兴奋性毒素β-N-草酰-L-α,β-二氨基丙酸对[3H]α-氨基-3-羟基-5-甲基-4-异恶唑丙酸结合的抑制作用。 - Suppr

Suppr

超能文献

Inhibition of [3H]alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid binding by the excitotoxin beta-N-oxalyl-L-alpha,beta-diaminopropionic acid.

作者信息

Bridges R J, Kadri M M, Monaghan D T, Nunn P B, Watkins J C, Cotman C W

机构信息

Department of Neurology, University of California, Irvine 92627.

出版信息

Eur J Pharmacol. 1988 Jan 19;145(3):357-9. doi: 10.1016/0014-2999(88)90442-6.

DOI:10.1016/0014-2999(88)90442-6

PMID:2895006

Abstract

摘要

相似文献

Inhibition of [3H]alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid binding by the excitotoxin beta-N-oxalyl-L-alpha,beta-diaminopropionic acid.兴奋性毒素β-N-草酰-L-α,β-二氨基丙酸对[3H]α-氨基-3-羟基-5-甲基-4-异恶唑丙酸结合的抑制作用。

Eur J Pharmacol. 1988 Jan 19;145(3):357-9. doi: 10.1016/0014-2999(88)90442-6.

Ibotenic acid analogues. Synthesis, molecular flexibility, and in vitro activity of agonists and antagonists at central glutamic acid receptors.鹅膏蕈氨酸类似物。中枢谷氨酸受体激动剂和拮抗剂的合成、分子柔性及体外活性

J Med Chem. 1985 May;28(5):668-72. doi: 10.1021/jm50001a022.

Effects of thiol-reagents on [3H]alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid binding to rat telencephalic membranes.硫醇试剂对[3H]α-氨基-3-羟基-5-甲基异恶唑-4-丙酸与大鼠端脑细胞膜结合的影响。

Mol Pharmacol. 1988 Aug;34(2):117-23.

Structure-function studies on N-oxalyl-diamino-dicarboxylic acids and excitatory amino acid receptors: evidence that beta-L-ODAP is a selective non-NMDA agonist.N-草酰二氨基二羧酸与兴奋性氨基酸受体的结构-功能研究：β-L-草酰基-3,4-二氨基丁酸是一种选择性非NMDA激动剂的证据

J Neurosci. 1989 Jun;9(6):2073-9. doi: 10.1523/JNEUROSCI.09-06-02073.1989.

Beta-N-oxalylamino-L-alanine action on glutamate receptors.β-N-草酰氨基-L-丙氨酸对谷氨酸受体的作用。

J Neurochem. 1989 Sep;53(3):710-5. doi: 10.1111/j.1471-4159.1989.tb11762.x.

N-Methyl-D-aspartate and quisqualate/DL-alpha-amino-3-hydroxy-5- methylisoxazole-4-propionic acid receptors: differential regulation by phospholipase C treatment.N-甲基-D-天冬氨酸和使君子氨酸/DL-α-氨基-3-羟基-5-甲基异恶唑-4-丙酸受体：磷脂酶C处理的差异调节

Mol Pharmacol. 1990 Feb;37(2):278-85.

Phosphatidylserine increases the affinity of the AMPA/quisqualate receptor in rat brain membranes.

Behav Neural Biol. 1991 Mar;55(2):137-40. doi: 10.1016/0163-1047(91)80134-z.

Modulation of DL-alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid/quisqualate receptors by phospholipase A2: a necessary step in long-term potentiation?磷脂酶A2对DL-α-氨基-3-羟基-5-甲基-4-异恶唑丙酸/使君子氨酸受体的调节作用：长时程增强中的必要步骤？

Proc Natl Acad Sci U S A. 1991 Mar 1;88(5):1893-7. doi: 10.1073/pnas.88.5.1893.

Multiple states of rat brain (RS)-alpha-amino-3-hydroxy-5-methylisoxazole-4-propionic acid receptors as revealed by quantitative autoradiography.定量放射自显影揭示大鼠脑（RS）-α-氨基-3-羟基-5-甲基异恶唑-4-丙酸受体的多种状态

Mol Pharmacol. 1992 May;41(5):832-8.

Excitatory amino acid receptors expressed in Xenopus oocytes: agonist pharmacology.非洲爪蟾卵母细胞中表达的兴奋性氨基酸受体：激动剂药理学

Mol Pharmacol. 1988 Sep;34(3):298-307.

引用本文的文献

In vitro activation of protein kinase C by beta-N-oxalyl-L-alpha,beta-diaminopropionic acid, the Lathyrus sativus neurotoxin.β-N-草酰-L-α,β-二氨基丙酸（即香豌豆神经毒素）对蛋白激酶C的体外激活作用。

Neurochem Res. 2004 Jul;29(7):1343-8. doi: 10.1023/b:nere.0000026395.25468.57.

Neurotoxic potential of three structural analogs of beta-N-oxalyl-alpha,beta-diaminopropanoic acid (beta-ODAP).β-N-草酰-α,β-二氨基丙酸（β-ODAP）三种结构类似物的神经毒性潜力。

Neurochem Res. 1999 Jun;24(6):791-7. doi: 10.1023/a:1020791815848.

Thiol oxidation and loss of mitochondrial complex I precede excitatory amino acid-mediated neurodegeneration.硫醇氧化和线粒体复合物I的丧失先于兴奋性氨基酸介导的神经退行性变。

J Neurosci. 1998 Dec 15;18(24):10287-96. doi: 10.1523/JNEUROSCI.18-24-10287.1998.

Receptor interactions of beta-N-oxalyl-L-alpha,beta-diaminopropionic acid, the Lathyrus sativus putative excitotoxin, with synaptic membranes.山黧豆潜在兴奋性毒素β-N-草酰-L-α,β-二氨基丙酸与突触膜的受体相互作用。

Neurochem Res. 1998 Sep;23(9):1191-6. doi: 10.1023/a:1020782119057.

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