4.6 Article

Modeling the chronotropic effect of isoprenaline on rabbit sinoatrial node

Journal

FRONTIERS IN PHYSIOLOGY
Volume 3, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphys.2012.00241

Keywords

sinoatrial node; isoprenaline; action potential

Categories

Funding

  1. Engineering and Physical Science Research Council UK [EP/J00958X/1, EP/I029826/1]
  2. British Heart Foundation [FS/08/021]
  3. Natural Science Foundation of China [61179009]
  4. Engineering and Physical Sciences Research Council [EP/I029826/1, EP/I029664/1, EP/I029664/2, EP/I030158/1, EP/J00958X/1] Funding Source: researchfish
  5. EPSRC [EP/J00958X/1, EP/I030158/1, EP/I029664/2, EP/I029664/1, EP/I029826/1] Funding Source: UKRI

Ask authors/readers for more resources

Introduction: beta-adrenergic stimulation increases the heart rate by accelerating the electrical activity of the pacemaker of the heart, the sinoatrial node (SAN). Ionic mechanisms underlying the actions of beta-adrenergic stimulation are not yet fully understood. lsoprenaline (ISO), a beta-adrenoceptor agonist, shifts voltage-dependent If activation to more positive potentials resulting in an increase of If, which has been suggested to be the main mechanism underlying the effect of beta-adrenergic stimulation. However, ISO has been found to increase the firing rate of rabbit SAN cells when If is blocked. ISO also increases kali ist, IKr, and IKs; and shifts the activation of IKr to more negative potentials and increases the rate of its deactivation. ISO has also been reported to increase the intracellular Ca2+ transient, which can contribute to chronotropy by modulating the Ca2+ clock. The aim of this study was to analyze the ionic mechanisms underlying the positive chronotropy of beta-adrenergic stimulation using two distinct and well established computational models of the electrical activity of rabbit SAN cells. Methods and results: We modified the Boyett et al. (2001) and Kurata et al. (2008) models of electrical activity for the central and peripheral rabbit SAN cells by incorporating equations for the known dose-dependent actions of ISO on various ionic channel currents f (kali ist, IKr, and IKs), kine tics of IKr and I, and the intracellular Ca2+ transient. These equations were constructed from experimental data. To investigate the ionic basis of the effects of ISO, we simulated the chronotropic effect of a range of ISO concentrations when ISO exerted all its actions or just a subset of them. Conclusion: In both the Boyett et al. and Kurata et al. SAN models, the chronotropic effect of ISO was found to result from an integrated action of ISO on Icab If, ISt, IKr, and IKs, among which an increase in the rate of deactivation of IKr plays a prominent role, though the effect of ISO on If and [Ca2+]; also plays a role.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available