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Effects of clomipramine hydrochloride on heart rate and rhythm in healthy dogs
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Abstract
Objective—To determine the effects of clomipramine
hydrochloride on heart rate and rhythm in dogs.
Animals—17 healthy Beagles.
Procedures—In experiment 1, 8 dogs received
placebo or clomipramine (20 mg/kg of body weight,
q 24 h, PO) for 7 days in a 2-way crossover design.
In experiment 2, 9 dogs were evaluated for 48
hours before and 24 hours after oral administration
of clomipramine (4 or 12 mg/kg) in a 2-way
crossover design. Electrocardiogram and heart rate
were monitored continuously by use of telemetry.
Results—A significant diurnal rhythm in heart rate
was detected; minimum values were recorded at
night. Administration of 20 mg of clomipramine/kg
induced a significant reduction in heart rate,
with peak effect achieved approximately 12
hours after dosing. Administration of 4 or 12 mg of
clomipramine/kg did not result in significant changes in
heart rate. Sinoatrial and second-degree atrioventricular
block and ventricular escape beats were
observed during periods of slow heart rate in more
dogs that received clomipramine (3 to 4 of 8 dogs),
compared with dogs that received placebo (1 to 2 of
8 dogs), but this difference was not significant.
Conclusions and Clinical Relevance—Short-term
administration of clomipramine induced benign
cardiovascular effects in dogs rather than the
potentially dangerous arrhythmias or tachycardia
reported following administration of tricyclic antidepressants
to humans. Precautions regarding
cardiovascular effects may not be needed for the use
of clomipramine in healthy dogs. (Am J Vet Res
2000;61:960–964)
American Veterinary Medical Association (AVMA)
Title: Effects of clomipramine hydrochloride on heart rate and rhythm in healthy dogs
Description:
Abstract
Objective—To determine the effects of clomipramine
hydrochloride on heart rate and rhythm in dogs.
Animals—17 healthy Beagles.
Procedures—In experiment 1, 8 dogs received
placebo or clomipramine (20 mg/kg of body weight,
q 24 h, PO) for 7 days in a 2-way crossover design.
In experiment 2, 9 dogs were evaluated for 48
hours before and 24 hours after oral administration
of clomipramine (4 or 12 mg/kg) in a 2-way
crossover design.
Electrocardiogram and heart rate
were monitored continuously by use of telemetry.
Results—A significant diurnal rhythm in heart rate
was detected; minimum values were recorded at
night.
Administration of 20 mg of clomipramine/kg
induced a significant reduction in heart rate,
with peak effect achieved approximately 12
hours after dosing.
Administration of 4 or 12 mg of
clomipramine/kg did not result in significant changes in
heart rate.
Sinoatrial and second-degree atrioventricular
block and ventricular escape beats were
observed during periods of slow heart rate in more
dogs that received clomipramine (3 to 4 of 8 dogs),
compared with dogs that received placebo (1 to 2 of
8 dogs), but this difference was not significant.
Conclusions and Clinical Relevance—Short-term
administration of clomipramine induced benign
cardiovascular effects in dogs rather than the
potentially dangerous arrhythmias or tachycardia
reported following administration of tricyclic antidepressants
to humans.
Precautions regarding
cardiovascular effects may not be needed for the use
of clomipramine in healthy dogs.
(Am J Vet Res
2000;61:960–964).
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