Langberg C W, Sauer T, Reitan J B, Hauer-Jensen M
Department of Oncology, Ullevål Hospital, Oslo, Norway.
Acta Oncol. 1996;35(1):81-7. doi: 10.3109/02841869609098484.
Intestinal fibrosis is a marked feature of late radiation enteropathy. This study assessed the time dose fractionation relationships of radiation-induced fibrosis in order to elucidate possible pathogenetic mechanisms. In 290 male Sprague-Dawley rats, a loop of small bowel was transposed to the left side of the scrotum. Three weeks later, the transposed segment was irradiated with either single dose or various fractionated regimens. The animals were observed for radiation-induced intestinal complications and killed in groups, 2 and 26 weeks after completion of irradiation. A semiquantitative histopathologic radiation injury score, morphometry of the submucosa, submucosal arterioles, intestinal surface area, and relative collagen content were used as endpoints. Fibrosis, measured by collagen assay and radiation injury score, increased with total dose, increasing fraction size and reduction in overall treatment time. This paralleled the results of morphometric assessment of mucosal surface area. Differences in vascular morphometry were only statistically significant in response to changes in total dose and fraction size and not with changes in overall treatment time. We conclude that fibrosis increases with increasing observation time, increasing fraction size, increasing total dose, and reduction of interfraction interval. Consequential injury, occurring as a result of disruption of mucosal integrity, seems to be an important mechanism for development of intestinal fibrosis. In contrast, vascular injury is relatively independent of this mechanism.
肠道纤维化是晚期放射性肠病的一个显著特征。本研究评估了辐射诱导纤维化的时间剂量分割关系,以阐明可能的发病机制。在290只雄性Sprague-Dawley大鼠中,将一段小肠襻转移至阴囊左侧。三周后,对转移段进行单次剂量或各种分割方案的照射。观察动物的辐射诱导肠道并发症,并在照射完成后2周和26周分批处死。使用半定量组织病理学辐射损伤评分、黏膜下层、黏膜下小动脉的形态计量学、肠表面积和相对胶原含量作为观察终点。通过胶原测定和辐射损伤评分测量的纤维化程度随总剂量、分次剂量增加以及总治疗时间缩短而增加。这与黏膜表面积的形态计量学评估结果一致。血管形态计量学的差异仅在总剂量和分次剂量变化时具有统计学意义,而在总治疗时间变化时无统计学意义。我们得出结论,纤维化程度随观察时间延长、分次剂量增加、总剂量增加以及分次间隔缩短而增加。由于黏膜完整性破坏而发生的继发性损伤似乎是肠道纤维化发展的一个重要机制。相比之下,血管损伤相对独立于这一机制。