King R H, Sarsilmaz M, Thomas P K, Jacobs J M, Muddle J R, Duncan I D
Royal Free Hospital School of Medicine, London.
Neuropathol Appl Neurobiol. 1993 Jun;19(3):224-32. doi: 10.1111/j.1365-2990.1993.tb00432.x.
The neuropathy produced by the hexacarbon 2,5-hexanedione (2,5-HD) resembles human and canine inherited giant axonal neuropathy (GAN) in the presence of giant axonal swellings that contain accumulations of neurofilaments. The accumulations are both paranodal and internodal in GAN and 2,5-HD induced neuropathy. Detailed morphometry on the neurofilaments reveals that the changes in human and canine GAN are closely similar and differ from those of 2,5-HD neuropathy, suggesting that the mechanisms underlying the formation of the axonal neurofilamentous accumulations differ between the two conditions. In both human and canine GAN, the neurofilaments are more closely spaced and are of greater diameter than in 2,5-HD neuropathy. The changes in the NF in GAN may be the consequence of flattening of the side-arms of the neurofilaments against the axis of the filaments.
己二酮(2,5-HD)所致的神经病变与人类和犬类遗传性巨轴索神经病(GAN)相似,均存在含有神经丝聚集的巨大轴突肿胀。在GAN以及2,5-HD诱导的神经病变中,神经丝聚集既出现在结旁也出现在结间。对神经丝进行的详细形态测量显示,人类和犬类GAN中的变化非常相似,与2,5-HD神经病变不同,这表明两种情况下轴突神经丝聚集形成的机制不同。在人类和犬类GAN中,神经丝的间距比2,5-HD神经病变中的更近,直径也更大。GAN中神经丝的变化可能是神经丝侧臂靠向细丝轴而变扁平的结果。