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GABA(A)自身受体增强人新皮质中GABA的释放:脑内高频刺激(HFS)机制的研究方向?

GABA(A) autoreceptors enhance GABA release from human neocortex: towards a mechanism for high-frequency stimulation (HFS) in brain?

作者信息

Mantovani Michela, Moser Andreas, Haas Carola A, Zentner Josef, Feuerstein Thomas J

机构信息

Section of Clinical Neuropharmacology, Department of Neurosurgery, University Hospital Freiburg, Breisacherstrasse 64, 79106 Freiburg, Germany.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2009 Jul;380(1):45-58. doi: 10.1007/s00210-009-0410-3. Epub 2009 Mar 19.

Abstract

High-frequency stimulation (HFS) in human neocortical slices induces gamma-aminobutyric acid (GABA) release via GABA(A) receptor (GABA(A)R) activation. The mechanism of this effect and the localization of these GABA(A)Rs were now studied. Fresh human neocortical slices were subjected to HFS (130 Hz) in the presence of veratridine (3 microM). As measured by high-performance liquid chromatography, only GABA but not glutamate outflow was affected by HFS/veratridine stimulation. The evoked GABA overflow was abolished by tetrodotoxin and furosemide, suggesting an involvement of action potentials and plasmalemmal chloride gradients. Double immunolabeling showed that GABA(A)Rs are localized on soma and dendrites of GABAergic neurons in the human neocortex. Moreover, in support of a terminal localization of GABA(A)Rs, the K+-evoked [3H]-GABA release from synaptosomes was enhanced by the GABA(A)R agonist muscimol (antagonized by GABA(A)R blockers). We conclude that HFS in human brain neocortex leads to a specific increase of GABA release, which is mediated by facilitatory GABA(A) autoreceptors located on soma, dendrites, and axon terminals of GABAergic neurons.

摘要

在人类新皮质切片中,高频刺激(HFS)通过激活γ-氨基丁酸(GABA)A受体(GABA(A)R)诱导GABA释放。现在对这种效应的机制以及这些GABA(A)R的定位进行了研究。将新鲜的人类新皮质切片在藜芦定(3 microM)存在的情况下进行HFS(130 Hz)处理。通过高效液相色谱法测量,只有GABA而不是谷氨酸外流受到HFS/藜芦定刺激的影响。河豚毒素和呋塞米消除了诱发的GABA溢出,表明动作电位和质膜氯化物梯度参与其中。双重免疫标记显示,GABA(A)R定位于人类新皮质中GABA能神经元的胞体和树突上。此外,为支持GABA(A)R的终末定位,GABA(A)R激动剂蝇蕈醇增强了从突触体中K+诱发的[3H]-GABA释放(被GABA(A)R阻滞剂拮抗)。我们得出结论,人类大脑新皮质中的HFS导致GABA释放特异性增加,这是由位于GABA能神经元的胞体、树突和轴突终末上的易化性GABA(A)自身受体介导的。

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