Abstract
Glycogen synthase kinase-3B (GSK-3B) is involved with important neuronal processes such as cell survival, gene regulation, mood and cognitive performance. This enzyme is inactivated by phosphorylation at the phospho-Ser9 site. We compared GSK-3B levels in patients with schizophrenia to a health control group. The levels of phosphorylated and total GSK-3B in platelets of ten drug-free patients, ten long-term olanzapine treated patients and 20 healthy controls were determined by means of an enzyme immunoassay kit. In drug-free patients, GSK-3B levels were accessed again after 8 weeks on treatment with olanzapine. At baseline, drug-free patients presented lower phosphorylated and total GSK-3B levels than healthy controls (p < 0.05). After 8 weeks on olanzapine treatment, phosphorylated and total GSK-3B levels were significantly increased (p < 0.01). Reduced phospho-Ser9-GSK-3B in schizophrenia may disrupt signal-transduction pathways and influence crucial cellular processes, such as transcription, apoptosis, stress response and cell proliferation. Further studies should clarify whether the increment of GSK-3B phosphorylation by olanzapine is related to its antipsychotic effects.
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Acknowledgments
This study was supported by the Fundação de Apoio à Pesquisa do Estado de Sao Paulo (FAPESP: process number 2009/05606-6). ASF received a scholarship from Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES). The Laboratory of Neuroscience receives financial support by Associação Beneficente Alzira Denise Hertzog da Silva (ABADHS).
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Ferreira, A.S., Raposo, N.R.B., Sallet, P.C. et al. Lower phosphorylated glycogen synthase kinase-3B levels in platelets of patients with schizophrenia: increment by olanzapine treatment. Eur Arch Psychiatry Clin Neurosci 265, 167–170 (2015). https://doi.org/10.1007/s00406-014-0505-9
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DOI: https://doi.org/10.1007/s00406-014-0505-9