Key result
Experimental MI in rabbits fails to alter passive elasticity over 10 days versus noninfarcted controls.
Why the study?
The inability of normal myocardium to sustain life after 30-50% LV necrosis despite substantial reserve and the role of infarct dyskinesia in initiating failure were unclear.
Following experimental cryogenic infarction in rabbits, the passive elasticity of the infarcted myocardial tissue remains unchanged over 10 days, indicating that contractile reserve falls rapidly with increasing infarct size.
Unchanged passive elasticity after rabbit infarction cautions against stiffness-driven remodeling assumptions; leaves open mechanisms of contractile reserve loss and human relevance.
Given the substantial reserve of normal myocardium, its inability to sustain life in the presence of 30-50% necrosis of the left ventricle (LV) seems a paradox. It is known that dyskinesia of the infarcted area probably plays a dominant role in initiating failure after an infarction. To study this problem, a well defined experimental infarction was produced by cryogenic means in 58 rabbits, and the animals were allowed to recover. Groups of rabbits were killed 4 hours and 1,2,5, or 10 days following infarction. As quickly as possible (within 4 minutes) a sample specimen from the infarcted area was removed from the LV and subjected to a force-elongation test while being bathed in Ringer solution at 37 degrees C equilibrated with 95% O2-5% CO2. The data were interpreted assuming an exponential stress-strain law with constants K and C. Mean values of K of 10.6 +/- 0.94 (SEM) were found for the noninfarcted control group, whereas, rather surprisingly, no significant trend in K over 10 days was found in the infarcted group. Mean values of K +/- SEM for the postinfarction groups were as follows: 4 hours, 9.51 +/- 0.63; 1 day 10.54 +/- 1.13; 2 days, 13.15 +/- 2.28; 5 days, 11.59 +/- 1.36; and over 10 days, 12.93 +/-1.02. The functional implications were estimated with a simple model of the shortening required of the viable muscle during the isovolumic phase. It was found that contractile reserve fell rapidly with increasing infarct size, reaching zero for a 60% infarct when K = 10. With K greater than 100, there was no appreciable reduction in reserve. With a constant infarct size, variation in reserve with the afterload-preload ration was found to be logarithmic.
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Laird et al. (1977) studied Experimental myocardial infarction (n=58). Experimental myocardial infarction vs. Noninfarcted control group was evaluated on Passive elasticity constant K. Experimental myocardial infarction in rabbits produced no significant trend in the passive elasticity constant K over 10 days compared to a noninfarcted control group mean of 10.6.
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