Skip to main content

Feasibility of cardiac microimpedance measurement using multisite interstitial stimulation.

Publication ,  Journal Article
Pollard, AE; Smith, WM; Barr, RC
Published in: American journal of physiology. Heart and circulatory physiology
December 2004

This study was designed to test the hypothesis that analyses of central interstitial potential differences recorded during multisite stimulation with a set of interstitial electrodes provide sufficient data for accurate measurement of cardiac microimpedances. On theoretical grounds, interstitial current injected and removed using electrodes in close proximity does not cross the membrane, whereas equilibration of intracellular and interstitial potentials occurs distant from electrodes widely separated. Multisite interstitial stimulation should therefore give rise to interstitial potential differences recorded centrally that depend on intracellular and interstitial microimpedances, allowing independent measurement. Simulations of multisite stimulation with fine (25 microm) and wide (400 microm) spacing in one-dimensional models that included Luo-Rudy dynamic membrane equations were performed. Constant interstitial and intracellular microimpedances were prescribed for initial analyses. Discrete myoplasmic and gap-junctional components were prescribed intracellularly in later simulations. With constant microimpedances, multisite stimulation using 29 total electrode combinations allowed interstitial and intracellular microimpedance measurements at errors of 0.30% and 0.34%, respectively, with errors of 0.05% and 0.40% achieved using 6 combinations and 10 total electrodes. With discrete myoplasmic and junctional components, comparable accuracy was maintained following adjustments to the junctions to reflect uncoupling. This allowed uncoupling to be quantified as relative increases in total junctional resistance. Our findings suggest development of microfabricated devices to implement the procedure would facilitate routine measurement as a component of cardiac electrophysiological study.

Duke Scholars

Published In

American journal of physiology. Heart and circulatory physiology

DOI

EISSN

1522-1539

ISSN

0363-6135

Publication Date

December 2004

Volume

287

Issue

6

Start / End Page

H2402 / H2411

Related Subject Headings

  • Ventricular Function
  • Myocytes, Cardiac
  • Models, Cardiovascular
  • Microelectrodes
  • Humans
  • Heart Ventricles
  • Heart
  • Gap Junctions
  • Feasibility Studies
  • Electric Stimulation
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Pollard, A. E., Smith, W. M., & Barr, R. C. (2004). Feasibility of cardiac microimpedance measurement using multisite interstitial stimulation. American Journal of Physiology. Heart and Circulatory Physiology, 287(6), H2402–H2411. https://doi.org/10.1152/ajpheart.00289.2004
Pollard, Andrew E., William M. Smith, and Roger C. Barr. “Feasibility of cardiac microimpedance measurement using multisite interstitial stimulation.American Journal of Physiology. Heart and Circulatory Physiology 287, no. 6 (December 2004): H2402–11. https://doi.org/10.1152/ajpheart.00289.2004.
Pollard AE, Smith WM, Barr RC. Feasibility of cardiac microimpedance measurement using multisite interstitial stimulation. American journal of physiology Heart and circulatory physiology. 2004 Dec;287(6):H2402–11.
Pollard, Andrew E., et al. “Feasibility of cardiac microimpedance measurement using multisite interstitial stimulation.American Journal of Physiology. Heart and Circulatory Physiology, vol. 287, no. 6, Dec. 2004, pp. H2402–11. Epmc, doi:10.1152/ajpheart.00289.2004.
Pollard AE, Smith WM, Barr RC. Feasibility of cardiac microimpedance measurement using multisite interstitial stimulation. American journal of physiology Heart and circulatory physiology. 2004 Dec;287(6):H2402–H2411.

Published In

American journal of physiology. Heart and circulatory physiology

DOI

EISSN

1522-1539

ISSN

0363-6135

Publication Date

December 2004

Volume

287

Issue

6

Start / End Page

H2402 / H2411

Related Subject Headings

  • Ventricular Function
  • Myocytes, Cardiac
  • Models, Cardiovascular
  • Microelectrodes
  • Humans
  • Heart Ventricles
  • Heart
  • Gap Junctions
  • Feasibility Studies
  • Electric Stimulation