首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >The effects of a series of omega-phosphonic alpha-carboxylic amino acids on electrically evoked and excitant amino acid-induced responses in isolated spinal cord preparations.
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The effects of a series of omega-phosphonic alpha-carboxylic amino acids on electrically evoked and excitant amino acid-induced responses in isolated spinal cord preparations.

机译:一系列ω-膦酸α-羧酸氨基酸对分离的脊髓制剂中电诱发和兴奋性氨基酸诱导的反应的影响。

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摘要

1 The depressant actions on evoked electrical activity and the excitant amino acid antagonist properties of a range of omega-phosphonic alpha-carboxylic amino acids have been investigated in the isolated spinal cord preparations of the frog or immature rat. 2 When tested on dorsal root-evoked ventral root potentials, members of the homologous series from 2- amino-5-phosphonovaleric acid to 2-amino-8-phosphonooctanoic acid showed depressant actions which correlated with the ability of the substances to antagonize selectivity motoneuronal depolarizations induced by N-methyl-D-aspartate. 3 2-Amino-5-phosphonovalerate was the most potent substance of the series giving an apparent KD of 1.4 microM for the antagonism of responses to N-methyl-D-aspartate. 4 A comparison of the (+)- and (-)-forms of 2-amino-5-phosphonovalerate indicated that the N-methyl-D-aspartate antagonist activity and the neuronal depressant action of this substance were both due mainly to the (-)-isomer. 5 The (-)- and (+)-forms of 2-amino-4-phosphonobutyrate had different actions. The (-)-forms of this substance had a relatively weak and non-selective antagonist action on depolarizations induced by N-methyl-D-aspartate, quisqualate and kainate and a similarly weak depressant effect when tested on evoked electrical activity. The (+)-form was more potent than he (-)-form in depressing electrically evoked activity but did not antagonize responses to amino acid excitants. At concentrations higher than those required to depress electrically evoked activity, the (+)-form produced depolarization. This action was blocked by 2-amino-5-phosphonovalerate.
机译:1在青蛙或未成熟大鼠的分离的脊髓制剂中,已经研究了一系列ω-膦酸α-羧酸氨基酸对诱发的电活性的抑制作用和兴奋性氨基酸拮抗剂特性。 2当对背根诱发的腹侧根电位进行测试时,从2-氨基-5-膦戊酸到2-氨基-8-膦酸辛酸的同源序列的成员显示出抑制作用,这与该物质拮抗选择性神经元的能力有关N-甲基-D-天冬氨酸诱导的去极化。 3 2-氨基-5-膦酸戊二酸酯是该系列中最有效的物质,它对N-甲基-D-天冬氨酸的应答具有明显的KD为1.4 microM。 4比较2-氨基-5-膦酸戊二酸酯的(+)-和(-)形式表明,该物质的N-甲基-D-天冬氨酸拮抗剂活性和神经元抑制作用均归因于( -)-异构体。 5 2-氨基-4-膦酰基丁酸酯的(-)-和(+)形式具有不同的作用。该物质的(-)形式对N-甲基-D-天冬氨酸,喹草酸酯和红藻氨酸引起的去极化具有相对弱的非选择性拮抗作用,对诱发的电活动进行测试时,其抑制作用也较弱。 (+)形式比他(-)形式在抑制电诱发的活性上更有效,但没有拮抗对氨基酸兴奋剂的反应。在高于抑制电激活活性所需的浓度时,(+)形式产生去极化。该作用被2-氨基-5-膦酸戊酸酯阻断。

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