The long range goal of our research program is to quantify intercellular coupling in acute and chronic heart dis- ease, which will lead to dramatically improved descriptions of arrhythmia substrates. Maintenance of coupling strength between cardiac myocytes is essential for normal electrical activity. That strength depends primarily on intracellular gap junction coupling and on interstitial coupling in the fibrillar collagen network. Each flow path is well recognized and there is considerable evidence to suggest microimpedance increases promote arrhyth- mias. Until recently, no procedure or standard instrument for measuring intracellular and interstitial impedances has been available, so information on their magnitudes is limited. The major near-term goal of this proposal is to apply our newly developed theoretical and experimental approach to measuring intracellular and intersti- tial microimpedances. That approach involves use of a precisely designed but very small set of electrodes for multisite stimulation and mathematical evaluation of the underlying tissue impedances from the set of recorded voltages. It has the potential to become a straightforward component of cardiac electrophysiologic study because no intracellular access is required to obtain the microimpedances. This RO1 scale Bioengineering Research Grant, which is responsive to PA-07-279, builds on expertise developed in our R21 scale Exploratory Bioengi- neering Research Grant. Studies will focus on rabbit left ventricular epicardium, providing quantitative details for this specific preparation. This revised application has the following aims: (1) to transition our microimpedance measurement approach from its developmental framework for application to heart preparations;(2) to measure spatial variabilities in directional interstitial microimpedances under normal conditions and during interstitial com- partment size adjustments;(3) to measure spatial variabilities in directional intracellular microimpedances under normal conditions and during interventions targeting gap junctions;and (4) to quantify microimpedance changes during development of ischemia-like conditions and subsequent reperfusion. The project is significant because the electrical properties of intracellular and interstitial pathways for cardiac excitation as they exist in vivo will be carefully measured on the size scale where propagation failure contributes to arrhythmia initiation and mainte- nance. Completion of the project's near-term objectives will have a longer-term impact because it will allow us to focus on adapting our approach for use with animal models of chronic heart disease, preparations that include interfaces between different tissue types and simultaneous stimulation and recording from multiple microelectrical mechanical systems arrays to obtain regional microimpedance measurements. Thesaurus Terms: electrical impedance, electrical measurement, heart electrical activity, interstitial, intracellular, method development, cardiac myocyte, electrical conductance, membrane model, myocardium, electrode.

Public Health Relevance

Intercellular uncoupling is broadly invoked as a mechanism for the initiation and maintenance of cardiac ar- rhythmias, although uncoupling as a term is used in a qualitative sense without precise definition. Successful completion of the objectives in this proposal will result, for the first time, in detailed quantitative descriptions of all directional intracellular and interstitial compartment microimpedances in rabbit left ventricular epicardium. This will impact public health by allowing integration of our knowledge of ion channel activity with the tissue's microimpedances in designing pharmacologic and electrical approaches to prevention and treatment of cardiac arrhythmias.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL092049-04
Application #
8257568
Study Section
Bioengineering, Technology and Surgical Sciences Study Section (BTSS)
Program Officer
Lathrop, David A
Project Start
2009-07-15
Project End
2015-02-28
Budget Start
2013-03-01
Budget End
2014-02-28
Support Year
4
Fiscal Year
2013
Total Cost
$280,131
Indirect Cost
$63,985
Name
University of Alabama Birmingham
Department
Biomedical Engineering
Type
Schools of Engineering
DUNS #
063690705
City
Birmingham
State
AL
Country
United States
Zip Code
35294
Yan, Jiajie; Thomson, Justin K; Wu, Xiaomin et al. (2014) Novel methods of automated quantification of gap junction distribution and interstitial collagen quantity from animal and human atrial tissue sections. PLoS One 9:e104357
Waits, Charlotte Mae K; Barr, Roger C; Pollard, Andrew E (2014) Sensor spacing affects the tissue impedance spectra of rabbit ventricular epicardium. Am J Physiol Heart Circ Physiol 306:H1660-8
Pollard, Andrew E; Barr, Roger C (2013) A new approach for resolution of complex tissue impedance spectra in hearts. IEEE Trans Biomed Eng 60:2494-503
Pollard, Andrew E; Barr, Roger C (2010) A biophysical model for cardiac microimpedance measurements. Am J Physiol Heart Circ Physiol 298:H1699-709