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γ-氨基丁酸(GABA)受体在大鼠成熟海马体中的功能作用证据。

Evidence for a functional role of GABA receptors in the rat mature hippocampus.

作者信息

Alakuijala Anniina, Alakuijala Jyrki, Pasternack Michael

机构信息

Institute of Biotechnology, PO Box 56, FI-00014 University of Helsinki, Finland.

出版信息

Eur J Neurosci. 2006 Jan;23(2):514-20. doi: 10.1111/j.1460-9568.2005.04572.x.

Abstract

Both gamma-aminobutyric acid (GABA)(C) receptor subunit mRNA and protein are expressed in the stratum pyramidale in the CA1 area of the adult rat hippocampus, but so far no conclusive evidence about functional hippocampal GABA(C) receptors has been presented. Here, the contribution of GABA(C) receptors to stimulus-evoked postsynaptic potentials was studied in the hippocampal CA1 area with extracellular and intracellular recordings at the age range of 21-47 postnatal days. Activation of GABA(C) receptors with the specific agonist cis-4-aminocrotonic acid (CACA) suppressed postsynaptic excitability and increased the membrane conductance. The GABA(C) receptor antagonist 1,2,5,6-tetrahydropyridine-4-ylmethylphosphinic acid (TPMPA), but not the GABA(A) receptor antagonist bicuculline, inhibited the effects of CACA. GABA-mediated long-lasting depolarizing responses evoked by high-frequency stimulation of local inhibitory interneurons in the CA1 area in the presence of ionotropic glutamate receptor and GABA(B) receptor blockers were prolonged by TPMPA, indicating that GABA(C) receptors are activated under these conditions. For weaker stimulation, the effect of TPMPA was enhanced after GABA uptake was inhibited. Our data demonstrate that GABA(C) receptors can be activated by endogenous synaptic transmitter release following strong stimulation or under conditions of reduced GABA uptake. The lack of GABA(C) receptor activation by less intensive stimulation under control conditions suggests that these receptors are extrasynaptic and activated via spillover of synaptically released GABA.

摘要

γ-氨基丁酸(GABA)(C)受体亚基的mRNA和蛋白在成年大鼠海马CA1区的锥体层均有表达,但迄今为止,尚未有关于海马GABA(C)受体功能的确凿证据。在此,利用细胞外和细胞内记录技术,在出生后21 - 47天的年龄范围内,研究了GABA(C)受体对海马CA1区刺激诱发的突触后电位的作用。用特异性激动剂顺式-4-氨基巴豆酸(CACA)激活GABA(C)受体可抑制突触后兴奋性并增加膜电导。GABA(C)受体拮抗剂1,2,5,6-四氢吡啶-4-基甲基次膦酸(TPMPA),而非GABA(A)受体拮抗剂荷包牡丹碱,可抑制CACA的作用。在离子型谷氨酸受体和GABA(B)受体阻滞剂存在的情况下,TPMPA可延长CA1区局部抑制性中间神经元高频刺激诱发的GABA介导的长时程去极化反应,表明在这些条件下GABA(C)受体被激活。对于较弱的刺激,抑制GABA摄取后TPMPA的作用增强。我们的数据表明,GABA(C)受体可在强烈刺激后或GABA摄取减少的条件下被内源性突触递质释放激活。在对照条件下,强度较低的刺激未能激活GABA(C)受体,这表明这些受体位于突触外,通过突触释放的GABA溢出而被激活。

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