Castel J C, Dorcier F, Caillé J M
Neuroradiology. 1987;29(2):206-10. doi: 10.1007/BF00327552.
After suboccipital injection of Iotrol and Iopamidol labelled with iodine 125 in rabbits, we measured residual radioactivity in the whole brain and optical density on autoradiographs of brain sections obtained 2, 8 and 24 h after injection. Residual radioactivity is higher with Iotrol than with Iopamidol after 8 h and 24 h. At densitometry, while the penetration of the cortex is the same with both media at 2 h (although subcortical passage of Iotrol is greater), by 8 h the concentration of Iopamidol is twice that of Iotrol, and at 24 h it is three times as high. A similar pattern was seen in the subcortical region. These densitometric findings are in agreement with previous electrophysiological studies, in which changes were less severe and more transient with Iotrol than with Iohexol. There is nevertheless an apparent lack of agreement between the studies of radioactivity and the electrical findings. The lower neurotoxicity of Iotrol may be explained by: a longer half-life in the subarachnoid space; its larger molecules, which inhibit diffusion in the extracellular fluid, and its more hydrophilic nature, which reduces intracellular penetration.
在兔枕下注射用碘125标记的碘曲仑和碘帕醇后,我们测量了注射后2小时、8小时和24小时获得的全脑残留放射性以及脑切片放射自显影片上的光密度。8小时和24小时后,碘曲仑的残留放射性高于碘帕醇。在密度测定中,尽管2小时时两种介质对皮质的穿透相同(尽管碘曲仑的皮质下通过率更高),但到8小时时碘帕醇的浓度是碘曲仑的两倍,24小时时则是其三倍。在皮质下区域也观察到类似模式。这些密度测定结果与先前的电生理学研究一致,在先前的研究中,碘曲仑引起的变化比碘海醇更轻微且更短暂。然而,放射性研究与电生理结果之间明显缺乏一致性。碘曲仑较低的神经毒性可能解释如下:在蛛网膜下腔的半衰期更长;其分子较大,抑制细胞外液中的扩散,且其亲水性更强,减少细胞内穿透。