Xu Y, Sladky J T, Brown M J
Department of Neurology, University of Pennsylvania School of Medicine, Philadelphia 19104.
Neurology. 1989 Aug;39(8):1077-83. doi: 10.1212/wnl.39.8.1077.
We examined the sequence of nervous system abnormalities that resulted when rats were given excess amounts of vitamin B6 (pyridoxine). High doses of pyridoxine (1,200 or 600 mg/kg/d) for 6 to 10 days caused a neuronopathy with necrosis of dorsal root ganglion (DRG) sensory neurons, accompanied by centrifugal axonal atrophy and breakdown of peripheral and central sensory axons. Large diameter neurons with long processes and large cytoplasmic volumes were especially affected. Smaller doses (300 to 150 mg/kg/d) for up to 12 weeks had minor effects on DRG neurons, but produced a neuropathy with axonal atrophy and degeneration. Guinea pigs given 1,800 mg/kg/d developed sensory neuronopathy, whereas mice given similar or higher doses did not have neuropathologic abnormalities. Multiple factors including rate of administration, differential neuronal vulnerability, and species susceptibility have bearing on the final expression of pyridoxine neurotoxicity.
我们研究了给大鼠过量服用维生素B6(吡哆醇)后所导致的神经系统异常序列。高剂量的吡哆醇(1200或600毫克/千克/天)持续6至10天会引发一种神经元病,伴有背根神经节(DRG)感觉神经元坏死,同时出现离心性轴突萎缩以及外周和中枢感觉轴突的断裂。具有长突起和大细胞质体积的大直径神经元尤其受到影响。较小剂量(300至150毫克/千克/天)持续长达12周对DRG神经元影响较小,但会产生伴有轴突萎缩和变性的神经病变。给予1800毫克/千克/天的豚鼠会出现感觉神经元病,而给予相似或更高剂量的小鼠则没有神经病理学异常。包括给药速率、神经元易感性差异和物种易感性在内的多种因素都与吡哆醇神经毒性的最终表现有关。