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大鼠大细胞基底前脑神经元中钙离子通透的非NMDA型谷氨酸受体

Ca2+-permeable non-NMDA glutamate receptors in rat magnocellular basal forebrain neurones.

作者信息

Waters D J, Allen T G

机构信息

Department of Pharmacology, University College London, Gower Street, London WC1E 6BT, UK.

出版信息

J Physiol. 1998 Apr 15;508 ( Pt 2)(Pt 2):453-69. doi: 10.1111/j.1469-7793.1998.453bq.x.

Abstract
  1. Ionotropic glutamate receptor-mediated responses were recorded from rat magnocellular basal forebrain neurones under voltage clamp from a somatically located patch-clamp pipette. Currents were recorded from both acutely dissociated neurones and neurones maintained in culture for up to 6 weeks. 2. Non-NMDA and NMDA receptor-mediated events could be distinguished pharmacologically using the selective agonists (S)-alpha-amino-3-hydroxy-5-methyl-isoxazolepropionic acid (AMPA), kainate and N-methyl-D-aspartate (NMDA), and antagonists 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) and D(-)-2-amino-5-phosphonopentanoic acid (AP5). 3. Responses to rapid application of AMPA displayed pronounced and rapid desensitization. Responses to kainate showed no desensitization. Steady-state EC50 values for AMPA and kainate were 2.7 +/- 0.4 microM (n = 5) and 138 +/- 25 microM (n = 10), respectively. Cyclothiazide markedly increased current amplitude of responses to both agonists, whereas concanavalin A had no clear effect on either response. The selective AMPA receptor antagonist GYKI 53655 inhibited responses to kainate with an IC50 of 1.2 +/- 0.08 microM (n = 5) at -70 mV. These data strongly suggest that AMPA receptors are the predominant non-NMDA receptors expressed by basal forebrain neurones. 4. At -70 mV, approximately 6 % of control current amplitude remained, at a maximally effective concentration of GYKI 53655. This residual response displayed desensitization, was insensitive to cyclothiazide and was potentiated by concanavalin A, suggesting that it was mediated by a kainate receptor. 5. Current-voltage relationships for non-NMDA receptor-mediated currents were obtained from both nucleated patches pulled from neurones in culture and from acutely dissociated neurones. With 30 microM spermine in the recording pipette, currents frequently displayed double-rectification characteristic of non-NMDA receptors with high Ca2+ permeabilities. Ca2+ permeability, relative to Na+ and Cs+, was investigated using constant field theory. The measured Ca2+ to Na+ permeability coefficient ratio was 0.26-3.6; median, 1.27 (n = 15). 6. Current flow through non-NMDA receptors was inhibited by Ca2+, Cd2+ and Co2+ ions. At a holding potential of -70 mV, a maximally effective concentration of Cd2+ (> 30 mM) reduced current amplitude by approximately 90 %, with an IC50 of 44 microM. In six out of seven cells tested, block by Cd2+ was voltage sensitive. 7. Ca2+ permeability of many of the non-NMDA receptors expressed by magnocellular basal forebrain neurones may underlie the unusual sensitivity of cholinergic basal forebrain neurones to non-NMDA receptor-mediated excitotoxicity.
摘要
  1. 在电压钳制下,使用位于体细胞的膜片钳微电极,记录大鼠大细胞基底前脑神经元中离子型谷氨酸受体介导的反应。电流记录来自急性解离的神经元以及在培养中维持长达6周的神经元。2. 非NMDA和NMDA受体介导的事件可通过药理学方法,使用选择性激动剂(S)-α-氨基-3-羟基-5-甲基异恶唑丙酸(AMPA)、海人酸和N-甲基-D-天冬氨酸(NMDA),以及拮抗剂6-氰基-7-硝基喹喔啉-2,3-二酮(CNQX)和D-(-)-2-氨基-5-膦酰戊酸(AP5)来区分。3. 对快速施加AMPA的反应表现出明显且快速的脱敏。对海人酸的反应未显示脱敏。AMPA和海人酸的稳态EC50值分别为2.7±0.4微摩尔(n = 5)和138±25微摩尔(n = 10)。环噻嗪显著增加了对两种激动剂的反应电流幅度,而伴刀豆球蛋白A对两种反应均无明显影响。选择性AMPA受体拮抗剂GYKI 53655在-70 mV时以1.2±0.08微摩尔(n = 5)的IC50抑制对海人酸的反应。这些数据强烈表明AMPA受体是基底前脑神经元表达的主要非NMDA受体。4. 在-70 mV时,在最大有效浓度的GYKI 53655下,约6%的对照电流幅度得以保留。这种残余反应表现出脱敏,对环噻嗪不敏感且被伴刀豆球蛋白A增强,表明它是由海人酸受体介导的。5. 非NMDA受体介导电流的电流-电压关系是从培养神经元中拉出的有核膜片以及急性解离的神经元中获得的。在记录微电极中加入30微摩尔精胺时,电流经常表现出具有高Ca2+通透性的非NMDA受体的双整流特性。使用恒定场理论研究了相对于Na+和Cs+的Ca2+通透性。测得的Ca2+与Na+通透性系数比为0.26 - 3.6;中位数为1.27(n = 15)。6. 通过非NMDA受体的电流受到Ca2+、Cd2+和Co2+离子的抑制。在-70 mV的钳制电位下,最大有效浓度的Cd2+(> 30 mM)使电流幅度降低约90%,IC50为44微摩尔。在测试的七个细胞中的六个中,Cd2+的阻断是电压敏感的。7. 大细胞基底前脑神经元表达的许多非NMDA受体的Ca2+通透性可能是胆碱能基底前脑神经元对非NMDA受体介导的兴奋性毒性异常敏感的基础。

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本文引用的文献

1
Sodium permeability in toad nerve and in squid nerve.
J Physiol. 1960 Jun;152(1):159-66. doi: 10.1113/jphysiol.1960.sp006477.
3
Dimensions and ion selectivity of recombinant AMPA and kainate receptor channels and their dependence on Q/R site residues.
J Physiol. 1996 Oct 1;496 ( Pt 1)(Pt 1):165-73. doi: 10.1113/jphysiol.1996.sp021674.
4
Calcium permeability of glutamate-gated channels in the central nervous system.
Curr Opin Neurobiol. 1996 Jun;6(3):311-7. doi: 10.1016/s0959-4388(96)80113-9.
5
Mechanisms of neuronal degeneration in Alzheimer's disease.
Neuron. 1996 May;16(5):921-32. doi: 10.1016/s0896-6273(00)80115-4.
6
Excitatory amino acid-induced currents in rat septal cholinergic neurons in culture.
Neuroscience. 1995 Nov;69(2):477-93. doi: 10.1016/0306-4522(95)00260-p.
8
Cloned glutamate receptors.
Annu Rev Neurosci. 1994;17:31-108. doi: 10.1146/annurev.ne.17.030194.000335.
9
Kainate injury to cultured basal forebrain cholinergic neurons is Ca2+ dependent.
Neuroreport. 1994 Jul 21;5(12):1477-80. doi: 10.1097/00001756-199407000-00017.
10
Metabotropic glutamate response in acutely dissociated hippocampal CA1 pyramidal neurones of the rat.
J Physiol. 1994 Mar 15;475(3):439-53. doi: 10.1113/jphysiol.1994.sp020084.

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