|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
1 Laboratory of Cardiac Energetics, National Heart, Lung and Blood Institute, Bethesda, MD, USA
* To whom correspondence should be addressed. E-mail: ashikagah{at}nhlbi.nih.gov.
To test the hypothesis that alterations in electrical activation sequence contribute to depressed systolic function in the infarct border zone, we examined the anatomical correlation of abnormal electromechanics and the infarct geometry in the canine post-myocardial infarction (MI) heart, using a high-resolution MR-based cardiac electromechanical mapping technique. Three to eight weeks after creating an MI in six dogs, a 247-electrode epicardial sock was placed over the ventricular epicardium under thoracotomy. MI location and geometry were evaluated with delayed hyperenhancement MRI. Three dimensional systolic strains in epicardial and endocardial layers were measured in five short axis slices using motion tracking MRI (DENSE). Epicardial electrical activation was determined from sock recordings immediately prior to and following the MR scans. The electrodes and MR images were spatially registered to create a total of 160 nodes per heart that contain mechanical, transmural infarct extent, and electrical data. The average depth of the infarct was 55±11% and the infarct covered 28±6% of the LV mass. Significantly delayed activation (>mean+2SD) was observed within the infarct zone. The strain map showed abnormal mechanics, including abnormal stretch and loss of the transmural gradient of radial, circumferential and longitudinal strains, in the region extending far beyond the infarct zone. We conclude that the border zone is characterized by abnormal mechanics directly coupled with normal electrical depolarization. This indicates that impaired function in the border zone is not contributed by electrical factors, but results from mechanical interaction between the ischemic and normal myocardium.
This article has been cited by other articles:
![]() |
Y. Liu, H. Wen, R. C. Gorman, J. J. Pilla, J. H. Gorman III, G. Buckberg, S. D. Teague, and G. S. Kassab Reconstruction of myocardial tissue motion and strain fields from displacement-encoded MR imaging Am J Physiol Heart Circ Physiol, September 1, 2009; 297(3): H1151 - H1162. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. P. O'Regan, R. Ahmed, C. Neuwirth, Y. Tan, G. Durighel, J. V. Hajnal, I. Nadra, S. J. Corbett, and S. A. Cook Cardiac MRI of myocardial salvage at the peri-infarct border zones after primary coronary intervention Am J Physiol Heart Circ Physiol, July 1, 2009; 297(1): H340 - H346. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Hasegawa, S. Nakatani, H. Kanzaki, H. Abe, and M. Kitakaze Heterogeneous Onset of Myocardial Relaxation in Subendocardial and Subepicardial Layers Assessed With Tissue Strain Imaging: Comparison of Normal and Hypertrophied Myocardium J. Am. Coll. Cardiol. Img., June 1, 2009; 2(6): 701 - 708. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. C. Shuros, R. W. Salo, V. G. Florea, J. Pastore, M. A. Kuskowski, Y. Chandrashekhar, and I. S. Anand Ventricular Preexcitation Modulates Strain and Attenuates Cardiac Remodeling in a Swine Model of Myocardial Infarction Circulation, September 4, 2007; 116(10): 1162 - 1169. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. C. Nguyen, A. Cheng, F. Langer, F. Rodriguez, R. A. Oakes, A. Itoh, D. B. Ennis, D. Liang, G. T. Daughters, N. B. Ingels Jr, et al. Altered Myocardial Shear Strains Are Associated With Chronic Ischemic Mitral Regurgitation Ann. Thorac. Surg., January 1, 2007; 83(1): 47 - 54. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Kilic, T. Li, T. D.C. Nolan, J. R. Nash, S. Li, D. J. Prastein, G. Schwartzbauer, S. L. Moainie, G. K. Yankey, C. DeFilippi, et al. Strain-related regional alterations of calcium-handling proteins in myocardial remodeling J. Thorac. Cardiovasc. Surg., October 1, 2006; 132(4): 900 - 908. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH |
| Visit Other APS Journals Online |