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Published on: April 13, 2015
Effect of chronotropic and inotropic stimulation on the coronary pressure-flow relation in left ventricular
1Thoraxcenter, Erasmus University Rotterdam, The Netherlands. duncker@tch.fgg.eur.nl
Insights
Left ventricular hypertrophy (LVH) impairs coronary blood flow, especially during exercise. Increased heart rate and contractility worsen this effect by raising coronary back pressure in hypertrophied hearts.
Area of Science:
- Cardiovascular Physiology
- Cardiac Hypertrophy Research
Background:
- Left ventricular hypertrophy (LVH) from chronic pressure overload increases susceptibility to myocardial hypoperfusion during increased cardiac workload.
- Understanding the coronary circulation's response to stimuli in LVH is crucial for managing ischemic events.
Purpose of the Study:
- To investigate the effects of chronotropic and inotropic stimulation on the coronary pressure-flow relationship in dogs with pressure-overload-induced LVH.
- To quantify the contributions of heart rate and contractility increases to exercise-induced coronary back pressure elevation in LVH.
Main Methods:
- Created LVH in dogs via ascending aortic banding, confirmed by increased LV to body weight ratio.
- Maximized coronary vasodilation using intracoronary adenosine infusion.
- Assessed coronary pressure-flow relations under resting, pacing (chronotropic), dobutamine (inotropic), and exercise conditions.
Main Results:
- Resting LVH hearts showed impaired maximal coronary blood flow due to increased pressure at zero flow (Pzf) and decreased coronary conductance.
- Atrial pacing caused similar rightward shifts in pressure-flow relations for both normal and LVH hearts, with LVH showing a blunted shift potentially due to filling and systolic pressure changes.
- Inotropic stimulation with dobutamine shifted the pressure-flow relation rightward in LVH hearts, correlating with increased LV systolic pressure.
- Exercise significantly increased Pzf more in LVH hearts than normal hearts, indicating limited myocardial perfusion.
Conclusions:
- LVH significantly impairs coronary conductance and increases resting Pzf.
- Both heart rate and contractility increases contribute to the exaggerated rise in coronary back pressure during exercise in LVH.
- These findings highlight the compromised coronary reserve and increased risk of ischemia in pressure-overloaded hypertrophied ventricles.
Abstract:
Left ventricular hypertrophy (LVH) secondary to chronic pressure overload is associated with increased susceptibility to myocardial hypoperfusion and ischemia during increased cardiac work. The present study was performed to study the effects of chronotropic and inotropic stimulation on the coronary pressure-flow relation of the hypertrophied left ventricle of dogs and to determine the individual contributions of increases in heart rate and contractility to the exaggerated exercise-induced increases in effective back pressure (pressure at zero flow; Pzf). Ascending aortic banding in seven dogs increased the LV to body weight ratio to 7.7 +/- 0.3 g/kg compared to 4.8 +/- 0.2 g/kg in 10 normal dogs (p < or = 0.01). Maximum coronary vasodilation was produced by intracoronary infusion of adenosine. During resting conditions maximum coronary blood flow in the pressure overloaded hypertrophied left ventricle was impaired by both an increase in Pzf (25.1 +/- 2.6 vs 13.8 +/- 1.2 mmHg in hypertrophied vs normal ventricles, respectively, p < or = 0.01) and a decrease in maximum coronary conductance (slope of the linear part of the pressure-flow relation, slopep > or = linear) (8.6 +/- 1.1 vs 12.7 +/- 0.9 ml/min/mmHg, p < or = 0.01). Right atrial pacing at 200 and 250 beats/min resulted in similar rightward shifts of the pressure-flow relation in hypertrophied and normal hearts with 3.1 +/- 0.8 and 4.7 +/- 0.8 mmHg increases in Pzf in LVH and normal dogs, respectively; stepwise multivariate regression analysis indicated that the exaggerated decrease in filling pressure (10 +/- 2 vs 6 +/-2 mmHg) and decrease in left ventricular systolic pressure (45 +/- 5 vs 3 +/- 3 mmHg, p < or = 0.01) may have blunted a greater rightward shift of the pressure-flow relation produced by atrial pacing in the hypertrophied hearts. Inotropic stimulation with dobutamine (10-20 micrograms/kg/min, i.v.) resulted in minimal flow changes in normal hearts but produced a 4.4 +/- 1.5 mmHg (p < or = 0.05) rightward shift of the pressure-flow relation in hypertrophied hearts. which correlated with a greater increase in left ventricular systolic pressure (83 +/- 16 vs 18 +/- 4 mmHg. p < or = 0.05). Exercise resulted in a rightward shift in both normal and hypertrophied left ventricles, but the increase in Pzf was significantly greater in the hypertrophied hearts (15.2 +/- 0.9 vs 10.3 +/- 0.9 mmHg. p < or = 0.05). Stepwise multivariate regression analysis indicated that not only increases in left ventricular filling pressure, but also increases in heart rate and LV systolic pressure contributed to the abnormally great increase in effective coronary back pressure which results in limitation of myocardial perfusion during exercise in the pressure overloaded hypertrophied left ventricle.
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