PMID- 28417199 OWN - NLM STAT- MEDLINE DCOM- 20180130 LR - 20191210 IS - 1433-8491 (Electronic) IS - 0940-1334 (Linking) VI - 267 IP - 5 DP - 2017 Aug TI - Intake of 7,8-dihydroxyflavone from pregnancy to weaning prevents cognitive deficits in adult offspring after maternal immune activation. PG - 479-483 LID - 10.1007/s00406-017-0802-1 [doi] AB - Brain-derived neurotrophic factor (BDNF) and its high-affinity receptor, tropomyosin receptor kinase B (TrkB) signaling plays a key role in the brain neurodevelopment. The exposure of pregnant mice to polyinosinic-polycytidylic acid [poly(I:C)] causes cognitive deficits in adult offspring. Supplementation with a TrkB agonist, 7,8-dihydroxyflavone, in poly(I:C)-treated pregnant mice from pregnancy to weaning could prevent the onset of cognitive deficits and reduced BDNF-TrkB signaling in the prefrontal cortex of their adult offspring. These findings suggest that supplementation with a TrkB agonist in pregnant women with an ultra-high risk of psychosis may reduce the development of psychosis in their offspring. FAU - Han, Mei AU - Han M AD - Division of Clinical Neuroscience, Chiba University Center for Forensic Mental Health, Chiba, 260-8670, Japan. AD - School of Medicine, Illawarra Health and Medical Research Institute (IHMRI), University of Wollongong, Wollongong, NSW, 2522, Australia. FAU - Zhang, Ji-Chun AU - Zhang JC AD - Division of Clinical Neuroscience, Chiba University Center for Forensic Mental Health, Chiba, 260-8670, Japan. FAU - Huang, Xu-Feng AU - Huang XF AD - School of Medicine, Illawarra Health and Medical Research Institute (IHMRI), University of Wollongong, Wollongong, NSW, 2522, Australia. FAU - Hashimoto, Kenji AU - Hashimoto K AD - Division of Clinical Neuroscience, Chiba University Center for Forensic Mental Health, Chiba, 260-8670, Japan. hashimoto@faculty.chiba-u.jp. LA - eng PT - Journal Article DEP - 20170417 PL - Germany TA - Eur Arch Psychiatry Clin Neurosci JT - European archives of psychiatry and clinical neuroscience JID - 9103030 RN - 0 (6,7-dihydroxyflavone) RN - 0 (Brain-Derived Neurotrophic Factor) RN - 0 (Flavones) RN - 0 (Interferon Inducers) RN - EC 2.7.10.1 (Receptor, trkB) RN - O84C90HH2L (Poly I-C) SB - IM MH - Analysis of Variance MH - Animals MH - Brain/drug effects/metabolism MH - Brain-Derived Neurotrophic Factor/metabolism MH - Cognition Disorders/*etiology/pathology/*prevention & control MH - Disease Models, Animal MH - Drug Administration Schedule MH - Female MH - Flavones/*administration & dosage MH - Interferon Inducers/toxicity MH - Locomotion/drug effects MH - Male MH - Mice MH - Poly I-C/toxicity MH - Pregnancy MH - Prenatal Exposure Delayed Effects/chemically induced/drug therapy/*physiopathology MH - Receptor, trkB/metabolism MH - Recognition, Psychology/drug effects MH - Signal Transduction/drug effects OTO - NOTNLM OT - BDNF-TrkB signaling OT - Cognitive deficits OT - Prevention OT - Psychosis EDAT- 2017/04/19 06:00 MHDA- 2018/01/31 06:00 CRDT- 2017/04/19 06:00 PHST- 2017/03/09 00:00 [received] PHST- 2017/04/11 00:00 [accepted] PHST- 2017/04/19 06:00 [pubmed] PHST- 2018/01/31 06:00 [medline] PHST- 2017/04/19 06:00 [entrez] AID - 10.1007/s00406-017-0802-1 [pii] AID - 10.1007/s00406-017-0802-1 [doi] PST - ppublish SO - Eur Arch Psychiatry Clin Neurosci. 2017 Aug;267(5):479-483. doi: 10.1007/s00406-017-0802-1. Epub 2017 Apr 17.