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Published on: March 25, 2016
Neonatal Immune Activation May Provoke Long-term Depressive Attributes
Simone H Schelder-Marzzani1, Paula Dias1, Viviane Freiberger1
1Research Group in Neurodevelopment of Childhood and Adolescence, Laboratory of Experimental Neuroscience, Postgraduate Program in Health Sciences, University of South Santa Catarina, Avenida Pedra Branca, 25, Pedra Branca, 88137-270 Palhoca, SC, Brazil.
Neonatal immune activation, triggered by endotoxemia, is linked to adult depression-like behaviors. Early life inflammation may increase vulnerability to developing psychiatric disorders later in life.
Area of Science:
- Neuroscience
- Immunology
- Psychiatry
Background:
- Neuroinflammation is linked to depressive symptoms.
- Limited research exists on neonatal neuroinflammation and adult psychiatric disorders.
Purpose of the Study:
- To investigate the association between neonatal immune activation and adult depressive-like behaviors using an animal model.
Main Methods:
- Neonatal C57BL/6 mice were exposed to lipopolysaccharides (LPS) or saline.
- Adult behavioral and physiological parameters, including sucrose preference, immobility, adrenal gland and hippocampus weight, plasma corticosterone, and hippocampal BDNF, were assessed.
- Imipramine treatment was administered to assess its effects.
Main Results:
- Neonatal LPS exposure led to decreased sucrose consumption, reduced hippocampus weight, increased immobility time, elevated adrenal gland weight, and higher plasma corticosterone levels in adulthood.
- Imipramine partially reversed the hippocampal weight reduction but did not affect BDNF levels.
- Hippocampal Brain-Derived Neurotrophic Factor (BDNF) levels remained unchanged.
Conclusions:
- Neonatal immune activation is associated with adult depressive-like parameters.
- Endotoxemia in early life may predispose individuals to depression by inducing physiological and behavioral changes.
- This study highlights a potential mechanism linking early-life inflammation to adult psychiatric vulnerability.
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