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P03-140 - Neurotransmitters Blood Level, ASR Prepulse Modification and Antisaccades Deficits in Schizophrenia: Implication for Identification of Schizophrenia Endophenotypes

Published online by Cambridge University Press:  17 April 2020

Z. Storozheva
Affiliation:
Laboratory of Clinical Neurophysiology, Serbsky National Research Centre for Social and Forensic Psychiatry, Moscow, Russia Laboratory of Functional Neurochemistry, P.K.Anokhin Institute of Normal Physiology RAMS, Moscow, Russia
A. Kirenskaya
Affiliation:
Laboratory of Clinical Neurophysiology, Serbsky National Research Centre for Social and Forensic Psychiatry, Moscow, Russia
K. Bogdanov
Affiliation:
Laboratory of Clinical Neurophysiology, Serbsky National Research Centre for Social and Forensic Psychiatry, Moscow, Russia
V. Novototsky-Vlasov
Affiliation:
Laboratory of Clinical Neurophysiology, Serbsky National Research Centre for Social and Forensic Psychiatry, Moscow, Russia
D. Samylkin
Affiliation:
Department of Endogenous Psychosis, Serbsky National Research Centre for Social and Forensic Psychiatry, Moscow, Russia

Abstract

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Objectives

Study of psychophysiological candidate schizophrenia endophenotypes in relation with neurotransmitters blood level and mental disorders.

Methods

23 patients with schizophrenia and 24 healthy subjects performed horizontal antisaccades. Acoustic startle response (ASR) prepulse modification was studied according to protocol, recommended by Consortium on the genetics of schizophrenia. Neurotransmitters blood plasma level was estimated using HPLC.

Results

Significant increase of errors and saccade latencies was revealed in patients compared to controls. ASR prepulse inhibition (PPI) at 60 ms lead interval and ASR prepulse facilitation (PPF) at 2500 ms lead interval were impaired in patients. Analysis didn’t reveal any correlations between ASR and antisaccades measures in patients while in healthy controls high initial ASR amplitude correlated with incorrect antisaccades number and PPF level correlated with antisaccades latencies. Significantly higher individual variability of plasma serotonin, glutamate and taurine content was found in patients compared to controls. Positive correlations of PPI with glutamate and taurine content were observed in patients but not in controls. At the same time, correlation between PPI and serotonine turnover ratio was positive in control group and negative in patients. Antisaccade latencies in controls displayed negative correlation with DOPAC and taurine level while in patients they positively correlated with dopamine and negatively with serotonine turnover ratio. It was also found that antisaccades parameters and ASR measures displayed correlations with different PANSS scales.

Conclusion

These data support the hypothesis that PPI and antisaccades are associated with different neural networks and have different genetic aetiology.

Type
Psychotic disorders / Schizophrenia
Copyright
Copyright © European Psychiatric Association 2010
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