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Published on: June 20, 2020
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.
Abstract:
Analysis of heart rate (HR) and heart rate variability (HRV) are powerful tools to investigate cardiac diseases, but current methods, including 24-h Holter monitoring, can be cumbersome and may be compromised by movement artefact. A commercially available data capture and analysis system was used in anaesthetised healthy cats to measure HR and HRV during pharmacological manipulation of HR. Seven healthy cats were subjected to a randomised crossover study design with a 7 day washout period between two treatment groups, placebo and atenolol (1mg/kg, IV), with the efficacy of atenolol to inhibit β1 adrenoreceptors challenged by epinephrine. Statistical significance for the epinephrine challenge was set at P<0.0027 (Holm-Bonferroni correction), whereas a level of significance of P<0.05 was set for other variables. Analysis of the continuous electrocardiography (ECG) recordings showed that epinephrine challenge increased HR in the placebo group (P=0.0003) but not in the atenolol group. The change in HR was greater in the placebo group than in the atenolol group (P=0.0004). Therefore, compared to cats pre-treated with placebo, pre-treatment with atenolol significantly antagonised the tachycardia while not significantly affecting HRV. The increased HR in the placebo group following epinephrine challenge was consistent with a shift of the sympathovagal balance towards a predominantly sympathetic tone. However, the small (but not significant at the critical value) decrease in the normalised high-frequency component (HFnorm) in both groups of cats suggested that epinephrine induced a parasympathetic withdrawal in addition to sympathetic enhancement (increased normalised low frequency component or LFnorm). In conclusion, this model is a highly sensitive and repeatable model to investigate HRV in anaesthetised cats that would be useful in the laboratory setting for short-term investigation of cardiovascular disease and subtle responses to pharmacological agents in this species.
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