Burkhardt J E, Hill M A, Turek J J, Carlton W W
Department of Pathobiology, Purdue University School of Veterinary Medicine, West Lafayette, IN.
Vet Pathol. 1992 May;29(3):230-8. doi: 10.1177/030098589202900307.
The ultrastructural features of quinolone-induced arthropathy were studied in the humeral and femoral heads of nine skeletally immature Beagle dogs (3 months old) that were dosed orally with difloxacin at 300 mg/kg body weight and euthanatized 24, 36, or 48 hours later in groups of three. Three age-matched dogs were given a placebo and euthanatized after 48 hours. Mitochondria in chondrocytes had significantly greater cross-sectional areas (P less than 0.05) in electron micrographs from dogs euthanatized after 48 hours of treatment than did those in other groups. There was also a significantly greater percentage of chondrocytes with swollen mitochondria in treated dogs than in the controls (P less than 0.05). These changes preceded the necrosis observed in some chondrocytes in the dogs of the 48-hour group. Disruption of extracellular matrix was first observed in the pericellular matrix of necrotic chondrocytes, indicating that this change was secondary to the changes in chondrocytes. Fissures within cartilages apparently resulted from the loss of the normal association of proteoglycans with collagen fibrils.
在9只骨骼未成熟的比格犬(3月龄)的肱骨头和股骨头中研究了喹诺酮诱导的关节病的超微结构特征。这些犬以300mg/kg体重口服地氟沙星,然后分三组在24、36或48小时后实施安乐死。3只年龄匹配的犬给予安慰剂,并在48小时后实施安乐死。在治疗48小时后实施安乐死的犬的电子显微照片中,软骨细胞中的线粒体横截面积显著更大(P<0.05),比其他组的线粒体横截面积大。与对照组相比,接受治疗的犬中出现线粒体肿胀的软骨细胞百分比也显著更高(P<0.05)。这些变化先于48小时组犬的一些软骨细胞中观察到的坏死。细胞外基质的破坏首先在坏死软骨细胞的细胞周基质中观察到,这表明这种变化是软骨细胞变化的继发结果。软骨内的裂隙显然是由于蛋白聚糖与胶原纤维的正常结合丧失所致。