Literature DB >> 12415549

Chronic treatment with both lithium and sodium valproate may normalize phosphoinositol cycle activity in bipolar patients.

Peter H Silverstone1, Ren H Wu, Tina O'Donnell, Michele Ulrich, Sheila J Asghar, Christopher C Hanstock.   

Abstract

BACKGROUND: It has been proposed that lithium may be clinically effective due to its actions on the phosphoinositol second messenger system (PI-cycle). Studies have also suggested that untreated manic patients may have raised myo-inositol and phosphomonoester (PME) concentrations and also that unmedicated euthymic bipolar patients may have lowered PME concentrations. The objective of the present study was to test the hypothesis that chronic treatment with either lithium or sodium valproate in patients with bipolar mood disorder leads to a normalization in the activity of the PI-cycle.
METHODS: This study had two parts each with different MRS methodology. The first part compared healthy controls (n = 19) with euthymic bipolar patients who were taking either lithium (n = 16) or sodium valproate (n = 11) using both (1)H-MRS and (31)P-MRS. In the second part we examined a separate group of euthymic bipolar disorder patients taking sodium valproate (n = 9) and compared these with age and sex-matched healthy controls (n = 11) using (1)H-MRS.
RESULTS: Both studies showed that there were no differences in either myo-inositol or phosphomonoester (PME) concentrations between controls and patients taking either medication.
CONCLUSIONS: These findings examine two key components of the PI-cycle in treated euthymic bipolar (myo-inositol and PME concentrations). The results from this study are consistent with the suggestion that chronic treatment with either lithium or sodium valproate in bipolar patients may normalize PI-cycle functioning. Copyright 2002 John Wiley & Sons, Ltd.

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Year:  2002        PMID: 12415549     DOI: 10.1002/hup.420

Source DB:  PubMed          Journal:  Hum Psychopharmacol        ISSN: 0885-6222            Impact factor:   1.672


  14 in total

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3.  Risperidone and divalproex differentially engage the fronto-striato-temporal circuitry in pediatric mania: a pharmacological functional magnetic resonance imaging study.

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4.  Neurochemical deficits in the cerebellar vermis in child offspring of parents with bipolar disorder.

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5.  Lithium treatment effects on Myo-inositol in adolescents with bipolar depression.

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Review 9.  Pharmacological treatment of bipolar disorder among children and adolescents.

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Review 10.  Neurochemical predictors of response to pharmacologic treatments for bipolar disorder.

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