• 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

甘氨酸相关氨基酸对豚鼠回肠中N-甲基-D-天冬氨酸受体介导的收缩产生立体选择性影响:与对大鼠皮层膜上士的宁不敏感的[3H]甘氨酸结合抑制作用的比较。

Glycine-related amino acids stereoselectively affect N-methyl-D-aspartate receptor-mediated contractions of guinea pig ileum: comparison with the inhibition of strychnine-insensitive [3H]glycine binding to rat cortical membranes.

作者信息

Galli A, Franchi-Micheli S, Mori F, Luzzi S, Zilletti L

机构信息

Department of Preclinical and Clinical Pharmacology, University of Florence, Firenze, Italy.

出版信息

Neuropharmacology. 1990 Feb;29(2):145-50. doi: 10.1016/0028-3908(90)90054-u.

DOI:10.1016/0028-3908(90)90054-u
PMID:2158634
Abstract

Ten microM glycine, D-serine and D-alanine potentiated L-glutamate (30 microM)-induced contractions of the guinea pig ileum by an average of 35, 53 and 24%, respectively. On the contrary, D-cysteine, at the same concentration, caused a 21% inhibition of the contractile response to L-glutamate. This inhibitory effect of D-cysteine was abolished by 10 microM glycine. The corresponding L-isomers of these amino acids, namely L-serine, L-alanine and L-cysteine and the other amino acids tested, possessed negligible activity or were inactive in this test. The IC50 values of the same compounds for strychnine-insensitive binding of [3H]glycine (20 nM) to cortical membranes from the brain of the rat were: 0.26 microM, glycine; 1.2 microM, D-serine; 2.1 microM, D-alanine; 8.6 microM, D-cysteine; 51 microM, L-serine; 90 microM, L-alanine; greater than 1000 microM, L-cysteine. On the whole, these results point out a strict requirement for stereoselectivity for both of the effects examined. In addition, the results obtained in the ileum preparation suggest that D-cysteine may act as an antagonist, rather than as an agonist at the glycine site which regulates the responses of N-methyl-D-aspartate receptors.

摘要

10微摩尔的甘氨酸、D-丝氨酸和D-丙氨酸分别使L-谷氨酸(30微摩尔)诱导的豚鼠回肠收缩平均增强了35%、53%和24%。相反,相同浓度的D-半胱氨酸使对L-谷氨酸的收缩反应受到21%的抑制。10微摩尔的甘氨酸可消除D-半胱氨酸的这种抑制作用。这些氨基酸的相应L-异构体,即L-丝氨酸、L-丙氨酸和L-半胱氨酸以及所测试的其他氨基酸,在此测试中活性可忽略不计或无活性。相同化合物对[3H]甘氨酸(20纳摩尔)与大鼠脑皮质膜上士的宁不敏感结合的IC50值分别为:甘氨酸0.26微摩尔;D-丝氨酸1.2微摩尔;D-丙氨酸2.1微摩尔;D-半胱氨酸8.6微摩尔;L-丝氨酸51微摩尔;L-丙氨酸90微摩尔;L-半胱氨酸大于1000微摩尔。总体而言,这些结果表明所研究的两种效应都严格要求立体选择性。此外,在回肠制备实验中获得的结果表明,D-半胱氨酸可能作为拮抗剂,而不是在调节N-甲基-D-天冬氨酸受体反应的甘氨酸位点上作为激动剂起作用。

相似文献

1
Glycine-related amino acids stereoselectively affect N-methyl-D-aspartate receptor-mediated contractions of guinea pig ileum: comparison with the inhibition of strychnine-insensitive [3H]glycine binding to rat cortical membranes.甘氨酸相关氨基酸对豚鼠回肠中N-甲基-D-天冬氨酸受体介导的收缩产生立体选择性影响:与对大鼠皮层膜上士的宁不敏感的[3H]甘氨酸结合抑制作用的比较。
Neuropharmacology. 1990 Feb;29(2):145-50. doi: 10.1016/0028-3908(90)90054-u.
2
Quinoxalines interact with the glycine recognition site of NMDA receptors: studies in guinea-pig myenteric plexus and in rat cortical membranes.喹喔啉与N-甲基-D-天冬氨酸受体的甘氨酸识别位点相互作用:豚鼠肠肌丛和大鼠皮层膜的研究
Br J Pharmacol. 1989 Dec;98(4):1281-6. doi: 10.1111/j.1476-5381.1989.tb12675.x.
3
Stereoselectivity for the (R)-enantiomer of HA-966 (1-hydroxy-3-aminopyrrolidone-2) at the glycine site of the N-methyl-D-aspartate receptor complex.HA-966(1-羟基-3-氨基吡咯烷-2)的(R)-对映体在N-甲基-D-天冬氨酸受体复合物甘氨酸位点的立体选择性。
J Neurochem. 1990 Oct;55(4):1346-51. doi: 10.1111/j.1471-4159.1990.tb03145.x.
4
Glycine and kynurenate modulate the glutamate receptors in the myenteric plexus and in cortical membranes.甘氨酸和犬尿氨酸调节肌间神经丛和皮质膜中的谷氨酸受体。
Eur J Pharmacol. 1989 Apr 12;163(1):123-6. doi: 10.1016/0014-2999(89)90404-4.
5
Thiokynurenates: a new group of antagonists of the glycine modulatory site of the NMDA receptor.硫代犬尿氨酸盐:一类新型N-甲基-D-天冬氨酸受体甘氨酸调节位点拮抗剂。
Eur J Pharmacol. 1991 Jun 25;199(2):227-32. doi: 10.1016/0014-2999(91)90461-x.
6
Glycine binding to rat cortex and spinal cord: binding characteristics and pharmacology reveal distinct populations of sites.甘氨酸与大鼠皮质和脊髓的结合:结合特性与药理学揭示不同的位点群体。
J Neurochem. 1989 Aug;53(2):503-12. doi: 10.1111/j.1471-4159.1989.tb07362.x.
7
Comparison of binding at strychnine-sensitive (inhibitory glycine receptor) and strychnine-insensitive (N-methyl-D-aspartate receptor) glycine binding sites.士的宁敏感型(抑制性甘氨酸受体)和士的宁不敏感型(N-甲基-D-天冬氨酸受体)甘氨酸结合位点的结合比较。
Neurosci Lett. 1992 Dec 14;148(1-2):199-201. doi: 10.1016/0304-3940(92)90838-x.
8
Characterization and regional distribution of strychnine-insensitive [3H]glycine binding sites in rat brain by quantitative receptor autoradiography.通过定量受体放射自显影法对大鼠脑中士的宁不敏感的[3H]甘氨酸结合位点进行表征及区域分布研究。
Neuroscience. 1990;35(3):653-68. doi: 10.1016/0306-4522(90)90336-3.
9
Pharmacological analysis of [3H]-senktide binding to NK3 tachykinin receptors in guinea-pig ileum longitudinal muscle-myenteric plexus and cerebral cortex membranes.[3H] - 速激肽与豚鼠回肠纵肌 - 肠肌间神经丛及大脑皮层膜中NK3速激肽受体结合的药理学分析
Br J Pharmacol. 1990 Apr;99(4):767-73. doi: 10.1111/j.1476-5381.1990.tb13004.x.
10
Agonists, antagonists and modulators of excitatory amino acid receptors in the guinea-pig myenteric plexus.豚鼠肠肌间神经丛中兴奋性氨基酸受体的激动剂、拮抗剂和调节剂
Br J Pharmacol. 1988 Dec;95(4):1271-7. doi: 10.1111/j.1476-5381.1988.tb11764.x.