Dimyristoyl Phosphatidylcholine/water Partitioning-dependent Modeling of Narcotic Toxicity toTetrahymena pyriformis

T. Schultz, J. Seward
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引用次数: 7

Abstract

Regression-type structure-toxicity relationships have been developed between Tetrahymena pyriformis population growth impairment toxicity data (log 1/IGC50) and the dimyristoyl phosphatidylcholine/water partition coefficient (log KDMPC) or the 1-octanol/water partition coefficient (log Kow). A statistically robust model [log(1/ IGC50)= 0.73 log (KDMPC)−1.62; n=23, r2=0.926, s=0.24, F=263, Pr/gt F=0.0001] was found for non-polar narcotics, polar narcotics, as well as esters with the DMPC partition coefficient. The above model was statistically better than the model [log(1/IGC50) = 0.71 (log Kow) − 1.60; n = 23, r2 = 0.828, s = 0.39, F = 101, Pr> F = 0.0001] developed for the same compounds with 1-octanol/water partitioning as the independent variable. The former equation does not explain the difference in the acute mechanisms of toxic action known to exist in fish for non-polar and polar narcotics. However, log KDMPC appears to correct for differences in the concentration of toxicant reaching the site of toxic action between narcotic mechanisms. Outliers to the log KDMPC model were primary aliphatic amines.
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二肉豆蔻酰磷脂酰胆碱/水分割依赖的梨形四膜虫麻醉毒性模型
梨形四膜虫种群生长损伤毒性数据(log 1/IGC50)与二肉豆蔻酰磷脂酰胆碱/水分配系数(log KDMPC)或1-辛醇/水分配系数(log Kow)之间建立了回归型结构-毒性关系。统计稳健性模型[log(1/ IGC50)= 0.73 log(KDMPC)−1.62;n=23, r2=0.926, s=0.24, F=263, Pr/gt F=0.0001]对非极性麻醉药、极性麻醉药以及具有DMPC分配系数的酯类均有显著性影响。上述模型在统计学上优于模型[log(1/IGC50) = 0.71 (log Kow)−1.60;n = 23, r2 = 0.828, s = 0.39, F = 101, Pr> F = 0.0001],以1-辛醇/水分配为自变量。前一个方程并不能解释已知存在于鱼类体内的非极性和极性麻醉品的急性毒性作用机制的差异。然而,log KDMPC似乎纠正了麻醉机制之间到达毒性作用部位的毒物浓度的差异。对数KDMPC模型的异常值是初级脂肪胺。
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