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人血清丁酰胆碱酯酶:小鼠体内外稳定性、药代动力学及安全性

Human serum butyrylcholinesterase: in vitro and in vivo stability, pharmacokinetics, and safety in mice.

作者信息

Saxena Ashima, Sun Wei, Luo Chunyuan, Doctor Bhupendra P

机构信息

Division of Biochemistry, Walter Reed Army Institute of Research, 503 Robert Grant Avenue, Silver Spring, MD 20910-7500, USA.

出版信息

Chem Biol Interact. 2005 Dec 15;157-158:199-203. doi: 10.1016/j.cbi.2005.10.028. Epub 2005 Nov 2.

DOI:10.1016/j.cbi.2005.10.028
PMID:16263104
Abstract

The use of exogenously administered cholinesterases (ChEs) as bioscavengers of highly toxic organophosphate (OP) nerve agents is now sufficiently well documented to make them a highly viable prophylactic treatment against this potential threat. Of the ChEs evaluated so far, human serum butyrylcholinesterase (HuBChE) is most suitable for human use. A dose of 200 mg (3 mg/kg) of HuBChE is envisioned as a prophylactic treatment in humans that can protect from an exposure of up to 2 x LD50 of soman. In addition to its use as a prophylactic for a variety of wartime scenarios, including covert actions, it also has potential use for first responders (civilians) reacting to terrorist nerve gas release. We recently, developed a procedure for the large-scale purification of HuBChE, which yielded approximately 6 g of highly purified enzyme from 120 kg of Cohn fraction IV-4. The enzyme had a specific activity of 700-750 U/mg and migrated as a single band on SDS-PAGE. To provide data for initiating an investigational new drug (IND) application for the use of this enzyme as a bioscavenger in humans, we established its pharmacokinetic properties, examined its safety in mice, and evaluated its shelf life at various temperatures. In mice administered various doses up to 90 mg/kg, enzyme activity reached peak levels in circulation at 10 and 24 h following i.p. and i.m. injections, respectively. The enzyme displayed a mean residence time (MRT) of 40-50 h, regardless of the route of administration or dose of injected enzyme. Mice were euthanized 2 weeks following enzyme administration and tissues were examined grossly or microscopically for possible toxic effects. Results suggest that HuBChE does not exhibit any toxicity in mice as measured by general observation, serum chemistry, hematology, gross or histologic tissue changes. The shelf life of this enzyme stored at 4, 25, 37, and 45 degrees C was determined in lyophilized form. The enzyme was found to be stable when stored in lyophilized form at -20, 4, 25, or 37 degrees C to date (2 years), as measured by specific activity and SDS polyacrylamide gel electrophoresis. The effect of storage on circulatory stability was determined by measuring MRT in mice; there was no change in the MRT of lyophilized enzyme stored at -20 degrees C to date (2 years). These results provide convincing data that HuBChE is a safe bioscavenger that can provide protection against all OP nerve agents. Efforts are now underway to prepare the required documentation for submission of an IND application to the United States Food and Drug Administration (USFDA).

摘要

将外源性施用的胆碱酯酶(ChEs)用作剧毒有机磷酸酯(OP)神经毒剂的生物清除剂,目前已有充分的文献记载,使其成为应对这一潜在威胁的极具可行性的预防性治疗方法。在迄今为止评估的胆碱酯酶中,人血清丁酰胆碱酯酶(HuBChE)最适合人类使用。预计200毫克(3毫克/千克)的HuBChE剂量可作为人类的预防性治疗药物,能保护人体免受高达2倍梭曼半数致死剂量(LD50)的暴露。除了用作各种战时场景(包括秘密行动)的预防药物外,它还可能用于应对恐怖分子释放神经毒气的急救人员(平民)。我们最近开发了一种大规模纯化HuBChE的方法,从120千克科恩IV-4组分中获得了约6克高度纯化的酶。该酶的比活性为700 - 750 U/毫克,在SDS-PAGE上迁移为单一条带。为了提供数据以启动将该酶用作人体生物清除剂的研究性新药(IND)申请,我们确定了其药代动力学特性,检测了其在小鼠中的安全性,并评估了其在不同温度下的保质期。在给小鼠注射高达90毫克/千克的不同剂量后,腹腔注射和肌肉注射后,酶活性分别在10小时和24小时达到循环峰值水平。无论给药途径或注射酶的剂量如何,该酶的平均驻留时间(MRT)为40 - 50小时。在酶给药后2周对小鼠实施安乐死,并对组织进行大体或显微镜检查以寻找可能的毒性作用。结果表明,通过一般观察、血清化学、血液学、大体或组织学组织变化测量,HuBChE在小鼠中未表现出任何毒性。以冻干形式测定了该酶在4℃, 25℃, 37℃和45℃下的保质期。通过比活性和SDS聚丙烯酰胺凝胶电泳测量发现,该酶以冻干形式储存在-20℃、4℃、25℃或37℃时至今(2年)是稳定的。通过测量小鼠中的MRT确定储存对循环稳定性的影响;至今(2年)储存在-20℃的冻干酶的MRT没有变化。这些结果提供了令人信服的数据,表明HuBChE是一种安全的生物清除剂,可以提供针对所有OP神经毒剂的保护。目前正在努力准备所需文件,以便向美国食品药品监督管理局(USFDA)提交IND申请。

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