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A comparison of the relative activities of a number of GABAB antagonists in the isolated vas deferens of the rat.

机译:大鼠离体输精管中多种GABA B拮抗剂相对活性的比较。

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摘要

1. A series of GABAB receptor antagonists were tested against (+/-)-baclofen for activity on the presynaptic GABAB receptor in the rat vas deferens. 2. All the antagonists tested caused a rightward shift in the concentration-response curve to (+/-)-baclofen. 3. pA2 values calculated from full Schild analysis were as follows: phaclofen, pA2 = 4.3; delta-amino valeric acid, pA2 = 4.4; 3-aminopropyl(diethoxymethyl)phosphinic acid (CGP 35348), pA2 = 5.0; 3-amino-propyl(n-hexyl)phosphinic acid (3-APHPA), pA2 = 4.5. 4. These results show that none of the above compounds possess potent antagonist activity at the GABAB receptor (i.e. pA2 > 6) in this peripheral tissue. In addition, the more recently available phosphinic acid antagonists, appear to offer no great advance over the GABAB antagonists previously available.
机译:1.测试了一系列GABA B受体拮抗剂对(+/-)-baclofen对大鼠输精管中突触前GABA B受体的活性。 2.所有测试的拮抗剂引起浓度-反应曲线向右移动至(+/-)-baclofen。 3.通过完全Schild分析计算出的pA2值如下:phclofen,pA2 = 4.3; δ-氨基戊酸,pA2 = 4.4; 3-氨基丙基(二乙氧基甲基)次膦酸(CGP 35348),pA2 = 5.0; 3-氨基丙基(正己基)次膦酸(3-APHPA),pA2 = 4.5。 4.这些结果表明,上述化合物均没有在该外周组织中对GABA B受体具有有效的拮抗活性(即,pA 2> 6)。另外,较以前可获得的次膦酸拮抗剂似乎没有比先前可获得的GABA B拮抗剂提供很大的进步。

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