Document Detail


Cholecystokinin regulates expression of Y2 receptors in vagal afferent neurons serving the stomach.
MedLine Citation:
PMID:  18987194     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The intestinal hormones CCK and PYY3-36 inhibit gastric emptying and food intake via vagal afferent neurons. Here we report that CCK regulates the expression of Y2R, at which PYY3-36 acts. In nodose ganglia from rats fasted up to 48 h, there was a fivefold decrease of Y2R mRNA compared with rats fed ad libitum; Y2R mRNA in fasted rats was increased by administration of CCK, and by refeeding through a mechanism sensitive to the CCK1R antagonist lorglumide. Antibodies to Y2R revealed expression in both neurons and satellite cells; most of the former (89 +/- 4%) also expressed CCK1R. With fasting there was loss of Y2R immunoreactivity in CCK1R-expressing neurons many of which projected to the stomach, but not in satellite cells or neurons projecting to the ileum or proximal colon. Expression of a Y2R promoter-luciferase reporter (Y2R-luc) in cultured vagal afferent neurons was increased in response to CCK by 12.3 +/- 0.1-fold and by phorbol ester (16.2 +/- 0.4-fold); the response to both was abolished by the protein kinase C inhibitor Ro-32,0432. PYY3-36 stimulated CREB phosphorylation in rat nodose neurons after priming with CCK; in wild-type mice PYY3-36 increased Fos labeling in brainstem neurons but in mice null for CCK1R this response was abolished. Thus Y2R is expressed by functionally distinct subsets of nodose ganglion neurons projecting to the stomach and ileum/colon; in the former expression is dependent on stimulation by CCK, and there is evidence that PYY3-36 effects on vagal afferent neurons are CCK dependent.
Authors:
Galina Burdyga; Guillaume de Lartigue; Helen E Raybould; Richard Morris; Rod Dimaline; Andrea Varro; David G Thompson; Graham J Dockray
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  The Journal of neuroscience : the official journal of the Society for Neuroscience     Volume:  28     ISSN:  1529-2401     ISO Abbreviation:  J. Neurosci.     Publication Date:  2008 Nov 
Date Detail:
Created Date:  2008-11-06     Completed Date:  2008-12-31     Revised Date:  2010-12-03    
Medline Journal Info:
Nlm Unique ID:  8102140     Medline TA:  J Neurosci     Country:  United States    
Other Details:
Languages:  eng     Pagination:  11583-92     Citation Subset:  IM    
Affiliation:
Physiological Laboratory, School of Biomedical Sciences and School of Preclinical Veterinary Science, University of Liverpool, Liverpool, United Kingdom.
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MeSH Terms
Descriptor/Qualifier:
Animals
Behavior, Animal / drug effects,  physiology
Cells, Cultured
Cholagogues and Choleretics / pharmacology*
Cholecystokinin / pharmacology*
Fasting / physiology
Gene Expression Regulation / drug effects*
Hormone Antagonists / pharmacology
Humans
Male
Mice
Mice, Knockout
Neurons, Afferent / drug effects*
Nodose Ganglion / cytology
Oncogene Proteins v-fos / metabolism
Proglumide / analogs & derivatives,  pharmacology
RNA, Messenger / metabolism
Rats
Receptor, Cholecystokinin A / deficiency
Receptors, Neuropeptide Y / genetics,  metabolism*
Satiety Response / drug effects,  physiology
Stomach / innervation*
Vagus Nerve / cytology*
Grant Support
ID/Acronym/Agency:
DK 41004/DK/NIDDK NIH HHS; R01 DK041004-19/DK/NIDDK NIH HHS; //Biotechnology and Biological Sciences Research Council; //Medical Research Council; //Wellcome Trust
Chemical
Reg. No./Substance:
0/Cholagogues and Choleretics; 0/Hormone Antagonists; 0/Oncogene Proteins v-fos; 0/RNA, Messenger; 0/Receptor, Cholecystokinin A; 0/Receptors, Neuropeptide Y; 0/neuropeptide Y2 receptor; 6620-60-6/Proglumide; 9011-97-6/Cholecystokinin; 97964-56-2/lorglumide
Comments/Corrections

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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