Source:http://linkedlifedata.com/resource/pubmed/id/15686481
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2005-2-2
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pubmed:abstractText |
In the present work, several experimental approaches were used to determine the presence of the glucagon-like peptide-1 receptor (GLP-1R) and the biological actions of its ligand in the human brain. In situ hybridization histochemistry revealed specific labelling for GLP-1 receptor mRNA in several brain areas. In addition, GLP-1R, glucose transporter isoform (GLUT-2) and glucokinase (GK) mRNAs were identified in the same cells, especially in areas of the hypothalamus involved in feeding behaviour. GLP-1R gene expression in the human brain gave rise to a protein of 56 kDa as determined by affinity cross-linking assays. Specific binding of 125I-GLP-1(7-36) amide to the GLP-1R was detected in several brain areas and was inhibited by unlabelled GLP-1(7-36) amide, exendin-4 and exendin (9-39). A further aim of this work was to evaluate cerebral-glucose metabolism in control subjects by positron emission tomography (PET), using 2-[F-18] deoxy-D-glucose (FDG). Statistical analysis of the PET studies revealed that the administration of GLP-1(7-36) amide significantly reduced (p < 0.001) cerebral glucose metabolism in hypothalamus and brainstem. Because FDG-6-phosphate is not a substrate for subsequent metabolic reactions, the lower activity observed in these areas after peptide administration may be due to reduction of the glucose transport and/or glucose phosphorylation, which should modulate the glucose sensing process in the GLUT-2- and GK-containing cells.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Glucagon,
http://linkedlifedata.com/resource/pubmed/chemical/Glucagon-Like Peptide 1,
http://linkedlifedata.com/resource/pubmed/chemical/Glucose,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Precursors,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Glucagon,
http://linkedlifedata.com/resource/pubmed/chemical/glucagon-like peptide receptor
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0022-3042
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pubmed:author |
pubmed-author:AlvarezElviraE,
pubmed-author:BlázquezEnriqueE,
pubmed-author:ChowenJulie AJA,
pubmed-author:DescoManuelM,
pubmed-author:García-CuarteroBeatrizB,
pubmed-author:GispertJuan DJD,
pubmed-author:MaldonadoAntonioA,
pubmed-author:MartínezM DoloresMD,
pubmed-author:PozoMiguel AngelMA,
pubmed-author:RonceroIsabelI,
pubmed-author:SanzCarmenC,
pubmed-author:VázquezPatriciaP,
pubmed-author:de CáceresJavierJ
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pubmed:issnType |
Print
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pubmed:volume |
92
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
798-806
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15686481-Adult,
pubmed-meshheading:15686481-Aged,
pubmed-meshheading:15686481-Aged, 80 and over,
pubmed-meshheading:15686481-Brain Stem,
pubmed-meshheading:15686481-Female,
pubmed-meshheading:15686481-Glucagon,
pubmed-meshheading:15686481-Glucagon-Like Peptide 1,
pubmed-meshheading:15686481-Glucose,
pubmed-meshheading:15686481-Humans,
pubmed-meshheading:15686481-Hypothalamus,
pubmed-meshheading:15686481-Male,
pubmed-meshheading:15686481-Middle Aged,
pubmed-meshheading:15686481-Peptide Fragments,
pubmed-meshheading:15686481-Protein Binding,
pubmed-meshheading:15686481-Protein Precursors,
pubmed-meshheading:15686481-RNA, Messenger,
pubmed-meshheading:15686481-Receptors, Glucagon
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pubmed:year |
2005
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pubmed:articleTitle |
The expression of GLP-1 receptor mRNA and protein allows the effect of GLP-1 on glucose metabolism in the human hypothalamus and brainstem.
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pubmed:affiliation |
Department of Biochemistry and Molecular Biology, Faculty of Medicine, Complutense University, Madrid, Spain.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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