Sidenius P
Brain. 1986 Oct;109 ( Pt 5):885-96. doi: 10.1093/brain/109.5.885.
The study was designed to investigate the changes in axonal transport that result from disturbances in protein synthesis. Doxorubicin, an antineoplastic drug which interferes with the function of DNA, has a selective effect on peripheral sensory nerves because of the high vascular permeability in the dorsal root ganglia. After the intravenous administration of a moderate dose (4 mg/kg) to male Wistar rats, the transport of slow component a (SCa) was found to be retarded, transport velocity being decreased by 17% (0.85 +/- 0.06 mm/day vs 1.03 +/- 0.06 mm/day in controls). The transport kinetics of the fast anterograde and retrograde components (aFC and rFC) were unchanged after the administration of a dose of 6 mg/kg, although the relative amount of aFC was decreased by 27% (3.2 +/- 0.9% vs 4.4 +/- 1.1% in controls). It is suggested that the neuronopathy induced by doxorubicin is mediated by changes in axonal transport.
本研究旨在调查蛋白质合成紊乱导致的轴突运输变化。阿霉素是一种干扰DNA功能的抗肿瘤药物,由于背根神经节血管通透性高,对周围感觉神经有选择性作用。给雄性Wistar大鼠静脉注射中等剂量(4mg/kg)后,发现慢成分a(SCa)的运输受阻,运输速度降低了17%(0.85±0.06mm/天,对照组为1.03±0.06mm/天)。给予6mg/kg剂量后,快速顺行和逆行成分(aFC和rFC)的运输动力学未发生变化,尽管aFC的相对量减少了27%(3.2±0.9%,对照组为4.4±1.1%)。提示阿霉素诱导的神经病变是由轴突运输变化介导的。