Modification of the baroreceptor control of atrio-ventricular conduction induced by digitalis in man

Cardiovasc Res. 1983 Oct;17(10):633-41. doi: 10.1093/cvr/17.10.633.

Abstract

Several studies in animals and in man have suggested that the inhibitory influence of baroreceptors on heart rate and peripheral circulation is enhanced by digitalis. Because the atrio-ventricular node represents a key site for the clinical action of digitalis we studied how baroreceptor control of atrio-ventricular conduction is modified by digitalis at therapeutical doses. In eight subjects heart rate was kept constant by atrial pacing to assess neural influences on atrio-ventricular conduction rate without the modifications caused by simultaneous changes in cardiac cycle length. Arterial baroreceptors were stimulated by increasing or reducing blood pressure (intra-arterial recording), via an iv bolus of phenylephrine or nitroglycerine. The baroreflex sensitivity was assessed in ms . mmHg-1 as the slope of the linear regressions relating the rise or fall in systolic blood pressure to the lengthening or shortening in St- (atrial stimulus artifact) Q interval (ECG recording). The study was performed before and 45 min after iv administration of digitalis (0.8 mg of Lanatoside C). Baroreflex sensitivity during baroreceptor stimulation was 2.9 +/- 1.1 ms . mmHg-1 (mean +/- SE) before digitalis, whereas after digitalis a significantly and markedly greater value of 5.6 +/- 1.5 ms . mmHg-1 was found. Baroreflex sensitivity during baroreceptor deactivation was 0.9 +/- 0.1 ms . mmHg-1 before digitalis, and was not significantly affected by the drug. Thus in man the baroreceptor control of atrio-ventricular conduction is strikingly potentiated by digitalis although this potentiation is only evident in the upper portion of the stimulus-response curve of the reflex.(ABSTRACT TRUNCATED AT 250 WORDS)

MeSH terms

  • Adult
  • Atrioventricular Node / physiology*
  • Blood Pressure / drug effects
  • Female
  • Heart Conduction System / physiology*
  • Humans
  • Hypertension / physiopathology
  • Lanatosides / pharmacology*
  • Male
  • Nitroglycerin / pharmacology
  • Phenylephrine / pharmacology
  • Pressoreceptors / drug effects*
  • Pressoreceptors / physiology
  • Reflex / drug effects
  • Sinoatrial Node / physiology

Substances

  • Lanatosides
  • Phenylephrine
  • lanatoside C
  • Nitroglycerin