Department of Orthopedic Surgery, Zhongnan Hospital of Wuhan University, Wuhan, China.
Toxicol Appl Pharmacol. 2011 Nov 15;257(1):67-73. doi: 10.1016/j.taap.2011.08.019. Epub 2011 Aug 27.
Articular cartilage, epiphyseal growth plate and tendons have been recognized as targets of fluoroquinolone-induced connective tissue toxicity. The effects of fluoroquinolones on ligament tissues are still unknown. The aim of this study was to investigate the effects of levofloxacin, a typical fluoroquinolone antibiotic drug, on rabbit anterior cruciate ligament (ACL) cells in vitro. Rabbit ACL cells were treated with levofloxacin at different concentrations (0, 14, 28, 56, 112 and 224 μM) and were assessed to determine the possible cytotoxic effects of levofloxacin on ACL cells. Levofloxacin, with concentrations ranging from 28 to 224 μM, induced dose-dependent ACL cell apoptosis. Characteristic markers of programmed cell death and degenerative changes were identified by electron microscopy in the ACL cells treated with 28 μM of levofloxacin. Moreover, levofloxacin significantly increased the mRNA expression of matrix metalloproteinase 3 (MMP-3) and MMP-13 and decreased the expression of tissue inhibitors of metalloproteinase 1 (TIMP-1) in a concentration-dependent manner; TIMP-3 and collagen type I alpha 1 (Col1A1) mRNA expression was not affected. Immunocytochemical analysis indicated that levofloxacin markedly increased the expression of active caspase-3 within a concentration range of 28 to 224 μM, whereas a clear-cut decrease in Col1A1 expression was found with levofloxacin treatment concentrations of 112 and 224 μM, compared to controls. Our data suggest that levofloxacin has cytotoxic effects on ACL cells characterized by enhanced apoptosis and decreased extracellular matrix, which suggest a potential adverse effect of fluoroquinolones.
关节软骨、骺板和肌腱已被认为是氟喹诺酮类药物引起的结缔组织毒性的靶标。氟喹诺酮类药物对韧带组织的影响尚不清楚。本研究旨在研究左氧氟沙星(一种典型的氟喹诺酮类抗生素药物)对兔前交叉韧带(ACL)细胞的体外影响。用不同浓度(0、14、28、56、112 和 224 μM)的左氧氟沙星处理兔 ACL 细胞,评估左氧氟沙星对 ACL 细胞的潜在细胞毒性作用。浓度为 28 至 224 μM 的左氧氟沙星诱导 ACL 细胞呈浓度依赖性凋亡。用 28 μM 左氧氟沙星处理的 ACL 细胞通过电子显微镜鉴定出程序性细胞死亡和退行性变化的特征性标记。此外,左氧氟沙星以浓度依赖的方式显著增加基质金属蛋白酶 3(MMP-3)和 MMP-13 的 mRNA 表达,并降低组织抑制剂的表达金属蛋白酶 1(TIMP-1);TIMP-3 和胶原类型 I alpha 1(Col1A1)mRNA 表达不受影响。免疫细胞化学分析表明,左氧氟沙星在 28 至 224 μM 的浓度范围内明显增加了活性半胱氨酸天冬氨酸蛋白酶-3 的表达,而与对照组相比,用左氧氟沙星处理的浓度为 112 和 224 μM 时,Col1A1 的表达明显下降。我们的数据表明,左氧氟沙星对 ACL 细胞具有细胞毒性作用,其特征为增强的凋亡和减少的细胞外基质,这表明氟喹诺酮类药物可能具有不良影响。