Crabos M, Coste P, Paccalin M, Tariosse L, Daret D, Besse P, Bonoron-Adele S
INSERM U441, Hôpital de Cardiologie Haut-Lévêque, Université de Bordeaux II, Pessac-Bordeaux, France.
J Mol Cell Cardiol. 1997 Jan;29(1):55-65. doi: 10.1006/jmcc.1996.0251.
Basal vasomotor tone in coronary vessels is, in part, maintained by nitric oxide (NO) production by endothelial constitutive NO synthase (ecNOS). Alteration of coronary circulation observed in left ventricular hypertrophy secondary to hypertension could be associated with a decrease in NO production. The aim of this study was to measure: (1) coronary flow in the Langendorff-perfused heart model at baseline, after maximum vasodilation in response to adenosine (10(-5) M), after endothelium-dependent vasodilation in response to bradykinin (10(-8) M) and after ecNOS inhibition by nitro-L-arginine methyl ester (L-NAME) (10(-4) M); (2) medial thickening of coronary microvessels and perivascular collagen on histological heart sections; and (3) ecNOS expression by immunohistochemical staining in these vessels using 20-week-old spontaneously hypertensive (SHR) and Wistar-Kyoto control rats (WKY). These measurements were determined by computer-directed color analysis. When SHR were compared with WKY rats, we found: (1) a decrease in basal flow (10.1+/-0.6 v 15.3+/-1.2 ml/min/g, n=10, P<0.0001), in maximum flow (15.4+/-0.7 v 24.3+/-1.3 ml/min/g, n=10, P<0.001), in bradykinin-induced flow increment (1.5+/-0.3 v 2.6+/-0.3 ml/min/g, n=5, P<0.05) and in L-NAME-sensitive flow (3.3+/-0.6 v 6.3+/-0.9 ml/min/g, n=7, P<0.05); (2) an increase in medial thickness (9.4+/-0.6 v 5.4+/-0.3 microm, n=8, P<0.001) and in perivascular collagen area (1509+/-311 v 462+/-120 microm2, n=8, P<0.01) of coronary arterioles; and (3) a decrease in ecNOS expression in the endothelium (ecNOS-stained cross-sectional area in arterioles: 40.0+/-9.1 v 84.6+/-9.0 microm2, n=7, P<O.005). These results suggest that in SHR the decrease in basal coronary flow can be related to a structural alteration of the microvessels with an increase of perivascular collagen but also to a decrease in ecNOS expression which might be associated with reduced NO production.
冠状动脉的基础血管舒缩张力部分由内皮型一氧化氮合酶(ecNOS)产生的一氧化氮(NO)维持。高血压继发左心室肥厚时观察到的冠状动脉循环改变可能与NO生成减少有关。本研究的目的是测量:(1)在Langendorff灌注心脏模型中,基线时、对腺苷(10⁻⁵ M)最大血管舒张后、对缓激肽(10⁻⁸ M)内皮依赖性血管舒张后以及用硝基-L-精氨酸甲酯(L-NAME)(10⁻⁴ M)抑制ecNOS后冠状动脉血流量;(2)心脏组织学切片上冠状动脉微血管的中层增厚和血管周围胶原;(3)使用20周龄自发性高血压大鼠(SHR)和Wistar-Kyoto对照大鼠(WKY),通过免疫组织化学染色测定这些血管中ecNOS的表达。这些测量通过计算机指导的颜色分析来确定。将SHR与WKY大鼠比较时,我们发现:(1)基础血流量减少(10.1±0.6对15.3±1.2 ml/min/g,n = 10,P<0.0001)、最大血流量减少(15.4±0.7对24.3±1.3 ml/min/g,n = 10,P<0.001)、缓激肽诱导的血流量增加减少(1.5±0.3对2.6±0.3 ml/min/g,n = 5,P<0.05)以及L-NAME敏感的血流量减少(3.3±0.6对6.3±0.9 ml/min/g,n = 7,P<0.05);(2)冠状动脉小动脉的中层厚度增加(9.4±0.6对5.4±0.3μm,n = 8,P<0.001)和血管周围胶原面积增加(1509±311对462±120μm²,n = 8,P<0.01);(3)内皮中ecNOS表达减少(小动脉中ecNOS染色的横截面积:40.0±9.1对84.6±9.0μm²,n = 7,P<0.005)。这些结果表明,在SHR中,基础冠状动脉血流量减少可能与微血管结构改变及血管周围胶原增加有关,也与ecNOS表达减少有关,而这可能与NO生成减少有关。