Flanagan M F, Fujii A M, Colan S D, Flanagan R G, Lock J E
Department of Cardiology, Children's Hospital, Boston, Mass.
Circ Res. 1991 May;68(5):1458-70. doi: 10.1161/01.res.68.5.1458.
In contrast to young growing animals, pressure-overload hypertrophy in adults is frequently associated with diminished myocardial capillary density and maximal coronary flow per gram. To determine the role of angiogenesis in maintaining perfusion capacity in the hypertrophying heart, the angiogenesis inhibitor protamine sulfate was administered to young lambs during the development of left ventricular (LV) pressure-overload hypertrophy. Baseline and maximum (adenosine) myocardial perfusion was measured in four groups of chronically instrumented 10-week-old lambs subjected to 1) ascending aortic bands since the age of 4 weeks (LVH group, n = 10), 2) sham operation at the age of 4 weeks (SHAM group, n = 8), 3) aortic bands and twice daily injections of protamine since the age of 4 weeks (LVH + P group, n = 9), 4) sham operation and injection of protamine (SHAM + P group, n = 8). Capillary density was measured postmortem. Peak LV pressure and the LV/body weight ratio were similarly increased in LVH and LVH + P compared with sham-operated lambs (p less than 0.001). In LVH lambs, LV capillary number increased by 32% compared with sham-operated lambs (p less than 0.05), and capillary density, coronary flow reserve, and minimal coronary resistance remained normal. In contrast, LVH + P lambs had no significant increase over SHAM lambs in LV capillaries and total maximum coronary flow. The LVH + P lambs had lower LV subendomyocardial capillary density and higher minimal coronary resistance per gram (p less than 0.05 versus LVH lambs). Right ventricular capillary density and minimal resistance were similar in all groups. These findings support the hypotheses that myocardial angiogenesis with pressure-overload hypertrophy is important in maintaining maximal LV coronary flow in the young and that impairment of angiogenesis results in diminished coronary flow capacity.
与生长中的幼龄动物不同,成年动物的压力超负荷肥大常伴有心肌毛细血管密度降低和每克心肌最大冠脉血流量减少。为了确定血管生成在维持肥大心脏灌注能力中的作用,在幼龄羔羊左心室(LV)压力超负荷肥大发展过程中给予血管生成抑制剂硫酸鱼精蛋白。对四组长期植入仪器的10周龄羔羊进行基线和最大(腺苷)心肌灌注测量,这些羔羊分别接受以下处理:1)自4周龄起进行升主动脉缩窄(LVH组,n = 10);2)4周龄时进行假手术(SHAM组,n = 8);3)自4周龄起进行主动脉缩窄并每日两次注射鱼精蛋白(LVH + P组,n = 9);4)假手术并注射鱼精蛋白(SHAM + P组,n = 8)。死后测量毛细血管密度。与假手术羔羊相比,LVH组和LVH + P组的左心室峰值压力和左心室/体重比均显著升高(p < 0.001)。与假手术羔羊相比,LVH组羔羊的左心室毛细血管数量增加了32%(p < 0.05),毛细血管密度、冠脉血流储备和最小冠脉阻力均保持正常。相比之下,LVH + P组羔羊的左心室毛细血管和总最大冠脉血流量与SHAM组羔羊相比无显著增加。LVH + P组羔羊的左心室心内膜下毛细血管密度较低,每克心肌的最小冠脉阻力较高(与LVH组羔羊相比,p < 0.05)。所有组的右心室毛细血管密度和最小阻力相似。这些发现支持以下假设:压力超负荷肥大时的心肌血管生成对维持幼龄动物左心室最大冠脉血流量很重要,血管生成受损会导致冠脉血流能力降低。