• 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

注射了哺乳动物和鸟类脑mRNA的非洲爪蟾卵母细胞中表达的非NMDA受体的物种依赖性功能特性。

Species-dependent functional properties of non-NMDA receptors expressed in Xenopus laevis oocytes injected with mammalian and avian brain mRNA.

作者信息

Bowie D, Smart T G

机构信息

Department of Pharmacology, School of Pharmacy, University of London.

出版信息

Br J Pharmacol. 1994 Mar;111(3):803-10. doi: 10.1111/j.1476-5381.1994.tb14809.x.

DOI:10.1111/j.1476-5381.1994.tb14809.x
PMID:7517329
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1910061/
Abstract
  1. Species-dependent variation in the functional properties of non-NMDA receptors was investigated by intracellular recording in Xenopus laevis oocytes injected with rat, chick and calf brain mRNA. 2. In all mRNA-injected oocytes, kainic acid (KA), domoic acid (Dom) and 5-bromowillardiine (BrW) evoked large, maintained membrane currents, in contrast to the smaller, desensitizing responses elicited by alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA), quisqualic acid (QA) and L-glutamic acid (L-Glu). Dose-response curves for KA in oocytes injected with calf (EC50 = 96.4 +/- 12.3 microM; mean +/- s.e. mean), chick (87.0 +/- 8.9 microM) or rat (88.7 +/- 4.3 microM) brain mRNA were similar. 3. Current-voltage (I-V) relationships determined with KA inwardly rectified in oocytes injected with calf or chick mRNA; whereas, outward rectification was observed in oocytes injected with rat brain mRNA. 4. In oocytes injected with rat brain mRNA, AMPA antagonized responses evoked by KA in a competitive manner. The absolute amplitudes of KA and AMPA responses in the same oocytes were significantly correlated, which is consistent with both agonists acting on the same receptor-ionophore complex. 5. In contrast, in oocytes injected with calf or chick brain mRNA, AMPA (QA and L-Glu) antagonized the response evoked by KA in a non-competitive manner. The response amplitudes of KA compared to AMPA, QA or L-Glu in the same oocytes were not correlated suggesting discrete receptor-ionophores. 6. This study favours the existence of distinct non-NMDA receptor subtypes that are equi-sensitive to KA. The expressed receptors from different species of mRNA may be distinguished by their voltage sensitivities and the type of antagonism exerted by AMPA on KA-activated responses. Our observations may reflect further heterogeneity of non-NMDA receptors in the central nervous system of different vertebrate species.
摘要
  1. 通过对注射了大鼠、鸡和小牛脑mRNA的非洲爪蟾卵母细胞进行细胞内记录,研究了非NMDA受体功能特性的物种依赖性差异。2. 在所有注射了mRNA的卵母细胞中,海藻酸(KA)、软骨藻酸(Dom)和5-溴威尔拉德啉(BrW)诱发了大的、持续的膜电流,这与α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)、quisqualic酸(QA)和L-谷氨酸(L-Glu)引发的较小的脱敏反应形成对比。注射小牛(EC50 = 96.4 +/- 12.3 microM;平均值 +/- 标准误平均值)、鸡(87.0 +/- 8.9 microM)或大鼠(88.7 +/- 4.3 microM)脑mRNA的卵母细胞中KA的剂量反应曲线相似。3. 在注射小牛或鸡mRNA的卵母细胞中,用KA测定的电流-电压(I-V)关系呈内向整流;而在注射大鼠脑mRNA的卵母细胞中观察到外向整流。4. 在注射大鼠脑mRNA的卵母细胞中,AMPA以竞争性方式拮抗KA诱发的反应。同一卵母细胞中KA和AMPA反应的绝对幅度显著相关,这与两种激动剂作用于同一受体-离子载体复合物一致。5. 相反,在注射小牛或鸡脑mRNA的卵母细胞中,AMPA(QA和L-Glu)以非竞争性方式拮抗KA诱发的反应。同一卵母细胞中KA与AMPA、QA或L-Glu的反应幅度不相关,表明存在离散的受体-离子载体。6. 本研究支持存在对KA同等敏感的不同非NMDA受体亚型。来自不同物种mRNA表达的受体可能通过其电压敏感性以及AMPA对KA激活反应的拮抗类型来区分。我们的观察结果可能反映了不同脊椎动物物种中枢神经系统中非NMDA受体的进一步异质性。

相似文献

1
Species-dependent functional properties of non-NMDA receptors expressed in Xenopus laevis oocytes injected with mammalian and avian brain mRNA.注射了哺乳动物和鸟类脑mRNA的非洲爪蟾卵母细胞中表达的非NMDA受体的物种依赖性功能特性。
Br J Pharmacol. 1994 Mar;111(3):803-10. doi: 10.1111/j.1476-5381.1994.tb14809.x.
2
Interaction of 5-bromowillardiine with non-NMDA receptors expressed in Xenopus laevis oocytes injected with chick brain mRNA.5-溴韦拉地丁与注射了鸡脑mRNA的非洲爪蟾卵母细胞中表达的非NMDA受体的相互作用。
Neurosci Lett. 1991 Jan 2;121(1-2):68-72. doi: 10.1016/0304-3940(91)90651-9.
3
Thiocyanate ions selectively antagonize AMPA-evoked responses in Xenopus laevis oocytes microinjected with rat brain mRNA.硫氰酸根离子可选择性拮抗在显微注射大鼠脑信使核糖核酸的非洲爪蟾卵母细胞中由α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)诱发的反应。
Br J Pharmacol. 1993 Jul;109(3):779-87. doi: 10.1111/j.1476-5381.1993.tb13642.x.
4
Thiocyanate ions inhibit AMPA-activated currents in recombinant non-NMDA receptors expressed in Xenopus laevis oocytes: the role of the GluR2 subunit.硫氰酸根离子抑制非洲爪蟾卵母细胞中表达的重组非NMDA受体的AMPA激活电流:GluR2亚基的作用。
Eur J Neurosci. 1996 Sep;8(9):1983-93. doi: 10.1111/j.1460-9568.1996.tb01342.x.
5
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.
6
Quinoxaline derivatives: structure-activity relationships and physiological implications of inhibition of N-methyl-D-aspartate and non-N-methyl-D-aspartate receptor-mediated currents and synaptic potentials.喹喔啉衍生物:抑制N-甲基-D-天冬氨酸和非N-甲基-D-天冬氨酸受体介导的电流及突触电位的构效关系和生理意义
Mol Pharmacol. 1992 Feb;41(2):337-45.
7
Horizontal cells isolated from catfish retina contain two types of excitatory amino acid receptors.从鲶鱼视网膜分离出的水平细胞含有两种兴奋性氨基酸受体。
J Neurophysiol. 1989 Jun;61(6):1097-109. doi: 10.1152/jn.1989.61.6.1097.
8
Gamma-D-glutamylaminomethyl sulfonic acid (GAMS) distinguishes kainic acid- from AMPA-induced responses in Xenopus oocytes expressing chick brain glutamate receptors.γ-D-谷氨酰胺甲基磺酸(GAMS)可区分在表达鸡脑谷氨酸受体的非洲爪蟾卵母细胞中,海人酸诱导的反应和AMPA诱导的反应。
Neuropharmacology. 1993 Aug;32(8):767-75. doi: 10.1016/0028-3908(93)90185-6.
9
A voltage-clamp study of isolated stingray horizontal cell non-NMDA excitatory amino acid receptors.
J Neurophysiol. 1989 Jan;61(1):162-72. doi: 10.1152/jn.1989.61.1.162.
10
Are chimeric kainate/N-methyl-D-aspartate receptors expressed in Xenopus oocytes from mammalian and amphibian RNA?嵌合的红藻氨酸盐/N-甲基-D-天冬氨酸受体是否由哺乳动物和两栖动物的RNA在非洲爪蟾卵母细胞中表达?
J Pharmacol Exp Ther. 1993 May;265(2):910-9.

引用本文的文献

1
Effect of pH on domoic acid toxicity in mice.pH对小鼠软骨藻酸毒性的影响。
Mol Cell Biochem. 1997 Feb;167(1-2):179-85. doi: 10.1023/a:1006862311940.

本文引用的文献

1
Cross-desensitization Reveals Pharmacological Specificity of Excitatory Amino Acid Receptors in Isolated Hippocampal Neurons.交叉脱敏揭示了离体海马神经元中兴奋性氨基酸受体的药理学特异性。
Eur J Neurosci. 1990;2(5):461-470. doi: 10.1111/j.1460-9568.1990.tb00437.x.
2
Mammalian ionotropic glutamate receptors.哺乳动物离子型谷氨酸受体。
Curr Opin Neurobiol. 1993 Jun;3(3):291-8. doi: 10.1016/0959-4388(93)90120-n.
3
Interplay between expressed non-NMDA receptors and endogenous calcium-activated chloride currents in Xenopus laevis oocytes.
Neurosci Lett. 1993 Mar 5;151(1):4-8. doi: 10.1016/0304-3940(93)90031-f.
4
Heterogeneity of synaptic glutamate receptors on CA3 stratum radiatum interneurones of rat hippocampus.大鼠海马CA3辐射层中间神经元突触谷氨酸受体的异质性
J Physiol. 1993 Mar;462:373-92. doi: 10.1113/jphysiol.1993.sp019560.
5
Thiocyanate ions selectively antagonize AMPA-evoked responses in Xenopus laevis oocytes microinjected with rat brain mRNA.硫氰酸根离子可选择性拮抗在显微注射大鼠脑信使核糖核酸的非洲爪蟾卵母细胞中由α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)诱发的反应。
Br J Pharmacol. 1993 Jul;109(3):779-87. doi: 10.1111/j.1476-5381.1993.tb13642.x.
6
The distribution of glutamate receptors in cultured rat hippocampal neurons: postsynaptic clustering of AMPA-selective subunits.谷氨酸受体在培养的大鼠海马神经元中的分布:AMPA 选择性亚基的突触后聚集。
Neuron. 1993 Jun;10(6):1055-68. doi: 10.1016/0896-6273(93)90054-u.
7
Evidence for more than one type of non-NMDA receptor in outside-out patches from cerebellar granule cells of the rat.大鼠小脑颗粒细胞外向膜片中存在不止一种非NMDA受体的证据。
J Physiol. 1993 Apr;463:193-226. doi: 10.1113/jphysiol.1993.sp019591.
8
Kainic acid produces depolarization of CA3 pyramidal cells in the vitro hippocampal slice.海人酸可使体外海马脑片中的CA3锥体细胞发生去极化。
Brain Res. 1981 Sep 21;221(1):117-27. doi: 10.1016/0006-8993(81)91067-2.
9
Mixed-agonist action of excitatory amino acids on mouse spinal cord neurones under voltage clamp.电压钳制下兴奋性氨基酸对小鼠脊髓神经元的混合激动剂作用。
J Physiol. 1984 Sep;354:29-53. doi: 10.1113/jphysiol.1984.sp015360.
10
The primary afferent depolarizing action of kainate in the rat.海人酸在大鼠中的初级传入去极化作用。
Br J Pharmacol. 1986 Feb;87(2):345-55. doi: 10.1111/j.1476-5381.1986.tb10823.x.