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Published on: March 25, 2016
Therapeutic Targets for Neurodevelopmental Disorders Emerging from Animal Models with Perinatal Immune Activation
Daisuke Ibi1,2, Kiyofumi Yamada3
1Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Meijo University, 150 Yagotoyama, Tenpaku-ku, Nagoya 468-8503, Japan. ibid@meijo-u.ac.jp.
Insights
Perinatal viral infections increase psychiatric disorder risk. Researchers are exploring molecules involved in astrocyte-neuron and gut microbiome interactions as potential therapeutic targets for brain dysfunction.
Area of Science:
- Neuroscience
- Immunology
- Psychiatry
Background:
- Epidemiological studies link perinatal viral infections to increased psychiatric disorder risk.
- Astrocyte-neuron and gut microbiome interactions are implicated in neurodevelopmental disorders following immune insults.
- Maternal immune activation and polyriboinosinic polyribocytidylic acid models identify molecules involved in brain dysfunction.
Purpose of the Study:
- To review the functions of candidate molecules in neurodevelopment and brain function.
- To discuss the potential of these molecules as therapeutic targets for psychiatric disorders.
Main Methods:
- Literature review of studies on perinatal infections, neurodevelopmental disorders, and candidate molecules.
- Analysis of the role of astrocytes, neurons, and gut microbiomes in disease pathogenesis.
- Examination of molecular mechanisms underlying brain dysfunction.
Main Results:
- Several candidate molecules have been identified in neurodevelopmental disorder models.
- These molecules play roles in neurodevelopment and overall brain function.
- Astrocyte-neuron and gut microbiome interactions are crucial pathways.
Conclusions:
- Understanding candidate molecules offers insights into psychiatric disorder development.
- Targeting specific molecules may provide novel therapeutic strategies for psychiatric disorders.
- Further research is needed to validate therapeutic potential.
Abstract:
Increasing epidemiological evidence indicates that perinatal infection with various viral pathogens enhances the risk for several psychiatric disorders. The pathophysiological significance of astrocyte interactions with neurons and/or gut microbiomes has been reported in neurodevelopmental disorders triggered by pre- and postnatal immune insults. Recent studies with the maternal immune activation or neonatal polyriboinosinic polyribocytidylic acid models of neurodevelopmental disorders have identified various candidate molecules that could be responsible for brain dysfunction. Here, we review the functions of several candidate molecules in neurodevelopment and brain function and discuss their potential as therapeutic targets for psychiatric disorders.
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