Literature DB >> 8993632

Anatomical relationship between vagal afferent fibers and CCK-immunoreactive entero-endocrine cells in the rat small intestinal mucosa.

H R Berthoud1, L M Patterson.   

Abstract

There is evidence for a pathway involving small intestinal CCK-producing entero-endocrine cells and visceral afferent nerve fibers in signaling the effect of luminal nutrients on gastrointestinal and food intake regulation. In order to investigate the type of anatomical apposition that exists between CCK cells and vagal afferents, CCK immunocytochemistry was performed on tissue from rats whose vagal afferent fibers to the abdomen had previously been labeled in vivo by injecting the fluorescent carbocyanine dye DiI into the nodose ganglia. CCK immunoreactive (CCK-IR) cells were more abundant than vagal afferent fibers, but both were present throughout the small intestine as well as in crypts and villi. Few CCK-IR cells were in close (< 5 microns) anatomical contact with vagal afferent axons, and the latter did not produce suspicious terminal specializations near CCK-IR cells. Most labeled vagal afferent axons, which distributed strictly within the crypt and villous lamina propria, were at distances of tens to hundreds of microns to the nearest CCK-IR cell. These findings strongly support the idea that CCK released from entero-endocrine cells acts on vagal sensory fibers in a paracrine fashion, but do not rule out the presence of a few very close, neurocrine-like contacts or a humoral mode of action. Possible implications of such an arrangement on CCK-mediated satiety are discussed.

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Year:  1996        PMID: 8993632     DOI: 10.1159/000147837

Source DB:  PubMed          Journal:  Acta Anat (Basel)        ISSN: 0001-5180


  33 in total

1.  Transduction sites of vagal mechanoreceptors in the guinea pig esophagus.

Authors:  V P Zagorodnyuk; S J Brookes
Journal:  J Neurosci       Date:  2000-08-15       Impact factor: 6.167

Review 2.  Visceral perception: sensory transduction in visceral afferents and nutrients.

Authors:  H E Raybould
Journal:  Gut       Date:  2002-07       Impact factor: 23.059

3.  Effects of cholecystokinin-8s in the nucleus tractus solitarius of vagally deafferented rats.

Authors:  V Baptista; K N Browning; R A Travagli
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2006-11-22       Impact factor: 3.619

Review 4.  Vagal and hormonal gut-brain communication: from satiation to satisfaction.

Authors:  H-R Berthoud
Journal:  Neurogastroenterol Motil       Date:  2008-05       Impact factor: 3.598

5.  Non-sulfated cholecystokinin-8 increases enteric and hindbrain Fos-like immunoreactivity in male Sprague Dawley rats.

Authors:  Amged I Dafalla; Thaer R Mhalhal; Kenneth Hiscocks; John Heath; Ayman I Sayegh
Journal:  Brain Res       Date:  2018-12-17       Impact factor: 3.252

6.  Paying the price for eating ice cream: is excessive GLP-1 signaling in the brain the culprit?

Authors:  Hans-Rudolf Berthoud
Journal:  Endocrinology       Date:  2008-10       Impact factor: 4.736

7.  Sensitivity to 5-hydroxytryptamine in different afferent subpopulations within mesenteric nerves supplying the rat jejunum.

Authors:  K Hillsley; D Grundy
Journal:  J Physiol       Date:  1998-06-15       Impact factor: 5.182

8.  In vitro analysis of the effects of cholecystokinin on rat brain stem motoneurons.

Authors:  Zhongling Zheng; Mark W Lewis; R Alberto Travagli
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2004-12-09       Impact factor: 4.052

9.  The role of CCK8 in the inhibition of glucose production.

Authors:  Christopher J Ramnanan; Dale S Edgerton; Alan D Cherrington
Journal:  Cellscience       Date:  2009-10-27

Review 10.  Upper intestinal lipids regulate energy and glucose homeostasis.

Authors:  Grace W C Cheung; Andrea Kokorovic; Tony K T Lam
Journal:  Cell Mol Life Sci       Date:  2009-06-10       Impact factor: 9.261

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