M. Rishniw et al., CHARACTERIZATION OF CHRONOTROPIC AND DYSRHYTHMOGENIC EFFECTS OF ATROPINE IN DOGS WITH BRADYCARDIA, American journal of veterinary research, 57(3), 1996, pp. 337-341
Objective-To characterize the magnitude, character, and time course of
chronotropic and dysrhythmogenic responses of dogs with vagally media
ted bradycardia to atropine sulfate. Design-Latin square design. Anima
ls-Seven clinically normal adult mixed-breed dogs. Procedure-Vagally m
ediated bradycardia was induced with morphine and fentanyl citrate. At
ropine (0.02 mg/kg of body weight) was administered IV, SC, or IM. Ele
ctrocardiograms were recorded continuously for 5 minutes before and fo
r 35 minutes after atropine administration or until a sustained parasy
mpatholytic response was observed. Data were digitized, analyzed indep
endently for changes in atrial and ventricular rate, and compared betw
een different routes of administration. Results-All dogs developed sec
ond-degree atrioventricular (AV) block after IV administration of atro
pine, and 71% of dogs developed AV block after SC or IM administration
. The AV block arose and resolved more rapidly with IV administration
than with SC or IM administration. The AV block was principally attrib
utable to an increase in the atrial rate prior to increases in the ven
tricular rate. Atropine, regardless of route of administration, potent
iated baseline ventricular bradycardia in 62% of the experiments (mean
heart rate decrease of 16 beats/min; decreased to < 20 beats/min in 2
dogs for less than or equal to 10 seconds). Duration of the bradycard
ic potentiation was longer with SC administration (9.1 minutes, SC, vs
1.4 minutes, IV, and 4.6 minutes, IM). Parasympatholytic rate was hig
her for IV than SC or IM administration (128 beats/min vs 92 beats/min
and 101 beats/min). Two dogs given atropine SC failed to resolve the
AV block and attain sinus rhythm. Conclusions-Administration of 0.02 m
g of atropine/kg by IV, IM, and SC routes for vagally mediated bradyca
rdia in dogs consistently induces AV block and occasional brief potent
iation of ventricular bradycardia. Clinical Relevance-Parasympathomime
tic effects occur and resolve most rapidly and consistently, and the s
table parasympatholytic effect is of greatest magnitude after IV admin
istration. Thus, vagally mediated bradycardia in clinically normal dog
s appears to be best abolished by IV administration of atropine.