Why the study?
Endothelin alters blood pressor responses, but whether it affects autonomic activity and arrhythmogenesis during acute emotional stress remains unclear.
Does chronically elevated plasma endothelin modulate autonomic responses and arrhythmogenesis during acute emotional stress in rats?
Does chronically elevated plasma endothelin modulate autonomic responses and arrhythmogenesis during acute emotional stress in rats?
Chronically elevated endothelin blunts sympathetic responses to acute emotional stress, promoting vagal dominance and bradyarrhythmias rather than tachyarrhythmias.
Endothelin modulation of autonomic stress responses remains unclear in rats; leaves open effects on arrhythmogenesis and human translation.
The ubiquitous peptide endothelin is currently under investigation as a modulatory factor of autonomic responses to acute emotional stress. Baseline plasma levels of endothelin alter blood pressor responses, but it remains unclear whether autonomic activity and arrhythmogenesis are affected. We recorded sympathetic and vagal indices (derived from heart rate variability analysis), rhythm disturbances, voluntary motion, and blood pressure after acute emotional stress in conscious rats with implanted telemetry devices. Two strains were compared, namely wild-type and ETB-deficient rats, the latter displaying elevated plasma endothelin. No differences in heart rate or blood pressure were evident, but sympathetic responses were blunted in ETB-deficient rats, contrasting prompt activation in wild-type rats. Vagal withdrawal was observed in both strains at the onset of stress, but vagal activity was subsequently restored in ETB-deficient rats, accompanied by low voluntary motion during recovery. Reflecting such distinct autonomic patterns, frequent premature ventricular contractions were recorded in wild-type rats, as opposed to sinus pauses in ETB-deficient rats. Thus, chronically elevated plasma endothelin levels blunt autonomic responses to acute emotional stress, resulting in vagal dominance and bradyarrhythmias. Our findings provide further insights into the pathophysiology of stress-induced tachyarrhythmias and syncope.
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Mouchtouri et al. (2023) studied this question.
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