Cwikiel M, Zhang B, Eskilsson J, Wieslander J B, Albertsson M
Department of Oncology, University Hospital, Lund, Sweden.
Scanning Microsc. 1995 Jun;9(2):561-76.
5-Fluorouracil (5-FU) is a widely used antineoplastic agent. 5-FU induced cardiotoxicity is a still relatively unknown side-effect of this drug. This phenomenon could be due to a direct cytotoxic effect on the endothelial cells. We tested this hypothesis in an experimental study in rabbits, by scanning or transmission electron microscopic evaluation of endothelium in small arteries (the central artery of the ear) after in vivo treatment with 5-FU. Both local and systemic effects of 5-FU on endothelium were studied 15, 30, 60 and 120 minutes after intra-arterial or intraperitoneal treatment. Perfusion fixation at physiological pressure and temperature was used in order to minimize damage to the endothelium during the preparation procedure. Eighteen rabbits weighing 2.5-3.0 kg were used, and 6 animals served as controls. The following parameters were evaluated: vessel wall and endothelial cell contraction, cell edema, cytolysis, occurrence of denuded areas, platelet adhesion/aggregation and fibrin formation. For the description of each parameter a scale of negative points was used. Irreversible cell damage was observed in 5-FU treated animals: disruption of the endothelial sheet and patchy exposure of the subendothelium, sometimes as a focus for thrombus formation. Our findings support the hypothesis that the thrombogenic effect of 5-FU secondary to its direct cytotoxic effect on endothelium might be one of the pathophysiological mechanisms behind 5-FU induced cardiotoxicity.
5-氟尿嘧啶(5-FU)是一种广泛使用的抗肿瘤药物。5-FU诱导的心脏毒性是这种药物一种仍相对不为人知的副作用。这种现象可能是由于对内皮细胞的直接细胞毒性作用。我们在一项针对兔子的实验研究中检验了这一假设,通过对5-FU体内治疗后小动脉(耳中央动脉)内皮进行扫描或透射电子显微镜评估。在动脉内或腹腔内给药后15、30、60和120分钟研究了5-FU对内皮的局部和全身作用。为了在制备过程中尽量减少对内皮的损伤,采用了生理压力和温度下的灌注固定。使用了18只体重2.5 - 3.0千克的兔子,6只动物作为对照。评估了以下参数:血管壁和内皮细胞收缩、细胞水肿、细胞溶解、剥脱区域的出现、血小板黏附/聚集以及纤维蛋白形成。对于每个参数的描述使用了负分制。在5-FU治疗的动物中观察到了不可逆的细胞损伤:内皮细胞层的破坏和内皮下的片状暴露,有时成为血栓形成的部位。我们的研究结果支持这样的假设,即5-FU对内皮的直接细胞毒性作用继发的血栓形成效应可能是5-FU诱导心脏毒性背后的病理生理机制之一。