The enzyme indoleamine 2,3-dioxygenase is induced in the mouse brain in response to peripheral administration of lipopolysaccharide and superantigen

Psychopharmacology: The Fourth Generation of Progress

Bloom, F. E., & Kupfer, D. J. (1995) · Medical Entomology and Zoology · Cited by 2,985

Relationship between interferon‐γ, indoleamine 2,3‐dioxygenase, and tryptophan catabolism

Taylor, M. W., & Feng, G. (1991) · The FASEB Journal · doi:10.1096/fasebj.5.11.1907934 · Cited by 1,060

Brain Serotonin Content: Physiological Dependence on Plasma Tryptophan Levels

Fernstrom, J. D., & Wurtman, R. J. (1971) · Science · doi:10.1126/science.173.3992.149 · Cited by 1,017

Cytokine-induced sickness behavior: where do we stand?

Dantzer, R. (2001) · Brain, Behavior, and Immunity · doi:10.1006/brbi.2000.0613 · Cited by 862

Brain Serotonin Content: Increase Following Ingestion of Carbohydrate Diet

Fernstrom, J. D., & Wurtman, R. J. (1971) · Science · doi:10.1126/science.174.4013.1023 · Cited by 734

Association between decreased serum tryptophan concentrations and depressive symptoms in cancer patients undergoing cytokine therapy

Capuron, L., Ravaud, A., Neveu, P. J., Miller, A. H., Maes, M., & Dantzer, R. (2002) · Molecular Psychiatry · doi:10.1038/sj.mp.4000995 · Cited by 473 · cited 2×

Mechanism of interferon-gamma action. Characterization of indoleamine 2,3-dioxygenase in cultured human cells induced by interferon-gamma and evaluation of the enzyme-mediated tryptophan degradation in its anticellular activity.

Takikawa, O., Kuroiwa, T., Yamazaki, F., & Kido, R. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)77982-4 · Cited by 472

The role of IFN-gamma in the pathology of experimental endotoxemia.

Heinzel, F. P. (1990) · The Journal of Immunology · doi:10.4049/jimmunol.145.9.2920 · Cited by 252

Toxic shock syndrome toxin 1 as an inducer of human tumor necrosis factors and gamma interferon.

Jupin, C., Anderson, S., Damais, C., ALOUF, J. E., & Parant, M. (1988) · The Journal of Experimental Medicine · doi:10.1084/jem.167.3.752 · Cited by 218

Nitric oxide inhibits indoleamine 2,3-dioxygenase activity in interferon-gamma primed mononuclear phagocytes.

Thomas, S. R., Mohr, D., & Stocker, R. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)36645-0 · Cited by 214

Identification and characterization of the kynurenine pathway in the pond snail Lymnaea stagnalis

Benatti, C., Rivi, V., Alboni, S., Andrea, G., Sara, C., Luca, P., Brunello, N., Johanna, B., Bicciato, S., & Tascedda, F. (2022) · Scientific Reports · doi:10.1038/s41598-022-19652-0 · Cited by 26

Intracerebroventricular Administration of Streptozotocin as an Experimental Approach to Depression: Evidence for the Involvement of Proinflammatory Cytokines and Indoleamine-2,3-Dioxygenase

Souza, L. C., Jessé, C. R., de Gomes, M. G., Viana, C. E., Mattos, E., Silva, N. C., & Boeira, S. P. (2017) · Neurotoxicity Research · doi:10.1007/s12640-016-9691-8 · Cited by 27

Latent toxoplasmosis and psychiatric symptoms – A role of tryptophan metabolism?

Bay-Richter, C., Buttenschøn, H. N., Mors, O. N., Eskelund, A., Budac, D. P., Kærlev, L., & Wegener, G. (2018) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2018.12.016 · Cited by 24

Proteomic analysis reveals energy metabolic dysfunction and neurogenesis in the prefrontal cortex of a lipopolysaccharide-induced mouse model of depression

Wang, Z., Li, W., Chen, J., Shi, H., Zhao, M., You, H., RAO, C., ZHAN, Y., Yang, Y., & Xie, P. (2015) · Molecular Medicine Reports · doi:10.3892/mmr.2015.4741 · Cited by 21

Suppression of pro-inflammatory cytokine expression and lack of anti-depressant-like effect of fluoxetine in lipopolysaccharide-treated old female mice

Duda, W., Kubera, M., Kreiner, G., Curzytek, K., Detka, J., Głombik, K., Ślusarczyk, J., Basta‐Kaim, A., Budziszewska, B., Lasoń, W., et al. (2017) · International Immunopharmacology · doi:10.1016/j.intimp.2017.04.021 · Cited by 22

Psychoneuroimmunology of Depressive Disorder: Mechanisms and Clinical Implications

Capuron, L., Miller, A. H., & Irwin, M. R. (2007) · Elsevier eBooks · doi:10.1016/b978-012088576-3/50030-7 · Cited by 22

Potential Inflammatory Biomarker in Patients with Attention Deficit Hyperactivity Disorder

Park, J. H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232113054 · Cited by 22

The Glutamate and the Immune Systems: New Targets for the Pharmacological Treatment of OCD

Marazziti, D., Albert, U., Mucci, F., & Piccinni, A. (2018) · Current Medicinal Chemistry · doi:10.2174/0929867324666171108152035 · Cited by 19

Not all depression is created equal: sex interacts with disease to precipitate depression

Nemeth, C. L., Harrell, C. S., Beck, K. D., & Neigh, G. N. (2013) · Biology of Sex Differences · doi:10.1186/2042-6410-4-8 · Cited by 19

Epileptic seizures as a manifestation of cow’s milk allergy: a studied relationship and description of our pediatric experience

Falsaperla, R., Pavone, P., Sopo, S. M., Mahmood, F., Scalia, F., Corsello, G., Lubrano, R., & Vitaliti, G. (2014) · Expert Review of Clinical Immunology · doi:10.1586/1744666x.2014.977259 · Cited by 18

Primary murine microglia are resistant to nitric oxide inhibition of indoleamine 2,3-dioxygenase

Wang, Y., Lawson, M. A., Kelley, K. W., & Dantzer, R. (2010) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2010.04.015 · Cited by 17

Augmentation of antidepressant effects of venlafaxine by agomelatine in mice are independent of kynurenine pathway

Thomas, J., Khanam, R., & Vohora, D. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.06.008 · Cited by 17

Tryptophan Catabolites and Their Impact on Multiple Sclerosis Progression

Watzlawik, J. O., Wootla, B., & Rodriguez, M. (2015) · Current Pharmaceutical Design · doi:10.2174/1381612822666151215095940 · Cited by 18

Mirtazapine for the treatment of interferon-induced psychopathology

Russo, S., Boon, J. C., Korf, J., & Haagsma, E. B. (2003) · General Hospital Psychiatry · doi:10.1016/s0163-8343(03)00091-4 · Cited by 17

Tryptophan Metabolism in Developmental Origins of Health and Disease

de Souza, S. L., Gomes, D. A., da Silva, C. M., Barros, W. M. A., Alves, S. M., & de Castro, R. M. (2025) · Nutrition Reviews · doi:10.1093/nutrit/nuaf127 · Cited by 15

T-cell activation or tolerization: the Yin and Yang of bacterial superantigens

Sähr, A., Foermer, S., Hildebrand, D., & Heeg, K. M. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01153 · Cited by 16

The cytokine profile of OCD: pathophysiological insights

Marazziti, D., Lombardi, A., Falaschi, V., Dell’Osso, L., & Mucci, F. (2015) · International Journal of Interferon Cytokine and Mediator Research · doi:10.2147/ijicmr.s76710 · Cited by 15

Cancer fatigue: a review for psychiatrists

Levy, M. R. (2008) · General Hospital Psychiatry · doi:10.1016/j.genhosppsych.2008.01.004 · Cited by 15

Cancer Fatigue: A Neurobiological Review for Psychiatrists

Levy, M. R. (2008) · Psychosomatics · doi:10.1176/appi.psy.49.4.283 · Cited by 13

Oxidative Processes and Antioxidative Metaloenzymes

Vašková, J., Vaško, L., & Kro, I. (2012) · InTech eBooks · doi:10.5772/50995 · Cited by 14

Central Nervous System Infection with Borna Disease Virus Causes Kynurenine Pathway Dysregulation and Neurotoxic Quinolinic Acid Production

Formisano, S., Hornig, M., Yaddanapudi, K., Vasishtha, M., Parsons, L., Briese, T., Lipkin, W., & Williams, B. L. (2017) · Journal of Virology · doi:10.1128/jvi.00673-17 · Cited by 13

Altered Tryptophan-Kynurenine Pathway in Delirium: A Review of the Current Literature

Ang, H. P., Makpol, S., Nasaruddin, M. L., Zaidi, W. A. W., Ahmad, N. S., & Embong, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065580 · Cited by 12

The Pharmacokinetic-Pharmacodynamic Model of Azithromycin for Lipopolysaccharide-Induced Depressive-Like Behavior in Mice

Hao, K., Qu, Q., Hao, H., Wang, G., Chen, Y., Liang, Y. L., & Xie, L. Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054981 · Cited by 13

Inflammation, sickness behaviour and depression

Dantzer, R., Castanon, N., Lestage, J., Moreau, M. M., & Capuron, L. (2006) · Cambridge University Press eBooks · doi:10.1017/cbo9780511544293.013 · Cited by 12

The role of cytokines and Indolamine-2.3 dioxygenase in experiencing a psycho-neurological symptom cluster in hematological cancer patients: IL-1alpha, IL-1beta, IL-4, IL-6, TNF-alpha, kynurenine, and tryptophan

Kim, H., Moon, J. H., Chung, S. W., & Abraham, I. L. (2023) · Journal of Psychosomatic Research · doi:10.1016/j.jpsychores.2023.111455 · Cited by 12

Neurological Infection, Kynurenine Pathway, and Parasitic Infection by Neospora caninum

Del’Arco, A. E., Argolo, D. S., Guillemin, G. J., Costa, M. D. F. D., Costa, S. L., & Pinheiro, A. M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2021.714248 · Cited by 11

Neuroinflammatory reactions in sickness behavior induced by bacterial infection: Protective effect of minocycline

Mansour, H. A., Hassan, W. A., & Georgy, G. S. (2017) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.22020 · Cited by 10

Gut microbiome metabolites as key actors in atherosclerosis co-depression disease

Liao, X.-X., Wu, X., Zhou, Y.-L., Li, J., Wen, Y.-L., & Zhou, J. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.988643 · Cited by 10

Dysregulation of the kynurenine pathway is related to persistent cognitive impairment in tick-borne encephalitis

Weidenfors, J. A., Griška, V., Li, X., Pranckevičienė, A., Pakalnienė, J., Atlas, A., Franzén‐Röhl, E., Piehl, F., Lindquist, L., Mickienė, A., et al. (2025) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2025.02.005 · Cited by 10

Indoleamine 2, 3-dioxygenase is responsible for low stress tolerance after intracerebral hemorrhage

Ohnishi, M., Akagi, M., Kotsuki, M., Yonemura, S., Aokawa, H., Yamashita-Ibara, M., Yokofujita, O., Maehara, S., Hata, T., & Inoue, A. (2023) · PLoS ONE · doi:10.1371/journal.pone.0273037 · Cited by 9

Inhibition of increased indoleamine 2,3-dioxygenase activity exacerbates neuronal cell death in various CNS disorders

Fujigaki, H., & Saito, K. (2007) · International Congress Series · doi:10.1016/j.ics.2007.07.050 · Cited by 8

Environment, the Immune System, and Depression: An Integrative Review and Discussion of the Infection-Defense Hypothesis

Tanaka, M., Anders, S. L., & Kinney, D. K. (2012) · Molecular and integrative toxicology · doi:10.1007/978-1-61779-812-2_14 · Cited by 7

A single prenatal lipopolysaccharide injection has acute, but not long‐lasting, effects on cerebral kynurenine pathway metabolism in mice

Notarangelo, F. M., & Schwarcz, R. M. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15416 · Cited by 8

First trimester human umbilical cord perivascular cells (HUCPVC) modulate the kynurenine pathway and glutamate neurotransmission in an LPS-induced mouse model of neuroinflammation

Siddiqui, F., Gallagher, D., Shuster-Hyman, H., Lopez, L., Gauthier-Fisher, A., & Librach, C. L. (2023) · Journal of Inflammation · doi:10.1186/s12950-023-00340-3 · Cited by 7

Rodent Models of Stress-Induced Depression: The Link Between Stress and Immune System Related Changes

McGuinness, B. W., & Harkin, A. (2015) · Current topics in neurotoxicity · doi:10.1007/978-3-319-13602-8_3 · Cited by 7

The Inflammatory Hypothesis of Depression

Soskin, D. P., Cassiello-Robbins, C. F., Isacoff, O. K., & D, M. F. M. (2012) · FOCUS The Journal of Lifelong Learning in Psychiatry · doi:10.1176/appi.focus.10.4.413 · Cited by 5

Vaccination and Immunotherapy for Major Depression

Evrensel, A., Ünsalver, B. Ö., Ceylan, M. E., & Tarhan, N. (2021) · Advances in experimental medicine and biology · doi:10.1007/978-981-33-6044-0_25 · Cited by 5

Circulating antibodies to conjugated tryptophan derivatives of the IDO pathway in amyotrophic lateral sclerosis, Alzheimer's, Parkinson's and multiple sclerosis patients

Duleu, S., Mangas, A., de Gannes, F. P., Tranchant, M., & Geffard, M. (2008) · Immuno-analyse & Biologie Spécialisée · doi:10.1016/j.immbio.2007.11.001 · Cited by 5

Cytokine-Induced Sickness Behavior and Depression

Chang, Q., Szegedi, S. S., O’Connor, J. C., Dantzer, R., & Kelley, K. W. (2008) · Springer eBooks · doi:10.1007/978-0-387-84851-8_9 · Cited by 5

Amine Precursors in Depressive Disorders and the Blood-Brain Barrier

Sharma, H. S., & Sharma, A. (2021) · Springer eBooks · doi:10.1007/978-3-319-56015-1_423-1 · Cited by 4

Effect of Acute Toxoplasmosis on Anxiety and Cortisol and Interleukin-17 Levels in Male Rats: An Experimental Study

Fallah, M., Shamsi-Ehsan, T., Salehi, I., Maghsood, A. H., Matini, M., & Pooyandehravan, A. (2021) · Zahedan Journal of Research in Medical Sciences · doi:10.5812/zjrms.95733 · Cited by 4

Biology of Depression and Cytokines in Cancer

Musselman, D. L., Miller, A. H., Royster, E. B., & McNutt, M. D. (2010) · Wiley eBooks · doi:10.1002/9780470972533.ch3 · Cited by 4

Quinolinic Acid Decreases Mental Activity in Mice by Damaging Brain Neurons through the Activation of N-methyl-D-aspartate Receptors: Proposed Relationship to Human Mental Fatigue

Morimoto, Y., Zhang, Q., & Adachi, K. (2011) · Eisei kagaku · doi:10.1248/jhs.57.153 · Cited by 3

Pancreas-brain axis: exploring the pathogenic mechanisms of pancreatic encephalopathy

Dai, N., Geng, Z., Wang, J., Bu, X., Gong, M.-Y., Qin, C., Zhang, Y., Fu, X.-Y., & Fu, B. (2026) · International Immunopharmacology · doi:10.1016/j.intimp.2026.116332 · Cited by 3

Animal Models to Study the Role of Kynurenine Pathway in Mood, Behavior, and Cognition

Castanon, N. (2015) · Springer eBooks · doi:10.1007/978-3-319-11870-3_25 · Cited by 2

Neuroinflammation in depression

Dobos, N. (2014) · University of Groningen research database (University of Groningen / Centre for Information Technology) · Cited by 2

The kynurenine pathway of tryptophan catabolism and schizophrenia

Marković, M., Nikolić, T., & Totić-Poznanović, S. (2023) · Medicinski podmladak · doi:10.5937/mp74-40330 · Cited by 1

Therapeutic Repurposing of Avanafil Against Lipopolysaccharide-induced Depression and Autoimmune Hepatitis: Gut-brain-liver Axis Orchestration Via Regulation of TLR4/NF-κB/IDO and Nrf2/HO-1 Pathways

Ibrahim, K. M., Ahmed, H. I., Ramadan, L. A. A., & Balah, A. (2026) · Molecular Neurobiology · doi:10.1007/s12035-026-05854-4 · Cited by 1

A circuit linking dentate gyrus and retrosplenial granular cortex regulates fracture healing in male mice

Zhang, W., Zhang, W., Guo, Y., Chen, D., Jiang, X., Zhang, J., Chen, E., Yuan, Y., Wu, W., Qian, Y., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-75340-x · Cited by 2

Diminished responses to monoaminergic antidepressants but not ketamine in a mouse model for neuropsychiatric lupus

Srikumar, B. N., Naidu, P. S., Kalidindi, N., Paschapur, M. S., Adepu, B., Subramani, S., Nagar, J., Srivastava, R., Sreedhara, M. V., Prasad, D. S., et al. (2018) · Journal of Psychopharmacology · doi:10.1177/0269881118812102 · Cited by 2

Role of Interferon-Gamma and Leucine-Rich Repeat Kinase 2 in Stress-Related Pathology

Litteljohn, D. (2016) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2016-11660

Inflammation and immune-mediated neurobehavioral alterations : a critical role for microglia

Lacabanne, C. (2018) · theses.fr (ABES) · doi:10.70675/41a4e2a3zdbb7z4aa0z899dz9553bb07954b · Cited by 1

Inflammatory processes and depressive-like behavior in a syngeneic model of ovarian cancer

Lamkin, D. M. (2010) · doi:10.17077/etd.s2tm95rd · Cited by 1

From inflammation to sickness and depression: the cytokine connection

Dantzer, R., & Kelley, K. W. (2010) · Cambridge University Press eBooks · doi:10.1017/cbo9780511780868.014

Role of Primed Microglia in the Aging Brain in Prolonged Sickness and Depressive Behavior Concomitant with Peripheral Immune Stimulation

Henry, C. J. (2011) · OhioLink ETD Center (Ohio Library and Information Network)

Analysis of rat brain lipids and metabolites after antidepressant drug treatment

Jaddoa, E. (2018) · DMU Open Research Archive (De Montfort University)

Stressor and cytokine interactions : implications in depressive-like pathology

Gibb, J. (2011) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2011-09658

Mental and Physiological Structures and Mechanisms of Overprotection in the Aetiology of Autoimmune Disease

Cristal-Lilov, A., Salmon, A. B., & Erez, O. (2021) · Journal of Medical - Clinical Research & Reviews · doi:10.33425/2639-944x.1238 · Cited by 1

First Trimester Human Umbilical Cord Perivascular cells (HUCPVC) Modulate the Kynurenine Pathway and Glutamate Neurotransmission in an LPS-induced Mouse Model of NeuroinflammationPreprint

Siddiqui, F., Gallagher, D., Shuster-Hyman, H., Lopez, L., Gauthier-Fisher, A., & Librach, C. L. (2022) · Research Square · doi:10.21203/rs.3.rs-2238679/v1

Amine Precursors in Depressive Disorders and the Blood-Brain Barrier

Sharma, H. S., & Sharma, A. (2022) · Springer eBooks · doi:10.1007/978-3-030-62059-2_423

Hypothesis of neuroinflammation in depression

Dolfi, A., & Talasman, A.-A. (2017) · Romanian Journal of Psychiatry & Psychotherapy · doi:10.37897/rjpp.2017.4.5

THE RESPONSES OF HUMAN PERIODONTAL LIGAMENT CELLS TO EXOGENOUS INTERLEUKIN-12

Ayuthaya, B. I. N. (2016) · doi:10.58837/chula.the.2016.1736

Impact of sanitary conditions and dietary amino acids on behaviour and brain monoamine levels in piglets

Minussi, I., Gerrits, W. J. J., Jansman, A. J. M., Troupakis, G., Bruin, M. D.-D., Vermeiren, Y., & Bolhuis, J. E. (2025) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2025.101076

Additional file 1 of First trimester human umbilical cord perivascular cells (HUCPVC) modulate the kynurenine pathway and glutamate neurotransmission in an LPS-induced mouse model of neuroinflammation

Siddiqui, F., Gallagher, D., Shuster-Hyman, H., Lopez, L., Gauthier-Fisher, A., & Librach, C. L. (2024) · Figshare · doi:10.6084/m9.figshare.26586243

Approche éthologique des modifications émotionnelles induites par les processus inflammatoires chez la souris domestique

Renault, J. (2008) · theses.fr (ABES) · doi:10.70675/bb0bebebzaaaaz4aa0z962aza9ae1033fff7

Etude du rôle de la voie de la kynurénine dans un modèle animale de dépression : le stress chronique imprédictible : approches biochimique et comportementale

Laugeray, A. (2010) · theses.fr (ABES) · doi:10.70675/b03b72f8zed45z46d0z997az0e920e97e824

Mise en évidence du potentiel thérapeutique de l’adiponectine et de son rôle dans les effets antidépresseurs de l’environnement enrichi

Nicolas, S. (2018) · theses.fr (ABES) · doi:10.70675/95c9bfb5zd68ez43b8zbbf8z73847b3cd3db

Etude de la voie de la kynurénine dans la symptomatologie du sujet obèse

Huet, L. (2019) · theses.fr (ABES) · doi:10.70675/ff26d7c8z4c5fz4c86z9e6ezd8d843268447

Inflamación, depresión y suicidio: Una aproximación al fenómeno biológico

Niño, N. B., Torres, A. C., Villanueva‐Alonzo, H. D. J., Arankowsky‐Sandoval, G., & Pineda, J. C. (2025) · Ediciones Comunicación Científica eBooks · doi:10.52501/cc.369.08

Tryptophan-Related Signaling Molecules: Targets and Functions

Engin, A. (2015) · Molecular and integrative toxicology · doi:10.1007/978-3-319-15630-9_1

Spatio-temporal differences in the profile of murine brain expression of proinflammatory cytokines and indoleamine 2,3-dioxygenase in response to peripheral lipopolysaccharide administration

André, C., O’Connor, J. C., Kelley, K. W., Lestage, J., Dantzer, R., & Castanon, N. (2008) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2008.06.011 · Cited by 116

Mechanisms of cytokine-induced activation of brain indoleamine 2,3-dioxygenase (IDO), a tryptophan-catabolizing enzyme, involved in behavioral and mood alterations observed in mice models of infection and obesity

Castanon, N., André, C., Dinel, A., Lestage, J., & Dantzer, R. (2006) · HAL

Intracerebroventricular administration of lipopolysaccharide induces indoleamine-2,3-dioxygenase-dependent depression-like behaviors

Lawson, M. A., Parrott, J. M., McCusker, R. H., Dantzer, R., Kelley, K. W., & O’Connor, J. C. (2013) · Journal of Neuroinflammation · doi:10.1186/1742-2094-10-87 · Cited by 166

Bacille Calmette‐Guérin Inoculation Induces Chronic Activation of Peripheral and Brain Indoleamine 2,3‐Dioxygenase in Mice

Moreau, M. M., Lestage, J., Verrier, D., Mormède, C., Kelley, K. W., Dantzer, R., & Castanon, N. (2005) · The Journal of Infectious Diseases · doi:10.1086/431603 · Cited by 104

Lipopolysaccharide-induced depressive-like behavior is mediated by indoleamine 2,3-dioxygenase activation in mice

O'Connor, J. C., Lawson, M. A., André, C., Moreau, M., Lestage, J., Castanon, N., Kelley, K. W., & Dantzer, R. (2009) · Molecular Psychiatry · doi:10.1038/sj.mp.4002148 · Cited by 1,278