Ghaleh B, Hittinger L, Kim S J, Kudej R K, Iwase M, Uechi M, Berdeaux A, Bishop S P, Vatner S F
Cardiovascular and Pulmonary Research Institute, Allegheny University of the Health Sciences, Pittsburgh, Pennsylvania 15212, USA.
Am J Physiol. 1998 Feb;274(2):H539-51. doi: 10.1152/ajpheart.1998.274.2.H539.
Coronary vascular responses to acetylcholine (ACh, 3 micrograms/kg i.v.), nitroglycerin (NTG, 25 micrograms/kg i.v.), and a 20-s coronary artery occlusion (reactive hyperemia, RH) were investigated in seven conscious dogs with severe left ventricular (LV) hypertrophy and chronic coronary pressure overload (CCPO) due to supravalvular aortic banding and in seven control dogs. All dogs were instrumented for measurement of ultrasonic coronary diameter (CD) and Doppler coronary blood flow (CBF). LV-to-body weight ratio was increased by 82% in CCPO dogs. In control dogs, ACh increased CD (+ 5.9 +/- 1.7%). This response was reduced (P < 0.05) in CCPO dogs (+ 1.9 +/- 0.9%). Similarly, flow-mediated increases in CD after RH were blunted (P < 0.01) in CCPO (+ 2.1 +/- 0.8) vs. control dogs (+ 6.8 +/- 1.8%). In contrast, ACh and RH increased CBF similarly in both groups. Increases in both CD and CBF to NTG were not different between control dogs and CCPO. Peak systolic CBF velocity was greater, P < 0.01, in CCPO (94 +/- 17 cm/s) compared with control (35 +/- 7 cm/s) dogs, most likely secondary to the increased systolic coronary perfusion pressure (215 vs. 130 mmHg). Histological analyses of large coronary arteries in CCPO revealed medial thickening, intimal thickening, and disruption of the internal elastic lamina and endothelium. In contrast, small intramyocardial arterioles failed to show the intimal and endothelial lesions. Thus, in CCPO selective to the coronary arteries, i.e., a model independent from systemic hypertension and enhanced levels of plasma renin activity, endothelial control was impaired for both flow-mediated and receptor-mediated large coronary artery function, which could be accounted for by the major morphological changes in the large coronary arteries sparing the resistance vessels. The mechanism may involve chronically elevated systolic coronary perfusion pressure, CBF velocity, and potential disruption of laminar flow patterns.
在七只因主动脉瓣上缩窄导致严重左心室(LV)肥厚和慢性冠状动脉压力超负荷(CCPO)的清醒犬以及七只对照犬中,研究了冠状动脉对乙酰胆碱(ACh,3微克/千克静脉注射)、硝酸甘油(NTG,25微克/千克静脉注射)和20秒冠状动脉闭塞(反应性充血,RH)的反应。所有犬均安装了用于测量超声冠状动脉直径(CD)和多普勒冠状动脉血流(CBF)的仪器。CCPO犬的左心室与体重比增加了82%。在对照犬中,ACh使CD增加(+5.9±1.7%)。在CCPO犬中这种反应减弱(P<0.05)(+1.9±0.9%)。同样,RH后由血流介导的CD增加在CCPO犬(+2.1±0.8)中比对照犬(+6.8±1.8%)减弱(P<0.01)。相比之下,ACh和RH在两组中对CBF的增加相似。对照犬和CCPO犬中CD和CBF对NTG的增加没有差异。CCPO犬的收缩期CBF峰值速度更高(P<0.01)(94±17厘米/秒),而对照犬为(35±7厘米/秒),这很可能继发于收缩期冠状动脉灌注压力的增加(215对130毫米汞柱)。CCPO犬大冠状动脉的组织学分析显示中膜增厚、内膜增厚以及内弹性膜和内皮的破坏。相比之下,心肌内小动脉未显示内膜和内皮病变。因此,在CCPO中,即一种独立于系统性高血压和血浆肾素活性升高水平的模型,对于冠状动脉具有选择性,血流介导和受体介导的大冠状动脉功能的内皮控制受损,这可能是由大冠状动脉的主要形态学改变所导致的,而阻力血管未受影响。其机制可能涉及收缩期冠状动脉灌注压力的长期升高、CBF速度以及层流模式的潜在破坏。