Effect of maternal immune activation on the kynurenine pathway in preadolescent rat offspring and on MK801-induced hyperlocomotion in adulthood: amelioration by COX-2 inhibition
Abstract
Infections during pregnancy and subsequent maternal immune activation (MIA) increase risk for schizophrenia in offspring. The progeny of rodents injected with the viral infection mimic polyI:C during gestation display brain and behavioural abnormalities but the underlying mechanisms are unknown. Since the blood kynurenine pathway (KP) of tryptophan degradation impacts brain function and is strongly regulated by the immune system, we tested if KP changes occur in polyI:C offspring at preadolescence. We also tested whether MK801-induced hyperlocomotion, a behaviour characteristic of adult polyI:C offspring, is prevented by adolescent treatment with celecoxib, a COX-2 inhibitor that impacts the KP. Pregnant rats were treated with polyI:C (4mg/kg, i.v.) or vehicle on gestational day 19. Serum levels of KP metabolites were measured in offspring of polyI:C or vehicle treated dams at postnatal day (PND) 31-33 using HPLC/GCMS. Additional polyI:C or vehicle exposed offspring were given celecoxib or vehicle between PND 35 and 46 and tested with MK801 (0.3mg/kg) in adulthood (PND>90). Prenatal polyI:C resulted in increases in the serum KP neurotoxic metabolite quinolinic acid at PND 31-33 (105%, p=0.014). In contrast, the neuroprotective kynurenic acid and its precursor kynurenine were significantly decreased (28% p=0.027, and 31% p=0.033, respectively). Picolinic acid, another neuroprotective KP metabolite, was increased (31%, p=0.014). Adolescent treatment with celecoxib (2.5 and 5mg/kg/day, i.p.) prevented the development of MK801-induced hyperlocomotion in adult polyI:C offspring. Our study reveals the blood KP as a potential mechanism by which MIA interferes with postnatal brain maturation and associated behavioural disturbances and emphasises the preventative potential of inflammation targeting drugs.
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Increased kynurenine metabolites have been reported in animal models of maternal inflammation.
“An increase in kynurenine metabolites has been reported in animal models of maternal inflammation (Pfaff et al., 2008; Zavitsanou et al., 2014).”
From Neuroinflammation as a risk factor for attention deficit hyperactivity disorder (2019) · cites this paper as Zavitsanou et al., 2014
Cites
Implications of Normal Brain Development for the Pathogenesis of Schizophrenia
Weinberger, D. R. (1987) · Archives of General Psychiatry · doi:10.1001/archpsyc.1987.01800190080012 · Cited by 3,724 · see citing works
Recent advances in the phencyclidine model of schizophrenia
(1991) · American Journal of Psychiatry · doi:10.1176/ajp.148.10.1301 · Cited by 2,904 · see citing works
Moghaddam, B., Adams, B., Verma, A., & Daly, D. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-08-02921.1997 · Cited by 1,793 · see citing works
Insel, T. R. (2010) · Nature · doi:10.1038/nature09552 · Cited by 1,783 · see citing works
Kynurenines in the mammalian brain: when physiology meets pathology
Schwarcz, R., Bruno, J. P., Muchowski, P. J., & Wu, H.-Q. (2012) · Nature Reviews Neuroscience · doi:10.1038/nrn3257 · Cited by 1,530 · see citing works
Adult Schizophrenia Following Prenatal Exposure to an Influenza Epidemic
Mednick, S. A. (1988) · Archives of General Psychiatry · doi:10.1001/archpsyc.1988.01800260109013 · Cited by 1,198 · see citing works
Blood–Brain Barrier Transport of Kynurenines: Implications for Brain Synthesis and Metabolism
Fukui, S., Schwarcz, R. M., Rapoport, S. I., Takada, Y., & Smith, Q. R. (1991) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1991.tb03460.x · Cited by 765 · see citing works
Boksa, P. (2010) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2010.03.005 · Cited by 603 · see citing works
Quinolinic acid, the inescapable neurotoxin
Guillemin, G. J. (2012) · The FEBS Journal · doi:10.1111/j.1742-4658.2012.08485.x · Cited by 595 · see citing works
Self-citationIncreased cortical kynurenate content in schizophrenia
Schwarcz, R., Rassoulpour, A., Wu, H.-Q., Medoff, D., Tamminga, C. A., & Roberts, R. C. (2001) · Biological Psychiatry · doi:10.1016/s0006-3223(01)01078-2 · Cited by 590 · see citing works
Kynurenine Pathway Metabolites in Humans: Disease and Healthy States
Chen, Y.-Q., & Guillemin, G. (2009) · International Journal of Tryptophan Research · doi:10.4137/ijtr.s2097 · Cited by 589 · see citing works
Self-citationCarboni, E., Impérato, A., Perezzani, L., & Chiara, G. D. (1989) · Neuroscience · doi:10.1016/0306-4522(89)90012-2 · Cited by 560 · see citing works
Kynurenine pathway metabolism in human astrocytes: a paradox for neuronal protection
Guillemin, G. J., Kerr, S. J., Smythe, G. A., Smith, D. G., Kapoor, V., Armati, P. J., Croitoru‐Lamoury, J., & Brew, B. J. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00498.x · Cited by 541 · see citing works
Self-citationProvocative tests with psychostimulant drugs in schizophrenia
Lieberman, J. A., Kane, J. M., & Alvir, J. (1987) · Psychopharmacology · doi:10.1007/bf00216006 · Cited by 535 · see citing works
Zuckerman, L., Rehavi, M., Nachman, R., & Weiner, I. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300248 · Cited by 501 · see citing works
Kynurenic acid levels are elevated in the cerebrospinal fluid of patients with schizophrenia.
Erhardt, S., Blennow, K., Nordin, C., Skogh, E., Lindström, L., & Engberg, G. (2001) · Neuroscience Letters · doi:10.1016/s0304-3940(01)02242-x · Cited by 478 · see citing works
Meyer, U., Nyffeler, M., Yee, B. K., Knuesel, I., & Feldon, J. (2008) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2007.09.012 · Cited by 457 · see citing works
Müller, N., Riedel, M. J., Scheppach, C., Brandstätter, B., Sokullu, S., Krampe, K., Ulmschneider, M., Engel, R. R., Möller, H., & Schwarz, M. (2002) · American Journal of Psychiatry · doi:10.1176/appi.ajp.159.6.1029 · Cited by 388 · see citing works
Epidemiology-driven neurodevelopmental animal models of schizophrenia
Meyer, U., & Feldon, J. (2009) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2009.10.018 · Cited by 366 · see citing works
Garay, P. A., Hsiao, E. Y., Patterson, P. H., & McAllister, A. K. (2013) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2012.07.008 · Cited by 366 · see citing works
Maternal immune activation leads to behavioral and pharmacological changes in the adult offspring
Zuckerman, L., & Weiner, I. (2004) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2004.08.008 · Cited by 352 · see citing works
Connecting inflammation with glutamate agonism in suicidality
Erhardt, S., Lim, C. K., Linderholm, K. R., Janelidze, S., Lindqvist, D., Samuelsson, M., Lundberg, K., Postolache, T. T., Träskman-Bendz, L., Guillemin, G. J., et al. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2012.248 · Cited by 345 · see citing works
Self-citationCharacterization of the Kynurenine Pathway in Human Neurons
Guillemin, G. J., Cullen, K. M., Lim, C. K., Smythe, G. A., Garner, B., Kapoor, V., Takikawa, O., & Brew, B. J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.4101-07.2007 · Cited by 325 · see citing works
Self-citationl-Kynurenine Its synthesis and possible regulatory function in brain
G�l, E. M., & Sherman, A. D. (1980) · Neurochemical Research · doi:10.1007/bf00964611 · Cited by 318 · see citing works
Developmental neuroinflammation and schizophrenia
Meyer, U. (2011) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2011.11.003 · Cited by 300 · see citing works
The kynurenine pathway as a therapeutic target in cognitive and neurodegenerative disorders
Stone, T. W., & Darlington, L. G. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12230 · Cited by 272 · see citing works
Elevated levels of kynurenic acid in the cerebrospinal fluid of male patients with schizophrenia.
Nilsson, L., Linderholm, K., Engberg, G., Paulson, L., Blennow, K., Lindström, L., Nordin, C., Karanti, A., Persson, P., & Erhardt, S. (2005) · Schizophrenia Research · doi:10.1016/j.schres.2005.07.013 · Cited by 257 · see citing works
Impaired Kynurenine Pathway Metabolism in The Prefrontal Cortex of Individuals With Schizophrenia
Sathyasaikumar, K. V., Stachowski, E. K., Wonodi, I., Roberts, R. C., Rassoulpour, A., McMahon, R. P., & Schwarcz, R. M. (2010) · Schizophrenia Bulletin · doi:10.1093/schbul/sbq112 · Cited by 253 · see citing works
Müller, N., Krause, D., Dehning, S., Musil, R., Schennach-Wolff, R., Obermeier, M., Möller, H., Klauß, V., Schwarz, M., & Riedel, M. J. (2010) · Schizophrenia Research · doi:10.1016/j.schres.2010.04.015 · Cited by 251 · see citing works
Fillman, S. G., Sinclair, D., Fung, S. J., Webster, M. J., & Shannon Weickert, C. (2014) · Translational Psychiatry · doi:10.1038/tp.2014.8 · Cited by 226 · see citing works
Self-citationElevations of Endogenous Kynurenic Acid Produce Spatial Working Memory Deficits
Chess, A. C., Simoni, M. K., Alling, T. E., & Bucci, D. J. (2006) · Schizophrenia Bulletin · doi:10.1093/schbul/sbl033 · Cited by 225 · see citing works
Schizophrenia as an inflammation-mediated dysbalance of glutamatergic neurotransmission
Müller, N., & Schwarz, M. (2006) · Neurotoxicity Research · doi:10.1007/bf03033242 · Cited by 214 · see citing works
Fineberg, A. M., & Ellman, L. M. (2013) · Biological Psychiatry · doi:10.1016/j.biopsych.2013.01.001 · Cited by 200 · see citing works
Endogenous kynurenic acid disrupts prepulse inhibition.
Erhardt, S., Schwieler, L., Emanuelsson, C., & Geyer, M. (2004) · Biological Psychiatry · doi:10.1016/j.biopsych.2004.06.006 · Cited by 187 · see citing works
Prenatal Exposure to Maternal Infection and Executive Dysfunction in Adult Schizophrenia
Brown, A. S., Vinogradov, S., Kremen, W. S., Poole, J. H., Deicken, R. F., Penner, J. D., McKeague, I. W., Kochetkova, A. S., Kern, D. M., & Schaefer, C. A. (2009) · American Journal of Psychiatry · doi:10.1176/appi.ajp.2008.08010089 · Cited by 177 · see citing works
Casolini, P., Catalani, A., Zuena, A. R., & Angelucci, L. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10192 · Cited by 174 · see citing works
Microglial activation in a neuroinflammational animal model of schizophrenia – a pilot study
Juckel, G., Manitz, M. P., Brüne, M., Friebe, A., Heneka, M. T., & Wolf, R. J. (2011) · Schizophrenia Research · doi:10.1016/j.schres.2011.06.018 · Cited by 165 · see citing works
Neural basis of psychosis-related behaviour in the infection model of schizophrenia
Meyer, U., & Feldon, J. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2008.12.022 · Cited by 158 · see citing works
Miller, D. W., & Abercrombie, E. D. (1996) · Brain Research Bulletin · doi:10.1016/0361-9230(95)02144-2 · Cited by 146 · see citing works
Piontkewitz, Y., Assaf, Y., & Weiner, I. (2009) · Biological Psychiatry · doi:10.1016/j.biopsych.2009.07.005 · Cited by 143 · see citing works
Piontkewitz, Y., Arad, M., & Weiner, I. (2010) · Schizophrenia Bulletin · doi:10.1093/schbul/sbq040 · Cited by 143 · see citing works
Celecoxib Augmentation of Continuously Ill Patients with Schizophrenia
Rapaport, M. H., Delrahim, K. K., Bresee, C. J., Maddux, R. E., Ahmadpour, O. A., & Dolnak, D. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.02.024 · Cited by 137 · see citing works
Shepard, P. D., Joy, B., Prendeville, L. C., & Schwarcz, R. M. (2003) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300188 · Cited by 131 · see citing works
Prenatal inflammation and neurodevelopment in schizophrenia: A review of human studies
Miller, B. J., Culpepper, N. H., Rapaport, M. H., & Buckley, P. F. (2012) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2012.03.010 · Cited by 124 · see citing works
Kynurenine pathway inhibition as a therapeutic strategy for neuroprotection
Stone, T. W., Forrest, C., & Darlington, L. (2012) · The FEBS Journal · doi:10.1111/j.1742-4658.2012.08487.x · Cited by 124 · see citing works
Myint, A.-M., Schwarz, M., Verkerk, R. M., Mueller, H. H., Zach, J., Scharpé, S., Steinbusch, H. W. M., Leonard, B. E., & Kim, Y. K. (2011) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2011.05.005 · Cited by 116 · see citing works
Meyer, U., Spoerri, E., Yee, B. K., Schwarz, M., & Feldon, J. (2008) · Schizophrenia Bulletin · doi:10.1093/schbul/sbn131 · Cited by 115 · see citing works
Tracing the development of psychosis and its prevention: what can be learned from animal models
Piontkewitz, Y., Arad, M., & Weiner, I. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.04.019 · Cited by 108 · see citing works
PRE- AND POSTNATAL EXPOSURE TO KYNURENINE CAUSES COGNITIVE DEFICITS IN ADULTHOOD
Pocivavsek, A., Wu, H., Elmer, G. I., Bruno, J. P., & Schwarcz, R. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08064.x · Cited by 105 · see citing works
Smythe, G. A., Braga, O., Brew, B. J., Grant, R., Guillemin, G. J., Kerr, S. J., & Walker, D. W. (2002) · Analytical Biochemistry · doi:10.1006/abio.2001.5490 · Cited by 101 · see citing works
Self-citationPiontkewitz, Y., Bernstein, H., Dobrowolny, H., Bogerts, B., Weiner, I., & Keilhoff, G. (2011) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2011.11.004 · Cited by 93 · see citing works
Erhardt, S., & Engberg, G. (2002) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.2002.00962.x · Cited by 91 · see citing works
Dean, B. (2010) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145710001410 · Cited by 89 · see citing works
Schwieler, L., Erhardt, S., Erhardt, C., & Engberg, G. (2004) · Journal of Neural Transmission · doi:10.1007/s00702-004-0231-y · Cited by 81 · see citing works
Wu, H., Okuyama, M., Kajii, Y., Pocivavsek, A., Bruno, J. P., & Schwarcz, R. M. (2014) · Schizophrenia Bulletin · doi:10.1093/schbul/sbt157 · Cited by 78 · see citing works
Effects of phencyclidine on ventral tegmental A10 dopamine neurons in the rat
French, E. D. (1986) · Neuropharmacology · doi:10.1016/0028-3908(86)90246-7 · Cited by 67 · see citing works
Priming of Metabolic Dysfunctions by Prenatal Immune Activation in Mice: Relevance to Schizophrenia
Pacheco‐López, G., Giovanoli, S., Langhans, W., & Meyer, U. (2011) · Schizophrenia Bulletin · doi:10.1093/schbul/sbr178 · Cited by 65 · see citing works
Dalton, V. S., Verdurand, M., Walker, A. K., Hodgson, D. M., & Zavitsanou, K. (2012) · ISRN Psychiatry · doi:10.5402/2012/451865 · Cited by 43 · see citing works
Self-citationMarkers of inflammation in the prefrontal cortex of individuals with schizophrenia
Fillman, S. G., Cloonan, N., Miller, L. C., & Weickert, C. S. (2013) · Molecular Psychiatry · doi:10.1038/mp.2012.199 · Cited by 41 · see citing works
Self-citationAltered GSK3β signaling in an infection-based mouse model of developmental neuropsychiatric disease
Willi, R., Harmeier, A., Giovanoli, S., & Meyer, U. (2013) · Neuropharmacology · doi:10.1016/j.neuropharm.2013.05.012 · Cited by 36 · see citing works
Immunological Treatment Options for Schizophrenia
Müller, N., Myint, A.-M., & Schwarz, M. (2012) · Current Pharmaceutical Biotechnology · doi:10.2174/138920112800784826 · Cited by 34 · see citing works
Characterization of the Kynurenine Pathway and Quinolinic Acid Production in Macaque Macrophages
Lim, C. K., Yap, M. M. C., Kent, S. J., Gras, G. S., Samah, B., Batten, J. C., Rose, R. D., Heng, B., Brew, B. J., & Guillemin, G. J. (2013) · International Journal of Tryptophan Research · doi:10.4137/ijtr.s11789 · Cited by 31 · see citing works
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Knuesel, I., Chicha, L., Britschgi, M., Schobel, S. A., Bodmer, M., Hellings, J. A., Toovey, S., & Prinssen, E. P. (2014) · Nature Reviews Neurology · doi:10.1038/nrneurol.2014.187 · Cited by 880 · see citing works
Altering the course of schizophrenia: progress and perspectives
Millan, M. J., Andrieux, A., Bartzokis, G., Cadenhead, K., Dazzan, P., Fusar-Poli, P., Gallinat, J., Giedd, J., Grayson, D. R., Heinrichs, M., et al. (2016) · Nature Reviews Drug Discovery · doi:10.1038/nrd.2016.28 · Cited by 516 · see citing works
Neuroinflammation as a risk factor for attention deficit hyperactivity disorder
Dunn, G. A., Nigg, J. T., & Sullivan, E. L. (2019) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2019.05.005 · Cited by 299 · see citing works
Kindler, J., Lim, C. K., Weickert, C., Boerrigter, D., Galletly, C., Liu, D., Jacobs, K. R., Balzan, R., Bruggemann, J. M., O'Donnell, M., et al. (2019) · Molecular Psychiatry · doi:10.1038/s41380-019-0401-9 · Cited by 267 · see citing works
Self-citationBrain changes in a maternal immune activation model of neurodevelopmental brain disorders
Bergdolt, L., & Dunaevsky, A. (2018) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2018.12.002 · Cited by 266 · see citing works
Maternal immune activation in neurodevelopmental disorders
Solek, C. M., Farooqi, N., Verly, M., Lim, T. K., & Ruthazer, E. S. (2018) · Developmental Dynamics · doi:10.1002/dvdy.24612 · Cited by 168 · see citing works
Gomes, F. V., Rincón‐Cortés, M., & Grace, A. A. (2016) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2016.05.030 · Cited by 128 · see citing works
Lim, C. K., Essa, M., Martins, R. D. P., Lovejoy, D. B., Bilgin, A. A., Waly, M., Al-Farsi, Y., Al-Sharbati, M., Al-Shaffae, M. A., & Guillemin, G. (2016) · Autism Research · doi:10.1002/aur.1565 · Cited by 95 · see citing works
Self-citationSchizophrenia and Depression Co-Morbidity: What We have Learned from Animal Models
Samsom, J. N., & Wong, A. (2015) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2015.00013 · Cited by 82 · see citing works
Kynurenine Pathway in Autism Spectrum Disorders in Children
Bryn, V., Verkerk, R. M., Skjeldal, O. H., Saugstad, O. D., & Ormstad, H. (2017) · Neuropsychobiology · doi:10.1159/000488157 · Cited by 67 · see citing works
Bauman, M. D., & de Water, J. V. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.104864 · Cited by 64 · see citing works
Notarangelo, F. M., & Schwarcz, R. M. (2016) · Developmental Neuroscience · doi:10.1159/000455228 · Cited by 62 · see citing works
Möller, M., Swanepoel, T., & Harvey, B. H. (2015) · ACS Chemical Neuroscience · doi:10.1021/cn5003368 · Cited by 59 · see citing works
Pocivavsek, A., Schwarcz, R. M., & Erhardt, S. (2024) · Pharmacological Reviews · doi:10.1124/pharmrev.124.000239 · Cited by 58 · see citing works
Kong, Q., Chen, Q., Mao, X., Wang, G., Zhao, J., Zhang, H., & Chen, W. (2022) · Nutrients · doi:10.3390/nu14081615 · Cited by 53 · see citing works
da Silveira, V. T., de Castro Medeiros, D., Ropke, J., Guidine, P. A., Rezende, G. H., Moraes, M. F. D., Mendes, E. M. A. M., Macedo, D., Moreira, F. A., & de Oliveira, A. C. P. (2017) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2017.01.009 · Cited by 51 · see citing works
Clark, S. M., Notarangelo, F. M., Li, X., Chen, S., Schwarcz, R. M., & Tonelli, L. H. (2018) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2018.09.011 · Cited by 50 · see citing works
Prenatal Dynamics of Kynurenine Pathway Metabolism in Mice: Focus on Kynurenic Acid
Goeden, N., Notarangelo, F. M., Pocivavsek, A., Beggiato, S., Bonnin, A., & Schwarcz, R. M. (2017) · Developmental Neuroscience · doi:10.1159/000481168 · Cited by 49 · see citing works
Graham, A. M., Doyle, O. J., Tilden, E. L., Sullivan, E. L., Gustafsson, H., Marr, M. C., Allen, M. C., & Seghete, K. L. M. (2021) · Biological Psychiatry Cognitive Neuroscience and Neuroimaging · doi:10.1016/j.bpsc.2021.10.012 · Cited by 54 · see citing works
Gene × Environment Interactions in Schizophrenia: Evidence from Genetic Mouse Models
Moran, P. M., Stokes, J., Marr, J., Bock, G., Desbonnet, L., Waddington, J. L., & O’Tuathaigh, C. M. P. (2016) · Neural Plasticity · doi:10.1155/2016/2173748 · Cited by 46 · see citing works
Murakami, Y., Imamura, Y., Kasahara, Y., Yoshida, C., Momono, Y., Fang, K., Sakai, D., Konishi, Y., & Nishiyama, T. (2023) · Cells · doi:10.3390/cells12071087 · Cited by 36 · see citing works
Schizophrenia and psychoneuroimmunology
Sperner‐Unterweger, B., & Fuchs, D. (2015) · Current Opinion in Psychiatry · doi:10.1097/yco.0000000000000153 · Cited by 37 · see citing works
Collier, M., Zhang, S.-W., Scrutton, N., & Giorgini, F. (2021) · Drug Discovery Today · doi:10.1016/j.drudis.2021.02.009 · Cited by 30 · see citing works
Goh, J.-Y., O’Sullivan, S. E., Shortall, S. E., Zordan, N., Piccinini, A. M., Potter, H. G., Fone, K. C. F., & King, M. V. (2020) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2020.05.076 · Cited by 33 · see citing works
Antiviral Inflammation during Early Pregnancy Reduces Placental and Fetal Growth Trajectories
Baines, K. J., Rampersaud, A. M., Hillier, D. M., Jeyarajah, M. J., Grafham, G. K., Eastabrook, G. D. M., Lacefield, J. C., & Renaud, S. J. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1900888 · Cited by 25 · see citing works
Aria, F., Bonini, S. A., Cattaneo, V., Premoli, M., Mastinu, A., Maccarinelli, G., & Memo, M. (2020) · Brain Sciences · doi:10.3390/brainsci10090620 · Cited by 28 · see citing works
Astrocytes as Pharmacological Targets in the Treatment of Schizophrenia
Pocivavsek, A., Notarangelo, F. M., Wu, H., Bruno, J., & Schwarcz, R. (2016) · Handbook of behavioral neuroscience · doi:10.1016/b978-0-12-800981-9.00025-0 · Cited by 33 · see citing works
Hasegawa, Y., Inoue, T., Kawaminami, S., & Fujita, M. (2016) · Asian Pacific Journal of Tropical Medicine · doi:10.1016/j.apjtm.2016.05.019 · Cited by 23 · see citing works
Allard, M., Brochu, M., Bergeron, J. D., & Sebire, G. (2018) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2018.06.005 · Cited by 22 · see citing works
Haider, S., Shahzad, S., Batool, Z., Sadir, S., Liaquat, L., Tabassum, S., & Perveen, T. (2021) · Life Sciences · doi:10.1016/j.lfs.2021.119417 · Cited by 17 · see citing works
MacDowell, K. S., Munarriz‐Cuezva, E., Meana, J. J., Leza, J. C., & Ortega, J. E. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.682602 · Cited by 15 · see citing works
Missault, S., Anckaerts, C., Ahmadoun, S., Blockx, I., Barbier, M., Bielen, K., Shah, D., Kumar‐Singh, S., Vos, W. H. D., der Linden, A. V., et al. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.02.040 · Cited by 14 · see citing works
Forrest, C. M., Kennedy, P. G. E., Rodgers, J., Dalton, R. N., Turner, C., Darlington, L. G., Cobb, S., & Stone, T. W. (2016) · Neurochemistry International · doi:10.1016/j.neuint.2016.09.012 · Cited by 14 · see citing works
Does the kynurenine pathway play a pathogenic role in autism spectrum disorder?
Santana‐Coelho, D. (2024) · Brain Behavior & Immunity - Health · doi:10.1016/j.bbih.2024.100839 · Cited by 10 · see citing works
Animal Models of Relevance to the Schizophrenia Prodrome
Petty, A. E., Howes, O. D., & Eyles, D. W. (2021) · Biological Psychiatry Global Open Science · doi:10.1016/j.bpsgos.2021.12.001 · Cited by 8 · see citing works
Notarangelo, F. M., & Schwarcz, R. (2021) · European Journal of Neuroscience · doi:10.1111/ejn.15416 · Cited by 5 · see citing works
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Murlanova, K., Begmatova, D., Weber‐Stadlbauer, U., Meyer, U., Pletnikov, M. V., & Pinhasov, A. (2021) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2021.09.004 · Cited by 6 · see citing works
Xu, Z., Hu, C., & Luo, Y. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1667164 · Cited by 4 · see citing works
Sonego, A. B., Prado, D. D. S., Uliana, D. L., Cunha, T. M., Grace, A. A., & Resstel, L. B. M. (2024) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2024.09.001 · Cited by 3 · see citing works
Yang, L.-R., Chen, H.-Y., Zeng, M.-L., Lu, Y.-F., Xu, C., Cao, Z.-J., Zhong, F.-C., Yang, X.-Y., Shen, A.-Y., Su, Y.-Q., et al. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1669845 · Cited by 2 · see citing works
Li, H., Shen, H., Duan, X., Guo, M., & Liu, X. (2026) · BMC Psychiatry · doi:10.1186/s12888-026-07774-y · Cited by 1 · see citing works
Developmental and psychoneuroimmunological mechanisms in depression
Pujol-Lopez, Y. (2015) · doi:10.26481/dis.20151030yp
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Küçükkarapınar, M., Karadağ, F., & Candansayar, S. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95650-5.00048-3
- Authors
- Zavitsanou, K., Lim, C. K., Purves-Tyson, T., Karl, T., Kassiou, M., Banister, S. D., Guillemin, G. J., & Weickert, C. S.
- Affiliations
- UNSW Sydney (AU)
- Macquarie University (AU)
- The University of Sydney (AU)
- Corresponding author
- Zavitsanou, Katerina
- ORCID
- Venue
- Brain Behavior and Immunity
- Publisher
- Elsevier BV
- Published
- 2014-10
- Volume
- 41
- Pages
- 173-181
- ISSN
- 0889-1591 (ISSN-L)
- OpenAlex
- W1989839225
- Cited by
- 46
- References
- 62
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 4 · 2023: 1 · 2022: 1 · 2021: 7 · 2020: 3 · 2019: 5 · 2018: 5 · 2017: 4 · 2016: 6 · 2015: 6 · 2014: 1
- FWCI
- 1.73
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Brain Behavior and Immunity (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Schizophrenia Research Institute
- Australian Research Council
- National Health and Medical Research Council
- University of New South Wales
- Neuroscience Research Australia
- Topics
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Immunology and Microbiology › Immunology › Immunotoxicology and immune responses
- Keywords
- maternal immune activation, kynurenine pathway, prenatal infection, poly(I:C), schizophrenia risk, quinolinic acid, kynurenic acid, picolinic acid, celecoxib, COX-2 inhibition, adolescent treatment, postnatal brain development, neuroinflammation, tryptophan metabolism
- MeSH terms
- Celecoxib, Animals, Brain, Disease Models, Animal, Female, Gestational Age, Hyperkinesis, Kynurenic Acid, Kynurenine, Male, Picolinic Acids, Poly I-C, Pregnancy, Prenatal Exposure Delayed Effects, Pyrazoles, Random Allocation, Schizophrenia, Sexual Maturation, Sulfonamides, Tryptophan, Dizocilpine Maleate, Rats, Wistar, Quinolinic Acid, Rats, Cyclooxygenase 2 Inhibitors
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