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5-HT4 受体与 CA1 海马突触可塑性内 GABA 能系统的相互作用。

Interplay between 5-HT4 Receptors and GABAergic System within CA1 Hippocampal Synaptic Plasticity.

机构信息

Normandie Univ, UNICAEN, INSERM, COMETE, GIP CYCERON, 14000 Caen, France.

PORSOLT, 53940 Le Genest Saint-Isle, France.

出版信息

Cereb Cortex. 2021 Jan 1;31(1):694-701. doi: 10.1093/cercor/bhaa253.

Abstract

The type 4 serotonin receptor (5-HT4R) is highly involved in cognitive processes such as learning and memory. Behavioral studies have shown a beneficial effect of its activation and conversely reported memory impairments by its blockade. However, how modulation of 5HT4R enables modifications of hippocampal synaptic plasticity remains elusive. To shed light on the mechanisms at work, we investigated the effects of the 5-HT4R agonist RS67333 on long-term potentiation (LTP) within the hippocampal CA1 area. Although high-frequency stimulation-induced LTP remained unaffected by RS67333, the magnitude of LTP induced by theta-burst stimulation was significantly decreased. This effect was blocked by the selective 5-HT4R antagonist RS39604. Further, 5-HT4R-induced decrease in LTP magnitude was fully abolished in the presence of bicuculline, a GABAAR antagonist; hence, demonstrating involvement of GABA neurotransmission. In addition, we showed that the application of a GABABR antagonist, CGP55845, mimicked the effect of 5-HT4R activation, whereas concurrent application of CGP55845 and RS67333 did not elicit an additive inhibition effect on LTP. To conclude, through investigation of theta burst induced functional plasticity, we demonstrated an interplay between 5-HT4R activation and GABAergic neurotransmission within the hippocampal CA1 area.

摘要

5-羟色胺受体 4 型(5-HT4R)在学习和记忆等认知过程中起着重要作用。行为研究表明,其激活具有有益作用,相反,其阻断则会导致记忆损伤。然而,5-HT4R 的调节如何使海马突触可塑性发生变化仍然难以捉摸。为了阐明起作用的机制,我们研究了 5-HT4R 激动剂 RS67333 对海马 CA1 区长时程增强(LTP)的影响。尽管高频刺激诱导的 LTP不受 RS67333 影响,但θ爆发刺激诱导的 LTP 幅度明显降低。这种效应被选择性 5-HT4R 拮抗剂 RS39604 阻断。此外,在 GABAAR 拮抗剂bicuculline 存在的情况下,5-HT4R 诱导的 LTP 幅度降低完全被消除;因此,表明涉及 GABA 神经传递。此外,我们表明,GABABR 拮抗剂 CGP55845 的应用模拟了 5-HT4R 激活的作用,而 CGP55845 和 RS67333 的同时应用对 LTP 没有产生附加的抑制作用。总之,通过研究θ爆发诱导的功能可塑性,我们证明了海马 CA1 区 5-HT4R 激活与 GABA 能神经传递之间的相互作用。

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