Literature DB >> 3835503

Morphology of synapses formed by cholecystokinin-immunoreactive axon terminals in regio superior of rat hippocampus.

S H Hendry, E G Jones.   

Abstract

Immunocytochemical and electron microscopic methods were used to examine neurons in regio superior of rat hippocampus displaying cholecystokinin octapeptide-like immunoreactivity. Cholecystokinin-immunoreactive synaptic terminals and somata are found in all layers of regio superior but are most numerous in stratum pyramidale. The vast majority of terminals form symmetric synaptic contacts onto the somata and proximal dendrites of hippocampal pyramidal cells and onto smaller dendrites which may also arise from pyramidal cells. A very small number of cholecystokinin-immunoreactive terminals form synapses that appear asymmetric and contact dendritic shafts or spines. The somata of some pyramidal cells receive symmetric synapses from cholecystokinin-immunoreactive terminals that are joined by cytoplasmic bridges to form parts of pericellular baskets. These and adjacent pyramidal cell somata are also contacted by terminals that are not immunoreactive for cholecystokinin. No cholecystokinin-positive terminals contacted the initial segments of pyramidal cell axons. Cholecystokinin-immunoreactive cells are found in all layers of regio superior. Their somata receive a few symmetric synapses, most of which are formed by terminals not immunoreactive for cholecystokinin. Their dendrites receive a greater number of both symmetric and asymmetric contacts, some of which are immunoreactive for cholecystokinin. We conclude the following: The localization of cholecystokinin immunoreactivity in synaptic terminals contacting the somata and dendrites of hippocampal pyramidal cells is consistent with the suggestion that cholecystokinin acts as a neurotransmitter at these sites and at sites in other parts of the cerebral cortex. Results from the present and previous studies suggest that cholecystokinin-like immunoreactivity may co-exist with gamma-aminobutyrate in some non-pyramidal neurons of regio superior. Cholecystokinin-immunoreactive terminals arise mainly from non-pyramidal cells intrinsic to the hippocampus, one class of which appears to be a type of basket cell.

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Year:  1985        PMID: 3835503     DOI: 10.1016/0306-4522(85)90047-8

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  7 in total

1.  Cortistatin is expressed in a distinct subset of cortical interneurons.

Authors:  L de Lecea; J A del Rio; J R Criado; S Alcántara; M Morales; P E Danielson; S J Henriksen; E Soriano; J G Sutcliffe
Journal:  J Neurosci       Date:  1997-08-01       Impact factor: 6.167

2.  CCK-immunoreactive terminals form different types of synapses in the rat and monkey hippocampus.

Authors:  C Leranth; M Frotscher; P Rakic
Journal:  Histochemistry       Date:  1988

3.  Immunocytochemical study of GABAergic neurons containing the calcium-binding protein parvalbumin in the rat hippocampus.

Authors:  H Katsumaru; T Kosaka; C W Heizmann; K Hama
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

4.  Functional specification of CCK+ interneurons by alternative isoforms of Kv4.3 auxiliary subunits.

Authors:  Viktor János Oláh; David Lukacsovich; Jochen Winterer; Antónia Arszovszki; Andrea Lőrincz; Zoltan Nusser; Csaba Földy; János Szabadics
Journal:  Elife       Date:  2020-06-03       Impact factor: 8.140

5.  Increased cholecystokinin labeling in the hippocampus of a mouse model of epilepsy maps to spines and glutamatergic terminals.

Authors:  M S Wyeth; N Zhang; C R Houser
Journal:  Neuroscience       Date:  2011-12-03       Impact factor: 3.590

6.  Bidirectional modulation of GABAergic transmission by cholecystokinin in hippocampal dentate gyrus granule cells of juvenile rats.

Authors:  Pan-Yue Deng; Saobo Lei
Journal:  J Physiol       Date:  2006-02-02       Impact factor: 5.182

7.  The 5-HT3 receptor is present in different subpopulations of GABAergic neurons in the rat telencephalon.

Authors:  M Morales; F E Bloom
Journal:  J Neurosci       Date:  1997-05-01       Impact factor: 6.167

  7 in total

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