Hu H-Z, Gao N, Zhu M X, Liu S, Ren J, Gao C, Xia Y, Wood J D
Department of Physiology and Cell Biology, The Ohio State University, Columbus, USA.
J Physiol. 2003 Jul 15;550(Pt 2):493-504. doi: 10.1113/jphysiol.2003.041731. Epub 2003 Jun 13.
Electrophysiological recording was used to study a type of slow excitatory postsynaptic potential (slow EPSP) that was mediated by release of ATP and its action at P2Y1 receptors on morphologically identified neurones in the submucosal plexus of guinea-pig small intestine. MRS2179, a selective P2Y1 purinergic receptor antagonist, blocked both the slow EPSP and mimicry of the EPSP by exogenously applied ATP. Increased conductance accounted for the depolarization phase of the EPSP, which occurred exclusively in neurones with S-type electrophysiological behaviour and uniaxonal morphology. The purinergic excitatory input to the submucosal neurones came from neighbouring neurones in the same plexus, from neurones in the myenteric plexus and from sympathetic postganglionic neurones. ATP-mediated EPSPs occurred coincident with fast nicotinic synaptic potentials evoked by the myenteric projections and with noradrenergic IPSPs evoked by sympathetic fibres that innervated the same neurones. The P2Y1 receptor on the neurones was identified as a metabotropic receptor linked to activation of phospholipase C, synthesis of inositol 1,4,5-trisphosphate and mobilization of Ca2+ from intracellular stores.
采用电生理记录法研究了一种慢兴奋性突触后电位(slow EPSP),该电位由三磷酸腺苷(ATP)释放介导,通过作用于豚鼠小肠黏膜下神经丛中形态学鉴定的神经元上的P2Y1受体发挥作用。选择性P2Y1嘌呤能受体拮抗剂MRS2179可阻断慢EPSP以及外源性应用ATP对EPSP的模拟。电导增加是EPSP去极化阶段的原因,该阶段仅发生在具有S型电生理行为和单轴突形态的神经元中。黏膜下神经元的嘌呤能兴奋性输入来自同一神经丛中的相邻神经元、肌间神经丛中的神经元以及交感神经节后神经元。ATP介导的EPSP与肌间神经丛投射诱发的快速烟碱样突触电位以及支配同一神经元的交感神经纤维诱发的去甲肾上腺素能抑制性突触后电位同时出现。神经元上的P2Y1受体被鉴定为一种与磷脂酶C激活、肌醇1,4,5-三磷酸合成以及细胞内钙库中钙离子释放相关的代谢型受体。