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有机磷抗胆碱酯酶对成年小鼠肌肉终板烟碱样受体离子通道的影响。

Effects of organophosphorus anticholinesterases on nicotinic receptor ion channels at adult mouse muscle endplates.

作者信息

Tattersall J E

机构信息

Biology Division, Chemical Defence Establishment, Salisbury, Wiltshire.

出版信息

Br J Pharmacol. 1990 Oct;101(2):349-57. doi: 10.1111/j.1476-5381.1990.tb12713.x.

DOI:10.1111/j.1476-5381.1990.tb12713.x
PMID:1701677
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1917701/
Abstract
  1. The effects of a range of organophosphorus anticholinesterases on the nicotinic acetylcholine receptor ion channel at the adult mouse muscle endplate were investigated by use of single-channel recording techniques. Diisopropylfluorophosphate (DFP), sarin and soman had no effect on open times at concentrations of up to 100 microM, but ecothiopate (Eco) and O-ethyl S-[2-(diisopropylamino)ethyl]methyl phosphonothiolate (VX) were found to have voltage- and concentration-dependent open channel-blocking actions at concentrations of 1-50 microM. In addition to its channel-blocking action, Eco (50 microM) had a weak agonist effect: it is suggested that this may be attributable to thiocholine produced by hydrolysis of Eco. 2. Rate constants for blockade by Eco and VX were determined according to a sequential model. The greater voltage-dependence of the block by Eco was due to a greater voltage sensitivity of the blocking rate constant compared to VX: the voltage-dependence of the unblocking rate constant was similar for both compounds. 3. In control recordings, the frequency of channel opening declined exponentially with time after formation of the gigaseal. Sarin and soman both increased the rate of this decline, indicating that they accelerated the rate of desensitization of the receptors. Eco and VX reduced the initial frequency of opening, which may have been due to enhancement of a fast phase of desensitization during gigaseal formation, or to blockade of closed channels. 4. It is concluded that the direct actions of organophosphates on nicotinic receptor ion channels are of little importance for their toxicity under normal conditions, since they occur only at much higher concentrations than those which cause inhibition of acetylcholinesterase. Such actions may become apparent, however, when therapies against the anticholinesterase effects of organophosphates increase their lethal dose sufficiently. These direct actions should also be taken into account when the effects of organophosphates on cholinergic transmission are studied.
摘要
  1. 运用单通道记录技术,研究了一系列有机磷抗胆碱酯酶对成年小鼠肌肉终板烟碱型乙酰胆碱受体离子通道的影响。在浓度高达100微摩尔时,二异丙基氟磷酸酯(DFP)、沙林和梭曼对开放时间无影响,但发现依可碘酯(Eco)和O - 乙基S - [2 - (二异丙氨基)乙基]甲基硫代膦酸酯(VX)在1 - 50微摩尔浓度时具有电压和浓度依赖性的开放通道阻断作用。除了其通道阻断作用外,Eco(50微摩尔)还有微弱的激动剂效应:提示这可能归因于Eco水解产生的硫代胆碱。2. 根据序贯模型测定了Eco和VX的阻断速率常数。Eco阻断的电压依赖性更强是因为与VX相比,其阻断速率常数的电压敏感性更高:两种化合物的解阻断速率常数的电压依赖性相似。3. 在对照记录中,形成千兆封接后,通道开放频率随时间呈指数下降。沙林和梭曼均增加了这种下降速率,表明它们加速了受体的脱敏速率。Eco和VX降低了初始开放频率,这可能是由于在千兆封接形成过程中增强了脱敏的快速相,或者是由于对关闭通道的阻断。4. 得出结论,在正常情况下,有机磷酸酯对烟碱型受体离子通道的直接作用对其毒性影响不大,因为它们仅在比导致乙酰胆碱酯酶抑制的浓度高得多的情况下才会发生。然而,当针对有机磷酸酯抗胆碱酯酶作用的治疗充分增加其致死剂量时,这些直接作用可能会变得明显。在研究有机磷酸酯对胆碱能传递的影响时,也应考虑这些直接作用。

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本文引用的文献

1
Toxicity of colchicine, di-isopropyl fluorophosphate, intocostrin, and potassium cyanide in mice at 4 degrees C.秋水仙碱、二异丙基氟磷酸酯、印防己毒素和氰化钾在4摄氏度下对小鼠的毒性
Proc Soc Exp Biol Med. 1951 Mar;76(3):536-8. doi: 10.3181/00379727-76-18547.
2
The use of therapeutic mixtures in the treatment of cholinesterase inhibition.治疗性混合物在胆碱酯酶抑制治疗中的应用。
Fundam Appl Toxicol. 1981 Mar-Apr;1(2):214-6. doi: 10.1016/s0272-0590(81)80060-7.
3
Factors modifying the toxicity of organophosphorous compounds including Soman and Sarin.影响包括梭曼和沙林在内的有机磷化合物毒性的因素。
Fundam Appl Toxicol. 1981 Mar-Apr;1(2):143-7. doi: 10.1016/s0272-0590(81)80050-4.
4
Anomalies in theories and therapy of intoxication by potent organophosphorus anticholinesterase compounds.强效有机磷抗胆碱酯酶化合物中毒的理论与治疗中的异常情况。
Gen Pharmacol. 1982;13(6):457-66. doi: 10.1016/0306-3623(82)90018-0.
5
The interaction of anticholinesterase agents with the acetylcholine receptor-ionic channel complex.抗胆碱酯酶药物与乙酰胆碱受体-离子通道复合物的相互作用。
Fundam Appl Toxicol. 1984 Apr;4(2 Pt 2):S27-33. doi: 10.1016/0272-0590(84)90135-0.
6
The charge carried by single-channel currents of rat cultured muscle cells in the presence of local anaesthetics.在局部麻醉剂存在的情况下,大鼠培养肌肉细胞单通道电流所携带的电荷。
J Physiol. 1983 Jun;339:663-78. doi: 10.1113/jphysiol.1983.sp014741.
7
Drug-induced modification of ionic conductance at the neuromuscular junction.药物引起的神经肌肉接头处离子电导的改变。
Annu Rev Pharmacol Toxicol. 1983;23:505-39. doi: 10.1146/annurev.pa.23.040183.002445.
8
Acetylcholine receptor.乙酰胆碱受体
Br J Anaesth. 1982 Feb;54(2):115-30. doi: 10.1093/bja/54.2.115.
9
The protective actions of some anticholinergic drugs in sarin poisoning.某些抗胆碱能药物在沙林中毒中的保护作用。
Br J Pharmacol. 1970 Aug;39(4):822-30. doi: 10.1111/j.1476-5381.1970.tb09909.x.
10
Diisopropylfluorophosphate: suppression of ionic conductance of the cholinergic receptor.二异丙基氟磷酸酯:对胆碱能受体离子电导的抑制作用。
Science. 1973 Aug 31;181(4102):853-6. doi: 10.1126/science.181.4102.853.