Duncker D J, Bache R J
Thoraxcenter, Erasmus University Rotterdam, The Netherlands.
Basic Res Cardiol. 1997 Aug;92(4):271-86. doi: 10.1007/BF00788522.
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.
继发于慢性压力超负荷的左心室肥厚(LVH)与心脏做功增加时心肌灌注不足和缺血的易感性增加有关。本研究旨在探讨变时性和变力性刺激对犬肥厚左心室冠状动脉压力-流量关系的影响,并确定心率和收缩力增加对运动诱导的有效背压(零流量时的压力;Pzf)过度增加的个体贡献。7只犬升主动脉缩窄后,左心室与体重之比增加至7.7±0.3 g/kg,而10只正常犬为4.8±0.2 g/kg(p≤0.01)。冠状动脉内注入腺苷可产生最大冠状动脉扩张。在静息状态下,压力超负荷肥厚左心室的最大冠状动脉血流量受损,这是由于Pzf增加(肥厚心室与正常心室分别为25.1±2.6 mmHg和13.8±1.2 mmHg,p≤0.01)以及最大冠状动脉传导性降低(压力-流量关系线性部分的斜率,slopep≥线性)(8.6±1.1 ml/min/mmHg与12.7±0.9 ml/min/mmHg,p≤0.01)。以200和250次/分钟的频率进行右心房起搏,导致肥厚和正常心脏的压力-流量关系类似地向右移位,LVH犬和正常犬的Pzf分别增加3.1±0.8 mmHg和4.7±0.8 mmHg;逐步多变量回归分析表明,充盈压过度降低(10±2 mmHg与6±2 mmHg)和左心室收缩压降低(45±5 mmHg与3±3 mmHg,p≤0.01)可能减弱了肥厚心脏中起搏引起的压力-流量关系更大的向右移位。用多巴酚丁胺(10 - 20微克/千克/分钟,静脉注射)进行变力性刺激,正常心脏的流量变化最小,但导致肥厚心脏的压力-流量关系向右移位4.4±1.5 mmHg(p≤0.05),这与左心室收缩压的更大增加相关(83±16 mmHg与18±4 mmHg,p≤0.05)。运动导致正常和肥厚左心室的压力-流量关系向右移位,但肥厚心脏中Pzf的增加明显更大(1