Key result
Endotoxin impairs biventricular function, triggering early LV dilation followed by delayed systolic depression.
Why the study?
The temporal sequence and distinct time courses of endotoxin-induced systolic and diastolic myocardial depression were not well characterized.
Does endotoxin induce systolic and diastolic myocardial depression with distinct time courses in anesthetized rabbits?
Does endotoxin induce systolic and diastolic myocardial depression with distinct time courses in anesthetized rabbits?
Endotoxin impairs systolic and diastolic LV function with distinct time courses, suggesting that contractility, relaxation, and passive LV properties are impaired by different endotoxin-mediated pathways.
Answers are grounded in this paper and cite their sources.
Phased LV changes in this rabbit model should not change practice; hypothesis-generating for distinct systolic-diastolic pathways in sepsis.
Twelve anesthetized rabbits received endotoxin (175 +/- 38 micrograms/kg i.v., mean +/- SD) to evaluate the temporal sequence of alterations in left ventricular (LV) function. LV volume was calculated from LV minor- and long-axis diameters, and wall thickness was measured with sonomicrometers. Hypotension, acidosis, and hypoxia were immediately corrected to eliminate these causes of myocardial depression. LV dilation developed early (1.2 +/- 0.5 h) with a significant (21 +/- 23%) increase in end-diastolic volume measured at a LV end-diastolic pressure of 5 +/- 6 mmHg. The LV stiffness did not change, and the LV dilation did not progressively worsen. Significant systolic depression developed later (2.8 +/- 1.0 h) with a 32 +/- 22% increase in end-systolic volume measured at a LV end-systolic pressure of 69 +/- 9 mmHg. The late preterminal phase (4.1 +/- 0.8 h) was characterized by a progressive increase in end-systolic volume (73 +/- 41% above control) and a significant (53 +/- 34%) increase in tau, the time constant of LV pressure fall. Diastolic abnormalities (LV dilation and increased tau) were not attributable to depressed contractility or altered hemodynamics. We conclude that endotoxin impairs systolic and diastolic LV function with distinct differences in time course. This suggests that contractility, relaxation, and passive LV properties are impaired by different endotoxin-mediated pathways and/or have different sensitivities to endotoxin.
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Hung et al. (1993) studied Endotoxin-induced myocardial depression (n=12). Endotoxin vs. Control (baseline) was evaluated on Temporal sequence of alterations in left ventricular (LV) function. Endotoxin administration in rabbits impaired systolic and diastolic left ventricular function with distinct differences in time course, showing early LV dilation and later systolic depression.
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