Ketamine Alleviates Depressive-Like Behaviors via Down-Regulating Inflammatory Cytokines Induced by Chronic Restraint Stress in Mice

Projections of Global Mortality and Burden of Disease from 2002 to 2030

Mathers, C. D., & Loncar, D. (2006) · PLoS Medicine · doi:10.1371/journal.pmed.0030442 · Cited by 11,386 · see citing works

Inflammation and Its Discontents: The Role of Cytokines in the Pathophysiology of Major Depression

Miller, A. H., Maletic, V., & Raison, C. L. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.11.029 · Cited by 3,848 · see citing works

Cytokines sing the blues: inflammation and the pathogenesis of depression

Raison, C. L., Capuron, L., & Miller, A. H. (2006) · Trends in Immunology · doi:10.1016/j.it.2005.11.006 · Cited by 3,009 · see citing works

mTOR-Dependent Synapse Formation Underlies the Rapid Antidepressant Effects of NMDA Antagonists

Li, N., Lee, B., Liu, R.-J., Banasr, M., Dwyer, J. M., Iwata, M., Li, X.-Y., Aghajanian, G., & Duman, R. S. (2010) · Science · doi:10.1126/science.1190287 · Cited by 2,881 · see citing works

Reduction of sucrose preference by chronic unpredictable mild stress, and its restoration by a tricyclic antidepressant

Willner, P., Towell, A., Sampson, D., Sophokleous, S., & Muscat, R. (1987) · Psychopharmacology · doi:10.1007/bf00187257 · Cited by 1,993 · see citing works

Regulation of the Hypothalamic‐Pituitary‐Adrenocortical Stress Response

Herman, J. P., McKlveen, J. M., Ghosal, S., Kopp, B., Wulsin, A., Makinson, R., Scheimann, J., & Myers, B. (2016) · Comprehensive Physiology · doi:10.1002/cphy.c150015 · Cited by 1,819 · 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

Replication of Ketamine's Antidepressant Efficacy in Bipolar Depression: A Randomized Controlled Add-On Trial

Zarate, C. A., Brutsche, N. E., Ibrahim, L., Franco-Chaves, J., Diazgranados, N., Cravchik, A., Selter, J., Marquardt, C. A., Liberty, V., & Luckenbaugh, D. A. (2012) · Biological Psychiatry · doi:10.1016/j.biopsych.2011.12.010 · Cited by 811 · see citing works

Immunological aspects in the neurobiology of suicide: Elevated microglial density in schizophrenia and depression is associated with suicide

Steiner, J., Bielau, H., Brisch, R., Danos, P., Ullrich, O., Mawrin, C., Bernstein, H.-G., & Bogerts, B. (2008) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2006.10.013 · Cited by 791 · see citing works

Chronic restraint stress causes anxiety- and depression-like behaviors, downregulates glucocorticoid receptor expression, and attenuates glutamate release induced by brain-derived neurotrophic factor in the prefrontal cortex

Chiba, S., Numakawa, T., Ninomiya, M., Richards, M. C., Wakabayashi, C., & Kunugi, H. (2012) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2012.05.018 · Cited by 673 · see citing works

Cytokine activation of the HPA axis

DUNN, A. J. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb05426.x · Cited by 352 · see citing works

Inflammation and Depression

Zunszain, P. A., Hepgul, N., & Pariante, C. M. (2012) · Current topics in behavioral neurosciences · doi:10.1007/7854_2012_211 · Cited by 317 · see citing works

Toll-like receptor 4 mediates microglial activation and production of inflammatory mediators in neonatal rat brain following hypoxia: role of TLR4 in hypoxic microglia

Yao, L., Kan, E. M., Lu, J., Hao, A., Dheen, S. T., Kaur, C., & Ling, E. (2013) · Journal of Neuroinflammation · doi:10.1186/1742-2094-10-23 · Cited by 296 · see citing works

Does Intraoperative Ketamine Attenuate Inflammatory Reactivity Following Surgery? A Systematic Review and Meta-Analysis

Dale, O., Somogyi, A. A., Li, Y., Sullivan, T., & Shavit, Y. (2012) · Anesthesia & Analgesia · doi:10.1213/ane.0b013e3182662e30 · Cited by 238 · see citing works

Prolonged Restraint Stress Increases IL-6, Reduces IL-10, and Causes Persistent Depressive-Like Behavior That Is Reversed by Recombinant IL-10

Voorhees, J. L., Tarr, A. J., Wohleb, E. S., Godbout, J. P., Mo, X., Sheridan, J. F., Eubank, T. D., & Marsh, C. B. (2013) · PLoS ONE · doi:10.1371/journal.pone.0058488 · Cited by 236 · see citing works

Inflammatory mechanisms in major depressive disorder

Raedler, T. J. (2011) · Current Opinion in Psychiatry · doi:10.1097/yco.0b013e32834b9db6 · Cited by 213 · see citing works

Microglia of Prefrontal White Matter in Suicide

Schnieder, T. P., Trencevska, I., Rosoklija, G., Stankov, A., Mann, J. J., Smiley, J., & Dwork, A. J. (2014) · Journal of Neuropathology & Experimental Neurology · doi:10.1097/nen.0000000000000107 · Cited by 202 · see citing works

Microglia: Proliferation and activation driven by the P2X7 receptor

Monif, M., Burnstock, G., & Williams, D. A. (2010) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2010.06.021 · Cited by 196 · see citing works

Stress-induced neuroinflammation is mediated by GSK3-dependent TLR4 signaling that promotes susceptibility to depression-like behavior

Cheng, Y., Pardo, M., Armini, R. D. S., Martinez, A., Mouhsine, H., Zagury, J.-F., Jope, R. S., & Beurel, E. (2016) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2015.12.012 · Cited by 174 · see citing works

HSP60 plays a regulatory role in IL-1β-induced microglial inflammation via TLR4-p38 MAPK axis

Swaroop, S., Sengupta, N., Suryawanshi, A. R., Adlakha, Y. K., & Basu, A. (2016) · Journal of Neuroinflammation · doi:10.1186/s12974-016-0486-x · Cited by 132 · see citing works

Case–control studies show that a non-conservative amino-acid change from a glutamine to arginine in the P2RX7 purinergic receptor protein is associated with both bipolar- and unipolar-affective disorders

McQuillin, A., Bass, N. J., Choudhury, K., Puri, V., Kosmin, M., Lawrence, J., Curtis, D., & Gurling, H. (2008) · Molecular Psychiatry · doi:10.1038/mp.2008.6 · Cited by 117 · see citing works

Schisandrin B exerts anti-neuroinflammatory activity by inhibiting the Toll-like receptor 4-dependent MyD88/IKK/NF-κB signaling pathway in lipopolysaccharide-induced microglia

Zeng, K.-W., Zhang, T., Fu, H., Liu, G.-X., & Wang, X.-M. (2012) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2012.05.030 · Cited by 116 · see citing works

Resilience and reduced c-Fos expression in P2X7 receptor knockout mice exposed to repeated forced swim test

Boucher, A. A., Arnold, J. C., Hunt, G. E., Spiro, A., Spencer, J., Brown, C., McGregor, I. S., Bennett, M. R., & Kassiou, M. (2011) · Neuroscience · doi:10.1016/j.neuroscience.2011.05.049 · Cited by 108 · see citing works

Inhibitory Effects of Ketamine on Lipopolysaccharide-Induced Microglial Activation

Chang, Y. F., Lee, J.-J., Hsieh, C., Hsiao, G., Chou, D., & Sheu, J. (2009) · Mediators of Inflammation · doi:10.1155/2009/705379 · Cited by 108 · see citing works

Stress-induced cytokine changes in rats

Himmerich, H., Fischer, J., Bauer, K., Kirkby, K. C., Sack, U., & Krügel, U. (2013) · European Cytokine Network · doi:10.1684/ecn.2013.0338 · Cited by 107 · see citing works

The Epidemiology of Depression and the Evolution of Treatment

Hirschfeld, R. M. A. (2012) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.11096su1c.01 · Cited by 100 · see citing works

Inflammation and increased IDO in hippocampus contribute to depression-like behavior induced by estrogen deficiency

Xu, Y., Sheng, H., Tang, Z., Lu, J., & Ni, X. (2015) · Behavioural Brain Research · doi:10.1016/j.bbr.2015.04.017 · Cited by 94 · see citing works

P2X7 as a new target for chrysophanol to treat lipopolysaccharide-induced depression in mice

Zhang, K., Liu, J., You, X., Kong, P., Song, Y., Cao, L., Yang, S. T., Wang, W., Fu, Q., & Ma, Z. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.12.043 · Cited by 90 · see citing works

Accelerating response to antidepressant treatment in depression: a review and clinical suggestions.

Nakajima, S., Suzuki, T., Watanabe, K., Kashima, H., & Uchida, H. (2010) · Progress in Neuro-psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2009.12.001 · Cited by 78 · see citing works

Inflammatory Markers and the Pathogenesis of Pediatric Depression and Suicide

Kim, J.-W., Szigethy, E., Melhem, N., Saghafi, E. M., & Brent, D. A. (2014) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.13r08898 · Cited by 76 · see citing works

Neuroinflammation and Depression

Sublette, M. E., & Postolache, T. T. (2012) · Psychosomatic Medicine · doi:10.1097/psy.0b013e318268de9f · Cited by 75 · see citing works

LIPOTEICHOIC ACID-INDUCED TNF-α AND IL-6 GENE EXPRESSIONS AND OXIDATIVE STRESS PRODUCTION IN MACROPHAGES ARE SUPPRESSED BY KETAMINE THROUGH DOWNREGULATING TOLL-LIKE RECEPTOR 2-MEDIATED ACTIVATION OF ERK1/2 AND NFκB

Chang, H.-C., Lin, K.-H., Tai, Y., Chen, J.-T., & Chen, R. (2010) · Shock · doi:10.1097/shk.0b013e3181c3cea5 · Cited by 74 · see citing works

Inflammation and Immune Regulation as Potential Drug Targets in Antidepressant Treatment

Schmidt, F. M., Kirkby, K. C., & Lichtblau, N. (2016) · Current Neuropharmacology · doi:10.2174/1570159x14666160115130414 · Cited by 72 · see citing works

Signal-transducing mechanisms of ketamine-caused inhibition of interleukin-1β gene expression in lipopolysaccharide-stimulated murine macrophage-like Raw 264.7 cells

Chen, T.-L., Chang, C., Lin, Y., Ueng, Y., & Chen, R. (2009) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2009.06.013 · Cited by 58 · see citing works

Cold stress induced morphological microglial activation and increased IL-1β expression in astroglial cells in rat brain

Sugama, S., Takenouchi, T., Fujita, M., Kitani, H., & Hashimoto, M. (2011) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2010.11.002 · Cited by 55 · see citing works

Depression Risk in Patients with Rheumatoid Arthritis in the United Kingdom

Jacob, L., Rockel, T., & Kostev, K. (2017) · Rheumatology and Therapy · doi:10.1007/s40744-017-0058-2 · Cited by 52 · see citing works

Effects of Ketamine on Endotoxin and Traumatic Brain Injury Induced Cytokine Production in the Rat

Ward, J. L., Harting, M. T., Cox, C. S., & Mercer, D. (2011) · The Journal of Trauma: Injury, Infection, and Critical Care · doi:10.1097/ta.0b013e31821c38bd · Cited by 46 · see citing works

Interleukin-1β induced activation of the hypothalamus–pituitary–adrenal axis is dependent on interleukin-1 receptors on non-hematopoietic cells

Matsuwaki, T., Eskilsson, A., Kugelberg, U. Ö., Jönsson, J., & Blomqvist, A. G. (2014) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2014.03.015 · Cited by 45 · see citing works

Endocrine and Neurobehavioral Abnormalities Induced by Propofol Administered to Neonatal Rats

Tan, S., Xu, C., Zhu, W., Willis, J., Seubert, C. N., Gravenstein, N. L., Sumners, C., & Martynyuk, A. E. (2014) · Anesthesiology · doi:10.1097/aln.0000000000000366 · Cited by 39 · see citing works

Depression Epidemiology and Its Treatment Evolution

Hirschfeld, R. M. A. (2012) · The Journal of Clinical Psychiatry · doi:10.4088/jcp.11096tx3c · Cited by 32 · see citing works

Immunomodulatory activity of ketamine in human astroglial A172 cells: Possible relevance to its rapid antidepressant activity

Yuhas, Y., Ashkenazi, S., Berent, E., & Weizman, A. (2015) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2015.03.012 · Cited by 28 · see citing works

Major depressive disorder is associated with subsequent adult-onset asthma: a population-based cohort study

Shen, T., Lin, C., Liao, C. H., Wei, C.-C., Fc, S., & Kao, C.-H. (2016) · Epidemiology and Psychiatric Sciences · doi:10.1017/s2045796016000664 · Cited by 23 · see citing works

Microglia in depression: an overview of microglia in the pathogenesis and treatment of depression

Wang, H., He, Y., Sun, Z., Ren, S., Liu, M., Wang, G., & Yang, J. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02492-0 · Cited by 591 · see citing works

Neurobiology of Resilience: Interface Between Mind and Body

Cathomas, F., Murrough, J. W., Nestler, E. J., Han, M.-H., & Russo, S. J. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.04.011 · Cited by 296 · see citing works

Chronic stress increases metastasis via neutrophil-mediated changes to the microenvironment

He, X., Gao, Y., Ng, D., Michalopoulou, E., George, S., Adrover, J. M., Sun, L., Albrengues, J., Daßler‐Plenker, J., Han, X., et al. (2024) · Cancer Cell · doi:10.1016/j.ccell.2024.01.013 · Cited by 307 · see citing works

Microglia in depression: current perspectives

Jia, X., Gao, Z., & Hu, H. (2020) · Science China Life Sciences · doi:10.1007/s11427-020-1815-6 · Cited by 283 · see citing works

Rapid inflammation modulation and antidepressant efficacy of a low-dose ketamine infusion in treatment-resistant depression: A randomized, double-blind control study

Chen, M.-H., Li, C.-T., Lin, W.-C., Hong, C.-J., Tu, P.-C., Bai, Y.-M., Cheng, C.-M., & Su, T.-P. (2018) · Psychiatry Research · doi:10.1016/j.psychres.2018.08.078 · Cited by 159 · see citing works

The P2X7 Receptor: Central Hub of Brain Diseases

Andrejew, R., Oliveira-Giacomelli, Á., Ribeiro, D. E., Glaser, T., Arnaud-Sampaio, V. F., Lameu, C., & Ulrich, H. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00124 · Cited by 162 · see citing works

Pro-Inflammatory Monocyte Profile in Patients with Major Depressive Disorder and Suicide Behaviour and How Ketamine Induces Anti-Inflammatory M2 Macrophages by NMDAR and MTOR

Nowak, W., Grendas, L. N., Sanmarco, L. M., Estecho, I. G., Arena, Á. R., Eberhardt, N., Rodante, D. E., Aoki, M. P., Daray, F. M., Carrera Silva, E. A., et al. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2019.10.063 · Cited by 159 · see citing works

Inflammation, Lifestyle Factors, and the Microbiome‐Gut‐Brain Axis: Relevance to Depression and Antidepressant Action

Donoso, F., Cryan, J. F., Olavarría‐Ramírez, L., Nolan, Y. M., & Clarke, G. A. (2022) · Clinical Pharmacology & Therapeutics · doi:10.1002/cpt.2581 · Cited by 147 · see citing works

Ketamine interactions with gut-microbiota in rats: relevance to its antidepressant and anti-inflammatory properties

Getachew, B., Aubee, J. I., Schottenfeld, R. S., Csoka, A. B., Thompson, K. M., & Tizabi, Y. (2018) · BMC Microbiology · doi:10.1186/s12866-018-1373-7 · Cited by 137 · see citing works

Neuroinflammation: The central enabler of postoperative cognitive dysfunction

Liu, Y., Yang, W., Xue, J., Chen, J., Liu, S., Zhang, S., Zhang, X., Gu, X., Dong, Y., & Qiu, P. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.115582 · Cited by 136 · see citing works

P2X7 Receptor Signaling in Stress and Depression

Ribeiro, D. E., Roncalho, A. L., Glaser, T., Ulrich, H., Wegener, G., & Joca, S. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20112778 · Cited by 129 · see citing works

The influence of ICAM1 rs5498 on diabetes mellitus risk: evidence from a meta-analysis

Mi, W., Xia, Y., & Bian, Y. (2019) · Inflammation Research · doi:10.1007/s00011-019-01220-4 · Cited by 128 · see citing works

Recent advances in CNS P2X7 physiology and pharmacology: Focus on neuropsychiatric disorders

Bhattacharya, A. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.00030 · Cited by 115 · see citing works

Inflaming sex differences in mood disorders

Rainville, J. R., & Hodes, G. E. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0124-7 · Cited by 106 · see citing works

The neuropsychiatric manifestations of COVID-19: Interactions with psychiatric illness and pharmacological treatment

van Vuren, E. J., Steyn, S. F., Brink, C. B., Möller, M., Viljoen, F. P., & Harvey, B. H. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2020.111200 · Cited by 105 · see citing works

Brain region–specific action of ketamine as a rapid antidepressant

Chen, M., Ma, S., Liu, H., Dong, Y., Tang, J., Ni, Z., Tan, Y. J., Duan, C.-C., Li, H., Huang, H., et al. (2024) · Science · doi:10.1126/science.ado7010 · Cited by 103 · see citing works

Ketamine’s effect on inflammation and kynurenine pathway in depression: A systematic review

Kopra, E. I., Mondelli, V., Pariante, C. M., & Nikkheslat, N. (2021) · Journal of Psychopharmacology · doi:10.1177/02698811211026426 · Cited by 102 · see citing works

The role of damage associated molecular pattern molecules (DAMPs) and permeability of the blood-brain barrier in depression and neuroinflammation

Serna-Rodríguez, M. F., Bernal‐Vega, S., de la Barquera, J. A. O.-S., Camacho‐Morales, A., & Pérez‐Maya, A. A. (2022) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2022.577951 · Cited by 101 · see citing works

Sericin alleviates restraint stress induced depressive- and anxiety-like behaviors via modulation of oxidative stress, neuroinflammation and apoptosis in the prefrontal cortex and hippocampus

Mohammadi, A. B., Torbati, M., Farajdokht, F., Sadigh‐Eteghad, S., Fazljou, S. M. B., Vatandoust, S. M., Golzari, S. E., & Mahmoudi, J. (2019) · Brain Research · doi:10.1016/j.brainres.2019.03.020 · Cited by 90 · see citing works

A P2X7 receptor antagonist reverses behavioural alterations, microglial activation and neuroendocrine dysregulation in an unpredictable chronic mild stress (UCMS) model of depression in mice

Farooq, R. K., Tanti, A., Ainouche, S., Roger, S., Belzung, C., & Camus, V. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2018.07.016 · Cited by 83 · see citing works

Neuropsychopharmacology of JNJ-55308942: evaluation of a clinical candidate targeting P2X7 ion channels in animal models of neuroinflammation and anhedonia

Bhattacharya, A., Lord, B., Grigoleit, J., He, Y., Fraser, I. C., Campbell, S. N., Taylor, N., Aluisio, L. E., O’Connor, J. C., Papp, M., et al. (2018) · Neuropsychopharmacology · doi:10.1038/s41386-018-0141-6 · Cited by 82 · see citing works

Alterations of multiple peripheral inflammatory cytokine levels after repeated ketamine infusions in major depressive disorder

Zhan, Y., Zhou, Y., Zheng, W., Liu, W., Wang, C., Lan, X., Deng, X., Xu, Y., Zhang, B., & Ning, Y. (2020) · Translational Psychiatry · doi:10.1038/s41398-020-00933-z · Cited by 81 · see citing works

Neuroimmune Mechanisms as Novel Treatment Targets for Substance Use Disorders and Associated Comorbidities

Namba, M. D., Leyrer-Jackson, J. M., Nagy, E. K., Olive, M. F., & Neisewander, J. L. (2021) · Frontiers in Neuroscience · doi:10.3389/fnins.2021.650785 · Cited by 76 · see citing works

Pathological ATPergic Signaling in Major Depression and Bipolar Disorder

Illés, P., Verkhratsky, A., & Tang, Y. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00331 · Cited by 77 · see citing works

Blood-based biomarkers of antidepressant response to ketamine and esketamine: A systematic review and meta-analysis

Medeiros, G. C., Gould, T. D., Prueitt, W. L., Nanavati, J., Grunebaum, M. F., Farber, N. B., Singh, B., Selvaraj, S., Machado-Vieira, R., Achtyes, E. D., et al. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01652-1 · Cited by 75 · see citing works

Tetramethylpyrazine ameliorates depression by inhibiting TLR4-NLRP3 inflammasome signal pathway in mice

Fu, S., Wang, J., Hao, C., Dang, H., & Jiang, S. (2019) · Psychopharmacology · doi:10.1007/s00213-019-05210-6 · Cited by 73 · see citing works

Targeting inflammation in depression: Ketamine as an anti-inflammatory antidepressant in psychiatric emergency

Nikkheslat, N. (2021) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2021.100383 · Cited by 71 · see citing works

The Anti-Depressive Effects of Hesperidin and the Relative Mechanisms Based on the NLRP3 Inflammatory Signaling Pathway

Xie, L., Gu, Z., Liu, H., Jia, B., Wang, Y., Cao, M., Song, R., Zhang, Z., & Bian, Y. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2020.01251 · Cited by 70 · see citing works

Ketamine may exert antidepressant effects via suppressing NLRP3 inflammasome to upregulate AMPA receptors

Li, J., Liu, L.-L., Su, W., Wang, B., Zhang, T., Zhang, Y., & Jiang, C. (2018) · Neuropharmacology · doi:10.1016/j.neuropharm.2018.11.022 · Cited by 67 · see citing works

Esketamine Prevents Postoperative Emotional and Cognitive Dysfunction by Suppressing Microglial M1 Polarization and Regulating the BDNF-TrkB Pathway in Ageing Rats with Preoperative Sleep Disturbance

Wen, Y., Xu, J., Shen, J., Tang, Z., Li, S., Zhang, Q., Li, J., & Sun, J. (2024) · Molecular Neurobiology · doi:10.1007/s12035-023-03860-4 · Cited by 71 · see citing works

Inflammation, stress and depression: An exploration of ketamine’s therapeutic profile

Johnston, J. N., Greenwald, M. S., Henter, I. D., Kraus, C., Mkrtchian, A., Clark, N. G., Park, L. T., Gold, P. W., Zarate, C. A., & Kadriu, B. (2023) · Drug Discovery Today · doi:10.1016/j.drudis.2023.103518 · Cited by 66 · see citing works

Finding intestinal fortitude: Integrating the microbiome into a holistic view of depression mechanisms, treatment, and resilience

Flux, M. C., & Lowry, C. A. (2019) · Neurobiology of Disease · doi:10.1016/j.nbd.2019.104578 · Cited by 68 · see citing works

Antidepressant Effects of Rosemary Extracts Associate With Anti-inflammatory Effect and Rebalance of Gut Microbiota

Guo, Y., Xie, J., Li, X., Yuan, Y., Zhang, L., Hu, W., Luo, H., Yu, H., & Zhang, R. (2018) · Frontiers in Pharmacology · doi:10.3389/fphar.2018.01126 · Cited by 64 · see citing works

An update on NMDA antagonists in depression

Pochwat, B., Nowak, G., & Szewczyk, B. (2019) · Expert Review of Neurotherapeutics · doi:10.1080/14737175.2019.1643237 · Cited by 65 · see citing works

SRT2104 attenuates chronic unpredictable mild stress-induced depressive-like behaviors and imbalance between microglial M1 and M2 phenotypes in the mice

Duan, C., Zhang, J., Wan, T.-F., Wang, Y., Chen, D., & Liu, L. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112296 · Cited by 66 · see citing works

Ghrelin exhibited antidepressant and anxiolytic effect via the p38-MAPK signaling pathway in hippocampus

Han, Q.-Q., Huang, H., Wang, Y., Liu, Y., Pilot, A., Zhu, X., Yu, R., Wang, J., Chen, X., Liu, Q., et al. (2019) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2019.02.013 · Cited by 53 · see citing works

Stress, pain, anxiety, and depression in endometriosis–Targeting glial activation and inflammation

Mokhtari, T., Irandoost, E., & Sheikhbahaei, F. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.111942 · Cited by 56 · see citing works

Mechanisms and Therapeutic Targets of Depression After Intracerebral Hemorrhage

Wu, Y., Wang, L., Hu, K., Yu, C., Zhu, Y., Zhang, S., & Shao, A. (2018) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2018.00682 · Cited by 49 · see citing works

Untitled work

Gürsel (2018) · doi:10.1016/j.neubiorev.2018.02.005 · Cited by 47 · see citing works

Antidepressant-like effects of Schisandrin on lipopolysaccharide-induced mice : Gut microbiota, short chain fatty acid and TLR4/NF-κB signaling pathway

Sun, Y., Yan, T., Gong, G., Li, Y., Zhang, J., Wu, B., Bi, K., & Jia, Y. (2020) · International Immunopharmacology · doi:10.1016/j.intimp.2020.107029 · Cited by 47 · see citing works

Whole blood transcriptional signatures associated with rapid antidepressant response to ketamine in patients with treatment resistant depression

Cathomas, F., Bevilacqua, L., Ramakrishnan, A., Kronman, H., Costi, S., Schneider, M., Chan, K. L., Li, L., Nestler, E. J., Shen, L., et al. (2022) · Translational Psychiatry · doi:10.1038/s41398-021-01712-0 · Cited by 45 · see citing works

The effects of anaesthetics and sedatives on brain inflammation

Dominguini, D., Steckert, A. V., Michels, M., Borges, M. S., Ritter, C., Barichello, T., Thompson, J. P., & Dal‐Pizzol, F. (2021) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2021.05.009 · Cited by 44 · see citing works

Mitochondria: A Connecting Link in the Major Depressive Disorder Jigsaw

Sharma, S., & Akundi, R. S. (2018) · Current Neuropharmacology · doi:10.2174/1570159x16666180302120322 · Cited by 42 · see citing works

Neurobiological biomarkers of response to ketamine

Kadriu, B., Ballard, E. D., Henter, I. D., Murata, S., Gerlus, N., & Zarate, C. A. (2020) · Advances in pharmacology · doi:10.1016/bs.apha.2020.05.003 · Cited by 36 · see citing works

Ginsenoside Rb1 exerts antidepressant-like effects via suppression inflammation and activation of AKT pathway

Guo, Y., Xie, J., Zhang, L., Yang, L., Ma, J., Bai, Y., Ma, W., Wang, X., Yu, H., Zeng, Y.-Q., et al. (2020) · Neuroscience Letters · doi:10.1016/j.neulet.2020.135561 · Cited by 36 · see citing works

Immunoregulation and antidepressant effect of ketamine

Zhang, N., Yao, L., Wang, P., & Liu, Z. (2021) · Translational Neuroscience · doi:10.1515/tnsci-2020-0167 · Cited by 35 · see citing works

Serum miR-221-3p as a new potential biomarker for depressed mood in perioperative patients

Feng, J., Wang, M., Li, M., Yang, J., Jia, J., Liu, L., Zhou, J. F., Zhang, C., & Wang, X. (2019) · Brain Research · doi:10.1016/j.brainres.2019.06.015 · Cited by 34 · see citing works

Ketamine – A New Antidepressant Drug with Anti-Inflammatory Properties

Jóźwiak-Bębenista, M., Sokołowska, P., Wiktorowska‐Owczarek, A., Kowalczyk, E., & Sienkiewicz, M. (2023) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.123.001823 · Cited by 32 · see citing works

PGE2/EP4 receptor and TRPV1 channel are involved in repeated restraint stress-induced prolongation of sensitization pain evoked by subsequent PGE2 challenge

Ma, W., Li, L., & Xing, S. (2019) · Brain Research · doi:10.1016/j.brainres.2019.146335 · Cited by 32 · see citing works

Chronic unpredictable restraint stress increases hippocampal pro-inflammatory cytokines and decreases motivated behavior in rats

Mograbi, K. D. M., Suchecki, D., da Silva, S. G., Covolan, L., & Hamani, C. (2020) · Stress · doi:10.1080/10253890.2020.1712355 · Cited by 32 · see citing works

Hypothalamus-pituitary-adrenal axis imbalance and inflammation contribute to sex differences in separation- and restraint-induced depression

Dong, Y., Wang, X., Zhou, Y., Zheng, Q., Chen, Z., Zhang, H., Sun, Z., Xu, G., & Hu, G. (2020) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104741 · Cited by 31 · see citing works

Brain immune cells characterization in UCMS exposed P2X7 knock-out mouse

Troubat, R., Leman, S., Pinchaud, K., Surget, A., Barone, P. R., Roger, S., Guisquet, A. L., Brizard, B., Belzung, C., & Camus, V. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.02.012 · Cited by 33 · see citing works

Anti-inflammatory and antioxidant effects of muscarinic acetylcholine receptor (mAChR) activation in the rat hippocampus

Frinchi, M., Nuzzo, D., Scaduto, P., Carlo, M. D., Massenti, M. F., Belluardo, N., & Mudò, G. (2019) · Scientific Reports · doi:10.1038/s41598-019-50708-w · Cited by 31 · see citing works

A Reciprocal Link Between Gut Microbiota, Inflammation and Depression: A Place for Probiotics?

Eltokhi, A., & Sommer, I. E. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.852506 · Cited by 32 · see citing works

Relationship between hippocampal volume and inflammatory markers following six infusions of ketamine in major depressive disorder

Zhou, Y., Wu, F., Wang, C., Zheng, W., Lan, X., Deng, X., & Ning, Y. (2020) · Journal of Affective Disorders · doi:10.1016/j.jad.2020.06.068 · Cited by 28 · see citing works

NLRP1-Mediated Antidepressant Effect of Ketamine in Chronic Unpredictable Mild Stress Model in Rats

Arıcıoğlu, F., Yalçınkaya, C., Özkartal, C. Ş., Tüzün, E., Şirvancı, S., Küçükali, C. İ., & Utkan, T. (2020) · Psychiatry Investigation · doi:10.30773/pi.2019.0189 · Cited by 27 · see citing works

Ketamine as a prophylactic resilience-enhancing agent

Evers, A. G., Murrough, J. W., Charney, D. S., & Costi, S. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.833259 · Cited by 27 · see citing works

Recent Advances in the Mechanisms of Postoperative Neurocognitive Dysfunction: A Narrative Review

Wang, T., Huang, X., Sun, S., Wang, Y., Han, L., Zhang, T., Zhang, T., & Chen, X. (2025) · Biomedicines · doi:10.3390/biomedicines13010115 · Cited by 26 · see citing works

Isoginkgetin treatment attenuated lipopolysaccharide-induced monoamine neurotransmitter deficiency and depression-like behaviors through downregulating p38/NF-κB signaling pathway and suppressing microglia-induced apoptosis

Li, P., Zhang, F., Li, Y., Zhang, C., Yang, Z., Zhang, Y., & Song, C. (2021) · Journal of Psychopharmacology · doi:10.1177/02698811211032473 · Cited by 26 · see citing works

Beyond Seizure Control: Treating Comorbidities in Epilepsy via Targeting of the P2X7 Receptor

Gil, B., Smith, J., Tang, Y., Illés, P., & Engel, T. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23042380 · Cited by 26 · see citing works

Ketamine: A Neglected Therapy for Alzheimer Disease

Smalheiser, N. (2019) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2019.00186 · Cited by 30 · see citing works

Low-dose ketamine inhibits neuronal apoptosis and neuroinflammation in PC12 cells via α7nAChR mediated TLR4/MAPK/NF-κB signaling pathway

Zhao, J., Zhang, R., Wang, W., Jiang, S., Liang, H., Guo, C., Qi, J., Zeng, H., & Song, H. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.109880 · Cited by 25 · see citing works

The Missing Piece? A Case for Microglia’s Prominent Role in the Therapeutic Action of Anesthetics, Ketamine, and Psychedelics

VanderZwaag, J., Halvorson, T., Dolhan, K., Šimončičová, E., Ben‐Azu, B., & Tremblay, M. (2022) · Neurochemical Research · doi:10.1007/s11064-022-03772-0 · Cited by 26 · see citing works

Astroglial Mechanisms of Ketamine Action Include Reduced Mobility of Kir4.1-Carrying Vesicles

Stenovec, M., Božić, M., Pirnat, S., & Zorec, R. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02744-1 · Cited by 25 · see citing works

Safflower extract improves depression in mice by inhibiting the TLR4-NLRP3 inflammation signaling pathway

Chen, H., Ma, Y., Chen, M., Chen, J., & Jin, C. (2021) · Annals of Palliative Medicine · doi:10.21037/apm-21-1728 · Cited by 23 · see citing works

Purinergic P2X7 receptor as a potential therapeutic target in depression

Wang, Q., Jin, X., & Guan, W. (2023) · Biochemical Pharmacology · doi:10.1016/j.bcp.2023.115959 · Cited by 22 · see citing works

Stress- and drug-induced neuroimmune signaling as a therapeutic target for comorbid anxiety and substance use disorders

Smiley, C. E., & Wood, S. K. (2022) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2022.108212 · Cited by 23 · see citing works

P2X7 Receptor as a Potential Target for Major Depressive Disorder

Huang, Z., & Tan, S. (2021) · Current Drug Targets · doi:10.2174/1389450122666210120141908 · Cited by 20 · see citing works

Molecular pathways of ketamine: A systematic review of immediate and sustained effects on PTSD

Wellington, N. J., Bouças, A. P., Lagopoulos, J., Quigley, B. L., & Kuballa, A. (2025) · Psychopharmacology · doi:10.1007/s00213-025-06756-4 · Cited by 21 · see citing works

Design, synthesis, and antidepressant/anticonvulsant activities of 3H-benzo[f]chromen chalcone derivatives

Tan, Q., He, L.-Y., He, Z., Liu, W., Zhang, S., Lin, L., Yang, H., & Guan, L. (2021) · Medicinal Chemistry Research · doi:10.1007/s00044-021-02742-5 · Cited by 19 · see citing works

Role of the GABA A receptors in the long-term cognitive impairments caused by neonatal sevoflurane exposure

Li, T., Huang, Z., Wang, X., Zou, J., & Tan, S. (2019) · Reviews in the Neurosciences · doi:10.1515/revneuro-2019-0003 · Cited by 19 · see citing works

Rapid anti‐depressant‐like effects of ketamine and other candidates: Molecular and cellular mechanisms

Peng, F., Fan, J., Ge, T., Liu, Q. Q., & Li, B. J. (2020) · Cell Proliferation · doi:10.1111/cpr.12804 · Cited by 18 · see citing works

Inhibition of Microglial GSK3β Activity Is Common to Different Kinds of Antidepressants: A Proposal for an In Vitro Screen to Detect Novel Antidepressant Principles

Kalkman, H. O. (2023) · Biomedicines · doi:10.3390/biomedicines11030806 · Cited by 18 · see citing works

The Neurochemical Changes Involved in Immobilization Stress-Induced Anxiety and Depression: Roles for Oxidative Stress and Neuroinflammation

Fekri, K., Nayebi, A. M., Sadigh‐Eteghad, S., Farajdokht, F., & Mahmoudi, J. (2020) · Neurochemical Journal · doi:10.1134/s181971242002004x · Cited by 19 · see citing works

Depression, Estrogens, and Neuroinflammation: A Preclinical Review of Ketamine Treatment for Mood Disorders in Women

Gagne, C., Piot, A., & Brake, W. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2021.797577 · Cited by 14 · see citing works

Reflections on the neuroscientific legacy of Jaak Panksepp (1943–2017)

Watt, D. F. (2017) · Neuropsychoanalysis · doi:10.1080/15294145.2017.1376549 · Cited by 18 · see citing works

Prevention and treatment of natural products from Traditional Chinese Medicine in depression: Potential targets and mechanisms of action

He, M., Feng, R., Wang, J., Xia, S., Wang, Y., & Zhang, Y. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.950143 · Cited by 17 · see citing works

A viewpoint on aldosterone and BMI related brain morphology in relation to treatment outcome in patients with major depression

Murck, H., Lehr, L., & Ježová, D. (2022) · Journal of Neuroendocrinology · doi:10.1111/jne.13219 · Cited by 17 · see citing works

Protection of p-Coumaric acid against chronic stress-induced neurobehavioral deficits in mice via activating the PKA-CREB-BDNF pathway

Cao, Y., Chen, H. L., Tan, Y., Yu, X., Xiao, C., Li, Y. Q., Reilly, J., He, Z., & Shu, X. (2023) · Physiology & Behavior · doi:10.1016/j.physbeh.2023.114415 · Cited by 17 · see citing works

Transcutaneous auricular vagal nerve stimulation inhibits limbic-regional P2X7R expression and reverses depressive-like behaviors in Zucker diabetic fatty rats

Yu, Y., He, X., Wang, Y., Zhang, J., Tang, C., & Rong, P. (2022) · Neuroscience Letters · doi:10.1016/j.neulet.2022.136562 · Cited by 16 · see citing works

P2RX7 gene variation mediates the effect of childhood adversity and recent stress on the severity of depressive symptoms

Kristóf, Z., Eszlári, N., Sütöri, S., Gál, Z., Török, D., Baksa, D., Petschner, P., Sperlágh, B., Anderson, I. M., Deakin, J. F. W., et al. (2021) · PLoS ONE · doi:10.1371/journal.pone.0252766 · Cited by 16 · see citing works

Antidepressant-like Effects of Combined Fluoxetine and Zinc Treatment in Mice Exposed to Chronic Restraint Stress Are Related to Modulation of Histone Deacetylase

Misztak, P., Sowa-Kućma, M., Pańczyszyn-Trzewik, P., Szewczyk, B., & Nowak, G. (2021) · Molecules · doi:10.3390/molecules27010022 · Cited by 15 · see citing works

Disordered gut microbiota and changes in short-chain fatty acids and inflammatory processes in stress-vulnerable mice

Han, W., Zheng, Y., Wang, L., & An, C. (2023) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2023.578172 · Cited by 15 · see citing works

Effect of General Anesthetic Agents on Microglia

Yang, Y., Hang, W., Li, J., Liu, T., Hu, Y., Fang, F., Yan, D., McQuillan, P. M., Wang, M., & Hu, Z. (2023) · Aging and Disease · doi:10.14336/ad.2023.1108 · Cited by 14 · see citing works

Association between peripheral biomarkers and clinical response to IV ketamine for unipolar treatment-resistant depression: An open label study

Kang, M. J. Y., & Vázquez, G. H. (2022) · Journal of Affective Disorders · doi:10.1016/j.jad.2022.08.047 · Cited by 13 · see citing works

Downregulation of iNOS, IL-1β, and P2X7 Expression in Mast Cells via Activation of PAR4 Contributes to the Inhibition of Visceral Hyperalgesia in Rats

Hao, Y., Niu, H., An, S., Wang, M., & Wang, Z. (2018) · Journal of Immunology Research · doi:10.1155/2018/3256908 · Cited by 13 · see citing works

Chronic restraint stress impairs voluntary wheel running but has no effect on food-motivated behavior in mice

Scott, K. A., Phan, T., Boukelmoune, N., Heijnen, C. J., & Dantzer, R. (2022) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2022.10.017 · Cited by 13 · see citing works

Ketamine exerts dual effects on the apoptosis of primary cultured hippocampal neurons from fetal rats in vitro

Wu, G.-H., Guo, Q.-H., Xu, X., Lin, J.-C., You, G.-T., Lin, C., & Zhang, L.-C. (2023) · Metabolic Brain Disease · doi:10.1007/s11011-023-01236-0 · Cited by 12 · see citing works

Magnesium and ketamine in the treatment of depression.

Górska, N., Słupski, J., Szałach, Ł. P., Włodarczyk, A., Szarmach, J., Jakuszkowiak‐Wojten, K., Gałuszko‐Węgielnik, M., Wilkowska, A., Wiglusz, M. S., & Cubała, W. J. (2019) · PubMed · Cited by 12 · see citing works

Inflammatory cytokines, cortisol, and anhedonia in patients with treatment-resistant depression after consecutive infusions of low-dose esketamine

Wang, Y., Yang, Q., Chen, C., Yao, Y., Yuan, X., & Zhang, K. (2024) · European Archives of Psychiatry and Clinical Neuroscience · doi:10.1007/s00406-024-01913-w · Cited by 11 · see citing works

Towards Novel Potential Molecular Targets for Antidepressant and Antipsychotic Pharmacotherapies

Kositsyn, Y. M., de Abreu, M. S., Kolesnikova, T. O., Lagunin, A. A., Poroikov, V., Harutyunyan, H. S., Yenkoyan, K. B., & Kalueff, A. V. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24119482 · Cited by 11 · see citing works

Ketamine abrogates sensorimotor deficits and cytokine dysregulation in a chronic unpredictable mild stress model of depression

Edem, E. E., Anyanwu, C.-K. C., Nebo, K. E., Akinluyi, E. T., Fafure, A. A., Ishola, A. O., & Enye, L. A. (2021) · Psychopharmacology · doi:10.1007/s00213-021-06021-4 · Cited by 10 · see citing works

Ketamine Reverses Chronic Stress‐Induced Behavioral Changes via the Expression of Ca 2+ ‐Permeable AMPA Receptors in Mice

Flowers, J. C., Vetter, P. E., Wiles, M. J., Roh, S. H., Black, E. R., Bouckova, E., Wustrau, M. H., Lee, R., Lee, S.-H., & Kim, S. (2025) · The FASEB Journal · doi:10.1096/fj.202501763r · Cited by 9 · see citing works

Chronic restraint stress alters rat behavior depending on sex and duration of stress

Pansarim, V., Leite‐Panissi, C. R. A., & Schmidt, A. (2023) · Behavioural Processes · doi:10.1016/j.beproc.2023.104856 · Cited by 9 · see citing works

Antidepressant and Anxiolytic Effect of Echium amoenum in Restraint Stress Model: The Role of Neuroinflammation in the Prefrontal Cortex and Hippocampus

Nouri, M., Farajdokht, F., Torbati, M., Ranjbar, F., Hamedyazdan, S., Sadigh‐Eteghad, S., & Araj‐Khodaei, M. (2019) · Iranian Red Crescent Medical Journal · doi:10.5812/ircmj.95438 · Cited by 9 · see citing works

Rice bran supplement ameliorates chronic restraint stress-induced depression-like behaviors in mice

Kim, M., Yoon, M., Cho, S., Kim, M. J., & Um, M. Y. (2024) · Food & Function · doi:10.1039/d4fo00718b · Cited by 8 · see citing works

Effects of stress on endophenotypes of suicide across species: A role for ketamine in risk mitigation

Lamontagne, S. J., Ballard, E. D., & Zarate, C. A. (2022) · Neurobiology of Stress · doi:10.1016/j.ynstr.2022.100450 · Cited by 9 · see citing works

Chronic salmon calcitonin exerts an antidepressant effect via modulating the p38 MAPK signaling pathway

Wenhui, Z., Li, W., Jiang, J., Wang, D., Mao, X., Zhang, J., Zhang, X., Chang, J., Yao, P., Yang, X., et al. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1071327 · Cited by 8 · see citing works

Serotonergic neurons in the treatment of mood disorders: The dialogue with astrocytes

Charvériat, M., & Guiard, B. P. (2021) · Progress in brain research · doi:10.1016/bs.pbr.2021.01.006 · Cited by 7 · see citing works

Involvement of proBDNF in Monocytes/Macrophages with Gastrointestinal Disorders in Depressive Mice

Yu, Y.-Q., Zhang, Y., Wang, Z., Liu, Y., Li, H., Zhou, X., Hu, Z., & Dai, R. (2020) · Neurotoxicity Research · doi:10.1007/s12640-020-00235-8 · Cited by 6 · see citing works

The rapid antidepressant effect of ketamine in rats is associated with down-regulation of pro-inflammatory cytokines in the hippocampus

Wang, N., Yu, H., Shen, X., Gao, Z., Yang, C., Yang, J., & Zhang, G.-F. (2015) · Upsala Journal of Medical Sciences · doi:10.3109/03009734.2015.1060281 · Cited by 101 · see citing works

The effect of ketamine on microglia and proinflammatory cytokines in the hippocampus of depression-like rat

Chen, Q., & Wang, X. (2017) · Neuropsychiatry · doi:10.5281/zenodo.14676702

Acute administration of ketamine inhibited stress induced pro-inflammatory cytokines in hippocampus of rats

Ünal, G., Terzioğlu, G., Şahin, C., Demirel, G. Y., & ARICIOĞLU, F. (2021) · Psychiatry and Clinical Psychopharmacology

Ketamine abrogates sensorimotor deficits and cytokine dysregulation in a chronic unpredictable mild stress model of depression

Edem, E. E., Anyanwu, C.-K. C., Nebo, K. E., Akinluyi, E. T., Fafure, A. A., Ishola, A. O., & Enye, L. A. (2021) · Psychopharmacology · doi:10.1007/s00213-021-06021-4 · Cited by 10 · see citing works

Ketamine reduces microglial activation and brain monocyte infiltration and promotes peripheral regulatory immune cells, relieving lipopolysaccharide (LPS)-induced depressive-like behavior in mice

Arena, Á. R., Rubinstein, M. R., Genaro, A. M., Tifner, V., Risnik, D., López-Carvajal, J. E., Daray, F. M., Silva, E. A. C., & Errasti, A. E. (2025) · Molecular Psychiatry · doi:10.1038/s41380-025-03338-w · Cited by 3 · see citing works