Key result
Imbalance of several PI3K elements is a leading cause of Autism and Schizophrenia, highlighting the PI3K signaling pathway as a plausible new pharmacological target.
The PI3K signaling pathway is implicated in synaptic dysfunction underlying Autism and Schizophrenia, presenting a potential pharmacological target.
No change to autism or schizophrenia management; leaves open PI3K pathway as hypothesis-generating research target.
This review is focused in PI3K’s involvement in two widespread mental disorders: Autism and Schizophrenia. A largebody of evidence points to synaptic dysfunction as a cause of these diseases, either during the initial phases ofbrain synaptic circuit’s development or later modulating synaptic function and plasticity. Autism related disordersand Schizophrenia are complex genetic conditions in which the identification of gene markers has proved difficult,although the existence of single-gene mutations with a high prevalence in both diseases offers insight into the roleof the PI3K signaling pathway. In the brain, components of the PI3K pathway regulate synaptic formation and plasticity;thus, disruption of this pathway leads to synapse dysfunction and pathological behaviors. Here, we recapitulate recentevidences that demonstrate the imbalance of several PI3K elements as leading causes of Autism and Schizophrenia,together with the plausible new pharmacological paths targeting this signaling pathway.
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Enriquez-barreto et al. (2016) conducted a review in Autism related disorders and Schizophrenia. PI3K signaling pathway targeted therapies was evaluated. Imbalance of several PI3K elements is a leading cause of Autism and Schizophrenia, highlighting the PI3K signaling pathway as a plausible new pharmacological target.
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