Ethemoglu M S, Kutlu S, Seker F B, Erdogan C S, Bingol C A, Yilmaz B
Yeditepe University, Medical School, Department of Physiology, Ataşehir, İstanbul, Turkey.
Necmettin Erbakan University, Meram Faculty of Medicine, Department of Physiology, Meram, Konya, Turkey.
Neurosci Lett. 2019 Jan 18;690:120-125. doi: 10.1016/j.neulet.2018.09.014. Epub 2018 Sep 10.
Agomelatine is a new antidepressant drug acting as an antagonist of 5-hydroxytryptamine receptor 2C (5-HTR) and agonist of melatonergic receptors 1 and 2 (MT and MT). Because of this dual action, it is an atypical antidepressant. The aim of this study was to investigate chronic anticonvulsant effects of agomelatine on penicillin-induced epilepsy model. Adult male Sprague-Dawley rats divided into four groups and were administered with tap water (vehicle), and agomelatine doses of 10 mg/kg, 50 mg/kg and 100 mg/kg for 14 days via oral gavage. After the last doses were given, epileptic seizures were induced by intracortical penicillin (500 IU/2.5 μl) application in rats under urethane (1.25 g/kg intraperitoneal) anesthesia. Electrocorticogram (ECoG) recordings were obtained from the somatomotor cortex through 90 min, and spike frequencies and amplitudes were analyzed. The spike frequency analyses revealed that only 50 mg/kg agomelatine administration decreased the spike frequencies of hypersynchronous discharge of neurons caused by penicillin (p < 0.05). No significant differences in amplitudes between experimental groups were observed. In addition, mRNA expressions of vesicular glutamate transporter 1 (VGLUT1) and vesicular gamma-aminobutyric acid transporter (VGAT) in response to the agomelatine active dose, 50 mg/kg, showed no significant effect of agomelatine on the mRNA expression. Our results indicate that chronic treatment with agomelatine may have potential anticonvulsant effects. Agomelatine may be a promising drug for epilepsy patients having depression due to its antiepileptic and antidepressant effects.
阿戈美拉汀是一种新型抗抑郁药物,它是5-羟色胺受体2C(5-HTR)的拮抗剂以及褪黑素能受体1和2(MT1和MT2)的激动剂。由于这种双重作用,它是一种非典型抗抑郁药。本研究的目的是调查阿戈美拉汀对青霉素诱导的癫痫模型的慢性抗惊厥作用。将成年雄性斯普拉格-道利大鼠分为四组,分别给予自来水(赋形剂),以及10毫克/千克、50毫克/千克和100毫克/千克剂量的阿戈美拉汀,通过灌胃给药14天。在给予最后一剂后,在乌拉坦(1.25克/千克腹腔注射)麻醉下,通过向大鼠大脑皮层内注射青霉素(500国际单位/2.5微升)诱导癫痫发作。通过90分钟从躯体运动皮层获得脑电图(ECoG)记录,并分析棘波频率和幅度。棘波频率分析显示,仅给予50毫克/千克阿戈美拉汀可降低青霉素引起的神经元超同步放电的棘波频率(p<0.05)。各实验组之间的幅度未观察到显著差异。此外,针对阿戈美拉汀的有效剂量50毫克/千克,囊泡谷氨酸转运体1(VGLUT1)和囊泡γ-氨基丁酸转运体(VGAT)的mRNA表达显示阿戈美拉汀对mRNA表达无显著影响。我们的结果表明,阿戈美拉汀的慢性治疗可能具有潜在的抗惊厥作用。由于其抗癫痫和抗抑郁作用,阿戈美拉汀可能是患有抑郁症的癫痫患者的一种有前景的药物。