Naseem S M
University of Maryland, School of Medicine, Baltimore 21201.
Biochem Int. 1990;20(4):799-806.
The effect of Soman, Sarin and Vx, known potent cholinesterase inhibitors, on the binding of several neurotransmitter receptors in various regions of brain was studied. Vx, exhibited considerable inhibition of binding of 3H-N-methylscopolamine (3H-NMS) to muscarinic receptors and of 3H-spiperone to dopamine D2 receptors in the striatum. 3H-NMS binding was 50% inhibited at 10(-6)M and 90% at 10(-3)M Vx. Inhibition of 3H-spiperone binding by Vx in striatum had an ID50 of 10(-5)M. KD of the treatment was affected more than Bmax. Binding inhibition of both 3H-NMS and 3H-spiperone in post-mortem brain of rats pre-treated with Vx confirmed the specificity of the organophosphates effect, since other organophosphates and ligands failed to show any activity.
研究了已知的强效胆碱酯酶抑制剂梭曼、沙林和维埃克斯对大脑不同区域几种神经递质受体结合的影响。维埃克斯对纹状体中3H-N-甲基东莨菪碱(3H-NMS)与毒蕈碱受体的结合以及3H-螺哌隆与多巴胺D2受体的结合表现出相当程度的抑制作用。在10^(-6)M的维埃克斯作用下,3H-NMS结合被抑制50%,在10^(-3)M时被抑制90%。维埃克斯对纹状体中3H-螺哌隆结合的抑制作用的半数抑制浓度(ID50)为10^(-5)M。治疗的解离常数(KD)比最大结合容量(Bmax)受影响更大。在用维埃克斯预处理的大鼠死后大脑中,3H-NMS和3H-螺哌隆的结合抑制证实了有机磷酸酯作用的特异性,因为其他有机磷酸酯和配体未显示任何活性。