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基于X射线照射和热疗后机械变化的病前小鼠空肠纤维化测定

Assay of premorbid murine jejunal fibrosis based on mechanical changes after X irradiation and hyperthermia.

作者信息

Peck J W, Gibbs F A

机构信息

Division of Radiation Oncology, University of Utah, Salt Lake City 84132.

出版信息

Radiat Res. 1987 Dec;112(3):525-43.

PMID:3423218
Abstract

Preparative surgery immobilized 15 mm of functional jejunum against the peritoneal surface of the ventral abdominal wall in C3H/HeJ mice. The surgery allowed subsequent treatments with single fractions of 44 degrees C hyperthermia and X irradiation to be selective to this portion of small intestine. With each doubling of time since treatment, 1 through 70 weeks, a sample of mice was killed and specimens of their intestines were excised and radially stretched in a tensile-testing apparatus that measured tension as a continuous function of circumference. Preconditioning with repeated cycles of stretch and relaxation before specimens were irreversibly stretched enabled measurement of the limit collagen placed on the extensibility of the intestinal wall by physiologic forces and the stiffness of the intestinal collagen once that limit was exceeded. Both kinds of measurements made possible dose-response characterization of radiation fibrosis for treatments that killed no mice. Response increased linearly with X-ray dose above a threshold. After X rays alone the threshold remained constant at 9.7 +/- 0.6 Gy for the assays at 1 through 8 weeks and subsequently decreased to about 6 Gy by 35 weeks. With adjuvant hyperthermia of 15 min at 44 degrees C beginning 10 min after X irradiation, the threshold of approximately 5 Gy at 2-4 weeks decreased to about 2 Gy by 17 weeks; the thermal enhancement ratio as calculated from slope-ratio analysis of the dose-response curves was 1.50 +/- 0.08 at 2-4 weeks post-treatment and 1.96 +/- 0.05 at 17-70 weeks post-treatment. Up to 20 min at 44 degrees C by itself was without effect. From comparisons of these data with results of crypt microcolony assays, it was concluded that intestinal fibrosis was both a chronic sequela of acute mucosal injury and a late effect of X irradiation. Adjuvant hyperthermia both hastened the expression of the late effect and increased its severity beyond that predicted from the acute injury.

摘要

在C3H/HeJ小鼠中,通过准备性手术将15毫米的功能性空肠固定在腹前壁的腹膜表面。该手术使得后续能用44摄氏度的单次高温治疗和X射线照射,且仅作用于小肠的这一部分。自治疗后,每经过一倍时间(从1周到70周),就处死一组小鼠,切除它们的肠标本,并在拉伸试验机中进行径向拉伸,该试验机可测量张力随周长的连续变化。在标本被不可逆拉伸之前,通过反复的拉伸和松弛循环进行预处理,能够测量生理力对肠壁可伸展性施加的极限胶原蛋白,以及超过该极限后肠胶原蛋白的硬度。这两种测量使得在未造成小鼠死亡的治疗情况下,能够对放射性纤维化进行剂量反应特性分析。反应在超过阈值后随X射线剂量呈线性增加。单独使用X射线时,在1至8周的检测中,阈值保持在9.7±0.6戈瑞不变,随后在35周时降至约6戈瑞。在X射线照射后10分钟开始进行15分钟的44摄氏度辅助高温治疗,2至4周时约5戈瑞的阈值在17周时降至约2戈瑞;根据剂量反应曲线的斜率比分析计算得出的热增强比,在治疗后2至4周为1.50±0.08,在治疗后17至70周为1.96±0.05。44摄氏度下长达20分钟的单独高温治疗没有效果。通过将这些数据与隐窝微菌落检测结果进行比较,得出结论:肠道纤维化既是急性黏膜损伤的慢性后遗症,也是X射线照射的晚期效应。辅助高温治疗既加速了晚期效应的表现,又使其严重程度超过了急性损伤所预测的程度。

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