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体外和体内乙撑双二硫代氨基甲酸酯类杀菌剂对大鼠脑膜 NMDA 受体的影响。

The effect ofin vitro andin vivo ethylenbis dithiocarbamate fungicides on NMDA receptors in rat brain membranes.

机构信息

Department of Public Health, Fukushima Medical University, School of Medicine, Hikarigaoka 1, 960-1295, Fukushima, Japan,

出版信息

Environ Health Prev Med. 2001 Apr;6(1):54-9. doi: 10.1007/BF02897310.

Abstract

To determine whether the ethlenbisdithiocarbamate fungicides, zineb, manzeb and maneb affect the N-methyl-D-aspartate (NMDA) receptor in rat brain membranes, we performed a binding assay using [(3)H]MK-801, a noncompetitive NMDA receptor antagonist. Displacement studies were conducted using well washed membranes to exclude the effect of endogenous acidic amino acids on the binding of [(3)H]MK-801. In both the presence or absence of added glutamate and glycine in the assay buffer, the dose-response curve indicated that zineb enhanced the binding in a concentration range of 100-500 μM. However, the displacement curves indicated that manzeb and maneb inhibited the binding in a concentration range of 10-500 μM. The addition of 50 μM glutamate and glycine to the assay medium increased binding by 5-20% above the control in a concentration range of 0.1-100 μM.No rats injected with zineb, manzeb, maneb (100 mg/kg, ip) showed any characteristic toxic signs or any significant weight changes within 24 hrs. Estimation of [(3)H]MK-801 binding to unwashed membranes from intoxicated rat brains revealed no marked change in Bmax or Kd values for 24 hrs following fungicide administration.

摘要

为了确定乙撑双硫代氨基甲酸酯类杀菌剂代森锰锌、代森锰和代森锌是否会影响大鼠脑膜上的 N-甲基-D-天冬氨酸(NMDA)受体,我们使用非竞争性 NMDA 受体拮抗剂 [(3)H]MK-801 进行了结合测定。通过使用充分洗涤的膜进行置换研究,排除了内源性酸性氨基酸对 [(3)H]MK-801 结合的影响。在测定缓冲液中存在或不存在添加的谷氨酸和甘氨酸的情况下,剂量反应曲线表明代森锰锌在 100-500 μM 的浓度范围内增强了结合。然而,置换曲线表明代森锰和代森锌在 10-500 μM 的浓度范围内抑制了结合。在 0.1-100 μM 的浓度范围内,向测定介质中添加 50 μM 的谷氨酸和甘氨酸会使结合增加 5-20%,超过对照。在 24 小时内,注射代森锰锌、代森锰和代森锌(100mg/kg,ip)的大鼠均未出现任何特征性毒性体征或明显体重变化。在接触杀真菌剂后 24 小时内,对中毒大鼠脑的未洗涤膜进行 [(3)H]MK-801 结合的估计显示,Bmax 或 Kd 值没有明显变化。

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