Frimmer M, Petzinger E, Ziegler K, Veil L B
Naunyn Schmiedebergs Arch Pharmacol. 1980 Feb;311(1):91-4. doi: 10.1007/BF00500308.
The uptake of trace amounts of 3H-demethylphalloin (3H-DMP) by isolated hepatocytes was studied in the presence of various concentrations of unlabeled demethylphalloin (DMP), of phalloin and of phalloidin. The addition of phalloidin (or phalloin) reduces the uptake of 3H-DMP more than the addition of the equivalent concentration of DMP. The error caused by dilution of 3H-DMP with phalloin or phalloidin is not constant and depends on the concentration of the unlabeled compound. The relative differences between the uptake of 3H-DMP in the presence of demethylphalloin and in the presence of either phalloin or phalloidin cannot be explained by a competitive model. Some consequences for the use of 3H-DMP in toxicokinetic experiments are discussed.
在存在不同浓度的未标记去甲基鬼笔环肽(DMP)、鬼笔环肽和鬼笔毒环肽的情况下,研究了分离的肝细胞对痕量3H-去甲基鬼笔环肽(3H-DMP)的摄取。加入鬼笔毒环肽(或鬼笔环肽)比加入等量浓度的DMP更能降低3H-DMP的摄取。用鬼笔环肽或鬼笔毒环肽稀释3H-DMP所引起的误差并不恒定,且取决于未标记化合物的浓度。在存在去甲基鬼笔环肽以及存在鬼笔环肽或鬼笔毒环肽的情况下,3H-DMP摄取之间的相对差异无法用竞争模型来解释。文中讨论了在毒代动力学实验中使用3H-DMP的一些后果。