Document Detail


Stimulation of incretin secretion by dietary lipid: is it dose dependent?
MedLine Citation:
PMID:  19520739     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
After the ingestion of nutrients, secretion of the incretin hormones glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1) by the enteroendocrine cells increases rapidly. Previous studies have shown that oral ingestion of fat stimulates secretion of both incretins; however, it is unclear whether there is a dose-dependent relationship between the amount of lipid ingested and the secretion of the hormones in vivo. Recently, we found a higher concentration of the incretin hormones in intestinal lymph than in peripheral or portal plasma. We therefore used the lymph fistula rat model to test for a dose-dependent relationship between the secretion of GIP and GLP-1 and dietary lipid. Under isoflurane anesthesia, the major mesenteric lymphatic duct of male Sprague-Dawley rats was cannulated. Each animal received a single, intraduodenal bolus of saline or varying amounts of the fat emulsion Liposyn II (0.275, 0.55, 1.1, 2.2, and 4.4 kcal). Lymph was continuously collected for 3 h and analyzed for triglyceride, GIP, and GLP-1 content. In response to increasing lipid calories, secretion of triglyceride, GIP, and GLP-1 into lymph increased dose dependently. Interestingly, the response to changes in intraluminal lipid content was greater in GLP-1- than in GIP-secreting cells. The different sensitivities of the two cell types to changes in intestinal lipid support the concept that separate mechanisms may underlie lipid-induced GIP and GLP-1 secretion. Furthermore, we speculate that the increased sensitivity of GLP-1 to intestinal lipid content reflects the hormone's role in the ileal brake reflex. As lipid reaches the distal portion of the gut, GLP-1 is secreted in a dose-dependent manner to reduce intestinal motility and enhance proximal fat absorption.
Authors:
Stephanie M Yoder; Qing Yang; Tammy L Kindel; Patrick Tso
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Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural     Date:  2009-06-11
Journal Detail:
Title:  American journal of physiology. Gastrointestinal and liver physiology     Volume:  297     ISSN:  1522-1547     ISO Abbreviation:  Am. J. Physiol. Gastrointest. Liver Physiol.     Publication Date:  2009 Aug 
Date Detail:
Created Date:  2009-07-22     Completed Date:  2009-08-25     Revised Date:  2010-09-27    
Medline Journal Info:
Nlm Unique ID:  100901227     Medline TA:  Am J Physiol Gastrointest Liver Physiol     Country:  United States    
Other Details:
Languages:  eng     Pagination:  G299-305     Citation Subset:  IM    
Affiliation:
University of Cincinnati, Department of Pathology and Laboratory Medicine, ML 0507, Cincinnati, OH 45237, USA. yodersy@email.uc.edu
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MeSH Terms
Descriptor/Qualifier:
Animals
Dose-Response Relationship, Drug
Duodenum / drug effects*,  metabolism,  secretion
Enteroendocrine Cells / drug effects*,  secretion
Fat Emulsions, Intravenous / administration & dosage*,  metabolism
Feedback, Physiological
Gastric Inhibitory Polypeptide / secretion*
Gastrointestinal Motility / drug effects
Glucagon-Like Peptide 1 / secretion*
Incretins / secretion*
Intestinal Absorption / drug effects
Intubation, Gastrointestinal
Lymph / drug effects*,  secretion
Male
Rats
Rats, Sprague-Dawley
Time Factors
Triglycerides / secretion
Grant Support
ID/Acronym/Agency:
DK-056863/DK/NIDDK NIH HHS; DK-059360/DK/NIDDK NIH HHS; DK-082205/DK/NIDDK NIH HHS
Chemical
Reg. No./Substance:
0/Fat Emulsions, Intravenous; 0/Incretins; 0/Triglycerides; 112353-79-4/liposyn II; 59392-49-3/Gastric Inhibitory Polypeptide; 89750-14-1/Glucagon-Like Peptide 1
Comments/Corrections

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


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