Institute of Cell Biophysics, Russian Academy of Sciences, Pushchino, 142290, Russia.
Institute of Cell Biophysics, Russian Academy of Sciences, Pushchino, 142290, Russia.
Biochem Biophys Res Commun. 2021 May 14;553:99-106. doi: 10.1016/j.bbrc.2021.02.149. Epub 2021 Mar 22.
Spontaneous burst firing is a hallmark attributed to the neuronal network activity. It is known to be accompanied by intracellular calcium [Са] oscillations within the bursting neurons. Studying mechanisms underlying regulation of burst firing is highly relevant, since impairment in neuronal bursting accompanies different neurological disorders. In the present study, the contribution of NMDA and GABA(A) receptors to the shape formation of spontaneous burst -was studied in cultured hippocampal neurons. A combination of inhibitory analysis with simultaneous registration of neuronal bursting by whole-cell patch clamp and calcium imaging was used to assess spontaneous burst firing and [Са] level. Using bicuculline and D-AP5 we showed that GABA(A) and NMDA receptors effectively modulate burst plateau phase and [Са] transient spike which can further affect action potential (AP) amplitudes and firing frequency within a burst. Bicuculline significantly elevated the amplitude and reduced the duration of both burst plateau phase and [Са] spike resulting in an increase of AP firing frequency and shortening of AP amplitudes within a burst. D-AP5 significantly decreases the amplitude of both plateau phase and [Са] spike along with a burst duration that correlated with an increase in AP amplitudes and reduced firing frequency within a burst. The effect of bicuculline was occluded by co-addition of D-AP5 revealing modulatory role of GABA(A) receptors to the NMDA receptor-mediated formation of the burst. Our results provide new evidence on importance of NMDA and GABA(A) receptors in shaping burst firing and Catransient spikes in cultured hippocampal neurons.
自发爆发放电是神经元网络活动的一个标志。已知它伴随着爆发神经元内的细胞内钙 [Ca] 振荡。研究调节爆发放电的机制非常重要,因为神经元爆发放电的损伤伴随着不同的神经障碍。在本研究中,使用全细胞膜片钳和钙成像同时记录神经元爆发的抑制分析,研究了 NMDA 和 GABA(A) 受体对自发爆发放电的形成的贡献。使用 Bicuculline 和 D-AP5,我们表明 GABA(A) 和 NMDA 受体有效地调节爆发平台期和 [Ca] 瞬时尖峰,这可能进一步影响爆发中的动作电位 (AP) 幅度和放电频率。Bicuculline 显著增加了爆发平台期和 [Ca] 尖峰的幅度,同时缩短了爆发中的 [Ca] 尖峰的持续时间,从而增加了 AP 放电频率并缩短了爆发中的 AP 幅度。D-AP5 显著降低了平台期和 [Ca] 尖峰的幅度以及爆发持续时间,这与爆发中的 AP 幅度增加和放电频率降低相关。Bicuculline 的作用被 D-AP5 的共同添加所阻断,这揭示了 GABA(A) 受体对 NMDA 受体介导的爆发形成的调节作用。我们的结果提供了新的证据,证明 NMDA 和 GABA(A) 受体在塑造培养海马神经元中的爆发放电和 [Ca] 瞬变中的重要作用。