Eren Ibrahim, Naziroğlu Mustafa, Demirdaş Arif, Celik Omer, Uğuz A Cihangir, Altunbaşak Ayşe, Ozmen Ismail, Uz Efkan
Department of Psychiatry, Medical Faculty, Suleyman Demirel University, Isparta, Turkey.
Neurochem Res. 2007 Mar;32(3):497-505. doi: 10.1007/s11064-006-9258-9.
Venlafaxine is an approved antidepressant that is an inhibitor of both serotonin and norepinephrine transporters. Medical treatment with oral venlafaxine can be beneficial to depression due to reducing free radical production in the brain and medulla of depression-induced rats because oxidative stress may a play role in some depression. We investigated the effect of venlafaxine administration and experimental depression on lipid peroxidation and antioxidant levels in cortex brain, medulla and erythrocytes of rats. Thirty male wistar rats were used and were randomly divided into three groups. Venlafaxine (20 mg/kg) was orally supplemented to depression-induced rats constituting the first group for four week. Second group was depression-induced group although third group was used as control. Depressions in the first and second groups were induced on day zero of the study by chronic mild stress. Brain, medulla and erythrocytes samples were taken from all animals on day 28. Depression resulted in significant decrease in the glutathione peroxidase (GSH-Px) activity and vitamin C concentrations of cortex brain, glutathione (GSH) value of medulla although their levels were increased by venlafaxine administration to the animals of depression group. The lipid peroxidation levels in the three tissues and nitric oxide value in cortex brain elevated although their levels were decreased by venlafaxine administration. There were no significant changes in cortex brain vitamin A, erythrocytes vitamin C, GSH-Px and GSH, medulla vitamin A, GSH and GSH-Px values. In conclusion, cortex brain within the three tissues was most affected by oxidative stress although there was the beneficial effect of venlafaxine in the brain of depression-induced rats on investigated antioxidant defenses in the rat model. The treatment of depression by venlafaxine may also play a role in preventing oxidative stress.
文拉法辛是一种已获批准的抗抑郁药,它是5-羟色胺和去甲肾上腺素转运体的抑制剂。口服文拉法辛进行药物治疗可能对抑郁症有益,因为它能减少抑郁症诱导大鼠大脑和延髓中的自由基生成,因为氧化应激可能在某些抑郁症中起作用。我们研究了给予文拉法辛和实验性抑郁症对大鼠大脑皮层、延髓和红细胞中脂质过氧化和抗氧化剂水平的影响。使用了30只雄性Wistar大鼠,并将它们随机分为三组。向构成第一组的抑郁症诱导大鼠口服补充文拉法辛(20毫克/千克),持续四周。第二组是抑郁症诱导组,而第三组用作对照组。在研究的第零天通过慢性轻度应激诱导第一组和第二组的抑郁症。在第28天从所有动物采集大脑、延髓和红细胞样本。抑郁症导致大脑皮层的谷胱甘肽过氧化物酶(GSH-Px)活性和维生素C浓度、延髓的谷胱甘肽(GSH)值显著降低,尽管对抑郁症组动物给予文拉法辛后这些水平有所升高。尽管给予文拉法辛后这三种组织中的脂质过氧化水平和大脑皮层中的一氧化氮值有所降低,但仍有所升高。大脑皮层中的维生素A、红细胞中的维生素C、GSH-Px和GSH、延髓中的维生素A、GSH和GSH-Px值没有显著变化。总之,在这三种组织中大脑皮层受氧化应激影响最大,尽管在大鼠模型中,文拉法辛对抑郁症诱导大鼠大脑中所研究的抗氧化防御有有益作用。文拉法辛治疗抑郁症可能在预防氧化应激方面也起作用。