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rdf:type |
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lifeskim:mentions |
umls-concept:C0005390,
umls-concept:C0028754,
umls-concept:C0032105,
umls-concept:C0043100,
umls-concept:C0205307,
umls-concept:C0376674,
umls-concept:C0681850,
umls-concept:C0871261,
umls-concept:C1550501,
umls-concept:C1704632,
umls-concept:C1706203,
umls-concept:C1706817,
umls-concept:C2349001,
umls-concept:C2697811,
umls-concept:C2911692
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pubmed:issue |
Pt 5
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pubmed:dateCreated |
2010-9-6
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pubmed:abstractText |
Bile acids can act as signalling molecules via various receptors including the nuclear farnesoid X receptor (FXR) and pregnane X receptor (PXR), and the cell surface G-protein-coupled receptor TGR5. The signalling has been implicated in the release of peptide YY (PYY) and glucagon-like peptide 1 (GLP-1), which improves glycaemic control and energy expenditure. We investigated whether morbidly obese subjects have altered postprandial bile acid responses in comparison to normal weight subjects.
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pubmed:grant |
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pubmed:commentsCorrections |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1758-1001
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
47
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
482-4
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pubmed:meshHeading |
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pubmed:year |
2010
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pubmed:articleTitle |
Postprandial plasma bile acid responses in normal weight and obese subjects.
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pubmed:affiliation |
Department of Clinical Biochemistry, King's College Hospital NHS Foundation Trust, Denmark Hill, London SE59RS, UK.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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