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Ejection has both positive and negative effects on left ventricular isovolumic relaxation
D S Berger1, K Vlasica, C M Quick
1Department of Medicine, University of Chicago, Illinois 60637, USA.
The American Journal of Physiology
|January 22, 1998
Summary
Ejection during heartbeats influences left ventricular relaxation speed. While current ejection hastens relaxation, prior ejection history slows it, with both effects potentially linked to myofilament calcium sensitivity.
Area of Science:
- Cardiovascular Physiology
- Cardiac Mechanics
Background:
- Left ventricular (LV) relaxation speed in isovolumic beats is determined by peak active stress.
- The relationship between ejection and LV relaxation is less understood, though ejection is generally believed to hasten relaxation.
Purpose of the Study:
- To investigate how cardiac ejection modifies the relationship between LV relaxation and peak active stress.
- To develop a model predicting LV relaxation during ejection beats.
Main Methods:
- Isolated rabbit hearts were subjected to varied loading conditions.
- Left ventricular pressure and volume were measured to calculate active stress.
- Relaxation time (Tr) was defined as the time for stress to fall from 75% to 25% of peak stress.
- A multiple regression model was developed using steady-state and transient isovolumic and ejection beat data.
Main Results:
- Peak active stress, current beat ejection, and previous beat ejection history were identified as independent predictors of relaxation time (Tr).
- The model accurately predicted relaxation in isovolumic beats (r2 > 0.98) and showed predictive capability for transient ejection beats (r2 = 0.30).
- Current ejection hastened relaxation (negative coefficient), while ejection history slowed it (positive coefficient), resulting in a net hastening effect.
Conclusions:
- Cardiac ejection significantly impacts LV relaxation dynamics, with both immediate and historical effects.
- The observed effects suggest non-mechanical mechanisms, possibly related to ejection-mediated alterations in myofilament calcium sensitivity.