Evidence map›Paper›PMID 16328433›Full record

ArticleHistochemistry and cell biology2006

Morphology of VIP/nNOS-immunoreactive myenteric neurons in the human gut.

A Brehmer, F Schrödl, W Neuhuber

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Article in Histochemistry and cell biology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

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0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

  1. Article
  2. Article
  3. Classification of human enteric neurons.Histochemistry and cell biology · 2021
    Review
  4. Article
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  18. Article
  19. Development of enteric neuron diversity.Journal of cellular and molecular medicine · 2009
    Review
  20. Article
4 · The record

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5 · Who and what money

Authors and funding

3 authors.

A BrehmerInstitute of Anatomy I, University of Erlangen-Nuremberg, Krankenhausstr. 9, 91054, Erlangen, Germany. axel.brehmer@anatomie1.med.uni-erlangen.de
F Schrödl
W Neuhuber

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we characterized human myenteric neurons co-immunoreactive for neuronal nitric oxide synthase (nNOS) and vasoactive intestinal peptide (VIP) by their morphology and their proportion as related to the putative entire myenteric neuronal population. Nine wholemounts (small and large intestinal samples) from nine patients were triple-stained for VIP, neurofilaments (NF) and nNOS. Most neurons immunoreactive for all three markers displayed radially emanating, partly branching dendrites with spiny endings. These neurons were called spiny neurons. The spiny character of their dendrites was more pronounced in the small intestinal specimens and differed markedly from enkephalinergic stubby neurons described earlier. Exclusively in the duodenum, some neurons displayed prominent main dendrites with spiny side branches. Of the axons which could be followed from the ganglion of origin within primary strands of the myenteric plexus beyond the next ganglion (70 out of 140 traced neurons), 94.3% run anally and 5.7% orally. Very few neurons reactive for both VIP and nNOS could not be morphologically classified due to weak or absent NF-immunoreactivity. Another six wholemounts were triple-stained for VIP, nNOS and Hu proteins (HU). The proportion of VIP/nNOS-coreactive neurons in relation to the number of HU-reactive neurons was between 5.8 and 11.5% in the small and between 10.6 and 17.5% in the large intestinal specimens. We conclude that human myenteric spiny neurons co-immunoreactive for VIP and nNOS represent either inhibitory motor or descending interneurons.

Indexed as

AdultAgedAged, 80 and overFemaleHumansIntestinal MucosaIntestine, LargeIntestinesIntestine, SmallMaleMiddle AgedMyenteric PlexusNeurofilament ProteinsNeuronsNitric Oxide Synthase Type IVasoactive Intestinal PeptideNeurofilament ProteinsNitric Oxide Synthase Type IVasoactive Intestinal Peptide

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.