Stone J D, Peterson A P, Eyer J, Oblak T G, Sickles D W
Department of Cellular Biology and Anatomy, Medical College of Georgia, Augusta, Georgia, 30912, USA.
Toxicol Appl Pharmacol. 1999 Nov 15;161(1):50-8. doi: 10.1006/taap.1999.8780.
Neurofilament modification and accumulation, occurring in toxicant-induced neuropathies, has been proposed to compromise fast axonal transport and contribute to neurological symptoms or pathology. The current study compares the effects of the neurotoxicants acrylamide (ACR) and 2,5-hexanedione (2,5-HD) on the quantity of fast, bidirectional vesicular traffic within isolated mouse sciatic nerve axons from transgenic mice lacking axonal neurofilaments (Eyer and Peterson, Neuron 12, 1-20, 1994) and nontransgenic littermates possessing neurofilaments. Fast anterograde and retrograde membrane bound organelle (MBO) traffic was quantitated within axons, before and after toxicant exposure, using video-enhanced differential interference contrast (AVEC-DIC) microscopy. Addition of 0.7 mM ACR to the buffer bathing the nerve produced a time-dependent reduction in bidirectional transport with a similar time to onset and magnitude in both transgenic and nontransgenic mice. 2,5-HD (4 mM) exposure reduced bidirectional vesicle traffic by a similar amount in both transgenic and nontransgenic animals. The time to onset of the transport reduction was less and the magnitude of the reduction was greater with 2,5-HD compared to ACR. A single 10-min exposure to ACR or 2,5-HD produced a similar reduction in transport to that produced by prolonged (1 h) exposure. Nonneurotoxic propionamide or 3,4-hexanedione (3,4-HD) produced no changes in bidirectional transport in either transgenic or nontransgenic animals. We conclude that ACR or 2,5-HD produces a rapid, saturable, nonreversible, neurotoxicant-specific reduction in fast bidirectional transport within isolated peripheral nerve axons. These actions are mediated through direct modification of axonal component(s), which are independent of toxicant-induced modifications of, or accumulations of, neurofilaments.
神经丝的修饰和积累发生在毒物诱导的神经病变中,有人提出这会损害快速轴突运输,并导致神经症状或病理变化。本研究比较了神经毒物丙烯酰胺(ACR)和2,5-己二酮(2,5-HD)对来自缺乏轴突神经丝的转基因小鼠(Eyer和Peterson,《神经元》12卷,1-20页,1994年)和具有神经丝的非转基因同窝小鼠的分离小鼠坐骨神经轴突内快速双向囊泡运输量的影响。在毒物暴露前后,使用视频增强微分干涉对比(AVEC-DIC)显微镜对轴突内的快速顺行和逆行膜结合细胞器(MBO)运输进行定量。向浸泡神经的缓冲液中添加0.7 mM ACR会导致双向运输随时间减少,转基因和非转基因小鼠的起始时间和幅度相似。暴露于2,5-HD(4 mM)会使转基因和非转基因动物的双向囊泡运输减少相似的量。与ACR相比,2,5-HD导致运输减少的起始时间更短,减少幅度更大。单次10分钟暴露于ACR或2,5-HD所产生的运输减少与长时间(1小时)暴露相似。非神经毒性的丙酰胺或3,4-己二酮(3,4-HD)在转基因或非转基因动物中均未引起双向运输的变化。我们得出结论,ACR或2,5-HD会在分离的外周神经轴突内快速、饱和、不可逆、特异性地减少快速双向运输。这些作用是通过轴突成分的直接修饰介导的,这与毒物诱导的神经丝修饰或积累无关。