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Altered inflammatory responsiveness in serotonin transporter mutant rats
Flavia Macchi1, Judith R Homberg, Francesca Calabrese
1Dipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, Milan, Italy. raffaella.molteni@unimi.it.
Journal of Neuroinflammation
|September 21, 2013
Summary
Altered serotonin transporter (SERT) gene expression in rats is linked to immune system changes and increased susceptibility to depression-like behaviors. These findings suggest a role for inflammation in depression pathogenesis.
Area of Science:
- Neuroscience
- Immunology
- Genetics
Background:
- Depression is increasingly linked to inflammatory and immune system dysregulation.
- Depressed individuals show elevated inflammatory markers and high comorbidity with inflammatory diseases.
- Investigating genetic models of depression vulnerability is crucial for understanding this link.
Purpose of the Study:
- To examine the inflammatory system in rats with serotonin transporter (SERT) gene deletion, a model for depression vulnerability.
- To characterize basal and LPS-induced inflammatory responses in SERT mutant rats.
Main Methods:
- Analysis of wild-type, heterozygous, and homozygous SERT rats.
- Assessment under basal conditions and after lipopolysaccharide (LPS) challenge.
- Measurement of cytokine expression and microglia activation markers in the hippocampus.
Main Results:
- SERT mutant rats exhibited altered basal cytokine expression in the hippocampus.
- Mutant rats showed an exacerbated cytokine response to LPS challenge.
- Differences in microglia activation markers were observed in SERT mutant rats.
Conclusions:
- Basal or functional alterations in immune/inflammatory systems may contribute to the SERT rat phenotype.
- These immune alterations could underlie the heightened susceptibility to depressive-like behavior in SERT rats.
- The study highlights a potential neuro-immune mechanism in depression.