Cannabidiol effects in predictive models for antipsychotic action
| Grant number: | 15/06515-8 |
| Support type: | Scholarships in Brazil - Doctorate |
| Effective date (Start): | August 01, 2015 |
| Effective date (End): | July 31, 2018 |
| Field of knowledge: | Biological Sciences - Pharmacology |
| Cooperation agreement: | Coordination of Improvement of Higher Education Personnel (CAPES) |
| Principal Investigator: | Elaine Aparecida Del Bel Belluz Guimarães |
| Grantee: | João Francisco Cordeiro Pedrazzi |
| Home Institution: | Faculdade de Odontologia de Ribeirão Preto (FORP). Universidade de São Paulo (USP). Ribeirão Preto , SP, Brazil |
Abstract Schizophrenia is a highly disabling disorder that affects about 1% of the population, involving imbalance of dopaminergic neurotransmission and a glutamatergic hypofunction. Patients with this disease have a deficiency of sensory-motor gating, characterized by disruption in prepulse inhibition test (PPI). This condition can be reproduced in experimental models, by treatment with psychostimulants such as amphetamine and attenuated / reversed by treatment with antipsychotics. Cannabidiol (CBD) a component of Cannabis sativa is devoid of psychotomimetic properties. Clinical and pre-clinical studies suggest that CBD has an antipsychotic profile, yet its mechanism of action has been little investigated to date. Recently, epigenetic mechanisms such as DNA methylation, have been linked to the schizophrenia pathophysiology. However, there is no investigation of the involvement of DNA methylation regulated by CBD on the behavioral responses induced by amphetamine. The aim of this study is to investigate the mechanisms of action of CBD in predictive models for antipsychotic action. Therefore, we will investigate: (I) the involvement of TRPV1 receptors, serotonin (5-HT1A) receptors and increased anandamide signaling in the PPI test and locomotor activity. (II) the participation of the prefrontal cortex as a possible neural substrates for the CBD antipsychotic profile on PPI test. (III) the global DNA methylation in brain structures (prefrontal cortex, hippocampus, striatum and ventral) after acute treatment with amphetamine. If changes will found we will investigate if pretreatment with clozapine or CBD modifies that condition. (AU) | |