Inter-breeder differences in prepulse inhibition deficits of C57BL/6J mice in a maternal immune activation model

Genetic and environmental factors interact with each other to influence the risk of various psychiatric diseases; however, the intensity and nature of their interactions remain to be elucidated. We established a maternal infection model using polyinosinic-polycytidylic acid (Poly(I:C)) to determine...

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Bibliographic Details
Main Authors: Inaba, H. (Author), Iwakura, Y. (Author), Iwamoto, K. (Author), Kobayashi, Y. (Author), Murata, Y. (Author), Namba, H. (Author), Nawa, H. (Author), Sotoyama, H. (Author)
Format: Article
Language:English
Published: John Wiley and Sons Inc 2021
Subjects:
Online Access:View Fulltext in Publisher
LEADER 03768nam a2200745Ia 4500
001 10.1002-npr2.12178
008 220427s2021 CNT 000 0 und d
020 |a 2574173X (ISSN) 
245 1 0 |a Inter-breeder differences in prepulse inhibition deficits of C57BL/6J mice in a maternal immune activation model 
260 0 |b John Wiley and Sons Inc  |c 2021 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1002/npr2.12178 
520 3 |a Genetic and environmental factors interact with each other to influence the risk of various psychiatric diseases; however, the intensity and nature of their interactions remain to be elucidated. We established a maternal infection model using polyinosinic-polycytidylic acid (Poly(I:C)) to determine the relationship between the maternal breeding environment and behavioral changes in the offspring. We purchased pregnant C57BL/6J mice from three breeders and administered Poly(I:C) (2 mg/kg) intravenously in their tail vein on gestation day 15. The offspring were raised to 8-12 weeks old and subjected to the acoustic startle tests to compare their startle response intensity, prepulse inhibition levels, and degree of the adaptation of the startle response. No statistical interaction between Poly(I:C) administration and sex was observed for prepulse inhibition; thus, male and female mice were analyzed together. There was a statistical interaction between the breeder origin of offspring and prepulse inhibition; the Poly(I:C) challenge significantly decreased prepulse inhibition levels of the offspring born to the pregnant dams from Breeder A but not those from the other breeders. However, we failed to detect significant inter-breeder differences in Poly(I:C) effects on startle response and on startle adaptation with the given number of mice examined. The rearing environment of mouse dams has a prominent effect on the Poly(I:C)-induced prepulse inhibition deficits in this maternal immune activation model. © 2021 The Authors. Neuropsychopharmacology Reports published by John Wiley & Sons Australia, Ltd on behalf of the Japanese Society of Neuropsychopharmacology 
650 0 4 |a adaptation 
650 0 4 |a adult 
650 0 4 |a animal 
650 0 4 |a animal experiment 
650 0 4 |a animal model 
650 0 4 |a Animals 
650 0 4 |a Article 
650 0 4 |a behavior change 
650 0 4 |a breed difference 
650 0 4 |a C57BL 6 mouse 
650 0 4 |a C57BL mouse 
650 0 4 |a controlled study 
650 0 4 |a environmental factor 
650 0 4 |a female 
650 0 4 |a Female 
650 0 4 |a gene-environment 
650 0 4 |a genotype environment interaction 
650 0 4 |a immunomodulation 
650 0 4 |a male 
650 0 4 |a Male 
650 0 4 |a maternal behavior 
650 0 4 |a maternal disease 
650 0 4 |a maturity 
650 0 4 |a Mice 
650 0 4 |a Mice, Inbred C57BL 
650 0 4 |a mouse 
650 0 4 |a nonhuman 
650 0 4 |a Poly I-C 
650 0 4 |a polyinosinic polycytidylic acid 
650 0 4 |a polyinosinic polycytidylic acid 
650 0 4 |a polyinosinic-polycytidylic acid 
650 0 4 |a pregnancy 
650 0 4 |a Pregnancy 
650 0 4 |a prepulse inhibition 
650 0 4 |a prepulse inhibition 
650 0 4 |a Prepulse Inhibition 
650 0 4 |a progeny 
650 0 4 |a Reflex, Startle 
650 0 4 |a schizophrenia 
650 0 4 |a schizophrenia 
650 0 4 |a startle reflex 
650 0 4 |a startle reflex 
650 0 4 |a startle response 
650 0 4 |a tail vein 
700 1 |a Inaba, H.  |e author 
700 1 |a Iwakura, Y.  |e author 
700 1 |a Iwamoto, K.  |e author 
700 1 |a Kobayashi, Y.  |e author 
700 1 |a Murata, Y.  |e author 
700 1 |a Namba, H.  |e author 
700 1 |a Nawa, H.  |e author 
700 1 |a Sotoyama, H.  |e author 
773 |t Neuropsychopharmacology Reports