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Preparation of Acute Hippocampal Slices from Rats and Transgenic Mice for the Study of Synaptic Alterations during Aging and Amyloid Pathology
Published on: March 23, 2011
Projection-specific deficits in synaptic transmission in adult Sapap3-knockout mice
Lotfi C Hadjas1, Michael M Schartner1, Jennifer Cand1
1Department of Basic Neurosciences, University of Geneva, Rue Michel-Servet 1, 1206, Geneva, Switzerland.
Abstract:
Obsessive-compulsive disorder (OCD) is a circuit disorder involving corticostriatal projections, which play a role in motor control. The Sapap3-knockout (KO) mouse is a mouse model to study OCD and recapitulates OCD-like compulsion through excessive grooming behavior, with skin lesions appearing at advanced age. Deficits in corticostriatal control provide a link to the pathophysiology of OCD. However, there remain significant gaps in the characterization of the Sapap3-KO mouse, with respect to age, specificity of synaptic dysfunction, and locomotor phenotype. We therefore investigated the corticostriatal synaptic phenotype of Sapap3-KO mice using patch-clamp slice electrophysiology, in adult mice and with projection specificity. We also analyzed grooming across age and locomotor phenotype with a novel, unsupervised machine learning technique (MoSeq). Increased grooming in Sapap3-KO mice without skin lesions was age independent. Synaptic deficits persisted in adulthood and involved the projections from the motor cortices and cingulate cortex to the dorsolateral and dorsomedial striatum. Decreased synaptic strength was evident at the input from the primary motor cortex by reduction in AMPA receptor function. Hypolocomotion, i.e., slowness of movement, was consistently observed in Sapap3-KO mice. Our findings emphasize the utility of young adult Sapap3-KO mice to investigate corticostriatal synaptic dysfunction in motor control.
Insights
Sapap3-knockout mice exhibit persistent corticostriatal synaptic deficits and age-independent excessive grooming, offering a valuable model for studying obsessive-compulsive disorder (OCD) and motor control.
Area of Science:
- Neuroscience
- Genetics
- Behavioral Science
Background:
- Obsessive-compulsive disorder (OCD) is linked to corticostriatal circuit dysfunction.
- The Sapap3-knockout (KO) mouse model displays OCD-like excessive grooming but requires further characterization regarding synaptic deficits and motor phenotype.
Purpose of the Study:
- To investigate the age-independent corticostriatal synaptic phenotype and locomotor behavior in Sapap3-KO mice.
- To clarify the specificity of synaptic dysfunction in Sapap3-KO mice relevant to OCD pathophysiology.
Main Methods:
- Patch-clamp slice electrophysiology was used to assess synaptic function in adult Sapap3-KO mice.
- Grooming behavior and locomotor activity were analyzed across ages using unsupervised machine learning (MoSeq).
Main Results:
- Sapap3-KO mice showed age-independent excessive grooming without skin lesions.
- Synaptic deficits were observed in corticostriatal projections, specifically a reduction in AMPA receptor function from the primary motor cortex.
- Sapap3-KO mice exhibited hypolocomotion (slowness of movement).
Conclusions:
- Young adult Sapap3-KO mice are a suitable model for studying corticostriatal synaptic dysfunction in motor control relevant to OCD.
- The findings highlight specific synaptic deficits in motor and cingulate cortex projections to the striatum in this OCD mouse model.

