Ilgin Sinem, Can Ozgur Devrim, Atli Ozlem, Ucel Umut Irfan, Sener Erol, Guven Ilkay
a Department of Pharmaceutical Toxicology .
b Department of Pharmacology , and.
Toxicol Mech Methods. 2015;25(5):374-81. doi: 10.3109/15376516.2015.1026008. Epub 2015 Apr 22.
Ciprofloxacin (CPX) is a fluoroquinolone antibiotic used for treating respiratory, urinary tract, gastrointestinal and abdominal infections. There are only a limited number of studies related to neurological adverse effects of this drug in therapeutic doses. Therefore, in the present study, we aimed to investigate the influence of CPX, when administered at pharmacological doses, on behavioral parameters of rats and the probable underlying mechanisms. CPX was administered in single oral daily doses of 20 and 50 mg/kg for 14 days in rats. CPX-induced depression and anxiety were evaluated by modified forced swimming test and elevated plus maze test, respectively. Also, spontaneous locomotor activity and motor coordination were assessed by activity cage and Rota-rod apparatus. Effects of CPX administration on brain serotonin, dopamine, γ-amino-butyric acid (GABA), glutamate, adrenaline and noradrenaline levels were determined by high performance liquid chromatography (HPLC) analysis. Contribution of oxidative stress to the changes induced by CPX administration was evaluated by measuring brain catalase, superoxide dismutase, glutathione (GSH) and malondialdehyde (MDA) levels. Our results indicated that depression-like and anxiety-like behaviors were observed only in the 50 mg/kg CPX-administered group with simultaneous decreases in the brain serotonin and GABA levels. In addition, in the brain homogenates of CPX-administered groups, increased MDA as well as decreased GSH and catalase activity with respect to their controls, indicated enhanced oxidative stress and weakened antioxidant defense system. In conclusion, repeated pharmacological doses of CPX were found to induce neurological toxicity. Also, altered brain neurotransmitter levels and increased oxidative stress observed in our study were thought to be the possible underlying mechanisms of ciprofloxacin-induced neurotoxicity.
环丙沙星(CPX)是一种氟喹诺酮类抗生素,用于治疗呼吸道、泌尿道、胃肠道和腹部感染。关于该药物治疗剂量下的神经不良反应的研究数量有限。因此,在本研究中,我们旨在研究以药理剂量给药的CPX对大鼠行为参数的影响以及可能的潜在机制。在大鼠中,以20和50mg/kg的单次口服日剂量给予CPX,持续14天。分别通过改良强迫游泳试验和高架十字迷宫试验评估CPX诱导的抑郁和焦虑。此外,通过活动笼和转棒仪评估自发运动活动和运动协调性。通过高效液相色谱(HPLC)分析测定CPX给药对脑血清素、多巴胺、γ-氨基丁酸(GABA)、谷氨酸、肾上腺素和去甲肾上腺素水平的影响。通过测量脑过氧化氢酶、超氧化物歧化酶、谷胱甘肽(GSH)和丙二醛(MDA)水平来评估氧化应激对CPX给药诱导的变化的贡献。我们的结果表明,仅在给予50mg/kg CPX的组中观察到抑郁样和焦虑样行为,同时脑血清素和GABA水平降低。此外,在给予CPX的组的脑匀浆中,与对照组相比,MDA增加,GSH和过氧化氢酶活性降低,表明氧化应激增强,抗氧化防御系统减弱。总之,发现重复给予药理剂量的CPX会诱导神经毒性。此外,我们研究中观察到的脑内神经递质水平改变和氧化应激增加被认为是环丙沙星诱导神经毒性的可能潜在机制。