Systemic and neurotoxic effects of epidural meloxicam in rabbits

The aim of this study was to assess systemic and neurotoxic changes following an epidural administration of meloxicamin to rabbits. Twelve adult rabbits four males and eight females; average mass, 1.9 ± 0.1kg were randomly divided into two groups: a control group (GC), which received a single dose of 0.9% NaCl epidurally in a volume of 0.3mL kg-1and a meloxicam group (GM), which received 0.2mg kg-1 meloxicam epidurally along with 0.9% NaCl in a total volume of 0.3mL kg-1. Heart rate, respiratory rate, body temperature, and neurological abnormalities were assessed prior to administration of anesthesia (H0), 1, 2, 3, 6, 12, and 24h following epidural puncture (H1, H2, H3, H6, H12, and H24, respectively), and every 24h afterward for 10 days after epidural puncture (D2, D3, D4, D5, D6, D7, D8, D9, and D10). The surface temperature of lumbosacral region was also measured at H0, H1, H6, H12, H24, D5 and D10. Three animals from each group were euthanized on days 15 and 30 after epidural puncture to assess possible spinal injuries. Variances observed in physiological parameters were not suggestive of adverse effects of meloxicam, as all were within the reference standards, and there were no physical or behavioral changes observed. Neurological function was similar between groups, with only difference between baseline values and values 1h after epidural administration in both groups. There were no histopathological changes in the GM group, and only one animal showed discrete lymphocytic infiltrate. Epidural lumbosacral administration of meloxicam at a dose of 0.2mg kg-1 caused no significant systemic or neurotoxic effects in rabbits. RESUMO: O objetivo desse estudo foi avaliar as alterações sistêmicas e neurotóxicas promovidas pelo meloxicam, administrado por via epidural, em coelhos. Foram utilizados 12 coelhos adultos, quatro machos e oito fêmeas, pensando em média 1,9 ± 0,1kg. Os animais foram divididos equitativa e aleatoriamente em dois grupos, os quais receberam dose única de solução de NaCl 0,9% no volume de 0,3mL kg-1, por via epidural (grupo controle - GC) ou meloxicam (0,2mg kg-1) associado à solução de NaCl 0,9%, compondo um volume total de 0,3mL kg-1 (grupo meloxicam - GM). Avaliaram-se frequências cardíaca e respiratória, temperatura corporal e alterações neurológicas, antes da administração da anestesia (H0), uma, duas, três, seis, 12 e 24 horas após a punção epidural (H1, H2, H3, H6, H12 e H24, respectivamente) e a cada 24 horas após o H24, até o 10º