Literature DB >> 10404414

Mucosa of the guinea pig gastric corpus is innervated by myenteric neurones with specific neurochemical coding and projection preferences.

D Reiche1, M Schemann.   

Abstract

The present study identified and characterised myenteric neurones involved in the innervation of the gastric mucosa. We applied retrograde neuronal tracing methods by using the dye DiI (1,1'-didodecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorat) in combination with the immunohistochemical demonstration of choline acetyltransferase (ChAT), enkephalin (ENK), neuropeptide Y (NPY), nitric oxide synthase (NOS), substance P (SP), and vasoactive intestinal peptide (VIP). This method showed distinct neurochemical coding of DiI-labelled neurones with projections to the mucosa (mucosa neurones): ChAT/- (indicating the presence of ChAT only, 32%), ChAT/NPY/ +/- VIP (22%), NOS/NPY/ +/- VIP (19%), ChAT/SP/ +/- ENK (12%), NOS/- (indicating the presence of NOS only, 8%), or ChAT/ENK (4.6%). DiI-labelled mucosa neurones did not contain calretinin, serotonin, or somatostatin. All ChAT population had primarily ascending projections, whereas the NOS populations had mainly descending projections. Both were further classified as longitudinally and circumferentially projecting neurones, the latter having projection preferences towards the lesser or greater curvature. All subpopulations exhibited projection preferences. Nitrergic projections primarily arose from cell bodies located at the lesser curvature. ChAT/- projections, which dominated the cholinergic pathway, mainly arose from cell bodies located at the greater curvature. The other major cholinergic pathway with the code ChAT/NPY/ +/- VIP consisted of neurones located mainly at the lesser curvature. The results suggest specific coding of gastric myenteric neurones with projections to the mucosa. Polarised projections consisted of ascending cholinergic and descending nitrergic neurones; the additional presence of NPY/VIP was a prominent feature in both pathways. Chemical coding, polarity, and projection preferences of enteric pathways to the gastric mucosa are remarkably different from those of other regions in the gut.

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Year:  1999        PMID: 10404414     DOI: 10.1002/(sici)1096-9861(19990802)410:3<489::aid-cne10>3.0.co;2-s

Source DB:  PubMed          Journal:  J Comp Neurol        ISSN: 0021-9967            Impact factor:   3.215


  6 in total

1.  Acute cold exposure induces vagally mediated Fos expression in gastric myenteric neurons in conscious rats.

Authors:  P Q Yuan; Y Taché; M Miampamba; H Yang
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2.  Age-dependent slowing of enteric axonal transport in insulin-resistant mice.

Authors:  Kathy J LePard; Joseph Cellini
Journal:  World J Gastroenterol       Date:  2013-01-28       Impact factor: 5.742

3.  Glycine activates myenteric neurones in adult guinea-pigs.

Authors:  M Neunlist; K Michel; D Reiche; G Dobreva; K Huber; M Schemann
Journal:  J Physiol       Date:  2001-11-01       Impact factor: 5.182

4.  Neuronal activation of brain vagal-regulatory pathways and upper gut enteric plexuses by insulin hypoglycemia.

Authors:  Pu-Qing Yuan; Hong Yang
Journal:  Am J Physiol Endocrinol Metab       Date:  2002-09       Impact factor: 4.310

Review 5.  Somatostatin as an Active Substance in the Mammalian Enteric Nervous System.

Authors:  Slawomir Gonkowski; Liliana Rytel
Journal:  Int J Mol Sci       Date:  2019-09-10       Impact factor: 5.923

6.  Mechanosensitive enteric neurons in the guinea pig gastric corpus.

Authors:  Gemma Mazzuoli-Weber; Michael Schemann
Journal:  Front Cell Neurosci       Date:  2015-11-03       Impact factor: 5.505

  6 in total

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