Homor G, Kása P
Acta Histochem. 1978;62(2):293-301. doi: 10.1016/S0065-1281(78)80095-6.
DFP (0.4 to 2.0 mg/kg) was injected into the rat spinal ganglion leads to N. ischiadicus model system and examinations were made of the AChE inhibitory affect and the influence on the transport and resynthesis of the enzyme. It was concluded that the intraganglionically administered DFP inhibits the enzyme activity of the pseudo-unipolar large ganglion cells, but the specific ChE remains in some of the small neurones. Autoradiographically, 3H-DFP could be demonstrated at the same morphological sites as the AChE histochemically. The labelled material migrates from the perikaryon towards the axon terminal by slow transport (10 mm/24 h). The intraganglionically administered DFP inhibits (96%) the AChE activity of the spinal ganglion. However, the enzyme activity of the ganglion cells begins to return 3 h later, and in 12 h it has attained 27% of the original activity. The enzyme undergoing transport from the perikaryon displays a proximo-distal gradient in the axon, and hence the results do not support the hypothesis of local axonal synthesis of AChE.
将二异丙基氟磷酸酯(DFP,0.4至2.0毫克/千克)注射到大鼠坐骨神经节模型系统中,并对乙酰胆碱酯酶(AChE)的抑制作用以及对该酶转运和再合成的影响进行了检测。结果表明,神经节内注射DFP可抑制假单极大型神经节细胞的酶活性,但某些小型神经元中仍保留特异性胆碱酯酶。放射自显影显示,3H-DFP在组织化学上与AChE处于相同的形态学部位。标记物质通过慢速运输(10毫米/24小时)从胞体向轴突终末迁移。神经节内注射DFP可抑制(96%)脊髓神经节的AChE活性。然而,神经节细胞的酶活性在3小时后开始恢复,12小时后达到原始活性的27%。从胞体运输的酶在轴突中呈现近端到远端的梯度,因此这些结果不支持AChE在轴突局部合成的假说。