Phillips S C
Acta Neuropathol. 1987;73(2):171-6. doi: 10.1007/BF00693784.
Groups of adult male mice were either fed a thiamine-deficient diet for 10 weeks and thereafter treated with ethanol by making them inhale vapourized cane spirit for 10 weeks, or given both treatments simultaneously. The brains of these mice were then searched for degeneration using both light and electron microscopy. No degenerating nerve cells were observed in any animal in the cerebral cortex, hippocampus, cerebellum, olfactory bulbs, midbrain or hindbrain. However, axon terminal degeneration was seen in the olfactory bulbs and deep cerebellar nuclei in mice given the combined treatment. No cerebellar degeneration was found and only little degeneration was present in the olfactory bulbs of mice given the two treatments at different times. Thus, the combined treatment of alcohol and thiamine deficiency produced more brain damage than the sum of that produced by the two treatments given separately. This represents the first experimental in vivo demonstration of a biochemical interaction between these two factors in alcohol-related brain damage. The findings of long-term animal treatment with models using thiamine antagonists are compared.
将成年雄性小鼠分成几组,一组喂食缺乏硫胺素的饮食10周,此后让它们吸入汽化的甘蔗酒来用乙醇处理10周;另一组则同时给予这两种处理。然后使用光学显微镜和电子显微镜对这些小鼠的大脑进行检查,以寻找退化情况。在任何一只动物的大脑皮层、海马体、小脑、嗅球、中脑或后脑均未观察到神经细胞退化。然而,在接受联合处理的小鼠的嗅球和小脑深部核团中发现了轴突终末退化。未发现小脑退化,且在不同时间接受两种处理的小鼠的嗅球中仅有少量退化。因此,酒精和硫胺素缺乏的联合处理比单独给予这两种处理所产生的脑损伤总和更多。这是首次在体内实验中证明这两种因素在酒精相关脑损伤中的生化相互作用。将该研究结果与使用硫胺拮抗剂模型对动物进行长期处理的研究结果进行了比较。