Nurgali K, Furness J B, Stebbing M J
Department of Anatomy and Cell Biology, University of Melbourne, Parkville, Vic 3010, Australia.
Neuroscience. 2003;116(2):335-47. doi: 10.1016/s0306-4522(02)00749-2.
Types and projections of neurons that received cholinergic, purinergic and other fast excitatory synaptic inputs in myenteric ganglia of the guinea-pig distal colon were identified using combined electrophysiological recording, application of selective antagonists, marker dye filling via the recording microelectrode, and immunohistochemical characterisation. Fast synaptic inputs were recorded from all major subtypes of uniaxonal neurons including Dogiel type I neurons, filamentous interneurons, circular muscle motor neurons and longitudinal muscle motor neurons. Fast excitatory postsynaptic potentials were completely blocked by the nicotinic receptor antagonists hexamethonium or mecamylamine in 62% of neurons tested and were partially inhibited in the remaining neurons. The P2 purine receptor antagonist, pyridoxal-phosphate-6-azophenyl-2',4'-disulfonic acid, reduced the amplitudes of fast excitatory postsynaptic potentials in 20% of myenteric neurons. The 5-hydroxytryptamine(3) receptor antagonist granisetron reduced the amplitude of fast excitatory postsynaptic potentials in only one of 15 neurons tested. In five of five neurons tested, the combination of a nicotinic antagonist, pyridoxal-phosphate-6-azophenyl-2',4'-disulfonic acid, granisetron and 6-cyano-7-nitroquinoxaline-2,3-dione did not completely block the fast excitatory postsynaptic potentials. Immunohistochemical studies of the neurons that had been identified electrophysiologically and morphologically imply that P2X(2) receptors may mediate fast transmission in some neurons, and that other P2X receptor subtypes may also be involved in fast synaptic transmission to myenteric neurons of the guinea-pig distal colon. Neurons with nicotinic and pyridoxal-phosphate-6-azophenyl-2',4'-disulfonic acid-sensitive fast excitatory postsynaptic potentials were present in both ascending and descending pathways in the distal colon. Thus, neither cholinergic nor mixed cholinergic/purinergic synaptic responses are confined to a particular class of neuron. The results indicate that acetylcholine and ATP are the major fast excitatory neurotransmitters in guinea-pig distal colon myenteric ganglia.
运用电生理记录、选择性拮抗剂应用、通过记录微电极进行标记染料填充以及免疫组织化学鉴定等方法,对豚鼠远端结肠肌间神经节中接受胆碱能、嘌呤能及其他快速兴奋性突触输入的神经元类型和投射进行了鉴定。从单轴突神经元的所有主要亚型记录到了快速突触输入,包括多极 I 型神经元、丝状中间神经元、环行肌运动神经元和纵行肌运动神经元。在62%的受试神经元中,快速兴奋性突触后电位被烟碱受体拮抗剂六甲铵或美加明完全阻断,其余神经元则被部分抑制。P2嘌呤受体拮抗剂磷酸吡哆醛 - 6 - 偶氮苯 - 2',4'-二磺酸可使20%的肌间神经元快速兴奋性突触后电位的幅度降低。5 - 羟色胺(3)受体拮抗剂格拉司琼仅使15个受试神经元中的1个快速兴奋性突触后电位的幅度降低。在5个受试神经元中,烟碱拮抗剂、磷酸吡哆醛 - 6 - 偶氮苯 - 2',4'-二磺酸、格拉司琼和6 - 氰基 - 7 - 硝基喹喔啉 - 2,3 - 二酮的组合并未完全阻断快速兴奋性突触后电位。对经电生理和形态学鉴定的神经元进行的免疫组织化学研究表明,P2X(2)受体可能介导某些神经元的快速传递,其他P2X受体亚型也可能参与豚鼠远端结肠肌间神经元的快速突触传递。在远端结肠的升支和降支通路中均存在具有烟碱和磷酸吡哆醛 - 偶氮苯 - 2',4'-二磺酸敏感的快速兴奋性突触后电位的神经元。因此,胆碱能或胆碱能/嘌呤能混合突触反应并不局限于某一特定类型的神经元。结果表明,乙酰胆碱和ATP是豚鼠远端结肠肌间神经节中的主要快速兴奋性神经递质。