Divisions of Psychiatry and Neurosciences, Walter Reed Army Institute of Research, Silver Spring, MD 20910-7500, USA.
Basic Clin Pharmacol Toxicol. 2010 May;106(5):428-34. doi: 10.1111/j.1742-7843.2009.00508.x. Epub 2009 Dec 29.
We evaluated the effects of conjugated enzyme-nerve agent product resulting from the inhibition of bioscavenger human serum butyrylcholinesterase (Hu BChE) by nerve agents soman or VX. Rats were trained on a multiple Fixed-Ratio 32, Extinction 30 sec. (FR32, Ext30) schedule of food reinforcement and then injected (i.m.) with Hu BChE (30 mg/kg), equivalent amounts of Hu BChE-soman conjugate (GDC), Hu BChE-VX conjugate, oxotremorine (OXO) (0.316 mg/kg) or vehicle (n = 8, each group). On the day of injection and on 10 subsequent daily sessions, performance was evaluated on the FR32, Ext30 schedule. Neither conjugates nor Hu BChE produced a performance deficit under the schedule. OXO produced a substantial decrease in responding on the day of administration, with complete recovery observed on subsequent sessions. None of the treatments affected circulating acetylcholinesterase (AChE) activity when evaluated 24-72 hr after injection. The dose of Hu BChE produced a 20,000-fold increase above baseline in circulating BChE activity. Pathological evaluation of organ systems approximately 2 weeks following administration of conjugates or Hu BChE alone did not show toxicity. Taken together, these results suggest that Hu BChE - nerve agent conjugates produced following bioscavenger protection against nerve agents soman and VX do not appear to be particularly toxic. These results add to the safety assessment of Hu BChE as a bioscavenger countermeasure against nerve agent exposure.
我们评估了生物清除剂人血清丁酰胆碱酯酶(Hu BChE)被神经毒剂梭曼或 VX 抑制后生成的共轭酶-神经毒剂产物的作用。大鼠在多重固定比率 32、30 秒消退(FR32,Ext30)的食物强化时间表上接受训练,然后肌肉注射 Hu BChE(30mg/kg)、等量的 Hu BChE-梭曼轭合物(GDC)、Hu BChE-VX 轭合物、氧托米农(OXO)(0.316mg/kg)或载体(n=8,每组)。在注射当天和随后的 10 天,根据 FR32,Ext30 时间表评估表现。轭合物或 Hu BChE 都没有在计划下产生表现缺陷。OXO 在给药当天导致反应明显减少,随后的课程中观察到完全恢复。在注射后 24-72 小时评估时,没有一种处理方法会影响循环乙酰胆碱酯酶(AChE)活性。Hu BChE 的剂量使循环 BChE 活性增加了 20000 倍。在单独给予轭合物或 Hu BChE 后约 2 周对器官系统进行的病理评估未显示毒性。总之,这些结果表明,生物清除剂保护免受梭曼和 VX 神经毒剂后产生的 Hu BChE-神经毒剂轭合物似乎没有特别毒性。这些结果增加了 Hu BChE 作为神经毒剂暴露的生物清除剂对策的安全性评估。