Document Detail


Sympathetic activity controls fat-induced oleoylethanolamide signaling in small intestine.
MedLine Citation:
PMID:  21490214     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Ingestion of dietary fat stimulates production of the small-intestinal satiety factors oleoylethanolamide (OEA) and N-palmitoyl-phosphatidylethanolamine (NPPE), which reduce food intake through a combination of local (OEA) and systemic (NPPE) actions. Previous studies have shown that sympathetic innervation of the gut is necessary for duodenal infusions of fat to induce satiety, suggesting that sympathetic activity may engage small-intestinal satiety signals such as OEA and NPPE. In the present study, we show that surgical resection of the sympathetic celiac-superior mesenteric ganglion complex, which sends projections to the upper gut, abolishes feeding-induced OEA production in rat small-intestinal cells. These effects are accounted for by suppression of OEA biosynthesis, and are mimicked by administration of the selective β2-adrenergic receptor antagonist ICI-118,551. We further show that sympathetic ganglionectomy or pharmacological blockade of β2-adrenergic receptors prevents NPPE release into the circulation. In addition, sympathetic ganglionectomy increases meal frequency and lowers satiety ratio, and these effects are corrected by pharmacological administration of OEA. The results suggest that sympathetic activity controls fat-induced satiety by enabling the coordinated production of local (OEA) and systemic (NPPE) satiety signals in the small intestine.
Authors:
Jin Fu; Nicholas V Dipatrizio; Ana Guijarro; Gary J Schwartz; Xiaosong Li; Silvana Gaetani; Giuseppe Astarita; Daniele Piomelli
Related Documents :
3579004 - Nutritional supplementation in ambulatory patients with chronic obstructive pulmonary d...
18620744 - Increase in inflammatory mediator concentrations in exhaled breath condensate after all...
15882384 - Comparison of energy and protein intakes of older people consuming a texture modified d...
19730424 - Preferences and self-efficacy for diet modification among primary care patients.
16636304 - Selective compensatory induction of hepatic hmg-coa reductase in response to inhibition...
18422334 - Polyphenolic transmission to segureno lamb meat from ewes' diet supplemented with the d...
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:  31     ISSN:  1529-2401     ISO Abbreviation:  J. Neurosci.     Publication Date:  2011 Apr 
Date Detail:
Created Date:  2011-04-14     Completed Date:  2011-06-13     Revised Date:  2011-10-13    
Medline Journal Info:
Nlm Unique ID:  8102140     Medline TA:  J Neurosci     Country:  United States    
Other Details:
Languages:  eng     Pagination:  5730-6     Citation Subset:  IM    
Affiliation:
Department of Pharmacology, School of Medicine, University of California, Irvine, Irvine, California 92697-4625, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Adrenergic Antagonists / pharmacology
Adrenergic beta-Agonists / pharmacology
Amidohydrolases / metabolism
Animals
Chromatography, High Pressure Liquid
Dietary Fats / pharmacology*
Eating / drug effects,  physiology
Feeding Behavior / drug effects,  physiology
Food
Ganglia, Sympathetic / physiology
Ganglionectomy
Intestine, Small / innervation*,  physiology*
Male
Oleic Acids / metabolism,  physiology*
Phospholipase D / metabolism
Propanolamines / pharmacology
Rats
Rats, Sprague-Dawley
Receptors, Adrenergic, beta-2 / drug effects,  physiology
Satiety Response / drug effects
Signal Transduction / physiology*
Sympathectomy
Sympathetic Nervous System / physiology*
Grant Support
ID/Acronym/Agency:
5P30DK026687/DK/NIDDK NIH HHS; DK047208/DK/NIDDK NIH HHS; DK073955/DK/NIDDK NIH HHS; P30 DK026687-26/DK/NIDDK NIH HHS; R01 DK073955-02/DK/NIDDK NIH HHS; R01 DK073955-02S1/DK/NIDDK NIH HHS; R01 DK073955-03/DK/NIDDK NIH HHS; R01 DK073955-04/DK/NIDDK NIH HHS
Chemical
Reg. No./Substance:
0/Adrenergic Antagonists; 0/Adrenergic beta-Agonists; 0/Dietary Fats; 0/Oleic Acids; 0/Propanolamines; 0/Receptors, Adrenergic, beta-2; 0/oleoylethanolamide; 72795-19-8/ICI 118551; EC 3.1.4.4/Phospholipase D; EC 3.5.-/Amidohydrolases; EC 3.5.1.-/fatty-acid amide hydrolase

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


Previous Document:  Deep brain stimulation of the subthalamic nucleus alters the cortical profile of response inhibition...
Next Document:  Calcium-permeable AMPA receptors are present in nucleus accumbens synapses after prolonged withdrawa...