AIM:The pathogenesis of delayed encephalopathy induced by heavy-ion irradiation was investigated experimentally in cats. The left cerebral hemispheres were irradiated with 15-40 Gy of heavy ions (carbon), and histologically and morphometrically examined 12 months later. RESULTS:In the irradiated cerebral white matter the following occurred as the dose increased: astrocytic swelling, then the dilatation of small blood vessels with a fibrous thickening of the wall, and then loosening of the white matter with cavity formation and diffuse albumin deposition. Pathological features of these cavities suggested that they are induced by long-standing edema. Although the dilated vessels were arteries, veins, and capillaries, arteriovenous shunt and damage of the smooth muscle cells of the arterial media were absent. Changes of the cerebral cortex were scarce. Morphometrically, the irradiated cerebral white matter was swollen, and the capillary density tended to be reduced in the deep cortex and subcortical white matter, but this effect was not dose dependent. CONCLUSION:Heavy-ion irradiation induces delayed encephalopathy in cats, preferentially involving the white matter. The cardinal pathogenesis was long-standing edema of the white matter due to vascular hyperpermeability, and the vascular dilatation seemed to be caused by a reduction in the vascular bed and/or hemoconcentration due to hyperpermeability.

译文

目的:通过实验研究猫重离子辐照引起的迟发性脑病的发病机理。左脑半球用15-40 Gy重离子(碳)照射,并在12个月后进行组织学和形态学检查。
结果:在受辐照的脑白质中,随着剂量的增加,会发生以下情况:星形胶质细胞肿胀,然后扩张小血管,使纤维壁增厚,然后使白质变松,形成空腔并扩散白蛋白沉积。这些腔的病理特征表明它们是由长期浮肿引起的。尽管扩张的血管是动脉,静脉和毛细血管,但没有动静脉分流和动脉中枢平滑肌细胞的损伤。大脑皮层的变化很少。从形态学上讲,受辐照的脑白质肿胀,并且在深皮层和皮层下白质中毛细血管密度趋于降低,但这种作用与剂量无关。
结论:重离子辐射可诱发猫的迟发性脑病,优先涉及白质。主要的发病机制是由于血管通透性过高引起的白质的长期水肿,并且血管扩张似乎是由于通透性过高导致的血管床减少和/或血液浓缩引起的。

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