Literature DB >> 11074451

Vagal afferent innervation of smooth muscle in the stomach and duodenum of the mouse: morphology and topography.

E A Fox1, R J Phillips, F A Martinson, E A Baronowsky, T L Powley.   

Abstract

Intraganglionic laminar endings (IGLEs) and intramuscular arrays (IMAs), the two putative mechanoreceptors that the vagus nerve supplies to the gastrointestinal smooth muscle, have been characterized almost exclusively in the rat. To provide normative inventories of these afferents for the mouse, the authors examined the endings in the stomach and small intestine of three strains used as backgrounds for gene manipulations (i.e., C57, 129/SvJ, and WBB6). Animals received nodose ganglion injections of wheat germ agglutinin-horseradish peroxidase or dextran-tetramethylrhodamine conjugated to biotin. The horseradish peroxidase tissue was processed with tetramethylbenzidine and was used to map the distributions and densities of the two endings; the dextran material was counterstained with c-Kit immunohistochemistry to assess interactions between intramuscular arrays and interstitial cells of Cajal. IGLEs and IMAs constituted the vagal innervation of mouse gastric and duodenal smooth muscle. IGLE morphology and distributions, with peak densities in the corpus-antrum, were similar in the three strains of mice and comparable to those observed in rats. IMAs varied in complexity from region to region but tended to be simpler (fewer telodendria) in mice than in rats. IMAs were most concentrated in the forestomach and sphincters in mice, as in rats, but the topographic distributions of the endings varied both between strains of mice (subtly) and between species (more dramatically). IMAs appeared to make appositions with both interstitial cells and smooth muscle fibers. This survey should make it practical to assay the effects of genetic (e.g., knockout) and experimental (e.g., regeneration) manipulations affecting visceral afferents and their target tissues. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 11074451     DOI: 10.1002/1096-9861(20001218)428:3<558::aid-cne11>3.0.co;2-m

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


  45 in total

1.  Mice deficient in brain-derived neurotrophic factor have altered development of gastric vagal sensory innervation.

Authors:  Michelle C Murphy; Edward A Fox
Journal:  J Comp Neurol       Date:  2010-08-01       Impact factor: 3.215

Review 2.  How many kinds of visceral afferents?

Authors:  M Costa; S H J Brookes; V Zagorodnyuk
Journal:  Gut       Date:  2004-03       Impact factor: 23.059

3.  Vagal Intramuscular Arrays: The Specialized Mechanoreceptor Arbors That Innervate the Smooth Muscle Layers of the Stomach Examined in the Rat.

Authors:  Terry L Powley; Cherie N Hudson; Jennifer L McAdams; Elizabeth A Baronowsky; Robert J Phillips
Journal:  J Comp Neurol       Date:  2015-10-13       Impact factor: 3.215

4.  Organization of vagal afferents in pylorus: mechanoreceptors arrayed for high sensitivity and fine spatial resolution?

Authors:  Terry L Powley; Cherie N Hudson; Jennifer L McAdams; Elizabeth A Baronowsky; Felecia N Martin; Jacqueline K Mason; Robert J Phillips
Journal:  Auton Neurosci       Date:  2014-03-06       Impact factor: 3.145

Review 5.  Age-related changes in vagal afferents innervating the gastrointestinal tract.

Authors:  Robert J Phillips; Gary C Walter; Terry L Powley
Journal:  Auton Neurosci       Date:  2009-08-07       Impact factor: 3.145

6.  Developmental corneal innervation: interactions between nerves and specialized apical corneal epithelial cells.

Authors:  James K Kubilus; Thomas F Linsenmayer
Journal:  Invest Ophthalmol Vis Sci       Date:  2009-09-09       Impact factor: 4.799

Review 7.  Extrinsic primary afferent signalling in the gut.

Authors:  Simon J H Brookes; Nick J Spencer; Marcello Costa; Vladimir P Zagorodnyuk
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2013-02-26       Impact factor: 46.802

8.  Neurotrophin-4 deficient mice have a loss of vagal intraganglionic mechanoreceptors from the small intestine and a disruption of short-term satiety.

Authors:  E A Fox; R J Phillips; E A Baronowsky; M S Byerly; S Jones; T L Powley
Journal:  J Neurosci       Date:  2001-11-01       Impact factor: 6.167

Review 9.  Roles for gut vagal sensory signals in determining energy availability and energy expenditure.

Authors:  Gary J Schwartz
Journal:  Brain Res       Date:  2018-08-15       Impact factor: 3.252

10.  Mechanism of hyperphagia contributing to obesity in brain-derived neurotrophic factor knockout mice.

Authors:  E A Fox; J E Biddinger; K R Jones; J McAdams; A Worman
Journal:  Neuroscience       Date:  2012-10-13       Impact factor: 3.590

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