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Page Background European Psychiatry 41S (2017) S365–S404

Available online at

ScienceDirect

www.sciencedirect.com

25th European congress of psychiatry

e-Poster walk part 5

e-Poster Walk: Psychopharmacology and

pharmacoeconomics and

psychoneuroimmunology

EW0752

Selective serotonine reuptake

inhibitors or dual antidepressants and

syndrome of inapropriate antidiuretic

hormone secretion: A systematic

search

I. Alberdi-Paramo

1 ,

, G .

Montero

1 , L. N

iell

1 , R. B

aena

1 ,

M. Tenorio

1 , A.

Carabias

1 , D.

Fuentes

1 , A. J

urado

1 , C. P

erez

1 ,

R. Carrillo

2 , A. F

raga

3 , M.

Fernandez De Aspe

4 , M.

Soto

5 ,

B. Gonzalez

6

1

Hospital Clinico San Carlos, Psiquiatria, Madrid, Spain

2

Complejo Hospitalario Insular Materno Infantil, Psiquiatria, Las

Palmas de Gran Canarias, Spain

3

Hospital Universitario La Paz, Psiquiatria, Madrid, Spain

4

Complexo Hospitalario de Ourense, Psiquiatria, Ourense, Spain

5

Hospital provincial de la misericordia, Psiquiatria, Toledo, Spain

6

Hospital Universitario de Alava, Psiquiatria, Vitoria-Gazteiz, Spain

Corresponding author.

Introduction

Depression is a diseasewith high prevalence all over

theworld. Selective serotonine reuptake inhibitors (SSRIs) and dual

antidepressants (DA) are worldwide used to treat the different

types of depressive episodes. Between the adverse events of these

compounds, an unusual but potentially severe side effect is the

syndrome of inapropriate antidiuretic hormone secretion (SIADH).

Results and discussion

Several cases published, and an amount of

cases series have documented the association of SIADH to the use

of SSRIs and DA. All SSRIs and DA are at risk of producing SIADH

(fluoxetine, paroxetine, fluvoxamine, sertraline, citalopram, esci-

talopram, venlafaxine and duloxetine). Old age has been found as a

risk factor for developing SIADH. There are not enough data to con-

clude that other risk factors can play a role in the development

of this adverse event. Treatment should include the immediate

withdrawal of the antidepressant. The introduction of other antide-

pressants is controversial, as SIADH has been related with all

antidepressive treatments; but the risk of relapse into a depressive

episode must be considered also. Between symptomatic treat-

ments, the control of water intake and the use of low doses of loop

diuretics can be recommended. Severe cases can be treated with

higher doses of loop diuretics and saline hypertonic solution.

Conclusions

SIADH has been related with SSRIs and DA antide-

pressants and it is an infrequent but severe adverse event. Its risk

must be considered when prescribing treatment with them. If this

adverse event is produced, the substitution of the antidepressant

should be done.

Disclosure of interest

The authors have not supplied their decla-

ration of competing interest.

http://dx.doi.org/10.1016/j.eurpsy.2017.02.366

EW0753

Anti-inflammatory properties of

brilliant blue G on chronic

unpredictable mild stress-induced

changes in rat hippocampus

F. Aricioglu

1 ,

, T. Bastaskin

1

, C. Kandemir

2

, S. Sirvanci

2

,

C. Ozkartal

1

, T. Utkan

3

1

Marmara University School of Pharmacy, Department of

Pharmacology and Psychopharmacology Research Unit, Istanbul,

Turkey

2

Marmara University School of Medicine, Department of Histology

Embriology, Istanbul, Turkey

3

Kocaeli University School of Medicine, Department of

Pharmacology, Kocaeli, Turkey

Corresponding author.

Objective

Purinergic 2X7 receptor (P2X7R) activation has

recently been considered to be involved in depression at least par-

tially by triggering microglial activation. The aim of the present

study was to examine whether the chronic administration of

brilliant blue G (BBG), a highly selective P2X7R antagonist, has

antidepressant-like effects and microglial (Iba-1) immunoreactiv-

ity in chronic unpredictable mild stress (CUMS) model in rats.

Methods

Male Wistar Albino rats (290–360 g) were divided

into groups such as control (saline), CUMS, CUMS + Imipramine

(20mg/kg; i.p.), CUMS + BBG25 (25mg/kg; i.p.), CUMS + BBG50

(50mg/kg; i.p.) groups (

n

= 10–12 in each). In CUMS model, vari-

ous stressors were applied for 40 days. On day 20, the treatment

of BBG was started for 20 days. At the end, sucrose preference and

forced swimming tests were performed. Then brains were removed

with paraformaldehyde perfusion for Iba-1 immunohistochemical

analysis in hippocampus. One-way analysis of variance and Tukey’s

test were used for statistical analysis.

Results

The time of immobility in forced swim test was sig-

nificantly reduced while sucrose preference was increased in

Imipramine and CUMS + BBG50 groups compared to control and

0924-9338/