Institute of Neurobiology, Bulgarian Academy of Sciences, Sofia, Bulgaria.
Cell Biochem Funct. 2010 Aug;28(6):497-502. doi: 10.1002/cbf.1682.
In vivo effects of the antidepressant fluoxetine on spleen antioxidant status of C57BL/6 mice were studied using a melanoma experimental model. After a 14-day treatment with fluoxetine (10 mg kg(-1) day(-1), i.p.), the endogenous antioxidant non-enzyme (glutathione) and enzyme (superoxide dismutase (SOD) and glutathione peroxidase (GPx)) defense systems in spleen of healthy animals were not changed; the lipid peroxidation (LP) was also unchanged. When B16F10 melanoma cells were introduced in C57BL/6 mice 2 h before fluoxetine treatment, a drug-protective effect against the melanoma-induced oxidative changes (increased LP and decreased total glutathione (GSH)-level, as well as antioxidant enzyme activities) in spleen was observed. Fluoxetine dose-dependently reduced the amounts of free oxygen radicals (hydroxyl and superoxide anion radicals), generated in chemical systems. Taken together, the present results suggest that fluoxetine, acting as antioxidant, prevents from melanoma-induced oxidative changes in mice spleen.
使用黑色素瘤实验模型研究了抗抑郁药氟西汀对 C57BL/6 小鼠脾脏抗氧化状态的体内影响。经过 14 天的氟西汀(10mg/kg/天,腹腔注射)治疗后,健康动物脾脏中的内源性抗氧化非酶(谷胱甘肽)和酶(超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GPx))防御系统没有变化;脂质过氧化(LP)也没有变化。当 B16F10 黑色素瘤细胞在氟西汀治疗前 2 小时引入 C57BL/6 小鼠时,观察到药物对黑色素瘤诱导的脾脏氧化变化(增加 LP 和降低总谷胱甘肽(GSH)水平以及抗氧化酶活性)的保护作用。氟西汀剂量依赖性地减少了化学系统中产生的游离氧自由基(羟基和超氧阴离子自由基)的量。总之,目前的结果表明,氟西汀作为抗氧化剂,可防止小鼠脾脏中黑色素瘤诱导的氧化变化。