Ligtenstein D A, Kossen S P
Toxicol Appl Pharmacol. 1983 Nov;71(2):177-83. doi: 10.1016/0041-008x(83)90334-4.
The kinetic profile of the oxime HI-6, a potent cholinesterase reactivator, after iv administration of 0.1325 mmol/kg (50 mg/kg) to rats is described. The blood concentrations measured over a period of 300 min can be described by a two-compartment open model. Excretion occurred only by the kidney. Approximately 60% was excreted in unmetabolized form. Brain tissue concentrations were significantly above the detection limit of the HPLC analysis procedure even when a correction was made for the amount of HI-6 present in brain blood. The concentration in brain tissue is built up according to a rapid equilibration mechanism. Disappearance of HI-6 from brain occurred slowly compared to the elimination of HI-6 from blood. These findings are discussed in the light of the existing knowledge on the kinetic behavior of polar solutes in the central nervous system. Whether the concentrations of HI-6 built up in the brain are relevant for the therapy of organophosphate intoxications cannot be determined from the experiments described.
描述了肟类化合物HI-6(一种有效的胆碱酯酶复活剂)以0.1325 mmol/kg(50 mg/kg)静脉注射给大鼠后的动力学特征。在300分钟内测得的血药浓度可用二室开放模型来描述。仅通过肾脏排泄。约60%以未代谢形式排泄。即使对脑血中存在的HI-6量进行校正后,脑组织浓度仍显著高于HPLC分析方法的检测限。脑组织中的浓度根据快速平衡机制建立。与HI-6从血液中的消除相比,HI-6从脑中的消失较慢。根据关于极性溶质在中枢神经系统中动力学行为的现有知识对这些发现进行了讨论。从所描述的实验中无法确定脑中积累的HI-6浓度是否与有机磷中毒的治疗相关。