Simonati A, Rizzuto N, Cavanagh J B
Acta Neuropathol. 1983;59(3):216-24. doi: 10.1007/BF00703206.
The pattern of recovery of myelinated axons in the posterior tibial nerve after crushing was studied in rats chronically intoxicated with 2,5-hexanedione. It was given for 2 weeks before crushing (200 mg/kg i.p. 5 times a week) or additionally for two further weeks after the nerve crush. Two animals were examined from each group at approximately 1,2,3,4 and 8 weeks later. Return of function in poisoned animals was slower than in the controls. The numbers of regenerating myelinated fibres was severely reduced in poisoned animals up to 4 weeks later, but by 8 weeks the numbers equalled those in the control nerves. Marked impairment of initiation of neurite outgrowth was found, but once begun, axonal growth was comparable to controls and myelination occurred normally. Above the crush for 10 mm, filament-filled axonal swellings were found in poisoned animals accompanied by varying amounts of retrograde axonal degeneration. These findings are discussed in relation to the role of normal neurofilaments in axonal growth and the effects of probably cross-linking of these by 2,5-hexanedione on regenerating neurites.
在长期用2,5 -己二酮中毒的大鼠中,研究了胫后神经挤压伤后有髓轴突的恢复模式。在挤压前2周给予该物质(腹腔注射200mg/kg,每周5次),或在神经挤压后再额外给予2周。每组在大约1、2、3、4和8周后检查2只动物。中毒动物的功能恢复比对照组慢。在中毒动物中,直至4周后再生有髓纤维的数量严重减少,但到8周时,数量与对照神经相等。发现神经突生长起始明显受损,但一旦开始,轴突生长与对照组相当,髓鞘形成正常。在挤压上方10mm处,在中毒动物中发现充满细丝的轴突肿胀,并伴有不同程度的逆行性轴突变性。结合正常神经丝在轴突生长中的作用以及2,5 -己二酮可能使其交联对再生神经突的影响,对这些发现进行了讨论。