Evaluation of a technique to measure heart rate variability in anaesthetised cats

Kuan Hua Khor1, Ian A Shiels2, Fiona E Campbell2

  • 1School of Veterinary Science, The University of Queensland, Gatton Campus, QLD 4343, Australia; Faculty of Veterinary Medicine, Universiti Putra Malaysia, 43400 UPM Serdang, Selangor, Malaysia.

Insights

Atenolol effectively blocks epinephrine-induced heart rate increases in cats, demonstrating its potential for studying cardiac responses and cardiovascular disease in laboratory settings without significantly altering heart rate variability.

Area of Science:

  • Cardiovascular Physiology
  • Pharmacology
  • Veterinary Cardiology

Background:

  • Heart rate (HR) and heart rate variability (HRV) analysis are crucial for diagnosing cardiac diseases.
  • Current monitoring methods like 24-h Holter can be inconvenient and prone to artifacts.
  • Anesthetized cats offer a controlled model for cardiovascular research.

Purpose of the Study:

  • To evaluate atenolol's efficacy in preventing epinephrine-induced tachycardia in cats.
  • To assess the impact of atenolol on heart rate variability (HRV) during sympathetic stimulation.
  • To validate a feline model for short-term cardiovascular and pharmacological studies.

Main Methods:

  • A randomized crossover study in seven healthy, anesthetized cats.
  • Administration of placebo or atenolol (1mg/kg, IV) followed by epinephrine challenge.
  • Continuous electrocardiography (ECG) for HR and HRV analysis.

Main Results:

  • Epinephrine significantly increased HR in the placebo group (P=0.0003) but not in the atenolol group.
  • Atenolol pre-treatment significantly antagonized epinephrine-induced tachycardia (P=0.0004).
  • HRV was not significantly affected by atenolol, though epinephrine suggested parasympathetic withdrawal.

Conclusions:

  • Atenolol effectively antagonizes tachycardia induced by sympathetic stimulation in anesthetized cats.
  • This feline model is sensitive and repeatable for investigating HRV and cardiovascular responses to drugs.
  • The model is suitable for short-term laboratory studies of cardiovascular disease and pharmacological agents.

Related Concept Videos