Suppr超能文献

γ-氨基丁酸(GABA)膦酸类似物对豚鼠离体回肠和输精管中GABAB受体介导反应的拮抗作用。

Antagonism of GABAB-receptor-mediated responses in the guinea-pig isolated ileum and vas deferens by phosphono-analogues of GABA.

作者信息

Kerr D I, Ong J, Prager R H

机构信息

Department of Physiology, University of Adelaide, South Australia.

出版信息

Br J Pharmacol. 1990 Feb;99(2):422-6. doi: 10.1111/j.1476-5381.1990.tb14719.x.

Abstract
  1. The phosphono-analogues of gamma-aminobutyric acid (GABA), 4-amino-butylphosphonic acid (4-ABPA), 3-amino-2-(4-chlorophenyl)-propylphosphonic acid (phaclofen) and 3-amino-2-cyclohexylpropyl-phosphonic acid, each antagonized the GABA- and baclofen-induced GABAB-receptor-mediated depression of twitch responses to transmural stimulation in the guinea-pig isolated ileum, in a concentration-dependent, reversible and surmountable manner (apparent pA2 = 4.0 +/- 0.1, 4 +/- 0.2 and 3.7 +/- 0.2 respectively, compared with 3.9 +/- 0.1 for delta-aminovaleric acid). No such activity was found in a variety of related analogues. 2. By contrast, 3-amino-propylphosphonic acid (3-APPA) behaved as a partial agonist, itself partly depressing ileal twitch contractions in a manner sensitive to 4-ABPA and phaclofen, as well as antagonizing the depression of the ileal twitch by GABA and baclofen (apparent pA2 = 4.0 +/- 0.2). 3. Both 4-ABPA and phaclofen also antagonized the baclofen-induced depression of the twitch in the guinea-pig isolated vas deferens (apparent pA2 = 4.0 +/- 0.1 for each), whilst 3-APPA behaved as a partial agonist, slightly depressing the vas twitch, and antagonised the baclofen-induced depression of the twitch (apparent pA2 = 3.9 +/- 0.1). 4. None of these phosphono-analogues exhibited any action at ileal GABAA-receptors, nor influenced the ileal twitch depression with morphine, adenosine or noradrenaline, suggesting their selectivity as antagonists at GABAB-receptors.
摘要
  1. γ-氨基丁酸(GABA)的膦酸类似物,4-氨基丁基膦酸(4-ABPA)、3-氨基-2-(4-氯苯基)-丙基膦酸(巴氯芬)和3-氨基-2-环己基丙基膦酸,均可拮抗GABA和巴氯芬诱导的豚鼠离体回肠对透壁刺激的抽搐反应的GABAB受体介导的抑制作用,呈浓度依赖性、可逆性和可克服性(表观pA2分别为4.0±0.1、4±0.2和3.7±0.2,相比之下,δ-氨基戊酸为3.9±0.1)。在多种相关类似物中未发现此类活性。2. 相比之下,3-氨基丙基膦酸(3-APPA)表现为部分激动剂,其本身以对4-ABPA和巴氯芬敏感的方式部分抑制回肠抽搐收缩,同时拮抗GABA和巴氯芬对回肠抽搐的抑制作用(表观pA2 = 4.0±0.2)。3. 4-ABPA和巴氯芬还拮抗巴氯芬诱导的豚鼠离体输精管抽搐抑制作用(每种的表观pA2 = 4.0±0.1),而3-APPA表现为部分激动剂,轻微抑制输精管抽搐,并拮抗巴氯芬诱导的抽搐抑制作用(表观pA2 = 3.9±0.1)。4. 这些膦酸类似物在回肠GABAA受体上均未表现出任何作用,也不影响吗啡、腺苷或去甲肾上腺素引起的回肠抽搐抑制,表明它们作为GABAB受体拮抗剂具有选择性。

相似文献

本文引用的文献

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验