Opanashuk L A, He D K, Lehning E J, LoPachin R M
Department of Anesthesiology, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, NY 10467, USA.
Neurotoxicology. 2001 Apr;22(2):215-20. doi: 10.1016/s0161-813x(00)00011-5.
Evidence suggests the morphologic hallmark of gamma-diketone neuropathy is axon atrophy and that this effect is associated with reduced neurofilament (NF) subunit protein content (Toxicol Appl Pharmacol 2000;165:141-7). To investigate the mechanism of diminished NF content, subunit (NF-L, -M and -H) gene expression was quantified in dorsal root ganglion (DRG) of slightly affected and moderately intoxicated groups of rats exposed to 2,5-hexanedione (HD) at one of three daily dosing rates (175, 250 and 400 mg/kg per day). Results show that sensory ganglia from slightly affected rats exhibited no changes in gene expression, whereas at a moderate level of neurotoxicity, each dosing protocol was associated with small but significant reductions (approximately 20%) in mean NF subunit mRNA. This was not a generalized effect on expression of cytoskeletal components in sensory ganglia since tubulin message levels were not affected. Although the observed reduction in NF gene expression might be related to diminished levels of subunit proteins in peripheral nerve, the actual contribution is likely to be minimal. The magnitude of effect was small and did not correspond to the dose-rate dependent effect of HD on respective isotype proteins. The mechanism of gamma-diketone-induced axon atrophy is unknown but might involve local changes in axonal NF phosphorylation and degradation.
有证据表明,γ-二酮神经病的形态学特征是轴突萎缩,且这种效应与神经丝(NF)亚基蛋白含量降低有关(《毒理学与应用药理学》2000年;165:141-147)。为了研究NF含量减少的机制,对以三种每日给药速率(每天175、250和400毫克/千克)之一暴露于2,5-己二酮(HD)的轻度中毒和中度中毒大鼠组的背根神经节(DRG)中的亚基(NF-L、-M和-H)基因表达进行了定量。结果表明,轻度中毒大鼠的感觉神经节基因表达没有变化,而在中度神经毒性水平下,每种给药方案均与平均NF亚基mRNA的小幅但显著降低(约20%)相关。这不是对感觉神经节中细胞骨架成分表达的普遍影响,因为微管蛋白信息水平未受影响。尽管观察到的NF基因表达降低可能与外周神经中亚基蛋白水平降低有关,但其实际作用可能很小。效应的大小很小,且与HD对各自同型蛋白的剂量率依赖性效应不对应。γ-二酮诱导轴突萎缩的机制尚不清楚,但可能涉及轴突NF磷酸化和降解的局部变化。