Cognitive deficits in Tsc1+/- mice in the absence of cerebral lesions and seizures
Annals of Neurology , Volume 62 - Issue 6 p. 648- 655
Objective: Tuberous sclerosis complex (TSC) is characterized by brain lesions, epilepsy, increased incidence of mental retardation and autism. The causal link between lesion load and epilepsy on cognitive disabilities has been debated, and these factors explain only part of the intelligence quotient variability. A Tsc2 rat model of the disease provided evidence that the TSC genes are directly involved in neuronal function. However, these lesion- and epilepsy-free animals did not show learning deficits, leaving open the possibility that the presence of brain lesions or epilepsy is a prerequisite for the cognitive deficits to fully develop. Here, we reinvestigated the relation among cerebral lesions, epilepsy, and cognitive function using Tsc1+/-mice. Methods: We used immunocytochemistry and high-resolution magnetic resonance imaging to study the presence of neuronal pathology in Tsc+/-mice. We used the Morris water maze, fear conditioning, social interaction, and nest building test to study the presence of cognitive and social deficits. Results: We observed no spontaneous seizures or cerebral lesions in the brains of Tsc1+/-mice. In addition, giant dysmorphic cells were absent, and spine number and dendritic branching appeared to be normal. Nevertheless, Tscl+/-mice showed impaired learning in the hippocampus-sensitive versions of the learning tasks and impaired social behavior. Interpretation: Tsc+/-mice show social and cognitive deficits in the absence of apparent cerebral pathology and spontaneous seizures. These findings support a model in which haploinsufficiency for the TSC genes leads to aberrations in neuronal functioning resulting in impaired learning and social behavior.
|Annals of Neurology
|Erasmus MC: University Medical Center Rotterdam
Goorden, S., van Woerden, G., van der Weerd, L., Cheadle, J., & Elgersma, Y. (2007). Cognitive deficits in Tsc1+/- mice in the absence of cerebral lesions and seizures. Annals of Neurology, 62(6), 648–655. doi:10.1002/ana.21317