Ka. Grimm et al., THE PHARMACODYNAMICS OF THIOPENTAL, MEDETOMIDINE, BUTORPHANOL AND ATROPINE IN BEAGLE DOGS, Journal of veterinary pharmacology and therapeutics, 21(2), 1998, pp. 133-137
This study evaluated the quality of anaesthesia and some of the haemod
ynamic effects induced by a combination of thiopental, medetomidine, b
utorphanol and atropine in healthy beagle dogs (n = 12). Following pre
medication with atropine (ATR, 0.022 mg/kg intravenously (i.v.)) and b
utorphanol (BUT, 0.22 mg/kg i.v.), medetomidine (MED, 22 mu g/kg intra
muscularly (i.m.)) was administered followed in 5 min by thiopental (T
HIO, 2.2 mg/kg i.v.). Heart rate, systolic blood pressure (SBP), diast
olic blood pressure (DBP) and mean arterial blood pressure (MBP) were
monitored continuously with an ECG and direct arterial blood pressure
monitor. Atipamezole (ATI, 110 mu g/kg i.v.) was administered to half
of the dogs (n = 6) following surgery to evaluate the speed and qualit
y of arousal from anaesthesia. Anaesthesia was characterized by excell
ent muscle relaxation, analgesia and absence of purposeful movement in
response to surgical castration. Arousal following antagonism of mede
tomidine was significantly faster (P < 0.05) than in unantagonized dog
s. Recoveries were smooth but recovery times following atipamezole adm
inistration were highly variable among dogs (sternal time range 6-38 m
in, standing time range 9-56 min). Medetomidine caused a significant (
P < 0.05) increase in SEP, DBP and MBP. Atropine prevented the medetom
idine induced bradycardia. In conclusion, this combination provided ad
equate surgical anaesthesia in healthy beagle dogs. At the dosages use
d in this study, it seems prudent that this combination should be rese
rved for dogs free of myocardial disease.