Yang Q, Michelson H B
Department of Physiology and Pharmacology, Box 29, SUNY Downstate Medical Center, 450 Clarkson Avenue, Brooklyn, NY 11203, USA.
Brain Res. 2001 Jul 13;907(1-2):139-43. doi: 10.1016/s0006-8993(01)02582-3.
The convulsant 4-aminopyridine (4AP) facilitates the synchronous firing of interneurons in the hippocampus, eliciting giant inhibitory postsynaptic potentials (IPSPs) in CA3 pyramidal cells. We used the gap junction blocker carbenoxolone to investigate the role of electrotonic coupling in both the initiation and the maintenance of 4AP-facilitated inhibitory circuit oscillations. Carbenoxolone abolished all synchronized IPSPs in CA3 cells elicited by 4AP in the presence of ionotropic glutamate receptor blockers. Carbenoxolone also blocked the isolated synchronized GABA(B) IPSPs generated in CA3 cells by a subpopulation of interneurons. These data confirm that: (1) the interneurons producing GABA(B) responses in CA3 cells are electrotonically coupled, and (2) gap junctions among interneurons are essential for initiating synchronized interneuron oscillatory firing in 4AP.
惊厥剂4-氨基吡啶(4AP)可促进海马中间神经元的同步放电,在CA3锥体细胞中引发巨大抑制性突触后电位(IPSPs)。我们使用缝隙连接阻滞剂羧苄青霉素来研究电紧张耦联在4AP促进的抑制性回路振荡的起始和维持中的作用。在离子型谷氨酸受体阻滞剂存在的情况下,羧苄青霉素消除了4AP在CA3细胞中引发的所有同步IPSPs。羧苄青霉素还阻断了由中间神经元亚群在CA3细胞中产生的孤立的同步GABA(B) IPSPs。这些数据证实:(1)在CA3细胞中产生GABA(B)反应的中间神经元是电紧张耦联的,(2)中间神经元之间的缝隙连接对于在4AP中启动同步中间神经元振荡放电至关重要。