Key result
A boosts heart rate variability ~58% vs control at 7 days.
Why the study?
The effects of chronic pyridostigmine administration on spontaneous atrial tachyarrhythmias in aging spontaneously hypertensive rats were unclear.
Absolute Event Rate: 12.8% vs 8.1%
p-value: p=<0.05
Supports parasympathetic role in atrial tachyarrhythmias in aging hypertensive rats; leaves open clinical translation to human AF.
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.
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Scridon et al. (2015) studied Acute myocardial infarction and renal inflammation (n=30). Pyridostigmine vs. Untreated acute myocardial infarction (AMI) and sham surgery was evaluated on Heart rate variability (RMSSD in ms) at 7 days (p=<0.05). A.
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