• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

通过拮抗剂谷氨酸二乙酯和D-α-氨基己二酸对兴奋性氨基酸进行排序。

Ranking of excitatory amino acids by the antagonists glutamic acid diethylester and D-alpha-aminoadipic acid.

作者信息

Hicks T P, Hall J G, McLennan H

出版信息

Can J Physiol Pharmacol. 1978 Dec;56(6):901-7. doi: 10.1139/y78-143.

DOI:10.1139/y78-143
PMID:743629
Abstract

A separation of the excitatory actions of the amino acids upon thalamic neurones of rats anaesthetized with urethane has been accomplished through the use of two antagonists. It has been possible to rank the excitatory compounds in their order of susceptibility to D-alpha-aminoadipic acid (DalphaAA) and L-glutamic acid diethylester (GDEE). The observation that the ranking orders of the excitants differ for these two antagonists permits an analysis of the types of receptors with which the amino acid excitants react. The results support the proposition that more than one neuronal receptor sensitive to the amino acids exists.

摘要

通过使用两种拮抗剂,已实现对用乌拉坦麻醉的大鼠丘脑神经元上氨基酸兴奋性作用的分离。已能够按照对D-α-氨基己二酸(DalphaAA)和L-谷氨酸二乙酯(GDEE)的敏感顺序对兴奋性化合物进行排序。这两种拮抗剂的兴奋性物质排序顺序不同这一观察结果,允许对氨基酸兴奋性物质所反应的受体类型进行分析。结果支持存在不止一种对氨基酸敏感的神经元受体这一观点。

相似文献

1
Ranking of excitatory amino acids by the antagonists glutamic acid diethylester and D-alpha-aminoadipic acid.通过拮抗剂谷氨酸二乙酯和D-α-氨基己二酸对兴奋性氨基酸进行排序。
Can J Physiol Pharmacol. 1978 Dec;56(6):901-7. doi: 10.1139/y78-143.
2
Selective antagonism of amino acid-induced and synaptic excitation in the cat spinal cord.猫脊髓中氨基酸诱导的和突触兴奋的选择性拮抗作用。
J Physiol. 1979 Dec;297(0):621-35. doi: 10.1113/jphysiol.1979.sp013060.
3
The action of D-alpha-aminoadipate on excitatory amino acid receptors of rat thalamic neurones.D-α-氨基己二酸对大鼠丘脑神经元兴奋性氨基酸受体的作用。
Brain Res. 1978 Jun 30;149(2):541-5. doi: 10.1016/0006-8993(78)90501-2.
4
The antagonism of amino acid-induced excitation of spinal neurones in the cat.猫体内氨基酸诱导的脊髓神经元兴奋的拮抗作用。
Brain Res. 1979 Jun 15;169(1):83-90. doi: 10.1016/0006-8993(79)90375-5.
5
Selective antagonist activity of 5-aminohex-2-enedioic acid on amino acid excitation of cat spinal neurones.5-氨基己-2-烯二酸对猫脊髓神经元氨基酸激发的选择性拮抗活性。
Neurosci Lett. 1980 Jan;16(1):17-20. doi: 10.1016/0304-3940(80)90094-4.
6
On the configuration of the receptors for excitatory amino acids.
Neuropharmacology. 1982 Jun;21(6):549-54. doi: 10.1016/0028-3908(82)90046-6.
7
Selective antagonism of amino acids by alpha-aminoadipate on pyramidal tract neurones but not Purkinje cells.α-氨基己二酸对锥体束神经元而非浦肯野细胞的氨基酸选择性拮抗作用。
Brain Res. 1979 Apr 20;166(1):217-20. doi: 10.1016/0006-8993(79)90668-1.
8
Depression of synaptic excitation and of amino acid induced excitatory responses of spinal neurones by D-alpha-aminoadipate, alpha,epsilon-diaminopimelic acid and HA-966.D-α-氨基己二酸、α,ε-二氨基庚二酸和HA-966对脊髓神经元突触兴奋及氨基酸诱导的兴奋性反应的抑制作用。
Eur J Pharmacol. 1977 Oct 1;45(3):315-6. doi: 10.1016/0014-2999(77)90017-6.
9
An evaluation of D-alpha-aminoadipate and D-(and DL-)alpha-aminosuberate as selective antagonists of excitatory amino acids in the substantia nigra and mesencephalic reticular formation of the rat.对D-α-氨基己二酸和D-(及DL-)α-氨基辛二酸作为大鼠黑质和中脑网状结构中兴奋性氨基酸选择性拮抗剂的评价。
Neuropharmacology. 1979 Feb;18(2):193-9. doi: 10.1016/0028-3908(79)90061-3.
10
The excitation of frog motoneurones in vitro by the glutamate analogue, DI-alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid (AMPA), and the effect of amino acid antagonists.体外培养的青蛙运动神经元由谷氨酸类似物二异亮氨酸-α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)激发及氨基酸拮抗剂的作用
Neurosci Lett. 1985 Mar 22;55(1):77-82. doi: 10.1016/0304-3940(85)90315-5.

引用本文的文献

1
The Discovery and Characterization of Targeted Perikaryal-Specific Brain Lesions With Excitotoxins.使用兴奋性毒素对靶向性核周特异性脑损伤的发现与特征描述
Front Neurosci. 2020 Sep 8;14:927. doi: 10.3389/fnins.2020.00927. eCollection 2020.
2
Antagonism of the hypermotility response induced by excitatory amino acids in the rat nucleus accumbens.兴奋性氨基酸诱导的大鼠伏隔核运动亢进反应的拮抗作用。
Naunyn Schmiedebergs Arch Pharmacol. 1984 Jan;325(1):1-7. doi: 10.1007/BF00507046.
3
Glutamate and aspartate agonists structurally related to ibotenic acid.
与鹅膏蕈氨酸结构相关的谷氨酸和天冬氨酸激动剂。
Mol Cell Biochem. 1981 Aug 11;38 Spec No(Pt 1):123-8. doi: 10.1007/BF00235691.
4
Blockade of amino acid-induced depolarizations and inhibition of excitatory post-synaptic potentials in rat dentate gyrus.大鼠齿状回中氨基酸诱导的去极化的阻断及兴奋性突触后电位的抑制
J Physiol. 1983 Aug;341:627-40. doi: 10.1113/jphysiol.1983.sp014829.
5
The antagonism of amino acid-induced excitations of rat hippocampal CA1 neurones in vitro.体外实验中氨基酸诱导的大鼠海马CA1神经元兴奋的拮抗作用
J Physiol. 1983 Jan;334:19-31. doi: 10.1113/jphysiol.1983.sp014477.
6
The action of six antagonists of the excitatory amino acids on neurones of the rat spinal cord.六种兴奋性氨基酸拮抗剂对大鼠脊髓神经元的作用。
Exp Brain Res. 1982;45(1-2):151-6. doi: 10.1007/BF00235774.
7
Inhibition of quisqualate-induced seizures by glutamic acid diethyl ester and anti-epileptic drugs.谷氨酸二乙酯和抗癫痫药物对喹啉酸诱发癫痫的抑制作用。
J Neural Transm. 1986;67(3-4):191-203. doi: 10.1007/BF01243347.
8
A comparison between the in vivo and in vitro activity of five potent and competitive NMDA antagonists.五种强效竞争性N-甲基-D-天冬氨酸拮抗剂的体内和体外活性比较。
Br J Pharmacol. 1988 Nov;95(3):957-65. doi: 10.1111/j.1476-5381.1988.tb11726.x.
9
A microiontophoretic study on the nature of the putative synaptic neurotransmitter involved in the pedunculopontine-substantia nigra pars compacta excitatory pathway of the rat.
Exp Brain Res. 1986;62(3):470-8. doi: 10.1007/BF00236025.
10
Excitatory amino acid receptor-mediated transmission of somatosensory evoked potentials in the rat thalamus.兴奋性氨基酸受体介导的大鼠丘脑体感诱发电位的传递
J Physiol. 1987 Dec;394:445-61. doi: 10.1113/jphysiol.1987.sp016880.