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点燃效应在齿状回-CA3投射中诱导短暂的快速抑制。

Kindling induces transient fast inhibition in the dentate gyrus--CA3 projection.

作者信息

Gutiérrez R, Heinemann U

机构信息

Departamento de Fisiología, Biofísica y Neurociencias del CINVESTAV-IPN, Apartado Postal 14-740, México D.F. 07000, México.

出版信息

Eur J Neurosci. 2001 Apr;13(7):1371-9. doi: 10.1046/j.0953-816x.2001.01508.x.

Abstract

The granule cells of the dentate gyrus (DG) send a strong glutamatergic projection, the mossy fibre tract, toward the hippocampal CA3 field, where it excites pyramidal cells and neighbouring inhibitory interneurons. Despite their excitatory nature, granule cells contain small amounts of GAD (glutamate decarboxylase), the main synthetic enzyme for the inhibitory transmitter GABA. Chronic temporal lobe epilepsy results in transient upregulation of GAD and GABA in granule cells, giving rise to the speculation that following overexcitation, mossy fibres exert an inhibitory effect by release of GABA. We therefore stimulated the DG and recorded synaptic potentials from CA3 pyramidal cells in brain slices from kindled and control rats. In both preparations, DG stimulation caused excitatory postsynaptic potential (EPSP)/inhibitory postsynaptic potential (IPSP) sequences. These potentials could be completely blocked by glutamate receptor antagonists in control rats, while in the kindled rats, a bicuculline-sensitive fast IPSP remained, with an onset latency similar to that of the control EPSP. Interestingly, this IPSP disappeared 1 month after the last seizure. When synaptic responses were evoked by high-frequency stimulation, EPSPs in normal rats readily summate to evoke action potentials. In slices from kindled rats, a summation of IPSPs overrides that of the EPSPs and reduces the probability of evoking action potentials. Our data show for the first time that kindling induces functionally relevant activity-dependent expression of fast inhibition onto pyramidal cells, coming from the DG, that can limit CA3 excitation in a frequency-dependent manner.

摘要

齿状回(DG)的颗粒细胞向海马CA3区发出强烈的谷氨酸能投射,即苔藓纤维束,在该区域它会兴奋锥体细胞和邻近的抑制性中间神经元。尽管颗粒细胞具有兴奋性,但它们含有少量的谷氨酸脱羧酶(GAD),这是抑制性神经递质γ-氨基丁酸(GABA)的主要合成酶。慢性颞叶癫痫会导致颗粒细胞中GAD和GABA短暂上调,这引发了一种推测,即苔藓纤维在过度兴奋后通过释放GABA发挥抑制作用。因此,我们刺激了齿状回,并记录了点燃大鼠和对照大鼠脑片中CA3锥体细胞的突触电位。在这两种标本中,齿状回刺激均引起兴奋性突触后电位(EPSP)/抑制性突触后电位(IPSP)序列。这些电位在对照大鼠中可被谷氨酸受体拮抗剂完全阻断,而在点燃大鼠中,一种对荷包牡丹碱敏感的快速IPSP仍然存在,其起始潜伏期与对照EPSP相似。有趣的是,这种IPSP在最后一次癫痫发作后1个月消失。当通过高频刺激诱发突触反应时,正常大鼠中的EPSP很容易总和以诱发动作电位。在点燃大鼠的脑片中,IPSP的总和超过了EPSP的总和,并降低了诱发动作电位的概率。我们的数据首次表明,点燃诱导了来自齿状回的对锥体细胞功能相关的、依赖活动的快速抑制表达,这种抑制可以以频率依赖的方式限制CA3区的兴奋。

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