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Poster Presentations<br />

[PP-033] Ref. No: 192<br />

Gender specific metabolic adverse effects in bipolar patients: A comparison<br />

between lithium, quetiapine and olanzapine<br />

Sermin Kesebir, Burak Baykaran, Burak Toprak, Ahmet Ertan Tezcan<br />

Erenkoy TEHMND, Istanbul, Turkey<br />

E-mail: serminkesebir@hotmail.com<br />

Objective: There is some evidence showing gender based differences in the side effects of atypical antipsychotic drugs. The aim of this<br />

study was to determine the differences between lithium, quetiapine and olanzapine with regard to their effects on metabolic variables in<br />

bipolar disorder and to assess the findings in terms of gender differences.<br />

Method: Twenty-eight female and 29 male cases diagnosed with bipolar disorder type I according to the DSM-IV, taking lithium or<br />

quetiapine or quetiapine+lithium or olanzapine or olanzapine+lithium, were evaluated consecutively. For evaluation, being in a remission<br />

period was set as a criterion for these cases. Patient interviews were carried out with SCID-I and SKIP-TURK. Blood samples were taken from<br />

the patients in order to determine PRL, blood lipids and HbA1c levels.<br />

Results: Mean age, mean age of onset, number of manic, depressive, and total episodes, functionality, and PRL levels were similar between<br />

female and male patients. BMI, HbA1c, cholesterol, triglycerides, LDL and HDL levels are found to be similar between the two groups. Both<br />

in female and male patients, no difference was found between the lithium, quetiapine and quetiapine+lithium and the olanzapine and<br />

olanzapine+lithium groups in terms of BMI, HbA1c, cholesterol, triglyceride, LDL and HDL levels. The only difference (although not significant)<br />

among the three groups was the level of cholesterol in women treated with lithium, which was found to be lower than in the other two groups.<br />

Conclusions: This insignificant difference was found while the clinical properties and PRL levels were similar among the lithium,<br />

quetiapine and quetiapine+lithium and the olanzapine and olanzapine+lithium groups. Future studies with a specific focus on this topic<br />

are needed in order to have a better understanding of the basic mechanisms of gender differences.<br />

Key words: Gender, metabolic side effect, psychotropics, bipolar disorder<br />

Bulletin of Clinical Psychopharmacology 2011;21(Suppl. 2):S140<br />

[PP-034] Ref. No: 161<br />

New model of psychogenic stress-induced depression and antioxidant system of rat brain<br />

Konstantin Chichinadze 1 , Tamar Domianidze 1 , Tamar Matitaishvili 1 , Ia Labadze 1 , Ann Lazarashvili 2 , Mikhail Khananashvili 1<br />

1Laboratory of Behavior and Cognitive Functions, Life Sciences Research Center, Tbilisi, Georgia<br />

2Department of Pathology, Tbilisi State University, Tbilisi, Georgia<br />

E-mail: k.chichinadze@lifescience.org.ge<br />

The present article describes results of investigation of lipid peroxidation and antioxidant enzyme activity in the brain cells of laboratory<br />

rats, that were subjected to a depression-like state. The above-mentioned state was achieved by means of a new model of depression<br />

elaborated by us. The model is based on the application of stressors of psychogenic nature.<br />

Our investigations demonstrated that in the depression-like state activity of lipid peroxidation processes increase, which was confirmed<br />

by increase of concentration of its end product – malondialdehyde, both in mitochondrial and cytosolic fractions of brain cells. In<br />

response to oxidative stress in mitochondria, activity of antioxidant system –namely the leading intracellular antioxidant superoxide<br />

dismutase (SOD) – increased. On the other hand, concentration of another important antioxidant –catalase– decreased. Most probably,<br />

the depletion of antioxidative potential of the cell, related to depression, proceeds at various speeds in various enzymatic systems.<br />

Administration of the antidepressant drug –fluoxetine– led to the normalization of intensity of lipid peroxidation and overall activity of<br />

antioxidative systems. Thus, if activity of these processes increases, antidepressants cause their down-regulation and in they decrease<br />

–antidepressants lead to their up-regulation. As a final result, this leads to normalization of cell functioning.<br />

Key words: Animal model of depression, lipid peroxidation, antidepressants<br />

Bulletin of Clinical Psychopharmacology 2011;21(Suppl. 2):S140<br />

S140 Bulletin of Clinical Psychopharmacology, Vol: 21, Supplement: 2, 2011 - www.psikofarmakoloji.org

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