Wetherell Janet, Price Matthew, Mumford Helen
Biomedical Sciences Department, Dstl Porton Down, Salisbury, Wiltshire SP4 0JQ, UK.
Neurotoxicology. 2006 Jul;27(4):485-91. doi: 10.1016/j.neuro.2006.01.006. Epub 2006 Feb 20.
This study forms part of a larger programme of work aimed at developing improved medical countermeasures for nerve agent poisoning with less reliance on pretreatment. Therapy with N(6)-cyclopentyladenosine (CPA), physostigmine, hyoscine and HI-6 protected guinea-pigs against the incapacitating and lethal effects of a supralethal challenge of soman (135 microg/kg) when given 1 min after poisoning. CPA, however has well-recognised side effects that are likely to preclude it being licensed for use in humans so further refinements were made to the doses of the other therapy components to improve efficacy in the absence of CPA. An immediate therapy comprising physostigmine (0.2 mg/kg), hyoscine (4 mg/kg) and HI-6 (93.6 mg/kg), when given 1 min after nerve agent, provided good protection against the lethal effects of GA, GB, GD, GF and VX poisoning and reduced the duration of the signs of incapacitation and hypothermia. In the case of GA and GB poisoning some animals exhibited a short period of substantial incapacitation. Most animals continued to gain weight over the following 6 days without the need for further medical intervention. In the case of GA poisoning further medical intervention would be needed to ensure the longer term survival of all animals and it is likely that in the battlefield situation further medical treatment would be available within 2-4 h. The drug combination described in this paper protects against supralethal doses of a range of nerve agents, with minimal incapacitation in the absence of any pretreatment. Further modification and refinement of this therapy is required for human use and it may provide a way forward for development of medical countermeasures for the treatment of organophosphate poisoning in the wider community should there be a need.
本研究是一个更大的工作计划的一部分,该计划旨在开发改进的抗神经毒剂中毒医学对策,减少对预处理的依赖。在中毒后1分钟给予N(6)-环戊基腺苷(CPA)、毒扁豆碱、东莨菪碱和HI-6进行治疗,可保护豚鼠免受索曼超致死剂量(135微克/千克)攻击所产生的失能和致死效应。然而,CPA具有公认的副作用,这可能使其无法获得用于人类的许可,因此对其他治疗成分的剂量进行了进一步优化,以在没有CPA的情况下提高疗效。在神经毒剂中毒后1分钟给予由毒扁豆碱(0.2毫克/千克)、东莨菪碱(4毫克/千克)和HI-6(93.6毫克/千克)组成的即时疗法,可有效预防GA、GB、GD、GF和VX中毒的致死效应,并缩短失能和体温过低症状的持续时间。在GA和GB中毒的情况下,一些动物出现了短时间的严重失能。大多数动物在接下来的6天里继续体重增加,无需进一步的医疗干预。在GA中毒的情况下,需要进一步的医疗干预以确保所有动物的长期存活,并且在战场情况下,可能在2至4小时内可获得进一步的医疗救治。本文所述的药物组合可预防一系列神经毒剂的超致死剂量,在没有任何预处理的情况下失能最小。该疗法用于人类还需要进一步的修改和完善,如果有需要,它可能为更广泛人群中治疗有机磷中毒的医学对策开发提供一条途径。