Dh. Dyson et Gr. Pettifer, EVALUATION OF THE ARRHYTHMOGENICITY OF A LOW-DOSE OF ACEPROMAZINE - COMPARISON WITH XYLAZINE, Canadian journal of veterinary research, 61(4), 1997, pp. 241-245
Alteration in the arrhythmogenic dose of epinephrine (ADE) was determi
ned in 6 healthy dogs under halothane anesthesia following the adminis
tration of xylazine at 1.1 mg/kg IV and acepromazine at 0.025 mg/kg IV
. The order of treatment was randomly assigned with each dog receiving
both treatments and testing was carried out on 2 separate occasions w
ith at least a 1 wk interval. The ADE determinations were made prior t
o drug administration during halothane anesthesia (CNTL) and then 20 m
in and 4 h following drug treatment. Epinephrine was infused for 3 min
at increasing dose rates (2.5, 5.0, 10.0 mu g/kg/min) until the arrhy
thmia criterion (4 or more intermittent or continuous premature ventri
cular contractions) was reached within the 3 min of infusion or the 1
min following cessation, The interinfusion interval was 20 min. There
was a significant difference (P = 0.0001) in the ADE determined follow
ing acepromazine administration at 20 min (20.95 mu g/kg +/- 2.28 SEM)
compared to CNTL (6.64 mu g/kg +/- 1.09), xylazine at 20 min (5.82 mu
g/kg +/- 0.95) and 4 h (6.13 mu g/kg +/- 1.05), and acepromazine at 4
h (7.32 mu g/kg +/- 0.34). No other significant differences existed (
P < 0.05). In this study we were unable to show any sensitization to e
pinephrine following xylazine administration during halothane anesthes
ia, while a protective effect was shown with a low dose of acepromazin
e.