Blast-Induced Neurotrauma Branch, Center for Military Psychiatry and Neuroscience, Walter Reed Army Institute of Research, Silver Spring, MD 20910, USA.
Toxicol Mech Methods. 2012 May;22(4):250-9. doi: 10.3109/15376516.2011.639817. Epub 2011 Dec 7.
Acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) activities were measured in the blood and tissues of animals that are treated with a number of endotracheally aerosolized therapeutics for protection against inhalation toxicity to sarin. Therapeutics included, aerosolized atropine methyl bromide (AMB), scopolamine or combination of AMB with salbutamol, sphingosine 1-phosphate, keratinocyte growth factor, adenosine A1 receptor antisense oligonucleotide (EPI2010), 2,3-diacetyloxybenzoic acid (2,3 DABA), oxycyte, and survanta. Guinea pigs exposed to 677.4 mg/m(3) or 846.5 mg/m(3) (1.2 LCt(50)) sarin for 4 min using a microinstillation inhalation exposure technique and treated 1 min later with the aerosolized therapeutics. Treatment with all therapeutics significantly increased the survival rate with no convulsions throughout the 24 h study period. Blood AChE activity determined using acetylthiocholine as substrate showed 20% activity remaining in sarin-exposed animals compare to controls. In aerosolized AMB and scopolamine-treated animals the remaining AChE activity was significantly higher (45-60%) compared to sarin-exposed animals (p < 0.05). Similarly, treatment with all the combination therapeutics resulted in significant increase in blood AChE activity in comparison to sarin-exposed animals although the increases varied between treatments (p < 0.05). BChE activity was increased after treatment with aerosolized therapeutics but was lesser in magnitude compared to AChE activity changes. Various tissues showed elevated AChE activity after therapeutic treatment of sarin-exposed animals. Increased AChE and BChE activities in animals treated with nasal therapeutics suggest that enhanced breathing and reduced respiratory toxicity/lung injury possibly contribute to rapid normalization of chemical warfare nerve agent inhibited cholinesterases.
乙酰胆碱酯酶(AChE)和丁酰胆碱酯酶(BChE)活性在接受多种经气管气溶胶化治疗药物治疗以预防沙林吸入毒性的动物的血液和组织中进行了测量。治疗药物包括气溶胶化的氨基甲酰溴化阿托品(AMB)、东莨菪碱或 AMB 与沙丁胺醇的组合、神经鞘磷脂 1-磷酸、角质细胞生长因子、腺苷 A1 受体反义寡核苷酸(EPI2010)、2,3-二乙酰氧基苯甲酸(2,3-DABA)、Oxycyte 和 Survanta。豚鼠使用微滴吸入暴露技术暴露于 677.4 mg/m(3)或 846.5 mg/m(3)(1.2 LCt(50))沙林 4 分钟,并在 1 分钟后用气溶胶化治疗药物治疗。所有治疗药物的治疗均显著提高了存活率,整个 24 小时研究期间无抽搐。使用乙酰硫代胆碱作为底物测定血液 AChE 活性显示,与对照相比,暴露于沙林中的动物的 AChE 活性剩余 20%。在气溶胶化的 AMB 和东莨菪碱治疗的动物中,剩余的 AChE 活性明显更高(45-60%),与暴露于沙林的动物相比(p<0.05)。同样,与暴露于沙林的动物相比,所有组合治疗药物的治疗均导致血液 AChE 活性显著增加,尽管治疗之间的增加幅度有所不同(p<0.05)。BChE 活性在接受气溶胶化治疗药物治疗后增加,但与 AChE 活性变化相比,增加幅度较小。各种组织在治疗暴露于沙林的动物后显示出升高的 AChE 活性。接受鼻用治疗药物治疗的动物中 AChE 和 BChE 活性的增加表明,增强呼吸和减少呼吸毒性/肺损伤可能有助于化学战剂抑制的胆碱酯酶的快速正常化。