| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6265744 | Brain Research | 2008 | 9 Pages |
The cellular prion protein (PrPC) has been implicated with the modulation of neuronal apoptosis, adhesion, neurite outgrowth and maintenance which are processes involved in the neocortical development. Malformations of cortical development (MCD) are frequently associated with neurological conditions including mental retardation, autism, and epilepsy. Here we investigated the behavioral performance of female adult PrPC-null mice (Prnp0/0) and their wild-type controls (Prnp+/+) presenting unilateral polymicrogyria, a MCD experimentally induced by neonatal freeze-lesion in the right hemisphere. Injured mice from both genotypes presented similar locomotor activity but Prnp0/0 mice showed a tendency to increase anxiety-related responses when compared to Prnp+/+ animals. Additionally, injured Prnp0/0 mice have a poorer performance in the social recognition task than sham-operated and Prnp+/+ injured ones. Moreover the step-down inhibitory avoidance task was not affected by the procedure or the genotype of the animals. These data suggest that the genetic deletion of PrPC confers increased susceptibility to short-term social memory deficits induced by neonatal freezing model of polymicrogyria in mice.
