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γ-氨基丁酸(GABA)结构类似物对神经元膜GABAB受体结合的抑制作用。

Inhibition of neuronal membrane GABAB receptor binding by GABA structural analogues.

作者信息

Tunnicliff G, Rogier C J, Youngs T L

机构信息

Laboratory of Neurochemistry, Indiana University School of Medicine, Evansville 47712.

出版信息

Int J Biochem. 1988;20(2):179-82. doi: 10.1016/0020-711x(88)90483-1.

Abstract
  1. A number of compounds structurally related to GABA were tested as inhibitors of baclofen-sensitive GABAB receptor binding to membranes from mouse brain. 2. In addition to two known inhibitors--baclofen and 5-aminovaleric acid--two analogues were shown to possess inhibitory activity. These compounds were 4-aminobutyryl-DL-alanine hydrobromide (IC50 = 3 microM) and trans-2-(aminomethyl)cyclopropane carboxylic acid (IC50 = 90 microM). 3. Both drugs also exhibited affinity for GABAA binding sites. 4. Further experiments are needed to establish if these analogues exert agonist or antagonist action at the GABAB receptor.
摘要
  1. 测试了多种与γ-氨基丁酸(GABA)结构相关的化合物,以研究它们作为巴氯芬敏感型GABAB受体与小鼠脑膜结合的抑制剂的作用。2. 除了两种已知的抑制剂——巴氯芬和5-氨基戊酸——两种类似物也显示出具有抑制活性。这些化合物是4-氨基丁酰-DL-丙氨酸氢溴酸盐(IC50 = 3 microM)和反式-2-(氨基甲基)环丙烷羧酸(IC50 = 90 microM)。3. 这两种药物对GABAA结合位点也表现出亲和力。4. 需要进一步的实验来确定这些类似物在GABAB受体上发挥激动剂还是拮抗剂作用。

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