Pyridostigmine enhances atrial tachyarrhythmias in aging spontaneously hypertensive rats

Clin Exp Pharmacol Physiol. 2015 Oct;42(10):1084-91. doi: 10.1111/1440-1681.12458.

Abstract

This study examined whether chronic administration of pyridostigmine, a reversible cholinesterase inhibitor, would exacerbate episodes of spontaneous atrial tachyarrhythmia (AT) in conscious, aging, spontaneously hypertensive rats (SHRs). Telemetric recordings of electrocardiogram (ECG, n = 5) and ECG/arterial pressure (n = 3) were performed in male 49-week old SHRs. After a 1-week period of continuous recording under baseline conditions, rats were implanted with osmotic minipumps that delivered pyridostigmine (15 mg/kg/day subcutaneously) for either 1 (n = 8) or 3 (n = 5) weeks. In the latter case, sympathovagal balance was assessed during the last infusion week by measuring heart rate (HR) changes in response to administration of cardiac autonomic blockers. An additional 1-week recording was performed after explantation of minipumps. Significant (P = 0.02) reductions in HR with no consistent changes in arterial pressure were observed. Frequency and duration of AT episodes were increased by pyridostigmine (0.01 ≤ P ≤ 0.07). This increase was sustained across the 3-week treatment period and reversible after cessation of treatment. Autonomic blockade revealed that intrinsic HR was above (P = 0.04) resting HR, pointing to a shift of sympathovagal balance towards vagal predominance. However, the respiratory-related component of HR variability (high-frequency power of RR interval) was lowered (P = 0.01) by pyridostigmine treatment, indicating reduced vagal modulation of HR. The results are consistent with a pathogenic role of the parasympathetic nervous system in the aging SHR model, and raise the possibility that sustained vagal activation may facilitate atrial arrhythmias.

Keywords: aging; atrial tachyarrhythmia; heart rate variability; hypertension; pyridostigmine; rat; sympathovagal balance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / physiology*
  • Animals
  • Autonomic Nervous System / drug effects
  • Autonomic Nervous System / physiopathology
  • Blood Pressure / drug effects
  • Cholinesterase Inhibitors / pharmacology*
  • Electrocardiography
  • Heart Atria / drug effects*
  • Heart Atria / physiopathology
  • Heart Rate / drug effects
  • Male
  • Motor Activity / drug effects
  • Pyridostigmine Bromide / pharmacology*
  • Rats
  • Rats, Inbred SHR
  • Tachycardia, Supraventricular / chemically induced
  • Tachycardia, Supraventricular / physiopathology*

Substances

  • Cholinesterase Inhibitors
  • Pyridostigmine Bromide