexibility impacts on coping and emotional responses in male mice submitted to social defeat stress

Rosado, A. F., Bevilacqua, L. M., Moreira, E. L. G., & Kaster, M. P. (2022) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2022.110696 · Cited by 8 · see citing works

The effects of different types of social interactions on the electrophysiology of neurons in the nucleus accumbens in rodents

Borland, J. M. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105809 · Cited by 7 · see citing works

Amelioration of gap junction dysfunction in a depression model by loganin: Involvement of GSK-3β/β-catenin signaling

Wang, M., Zuo, G., Wang, X., Han, Y., Xia, C., Pan, C., Guo, Y., Wang, Y., Yang, H., Zhang, W., et al. (2024) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2024.119288 · Cited by 8 · see citing works

Neuropeptide-mediated activation of astrocytes improves stress resilience in mice by modulating cortical neural synapses

Cui, J., Wang, X., Yu, J. Z., Zhang, B., Shi, Y., So, K., Zhang, L., & Wei, J. (2024) · Acta Pharmacologica Sinica · doi:10.1038/s41401-024-01420-7 · Cited by 7 · see citing works

Activity‐Dependent Synaptic Plasticity in the Medial Prefrontal Cortex of Male Rats Underlies Resilience‐Related Behaviors to Social Adversity

Montes-Rodríguez, C. J., Hernández‐Reyes, E. D., Piña‐Díaz, V., Muñoz‐Torres, Z., Pérez‐Zarazúa, I., Urías, E. U., & Prospero-Garcia, O. E. (2024) · Journal of Neuroscience Research · doi:10.1002/jnr.25377 · Cited by 4 · see citing works

Stress-Induced Dysregulation of the Guidance Cue Receptor DCC Alters Corticolimbic Circuit Architecture

Mahmud, A., Hernández, G., Abboud, F., & Flores, C. (2025) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2025.100629 · Cited by 3 · see citing works

Stress-induced alterations of mesocortical and mesolimbic dopaminergic pathwaysPreprint

Quessy, F., Bittar, T. P., Blanchette, L.-J., Lévesque, M., & Labonté, B. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.01.04.425341 · Cited by 3 · see citing works

Prenatal maternal stress induces increased avoidance behavior in adolescent mice offspring

Yin, X., Jiang, R., Liu, X., Liu, Y., Liu, X., Zhou, F., Xi, Y., Yan, S., Li, Y., Du, Y., et al. (2025) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2025.174029 · Cited by 2 · see citing works

Characterization of Neurensin-2 knockout mice: insights into stress-resilience mechanisms

Hovav, H. C., Kashi, O. Y., Ghanem, Y. A., Stochinsky, N., Agbariya, L., Yehuda, H., Weitz, M., Baraghithy, S., Tam, J., Yaka, R., et al. (2025) · Translational Psychiatry · doi:10.1038/s41398-025-03448-7 · Cited by 2 · see citing works

Ghrelin mechanisms of food reward. Part 2. Interaction of ghrelin with hormones, neuropeptides and other endogenous ligands

Reikhardt, B. A., & Shabanov, P. D. (2022) · Reviews on Clinical Pharmacology and Drug Therapy · doi:10.17816/rcf203229-254 · Cited by 2 · see citing works

Stress-induced Alterations of Mesocortical and Mesolimbic Dopaminergic PathwaysPreprint

Quessy, F., Bittar, T. P., Blanchette, L.-J., Lévesque, M., & Labonté, B. (2021) · Research Square · doi:10.21203/rs.3.rs-140843/v1 · Cited by 2 · see citing works

Gut-brain axis modulation by sudachi peel extract enhances resilience to chronic social defeat stress in mice.

Shan, J., Qu, Y., & Hashimoto, K. (2025) · Journal of Affective Disorders · doi:10.1016/j.jad.2025.04.027 · Cited by 1 · see citing works

Sex difference in stress susceptibility and resilience in a restraint stress-induced depression mouse model: A proteomic investigation of the hippocampal dentate gyrus

Vijay, V., Ray, S., Kingsly, R., Sharma, P., Kumar, A., & Chakravarty, S. (2026) · Physiology & Behavior · doi:10.1016/j.physbeh.2026.115288 · Cited by 1 · see citing works

Prelimbic-amygdala overexcitability mediates trait vulnerability in a novel mouse model of acute social defeat stressPreprint

Grossman, Y. S., Fillinger, C., Manganaro, A., Voren, G., Waldman, R. N., Zou, T., Janssen, W. G. M., Kenny, P. J., & Dumitriu, D. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.11.147231 · Cited by 1 · see citing works

Efeitos comportamentais e neuroplásticos da combinação de escitalopram e canabinóides

Scarante, F. F. (2018) · doi:10.11606/d.17.2018.tde-25072018-103829

Aberrant ventral dentate gyrus structure and function in individuals susceptible to post-traumatic stress disorderPreprint

Dirven, B. C. J., van der Geugten, D., van Bodegom, M., Madder, L., van Agen, L., Homberg, J. R., Kozicz, T., & Henckens, M. J. A. G. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.10.01.321893

Effect of regulating Piezo2 expression in DRG on core phenotype, S1 and mPFC neuron functions in ASD mouse modelPreprint

Zhai, J., Hao, H., Xu, Z., Tomoda, A., Zhang, X., Wang, X., Cao, X., Li, D., Li, X., Fan, L., et al. (2023) · Research Square · doi:10.21203/rs.3.rs-3517747/v1

Additional file 2 of Circuit- and laminar-specific regulation of medial prefrontal neurons by chronic stress

Liu, W.-Z., Wang, C., Wang, Y., Cai, M.-T., Zhong, W.-X., Liu, T., Wang, Z.-H., Pan, H., Zhang, W., & Pan, B. (2023) · Figshare · doi:10.6084/m9.figshare.22978259

NLRP3-caspase 1 and caspase 11-gasdermin D pathways jointly promote IL1β-mediated neuroinflammation and behavioral deficits in a rat model of psychosocial stressPreprint

Tiwari, S., Mohammed, Z., Yadav, E., Atta, S. R., Kaushik, S., Tiwari, A., Chopra, A., Singh, I., & Ghosh, S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.02.02.636090

Longitudinal Genome-Wide Study Reveals Genetic Architecture of Resilience Using a Novel PhenotypePreprint

Cahill, S., Mekli, K., & Hager, R. (2025) · Research Square · doi:10.21203/rs.3.rs-4861048/v1

Sex Difference in Stress Susceptibility and Resilience in a Restraint Stress-induced Depression Mouse Model: A Proteomic Investigation of the Hippocampal Dentate GyrusPreprint

Vijay, V., Ray, S., Kingsly, R., Sharma, P., Kumar, A., & Chakravarty, S. (2025) · Research Square · doi:10.21203/rs.3.rs-8056455/v1

Chronic social defeat stress impairs polysialic acid levels in the hippocampus of mice

Ohno, H., & Aizawa, S. (2025) · Neuroreport · doi:10.1097/wnr.0000000000002228

Additional file 1 of Circuit- and laminar-specific regulation of medial prefrontal neurons by chronic stress

Liu, W.-Z., Wang, C.-Y., Wang, Y., Cai, M.-T., Zhong, W.-X., Liu, T., Wang, Z.-H., Pan, H.-Q., Zhang, W.-H., & 潘秉兴 (2023) · Figshare · doi:10.6084/m9.figshare.22978256

The caspase 11/gasdermin D pathway is a key driver of stress-induced neuroinflammation and behavioral dysfunction in rats

Tiwari, S., Mohammed, Z., Tiwari, A., Yadav, E., Atta, S. R., Kaushik, S., Chopra, A., Singh, I., & Ghosh, S. (2026) · Neurochemistry International · doi:10.1016/j.neuint.2026.106139

Dynamic dopamine signaling, prediction error, and microcircuit mechanisms in stress-induced depression-like behaviors

Mahmud, A., & Efremov, L. (2026) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2026.1948686

Vitamin D binding protein in ventral CA3 of the hippocampus drives stress-induced depression

Kong, Y., Huang, Z., Zeng, C., Xu, Y., & Zhang, Z. (2026) · Science Advances · doi:10.1126/sciadv.aeh9563

Chronic social defeat stress induces sustained synaptic structural changes in the prefrontal cortex and amygdala

Colyn, L., Venzala, E., Marco, S., Perez-Otaño, I., & Tordera, R. M. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112079 · Cited by 89 · see citing works

Dendritic spine density is increased on nucleus accumbens D2 neurons after chronic social defeat

Fox, M. E., Figueiredo, A. M. P. D., Menken, M. S., & Lobo, M. K. (2020) · Scientific Reports · doi:10.1038/s41598-020-69339-7 · Cited by 43 · see citing works

Stress-Induced Dysregulation of the Guidance Cue Receptor DCC Alters Corticolimbic Circuit Architecture

Mahmud, A., Hernández, G., Abboud, F., & Flores, C. (2025) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2025.100629 · Cited by 3 · see citing works

Chronic Social Defeat Stress Modulates Dendritic Spines Structural Plasticity in Adult Mouse Frontal Association Cortex

Shu, Y., & Xu, T. (2017) · Neural Plasticity · doi:10.1155/2017/6207873 · Cited by 34 · see citing works

Differential mechanisms of synaptic plasticity for susceptibility and resilience to chronic social defeat stress in male mice

Lee, C. J., Fang, Y.-P., Chu, M.-C., Chung, Y.-J., Chi, H., Tang, C., So, E. C., Lin, H.-C., & Lin, H.-C. (2021) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2021.05.064 · Cited by 26 · see citing works