Weidinger F F, McLenachan J M, Cybulsky M I, Gordon J B, Rennke H G, Hollenberg N K, Fallon J T, Ganz P, Cooke J P
Division of Cardiology, Brigham and Women's Hospital, Boston, MA 02115.
Circulation. 1990 May;81(5):1667-79. doi: 10.1161/01.cir.81.5.1667.
This study investigated the vasodilator function of endothelium that regenerated after balloon angioplasty and the relation of this function to the extent of vascular injury and to subsequent intimal proliferation. Balloon angioplasty was performed in the left iliac artery of 47 New Zealand White rabbits. Vascular responses were examined in vitro 2 and 4 weeks after a "severe" injury (3.0-mm balloon) or a "moderate" injury (2.5-mm balloon). Both degrees of balloon injury caused complete endothelial denudation. Endothelial regrowth 2 weeks after either injury was confirmed histologically. Although the regenerated cells had irregular sizes and polygonal shapes and lacked the typical alignment in the direction of blood flow, immunocytochemical staining for factor VIII-related antigen identified these cells as endothelium. To study the vasodilator function of regenerated endothelium, rings of balloon-injured and control (contralateral) iliac arteries were suspended in organ chambers for recording of isometric force. Endothelium-dependent relaxation of balloon-injured vessels to acetylcholine and to the calcium ionophore A23187 were reduced at 2 and at 4 weeks after severe injury. After moderate injury, endothelium-dependent relaxations to these agents were reduced at 2 weeks but had normalized by 4 weeks. Endothelium-independent relaxation to sodium nitroprusside, however, was preserved in all study groups. Morphometric analysis revealed an inverse correlation between the degree of intimal thickening and maximal relaxation to acetylcholine (r = 0.45, p less than 0.01). Thus, there is a persistent attenuation of receptor- and nonreceptor-mediated endothelium-dependent relaxations after arterial injury. The regenerated cells have an altered morphological appearance, but staining for factor VIII-related antigen confirms their endothelial origin. The degree and duration of endothelial dysfunction depends on the severity of the initial injury and is related to the extent of intimal thickness.
本研究调查了球囊血管成形术后再生内皮的血管舒张功能,以及该功能与血管损伤程度和随后内膜增生的关系。对47只新西兰白兔的左髂动脉进行球囊血管成形术。在“重度”损伤(3.0毫米球囊)或“中度”损伤(2.5毫米球囊)后2周和4周,体外检测血管反应。两种程度的球囊损伤均导致内皮完全剥脱。组织学证实两种损伤后2周内皮均有再生。尽管再生细胞大小不规则、呈多边形,且缺乏沿血流方向的典型排列,但因子VIII相关抗原的免疫细胞化学染色将这些细胞鉴定为内皮细胞。为研究再生内皮的血管舒张功能,将球囊损伤和对照(对侧)髂动脉环悬挂于器官浴槽中记录等长力。重度损伤后2周和4周,球囊损伤血管对乙酰胆碱和钙离子载体A23187的内皮依赖性舒张反应降低。中度损伤后,对这些药物的内皮依赖性舒张反应在2周时降低,但在4周时恢复正常。然而,所有研究组对硝普钠的非内皮依赖性舒张反应均得以保留。形态学分析显示内膜增厚程度与对乙酰胆碱的最大舒张反应呈负相关(r = 0.45,p < 0.01)。因此,动脉损伤后受体介导和非受体介导的内皮依赖性舒张反应持续减弱。再生细胞形态外观改变,但因子VIII相关抗原染色证实其内皮来源。内皮功能障碍的程度和持续时间取决于初始损伤的严重程度,并与内膜厚度相关。