Ka. Lemke et al., ALTERATIONS IN THE ARRHYTHMOGENIC DOSE OF EPINEPHRINE AFTER XYLAZINE OR MEDETOMIDINE ADMINISTRATION IN HALOTHANE-ANESTHETIZED DOGS, American journal of veterinary research, 54(12), 1993, pp. 2132-2138
Eight dogs (12.5 to 21.5 kg) were assigned at random to each of 3 grou
ps that were not given glycopyrrolate (HS, HX, HM) and to each of 3 gr
oups that were given glycopyrrolate (HGS, HGX, HGM). Dogs were anesthe
tized with halothane (1.31% end-tidal concentration), and ventilation
was controlled (P-CO2 35 to 40 mm of Hg end-tidal concentration). Glyc
opyrrolate was administered IV and IM at a dosage of 11 mu g/kg of bod
y weight, each. Saline solution, xylazine (1.1 mg/kg, IM), or medetomi
dine (15 mu g/ kg, IM) was administered 10 minutes after baseline arrh
ychmogenic dose of epinephrine (ADE) determination. Redetermination of
the ADE at the same infusion rate was stared 10 minutes after drug ad
ministration. Arrhythmogenic dose was determined by constant infusion
of epinephrine at rates of 1.0 and 2.5 mu g/kg/min. The ADE was define
d as the total dose of epinephrine inducing at least 4 ectopic ventric
ular depolarizations within 15 seconds during a 3-minute infusion or w
ithin 1 minute after the end of the infusion. Total dose was calculate
d as the product of infusion rate and time to arrhythmia. Statistical
analysis of the differences between baseline ADE and posttreatment ADE
for groups HS, Hx, and HM was performed by use of one-way ANOVA. Mean
+/- SEM baseline ADE values for groups HS, Hx, and HM were 1.50 +/- 0
.11, 1.49 +/- 0.10, and 1.57 +/- 0.22 mu g/kg, respectively, and for g
roups HGS, HGX, and HGM were 3.37 +/- 0.61, 3.10 +/- 0.75, and 3.04 +/
- 0.94 mu g/kg, respectively. Differences for groups HS, HX, and HM we
re -0.02 +/- 0.15, -0.00 +/- 0.14, and -0.21 +/- 0.17 mu g/kg, respect
ively, and for groups HGS, HGX, and HGM, were -0.59 +/- 0.26, -0.41 +/
- 0.15, and -0.58 +/- 0.20 mu g/kg, respectively. Differences among gr
oups HS, Hx, and HM, or among groups HGS, HGX, and HGM were not signif
icant. Me conclude that without and with cholinergic blockade in halot
hane-anesthetized dogs: preanesthetic dosages of xylazine (1.1 mg/kg,
IM) or medetomidine (15 mu g/kg, IM) do not enhance arrhythmogenicity,
and at these dosages, there is no difference in the arrhythmogenic po
tential of either alpha(2)-adrenoceptor agonist.