Cited by 46Tryptophan and brain disordersStress Responses and CortisolImmunotoxicology and immune responses

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

Zavitsanou, Katerina, Lim, Chai K., Purves-Tyson, Tertia, Karl, Tim, Kassiou, Michael, Banister, Samuel D., Guillemin, Gilles J., Weickert, Cynthia Shannon·2014·Brain Behavior and Immunity

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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Crossref · 10.1016/j.bbi.2014.05.011

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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
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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