van der Sanden B P, Heerschap A, Simonetti A W, Rijken P F, Peters H P, Stüben G, van der Kogel A J
Department of Radiology, University Hospital, Nijmegen, The Netherlands.
Int J Radiat Oncol Biol Phys. 1999 Jun 1;44(3):649-58. doi: 10.1016/s0360-3016(98)00555-0.
The aim of this study was to characterize and to validate noninvasive 19F-magnetic resonance relaxometry for the measurement of oxygen tensions in human glioma xenografts in nude mice. The following three questions were addressed: 1. When perfluorocarbon compounds (PFCs) are administrated intravenously, which tumor regions are assessed by 19F-MR relaxometry? 2. Are oxygen tension as detected by 19F-MR relaxometry (pO2/relaxo) comparable to Eppendorf O2-electrode measurements (pO2/electrode)? 3. Can 19F-MR relaxometry be used to detect oxygen tension changes in tumor tissue during carbogen breathing?
Slice-selective 19F-MR relaxometry was carried out with perfluoro-15-crown-5-ether as oxygen sensor. The PFC was injected i.v. 3 days before the 19F-MR experiments. Two datasets were acquired before and two after the start of carbogen breathing. The distribution of PFCs and necrotic areas were analyzed in 19F-Spin Echo (SE) density MR images and T2-weighted 1H-SE MR images, respectively. One day after the MR investigations, oxygen tensions were measured by oxygen electrodes in the same slice along two perpendicular tracks. These measurements were followed by (immuno)histochemical analysis of the 2D distribution of perfused microvessels, hypoxic cells, necrotic areas, and macrophages.
The PFCs mainly became sequestered in perfused regions at the tumor periphery; thus, 19F-MR relaxometry probed mean oxygen tensions in these regions throughout the selected MR slice. In perfused regions of the tumor, mean PO2/relaxo values were comparable to mean PO2/electrode values, and varied from 0.03 to 9 mmHg. Median pO2/electrode values of both tracks were lower than mean pO2/relaxo values, because low pO2 electrode values that originate from hypoxic and necrotic areas were also included in calculations of median pO2/electrode values. After 8-min carbogen breathing, the average PO2/relaxo increase was 3.3 +/- 0.8 (SEM) mmHg and 2.1 +/- 0.6 (SEM) after 14 min breathing.
We have demonstrated that PFCs mainly became sequestered in perfused regions of the tumor. Here, mean PO2/relaxo values were comparable to mean PO2electrode values. In these areas, carbogen breathing was found to increase the PO2/relaxo values significantly.
本研究旨在表征和验证用于测量裸鼠人胶质瘤异种移植瘤中氧张力的非侵入性19F磁共振弛豫测量法。探讨了以下三个问题:1. 静脉注射全氟碳化合物(PFCs)后,19F磁共振弛豫测量法评估的是哪些肿瘤区域?2. 19F磁共振弛豫测量法检测到的氧张力(pO2/relaxo)与Eppendorf氧电极测量值(pO2/electrode)是否可比?3. 19F磁共振弛豫测量法能否用于检测碳合气呼吸期间肿瘤组织中的氧张力变化?
以全氟-15-冠-5-醚作为氧传感器进行切片选择性19F磁共振弛豫测量。在19F磁共振实验前3天静脉注射PFC。在碳合气呼吸开始前和开始后分别采集两组数据集。分别在19F自旋回波(SE)密度磁共振图像和T2加权1H-SE磁共振图像中分析PFCs的分布和坏死区域。磁共振检查后一天,沿两条垂直轨迹在同一切片中用氧电极测量氧张力。随后对灌注微血管、缺氧细胞、坏死区域和巨噬细胞的二维分布进行(免疫)组织化学分析。
PFCs主要潴留在肿瘤周边的灌注区域;因此,19F磁共振弛豫测量法在所选磁共振切片中探测这些区域的平均氧张力。在肿瘤的灌注区域,平均pO2/relaxo值与平均pO2/electrode值相当,范围为0.03至9 mmHg。两条轨迹的pO2/electrode中位数均低于平均pO2/relaxo值,因为缺氧和坏死区域产生的低pO2电极值也包含在pO2/electrode中位数的计算中。碳合气呼吸8分钟后,平均pO2/relaxo增加3.3±0.8(标准误)mmHg,呼吸14分钟后增加2.1±0.6(标准误)mmHg。
我们已证明PFCs主要潴留在肿瘤的灌注区域。在此,平均pO2/relaxo值与平均pO2电极值相当。在这些区域,发现碳合气呼吸可显著提高pO2/relaxo值。