Vehovszky A, Elliott C J
Department of Biology, University of York, UK.
Invert Neurosci. 1995;1(1):67-74. doi: 10.1007/BF02331833.
This study examines neurotransmission between identified buccal interneurons in the feeding system of the snail Lymnaea stagnalis. We compare the pharmacology of the individual synaptic connections from a hybrid modulatory/pattern generating interneuron (N1L) to a pattern generating interneuron (N1M) with that from a modulatory interneuron (SO) to the same follower cell (N1M). The pharmacological properties of the N1L to N1M and the SO to N1M connections closely resemble each other. Both interneurons produce fast cholinergic EPSPs as judged by the blocking effects of cholinergic antagonists hexamethonium, d-tubocurarine and the cholinergic neurotoxin AF-64A. A slower, more complex but non-cholinergic component of the synaptic response is also present after stimulating either the presynaptic N1L or SO interneurons. This second component of the postsynaptic response is not dopaminergic, on the basis of its persistence in the presence of dopaminergic antagonists ergometrine and fluphenazine and the dopaminergic neurotoxin MPP+. We conclude that, although there has been an evolutionary divergence in function, the modulatory SO and the hybrid modulatory/pattern generating N1L are pharmacologically similar. Neither of them contributes directly to dopaminergic modulation of the feeding activity. These neurons also resemble the N1M protraction phase pattern generating neurons which are cholinergic (Elliott and Kemenes, 1992).
本研究考察了椎实螺(Lymnaea stagnalis)摄食系统中已确定的颊部中间神经元之间的神经传递。我们比较了从一个混合调节/模式生成中间神经元(N1L)到一个模式生成中间神经元(N1M)的单个突触连接的药理学特性,以及从一个调节中间神经元(SO)到同一个跟随细胞(N1M)的药理学特性。从N1L到N1M以及从SO到N1M连接的药理学特性彼此非常相似。根据胆碱能拮抗剂六甲铵、d - 筒箭毒碱和胆碱能神经毒素AF - 64A的阻断作用判断,这两种中间神经元均产生快速胆碱能兴奋性突触后电位(EPSP)。在刺激突触前N1L或SO中间神经元后,突触反应中还存在一个较慢、更复杂但非胆碱能的成分。基于其在多巴胺能拮抗剂麦角新碱和氟奋乃静以及多巴胺能神经毒素MPP⁺存在时的持续性,突触后反应的这第二个成分不是多巴胺能的。我们得出结论,尽管在功能上存在进化差异,但调节性的SO和混合调节/模式生成的N1L在药理学上是相似的。它们都不直接参与摄食活动的多巴胺能调节。这些神经元也类似于胆碱能的N1M伸展相模式生成神经元(Elliott和Kemenes,1992)。