Correlated morphological and neurochemical features identify different subsets of vasoactive intestinal polypeptide-immunoreactive interneurons in rat hippocampus

被引:162
作者
Acsady, L
Arabadzisz, D
Freund, TF
机构
[1] Institute of Experimental Medicine, Hungarian Academy of Sciences, Budapest, H-1450
基金
匈牙利科学研究基金会;
关键词
hippocampus; interneuron; GABA; VIP; co-localization; neuropeptides;
D O I
10.1016/0306-4522(95)00610-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Vasoactive intestinal polypeptide-immunoreactive interneurons have been classified according to their axonal and dendritic patterns and neurochemical features in the hippocampus of the rat. A correlation of these characteristics unravelled three distinct types of vasoactive intestinal polypeptide-containing cells. Interneurons forming a dense axonal plexus at the border of stratum oriens and alveus always contain the calcium binding protein, calretinin, but lack the neuropeptide cholecystokinin. The axon of another type of vasoactive intestinal polypeptide-positive interneuron surrounds pyramidal cell bodies in a basket-like manner, and co-localizes cholecystokinin but not calretinin. Vasoactive intestinal polypeptide-containing cells projecting to stratum radiatum form two subsets distinguished by dendritic morphology. Those with dendrites restricted to stratum lacunosum-moleculare lack both calretinin and cholecystokinin, whereas the other subtype with dendrites spanning all layers contains calretinin in 40% of the cases and occasionally also cholecystokin. GABA was shown to be present, and the calcium binding proteins calbindin D-28k and parvalbumin absent from all three types of vasoactive intestinal polypeptide-positive interneurons. The specific dendritic and axonal arbours imply different input and output properties for the three interneuron types. The correlation of these features with the content of neurochemical markers strongly suggests that they are specialized for distinct inhibitory functions in the hippocampal network. Copyright (C) 1996 IBRO. Published by Elsevier Science Ltd.
引用
收藏
页码:299 / 315
页数:17
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