Objective-To determine whether enrofloxacin has detrimental, dose-dependent
effects on equine articular cartilage in vitro.
Animals-Cartilage explants were developed from 6 healthy horses between 0 a
nd 96 months old.
Procedure-Patellar cartilage explants were incubated in 5 concentrations of
enrofloxacin (2 mu/ml, 10 mu g/ml, 1.000 mu g/ml, 10,000 mu g/ml, and 50,0
00 mu g/ml) for 72 hours, Proteoglycan synthesis ((NaSO4)-S-35 incorporatio
n for 24 hours), proteoglycan degradation ((NaSO4)-S-35 release for 72 hour
s), endogenous proteoglycan content (dimethylmethiene blue assay), and tota
l protein content were determined. Cartilage explants were evaluated by use
of histomorphologic and histomorphometric techniques (toluidine blue stain
) for cytologic and matrix characteristics. Quantitative data were analyzed
with a one-way ANOVA to compare results among various enrofloxacin concent
ration groups and the control group. A general linear model was used to det
ermine whether age had an effect.
Result-Proteoglycan synthesis was excellent in control specimens and in spe
cimens incubated in low concentrations of enrofloxacin (2 mu g/ml and 10 mu
g/ml). High concentrations of enrofloxacin (> 1,000 mu g/ml) effectively e
liminated proteoglycan synthesis regardless of horse age. Proteoglycan degr
adation at low concentrations (2 mu g/ml and 10 mu g/ml) was not different
than control. High concentrations of enrofloxacin (> 1,000 mu g/ml) caused
significant degradation. Different concentrations of enrofloxacin did not a
ffect endogenous proteoglycan. High concentrations of enrofloxacin were ass
ociated with a significant increase in number of pyknotic nuclei.
Conclusion-Concentrations of enrofloxacin that might be achieved following
systemic administration did not suppress chondrocyte metabolism in vitro, H
igh concentrations of enrofloxacin (> 1,000 mu g/ml) were toxic to chondroc
ytes.