Bache R J, Stark R P, Duncker D J
Cardiovascular Division, University of Minnesota Medical School, Minneapolis 55455.
Circulation. 1992 Nov;86(5):1559-65. doi: 10.1161/01.cir.86.5.1559.
The coronary circulation has been shown to remain responsive to vasodilator and vasoconstrictor stimuli during myocardial ischemia. Because serotonin possesses both vasodilator and vasoconstrictor properties, we examined its effect in the coronary circulation distal to an arterial stenosis that resulted in myocardial hypoperfusion during exercise.
Seven chronically instrumented dogs were studied during treadmill exercise in the presence of a stenosis that reduced distal left circumflex coronary artery perfusion pressure to 42 +/- 1 mm Hg. Myocardial blood flow was assessed with radioactive microspheres during exercise before and during intracoronary infusion of 0.4 and 2.0 micrograms/kg-1.min-1 serotonin. The stenosis was adjusted to maintain distal coronary pressure constant during control exercise and with the two doses of serotonin. In seven dogs, the effect of serotonin (2.0 micrograms/kg-1.min-1) was also studied during exercise with normal arterial inflow. During control exercise, the stenosis decreased mean myocardial blood flow to 45% of flow in the normally perfused region. This decrease was most pronounced in the subendocardium (endocardial/epicardial ratio 0.36 +/- 0.06 versus 1.46 +/- 0.14 in the control region; p < 0.01). With no change in pressure distal to the stenosis, serotonin decreased subendocardial flow from 0.51 +/- 0.09 ml/min-1.g-1 to 0.41 +/- 0.12 (p < 0.05) and then to 0.35 +/- 0.08 ml/min-1.g-1 (p < 0.05) and tended to increase subepicardial flow from 1.47 +/- 0.17 to 1.91 +/- 0.23 and 1.85 +/- 0.21 ml/min-1.g-1 (p = 0.08) during infusions of 0.5 and 2.0 micrograms/kg-1.min-1, respectively, with no change in total arterial inflow. In contrast, in the absence of a stenosis, serotonin (2.0 micrograms/kg-1.min-1) increased subendocardial flow from 2.43 +/- 0.25 to 3.73 +/- 0.25 ml/min-1.g-1 (p < 0.01) and subepicardial flow from 1.88 +/- 0.20 to 5.29 +/- 0.38 ml/min-1.g-1 (p < 0.01).
During normal arterial inflow, serotonin dilated coronary resistance vessels and increased flow to all myocardial layers. During hypoperfusion, a vasodilator response was still present in the subepicardium, but vasoconstriction was then observed in the subendocardium. Our data suggest that serotonin constricts the intramural penetrating arteries, thereby selectively increasing resistance to subendocardial blood flow.
研究表明,在心肌缺血期间,冠状动脉循环对血管舒张剂和血管收缩剂刺激仍有反应。由于血清素兼具血管舒张和收缩特性,我们研究了其在运动期间导致心肌灌注不足的动脉狭窄远端的冠状动脉循环中的作用。
对7只长期植入仪器的犬在跑步机运动期间进行研究,存在使左回旋支冠状动脉远端灌注压降至42±1mmHg的狭窄。在冠状动脉内输注0.4和2.0微克/千克-1·分钟-1血清素之前和期间运动时,用放射性微球评估心肌血流量。在对照运动期间以及使用两剂血清素时,调整狭窄以维持冠状动脉远端压力恒定。在7只犬中,还研究了血清素(2.0微克/千克-1·分钟-1)在正常动脉血流运动期间的作用。在对照运动期间,狭窄使平均心肌血流量降至正常灌注区域血流量的45%。这种减少在心肌内膜下最为明显(心肌内膜/心肌外膜比率为0.36±0.06,而对照区域为1.46±0.14;p<0.01)。在狭窄远端压力无变化的情况下,血清素使心肌内膜下血流从0.51±0.09毫升/分钟-1·克-1降至0.41±0.12(p<0.05),然后降至0.35±0.08毫升/分钟-1·克-1(p<0.05),并且在分别输注0.5和2.0微克/千克-1·分钟-1血清素期间,心肌外膜下血流倾向于从1.47±0.17增加至1.91±0.23和1.85±0.21毫升/分钟-1·克-1(p=0.08),总动脉血流量无变化。相比之下,在无狭窄的情况下,血清素(2.0微克/千克-1·分钟-1)使心肌内膜下血流从2.43±0.25增加至3.73±0.25毫升/分钟-1·克-1(p<0.01),心肌外膜下血流从1.88±0.20增加至5.29±0.38毫升/分钟-1·克-1(p<0.01)。
在正常动脉血流期间,血清素使冠状动脉阻力血管扩张并增加所有心肌层的血流。在灌注不足期间,心肌外膜下仍存在血管舒张反应,但在心肌内膜下则观察到血管收缩。我们的数据表明,血清素使壁内穿通动脉收缩,从而选择性增加对心肌内膜下血流的阻力。