Rannels D E, Pegg A E, Clark R S, Addison J L
Am J Physiol. 1985 Nov;249(5 Pt 1):E506-13. doi: 10.1152/ajpendo.1985.249.5.E506.
The kinetics of [14C]paraquat (N,N-di[14C]methyl-4,4'-bipyridylium) uptake from the pulmonary circulation were investigated in rat lungs perfused in situ. During the 1st h of exposure to the herbicide paraquat entered the lungs primarily by diffusion; no evidence was obtained from concentrative uptake, saturation kinetics (1-3,500 microM paraquat), or inhibition by the amines methyl-glyoxal bis(guanylhydrazone) or spermidine, both of which were expected to compete for paraquat transport sites. In contrast, after 60 min of exposure, uptake rates increased two- to three-fold, and paraquat was accumulated to an apparent intracellular concentration greater than that in the perfusate. The latter phase of paraquat uptake was saturable and was inhibited by methylglyoxal bis(guanylhydrazone); it did not appear to reflect a progressive paraquat-induced alteration in cellular permeability but rather predominance of a rapid, carrier-mediated uptake pathway.
在原位灌注的大鼠肺中研究了[14C]百草枯(N,N-二[14C]甲基-4,4'-联吡啶鎓)从肺循环摄取的动力学。在接触除草剂的第1小时内,百草枯主要通过扩散进入肺;未从浓缩摄取、饱和动力学(1-3500 microM百草枯)或胺甲基乙二醛双(胍腙)或亚精胺的抑制作用中获得证据,这两种物质预计会竞争百草枯转运位点。相反,接触60分钟后,摄取率增加了两到三倍,百草枯在细胞内的表观浓度高于灌注液中的浓度。百草枯摄取的后期是可饱和的,并受到甲基乙二醛双(胍腙)的抑制;它似乎并不反映百草枯诱导的细胞通透性的渐进性改变,而是反映了一种快速的、载体介导的摄取途径占主导地位。