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吡啶斯的明和毒扁豆碱联合阿托品和美加明对二异丙基氟磷酸酯中毒的防护作用

Protection against diisopropylfluorophosphate intoxication by pyridostigmine and physostigmine in combination with atropine and mecamylamine.

作者信息

Harris L, Stitcher D

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1984 Aug;327(1):64-9. doi: 10.1007/BF00504993.

DOI:10.1007/BF00504993
PMID:6493352
Abstract

Atropine (A), mecamylamine (M), pyridostigmine (Py) and physostigmine (Ph) are pretreatment components of Mix I (A = 0.79, M = 0.79, Py = 0.056 mg/kg) and Mix II (A = 0.79, M = 0.79, Ph = 0.026 mg/kg). They have been successfully used in antagonizing Soman intoxication in experimental animals. Rats were pretreated with either Mix I or Mix II and subsequently exposed to diisopropylfluorphosphate (DFP). Pretreatment with Mix I or Mix II (i.m.) 30 min before DFP (i.v.) protected rats from the lethal effects of DFP. The protective ratios were 2.8 (Mix I) and 6.9 (Mix II). Changes in brain levels of acetylcholine (ACh) were measured to help understand the basis for effectiveness of these pretreatments. In the absence of DFP, pretreatments had no significant (P greater than 0.05) effect on bound or free ACh. Pretreatment did not prevent the DFP-induced rise in bound and free ACh nor the agent-induced physical incapacitation at 30 min post exposure. At 2 h after DFP exposure, rats pretreated with Mix II, but not Mix I, showed significant recovery from signs of physical incapacitation. At 30 min after the administration of 3.3 mg/kg of DFP (i.v.), the levels of free and bound ACh in rats given Mix I or Mix II pretreatment increased above control levels by 705% and 116% and 120% and 43%, respectively. By 2 h after DFP, cerebral ACh levels had changed to 437% and 91% with Mix I pretreatment and 26% and 50% with Mix II pretreatment. These data suggest a correlation between DFP-induced increases in the levels of cerebral ACh, possibly free, and physical incapacitation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

阿托品(A)、美加明(M)、吡啶斯的明(Py)和毒扁豆碱(Ph)是混合物I(A = 0.79、M = 0.79、Py = 0.056毫克/千克)和混合物II(A = 0.79、M = 0.79、Ph = 0.026毫克/千克)的预处理成分。它们已成功用于拮抗实验动物中的梭曼中毒。大鼠用混合物I或混合物II进行预处理,随后暴露于二异丙基氟磷酸酯(DFP)。在静脉注射DFP前30分钟肌肉注射混合物I或混合物II可保护大鼠免受DFP的致死作用。保护率分别为2.8(混合物I)和6.9(混合物II)。测量脑内乙酰胆碱(ACh)水平的变化以帮助理解这些预处理有效性的基础。在没有DFP的情况下,预处理对结合型或游离型ACh没有显著(P大于0.05)影响。预处理不能阻止DFP诱导的结合型和游离型ACh升高,也不能阻止暴露后30分钟时药物诱导的身体失能。在DFP暴露后2小时,用混合物II预处理的大鼠,但不是混合物I,显示出身体失能体征的显著恢复。在静脉注射3.3毫克/千克DFP后30分钟,接受混合物I或混合物II预处理的大鼠中游离型和结合型ACh水平分别比对照水平升高了705%和116%以及120%和43%。到DFP暴露后2小时,混合物I预处理时脑内ACh水平变为437%和91%,混合物II预处理时变为26%和50%。这些数据表明DFP诱导的脑内ACh水平升高(可能是游离型)与身体失能之间存在相关性。(摘要截于250字)

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本文引用的文献

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