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Neurotoxic lesions of serotonin cells in the dorsal raphe reduce compulsive-like nest building in mice

Greene DM, Castillo MR, Alexander KA, McMahan A, Raap DK, Bult-Ito A (2005) Neurotoxic lesions of serotonin cells in the dorsal raphe reduce compulsive-like nest building in mice. Neuroscience 2005 Abstracts 796.10. Society for Neuroscience, Washington, DC.

Summary: Bi-directional selection for thermoregulatory nest-building behavior in house mice (Mus musculus) has resulted in a 40-fold difference in the amount of cotton used for nest-building between the high and the low selected lines (big and small nest-builders, respectively). The efficacy of serotonin re-uptake inhibitors (SSRIs), especially fluoxetine, for the treatment of obsessive-compulsive disorder (OCD) indicates a serotonergic involvement in the disorder. The repetitive nest-building behavior, characteristic of the big nest-builders, is a compulsive-like behavior that is responsive to SSRI treatment. We investigated the functional involvement of serotonergic pathways in excessive, repetitive nest-building behavior in mice by lesioning serotonergic cells in the dorsal raphe using the neurotoxin 5,7-dihydroxytryptamine (5,7-DHT) or SERT-saporin (Advanced Targeting Systems). 5,7-DHT lesioned mice had a significant decrease in the number of serotonin-stained cells in the dorsal raphe. No decrease was noted in serotonin staining after lesions performed with the SERT-saporin neurotoxin. Mice with successful 5,7-DHT lesions also significantly decreased compulsive-like nest-building as compared to sham and non-surgery controls. These data taken together with additional findings in these mice support the involvement of serotonin pathways in OCD. This data further supports the big nest-builders as a potentially valuable animal model of compulsive behaviors in humans and a means to more clearly identify neurobiological pathways involved in OCD.

Related Products: Anti-SERT-SAP (Cat. #IT-23)

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