Bai Zhi-Long, Chen Qian, Yang Si-Dong, Zhang Feng, Wang Hai-Ying, Yang Da-Long, Ding Wen-Yuan
Department of Spine Surgery, Third Hospital of Hebei Medical University, Shijiazhuang, Hebei, China (mainland).
Department of Rehabilitation Medicine, Third Hospital of Hebei Medical University, Shijiazhuang, Hebei, China (mainland).
Med Sci Monit. 2014 Nov 8;20:2205-12. doi: 10.12659/MSM.892610.
Fluoroquinolones are in wide clinical use as safe and effective antibiotics. Articular cartilage, tendons, and epiphyseal growth plates have been recognized as targets of fluoroquinolone-induced connective tissue toxicity. However, the effects of fluoroquinolones on annulus fibrosus (AF) cells are still unknown.
MATERIAL/METHODS: The main objective of this study was to investigate the effects of levofloxacin, a typical fluoroquinolone antibiotic drug, on rat AF cells in vitro. Rat annulus fibrosus (RAF) cells were treated with levofloxacin at different concentrations (0, 10, 20, 30, 40, 60, 80, and 90 μg/ml) and were assessed to determine the possible cytotoxic effects of levofloxacin. Inverted phase-contrast microscopy was used to accomplish the morphological observation of apoptosis of treated cells. Western blot and real-time quantitative RT-PCR (qPCR) was used to explore the expression of active caspase-3 and MMP-3. Flow cytometry was used to measure the apoptotic incidences.
Our study showed that levofloxacin, with concentrations at 30, 60, and 90 μg/ml, induced dose-dependent RAF cell apoptosis and higher expression of caspase-3 and MMP-3. More apoptotic cells were observed by inverted phase-contrast microscopy. Moreover, levofloxacin increased the activity of caspase-3, and it also reduced cell viability with different concentrations ranging from 10 to 80 μg/ml.
Our study results suggest that levofloxacin has cytotoxic effects on RAF cells, characterized by enhancing apoptosis and reducing cell viability, and indicate a potential toxic effect of fluoroquinolones on RAF cells.
氟喹诺酮类药物作为安全有效的抗生素在临床中广泛使用。关节软骨、肌腱和骨骺生长板已被认为是氟喹诺酮类药物诱导的结缔组织毒性的靶点。然而,氟喹诺酮类药物对纤维环(AF)细胞的影响仍不清楚。
材料/方法:本研究的主要目的是在体外研究典型的氟喹诺酮类抗生素药物左氧氟沙星对大鼠AF细胞的影响。用不同浓度(0、10、20、30、40、60、80和90μg/ml)的左氧氟沙星处理大鼠纤维环(RAF)细胞,并评估其对左氧氟沙星可能的细胞毒性作用。采用倒置相差显微镜对处理后的细胞凋亡进行形态学观察。采用蛋白质免疫印迹法和实时定量逆转录聚合酶链反应(qPCR)检测活性半胱天冬酶-3和基质金属蛋白酶-3的表达。采用流式细胞术检测细胞凋亡发生率。
我们的研究表明,浓度为30、60和90μg/ml的左氧氟沙星可诱导RAF细胞呈剂量依赖性凋亡,并使半胱天冬酶-3和基质金属蛋白酶-3的表达升高。通过倒置相差显微镜观察到更多的凋亡细胞。此外,左氧氟沙星增加了半胱天冬酶-3的活性,并且在10至80μg/ml的不同浓度范围内也降低了细胞活力。
我们的研究结果表明,左氧氟沙星对RAF细胞具有细胞毒性作用,其特征为增强细胞凋亡和降低细胞活力,并提示氟喹诺酮类药物对RAF细胞具有潜在的毒性作用。