Lanzen J L, Braun R D, Ong A L, Dewhirst M W
Department of Radiation Oncology, Duke University Medical Center, Durham, NC 27710, USA.
Int J Radiat Oncol Biol Phys. 1998 Nov 1;42(4):855-9. doi: 10.1016/s0360-3016(98)00312-5.
There is speculation that the CO2 in carbogen (95% O2, 5% CO2) can block the vasoconstrictive effects of oxygen. However, it has recently been shown that blood flow in human tumors is variable while patients breathe carbogen. Furthermore, we have shown a consistent decrease in tumor blood flow (TBF) with carbogen breathing in the rat window chamber model. Also, we have previously shown that there is no significant difference in tumor growth time after radiation with air vs. carbogen breathing. This study was designed to investigate the effects of carbogen breathing on blood flow and oxygen levels in a solid tumor.
Measurements were made in Fischer-344 rats with 8-10 mm diameter R3230Ac tumors transplanted either within the quadriceps muscle (n = 16) or subcutis (n = 14). Nontumor-bearing quadriceps muscle was studied in six other rats. After a 20-minute air-breathing baseline, rats breathed carbogen for an additional 40 minutes. Partial pressure of oxygen (pO2) was continuously monitored at one position for 60 minutes using 9-12 microm diameter oxygen microelectrodes. Blood flow was simultaneously monitored in all animals using laser Doppler flowmetry (1-2 probes/tumor).
Blood flow changes during carbogen breathing were variable in all tissues and intratumoral heterogeneity was observed. Despite variability in blood flow, pO2 consistently increased in normal muscle but varied in both tumor sites. During carbogen breathing, the percent pO2 measurements greater than the baseline average were 99.5% +/- 0.4% (mean +/- SEM), 42.7% +/- 13.8%, and 79.8% +/- 11.0% in normal muscle, subcutaneous tumor, and muscle tumor, respectively. To show the magnitude of change, average pO2 values during air and carbogen breathing were calculated for each site. Normal muscle increased from 14.9 +/- 2.3 to 39.0 +/- 6.4 mm Hg (paired t-test; p = 0.009). Muscle tumors showed a rise from 14.6 +/- 3.2 to 34.5 +/- 8.2 mm Hg (p = 0.019). However, pO2 in subcutaneous tumors remained unchanged, with a pO2 of 7.3 +/- 2.0 mm Hg on air and 7.3 +/- 4.1 mm Hg (p = 0.995) during carbogen breathing.
Carbogen had no consistent effect on blood flow and was ineffective at increasing tumor pO2. These results may partially explain why carbogen breathing failed to improve the efficacy of radiation in this tumor model when transplanted subcutaneously.
有人推测,卡波金(95%氧气,5%二氧化碳)中的二氧化碳可阻断氧气的血管收缩作用。然而,最近研究表明,在患者呼吸卡波金时,人体肿瘤中的血流是可变的。此外,我们已经证实在大鼠窗室模型中,呼吸卡波金会使肿瘤血流(TBF)持续减少。而且,我们之前已经表明,在空气呼吸与卡波金呼吸条件下接受放疗后,肿瘤生长时间并无显著差异。本研究旨在探讨呼吸卡波金对实体瘤血流和氧水平的影响。
在Fischer-344大鼠中进行测量,这些大鼠的股四头肌(n = 16)或皮下组织(n = 14)移植了直径8 - 10毫米的R3230Ac肿瘤。另外对6只大鼠的非荷瘤股四头肌进行了研究。在20分钟的空气呼吸基线期后,大鼠再呼吸卡波金40分钟。使用直径9 - 12微米的氧微电极在一个位置连续监测氧分压(pO2)60分钟。使用激光多普勒血流仪(每个肿瘤1 - 2个探头)同时监测所有动物的血流。
在所有组织中,呼吸卡波金期间的血流变化是可变的,并且观察到肿瘤内的异质性。尽管血流存在变化,但正常肌肉中的pO2持续升高,而在两个肿瘤部位pO2有所不同。在呼吸卡波金期间,正常肌肉、皮下肿瘤和肌肉肿瘤中pO2测量值高于基线平均值的百分比分别为99.5%±0.4%(平均值±标准误)、42.7%±13.8%和79.8%±11.0%。为了显示变化幅度,计算了每个部位在空气呼吸和卡波金呼吸期间的平均pO2值。正常肌肉从14.9±2.3毫米汞柱升至39.0±6.4毫米汞柱(配对t检验;p = 0.009)。肌肉肿瘤从14.6±3.2毫米汞柱升至34.5±8.2毫米汞柱(p = 0.019)。然而,皮下肿瘤中的pO2保持不变,空气呼吸时pO2为7.3±2.0毫米汞柱,呼吸卡波金时为7.3±4.1毫米汞柱(p = 0.995)。
卡波金对血流没有一致的影响,并且在提高肿瘤pO2方面无效。这些结果可能部分解释了为什么在皮下移植的这种肿瘤模型中,呼吸卡波金未能提高放疗疗效。