Sugihara T, Hattori Y, Yamamoto Y, Qi F, Ichikawa R, Sato A, Liu M Y, Abe K, Kanno M
Department of Plastic and Reconstructive Surgery, Hokkaido University School of Medicine, Sapporo, Japan.
Circulation. 1999 Aug 10;100(6):635-41. doi: 10.1161/01.cir.100.6.635.
Vascular abnormalities are a major cause of postoperative complications in irradiated tissues. Endothelial cell dysfunction characterized by diminished endothelium-dependent relaxation may be involved. We examined the endothelium-dependent relaxation and morphology of the endothelium in irradiated human cervical arteries.
Irradiated arteries were taken from the neck region of patients who had radiation therapy. Arteries from patients who did not receive radiation therapy were used as controls. Endothelium-dependent relaxation to acetylcholine and A23187 was impaired in irradiated arteries. Norepinephrine-induced contraction and sodium nitroprusside-induced relaxation were unchanged. In control arteries, N(omega)-nitro-L-arginine and indomethacin each caused a partial inhibition of endothelium-dependent relaxation. In irradiated arteries, the impaired endothelium-dependent relaxation was unaffected by these agents, but it was abolished by high K(+). Acetylcholine produced similar degrees of hyperpolarization in control and irradiated arteries. Immunohistochemical examination for endothelial nitric oxide synthase indicated no expression in the endothelium of irradiated arteries. Electron scanning microscopy showed morphologically intact endothelial cells in irradiated arteries.
In irradiated human cervical arteries, the nitric oxide- and prostacyclin-mediated endothelium-dependent relaxation, but not endothelium-derived hyperpolarizing factor-mediated relaxation, are specifically impaired, without significant morphological damage of the endothelium. The impaired nitric oxide-mediated relaxation was associated with a lack of endothelial nitric oxide synthase expression. Our results suggest the importance of impaired endothelial function in irradiated human blood vessels, which may partly explain the development of vascular stenosis and poor surgical wound healing in irradiated tissues.
血管异常是放疗组织术后并发症的主要原因。可能涉及以内皮依赖性舒张功能减弱为特征的内皮细胞功能障碍。我们研究了放疗后人类颈动脉的内皮依赖性舒张功能及内皮形态。
放疗后的动脉取自接受放射治疗患者的颈部区域。未接受放射治疗患者的动脉用作对照。放疗后的动脉对乙酰胆碱和A23187的内皮依赖性舒张功能受损。去甲肾上腺素诱导的收缩和硝普钠诱导的舒张功能未改变。在对照动脉中,N(ω)-硝基-L-精氨酸和吲哚美辛各自部分抑制内皮依赖性舒张。在放疗后的动脉中,受损的内皮依赖性舒张不受这些药物影响,但高钾可消除该作用。乙酰胆碱在对照和放疗后的动脉中产生相似程度的超极化。内皮型一氧化氮合酶的免疫组织化学检查显示放疗后的动脉内皮中无表达。电子扫描显微镜显示放疗后的动脉内皮细胞形态完整。
在放疗后的人类颈动脉中,一氧化氮和前列环素介导的内皮依赖性舒张功能,而非内皮衍生超极化因子介导的舒张功能,受到特异性损害,而内皮无明显形态学损伤。一氧化氮介导的舒张功能受损与内皮型一氧化氮合酶表达缺失有关。我们的结果提示放疗后人类血管内皮功能受损的重要性,这可能部分解释了放疗组织中血管狭窄的发生及手术伤口愈合不良的原因。