4.5 Article

Spinophilin expression in postmortem prefrontal cortex of schizophrenic subjects: Effects of antipsychotic treatment

Journal

EUROPEAN NEUROPSYCHOPHARMACOLOGY
Volume 42, Issue -, Pages 12-21

Publisher

ELSEVIER
DOI: 10.1016/j.euroneuro.2020.11.011

Keywords

Spinophilin; Schizophrenia; Antipsychotics; Prefrontal cortex; Human brain; Postmortem

Funding

  1. Spanish MINECO [SAF2013-48586-R, RTI2018-094414-A-I00]
  2. Basque Government [IT1211/19]

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Schizophrenia is associated with alterations in neurotransmission and synaptic dysfunction, with spinophilin protein expression showing a significant decrease in individuals with schizophrenia compared to controls. The study suggests that antipsychotic medications may produce alterations in spinophilin expression, potentially underlying some side effects of antipsychotics.
Schizophrenia has been associated with alterations in neurotransmission and synaptic dysfunction. Spinophilin is a multifunctional scaffold protein that modulates excitatory synaptic transmission and dendritic spine morphology. Spinophilin can also directly interact with and regulate several receptors for neurotransmitters, such as dopamine D-2 receptors, which play a role in the pathophysiology of schizophrenia and are targets of antipsychotics. Several studies have thus suggested an implication of spinophilin in schizophrenia. In the present study spinophilin protein expression was determined by western blot in the postmortem dorsolateral prefrontal cortex of 24 subjects with schizophrenia (12 antipsychotic-free and 12 antipsychotic-treated subjects) and 24 matched controls. Experiments were performed in synaptosomal membranes (SPM) and in postsynaptic density fractions (PSD). As previously reported, two specific bands for this protein were observed: an upper 120-130 kDa band and a lower 80-95 kDa band. The spinophilin lower band showed a significant decrease in schizophrenia subjects compared to matched controls, both in SPM and PSD fractions (-15%, p = 0.007 and-15%, p = 0.039, respectively). When schizophrenia subjects were divided by the presence or absence of antipsychotics in blood at death, the lower band showed a significant decrease in antipsychotictreated schizophrenia subjects (-24%, p = 0.003 for SPM and-26%, p = 0.014 for PSD), but not in antipsychotic-free subjects, compared to their matched controls. These results suggest that antipsychotics could produce alterations in spinophilin expression that do not seem to be related to schizophrenia per se. These changes may underlie some of the side effects of antipsychotics. (c) 2020 Elsevier B.V. and ECNP. All rights reserved.

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