Ludwig R, Calvo W, Kober B, Brandeis W E
J Cancer Res Clin Oncol. 1987;113(3):235-40. doi: 10.1007/BF00396379.
Brain damage following cranial radiation therapy can be crippling or even life-threatening and has been studied in both patients and animals. An additional toxic effect of chemotherapy has been found in children, who died following brain irradiation and systemic chemotherapy for the treatment of acute lymphoblastic leukemia. To study the interaction of radiation and drugs on brain tissue, we treated rabbits with brain irradiation and/or i.v. methotrexate. For a period of up to 3 months following radiation therapy, brain morphology was compared in seven treatment groups. Weekly doses of methotrexate administered i.v. produced no brain damage. Histological examination showed myelin swelling and beading 14 weeks after fractionated brain irradiation with 24 Gy. Combination of brain irradiation and methotrexate produced additional hypertrophy of microglia and pyknosis of adventitial cells. In none of these groups, even after doses of 48 Gy brain irradiation, was calcification or brain necrosis observed during the first 14 weeks following irradiation.
颅脑放射治疗后的脑损伤可能会导致残疾甚至危及生命,并且已经在患者和动物身上进行了研究。在接受脑照射和全身化疗以治疗急性淋巴细胞白血病的儿童中,发现了化疗的另一种毒性作用。为了研究辐射和药物对脑组织的相互作用,我们对兔子进行了脑照射和/或静脉注射甲氨蝶呤治疗。在放射治疗后的长达3个月的时间里,对七个治疗组的脑形态进行了比较。静脉注射甲氨蝶呤的每周剂量未产生脑损伤。组织学检查显示,在24 Gy分次脑照射14周后,髓鞘肿胀和串珠样改变。脑照射和甲氨蝶呤联合使用导致小胶质细胞进一步肥大和外膜细胞固缩。在这些组中,即使在脑照射剂量达到48 Gy后,在照射后的前14周内也未观察到钙化或脑坏死。