The effect of duloxetine on ECoG activity of absence-epilepsy model in WAG/Rij rats
Öz
Aim: Many
epidemiological studies have found a high
incidence of depression and anxiety in people with epilepsy. Duloxetine is a selective
inhibitor of serotonin and norepinephrine reuptake (SNRI) and commonly prescribed in a patient with major depressive
disorder. The aim of this study was to investigate
the effect of duloxetine on the WAG/Rij rat in an experimental rat model
of absence-epilepsy.
Methods: WAG/Rij
rats were randomly assigned into 5 groups with 7 animals in each group. Tripolar
electrodes were placed on the skull to
perform electrocorticography (ECoG) evaluation. Then, following the recovery
period, ECoGs were recorded at 09:00 am for 3 hours every day. Subsequently, duloxetine (1, 5, 10
and 30 mg/kg) was injected
intraperitoneally (i.p). After
the treatment program, ECoG recordings were taken for 3 hours. And then all
animal anxiety-like behavior by using the
behavioral test, open field test (OFT) was performed after duloxetine (1,5,10
and 30 mg/kg) treatment. The total number and
the total duration of the spike-wave
discharges (SWDs) were
calculated offline. The
number of squares crossed (locomotor activity) and the duration of grooming
episodes were analyzed in OFT.
Results: The doses of duloxetine (1 mg/kg) did not alter ECoG and OFT parameters. The 5, 10 and 30 mg/kg doses of duloxetine decreased the total number and the total duration of
SWDs, (p<0.05) and increased the number of squares crossed when
compared to with control group (p <0.05) without changing duration of
grooming episodes (p> 0.05). Intraperitoneal administering of 1 mg/kg
duloxetine did not show any statistically
significant change in regard to the number and duration of SWDs.
Conclusions: In the present study, duloxetine reduce
dose-dependent absences-like seizures and
anxiety-like behavior.
Anahtar Kelimeler
Kaynakça
- 1- Zupec-Kania BA, Spellman E. An overview of the ketogenic diet for pediatric epilepsy. Nutr Clin Pract. 2009;23(6):589-596.
- 2- Barry JJ, Ettinger AB, Friel P, et al. Consensus statement: the evaluation and treatment of people with epilepsy and affective disorders. Epilepsy Behav 2008;13(Suppl. 1): S1–29.
- 3- Tellez-Zenteno JF, Patten SB, Jetté N, et al. Psychiatric comorbidity in epilepsy: a population-based analysis. Epilepsia 2007;48:2336-2344.
- 4- Sillanpää M, Schmidt D. Natural history of treated childhood-onset epilepsy: prospective, long-term population-based study. Brain 2006;129(Pt 3):617-624.
- 5- Cardamone L, Salzberg MR, O'brien TJ, Jones NC. Antidepressant therapy in epilepsy: can treating the comorbidities affect the underlying disorder?. British J Pharmacol 2013;168(7):1531-1554.
- 6- Citraro R, Leo A, De Fazio P, et al. Antidepressants but not antipsychotics have antiepileptogenic effects with limited effects on comorbid depressive‐like behavior in the WAG/Rij rat model of absence epilepsy. Br J Pharmacol 2015;172(12):3177-3188.
- 7- Esen M, Aygun H. The effect of duloxetine on penicillin-induced epileptiform activity in rats. Neurological Res 2019;41(4):298-305.
- 8- Wong DT, Bymaster FP, Mayle DA, et al. LY248686, a new inhibitor of serotonin and norepinephrine uptake. Neuropsychopharmacol 1993;8(1):23–33.
Ayrıntılar
Birincil Dil
İngilizce
Konular
Sağlık Kurumları Yönetimi
Bölüm
Araştırma Makalesi
Yazarlar
Hatice Aygün
*
0000-0002-4272-0562
Türkiye
Yayımlanma Tarihi
30 Eylül 2019
Gönderilme Tarihi
18 Mart 2019
Kabul Tarihi
11 Temmuz 2019
Yayımlandığı Sayı
Yıl 2019 Cilt: 9 Sayı: 3