Source:http://linkedlifedata.com/resource/pubmed/id/12769729
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
17
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pubmed:dateCreated |
2003-5-28
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pubmed:abstractText |
Modern societies have moved from famine to feast and obesity and its co-morbidities now sweep the world as a global epidemic. Numerous scientific laboratories and pharmaceutical companies have taken the challenge and are now exploiting novel molecular targets for treatment of obesity. The pre-proglucagon system constitutes interesting candidates as potential targets for new anti-obesity drugs. In the periphery, pre-proglucagon derived peptides, Glucagon-Like Peptide-1 (GLP-1), Glucagon-Like Peptide-2 (GLP-2) and oxyntomodulin (OXM) are involved in a wide variety of physiological functions, including glucose homeostasis, gastric emptying, intestinal growth, insulin secretion as well as the regulation of food intake. Peripheral administration of GLP-1 derivatives and analogues to both rodents and man have shown promising effects on food intake and body weight suggesting that such therapies constitute potential anti-obesity treatment. In the central nervous system, pre-proglucagon and hence GLP-1, GLP-2 and OXM are exclusively found in a small population of nerve cells in the nucleus of the solitary tract. These constitute a neural pathway linking the "viscero-sensory" brainstem to hypothalamic nuclei involved in energy homeostasis. Intracerebroventricular administration of all of the three derived peptides robustly decrease food intake. It is evident that central GLP-1 agonism probably in combination with GLP-2 and/or OXM agonism constitute a potential pharmacological tool to reduce food intake and maybe also enhance energy expenditure. This and other aspects of the current state of the role of central pre-proglucagon in energy homeostasis are reviewed.
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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/Glucagon-Like Peptide 2,
http://linkedlifedata.com/resource/pubmed/chemical/Glucagon-Like Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Oxyntomodulin,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Proglucagon,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Precursors,
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:issn |
1381-6128
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
9
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1373-82
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12769729-Animals,
pubmed-meshheading:12769729-Behavior, Animal,
pubmed-meshheading:12769729-Central Nervous System,
pubmed-meshheading:12769729-Eating,
pubmed-meshheading:12769729-Glucagon,
pubmed-meshheading:12769729-Glucagon-Like Peptide 1,
pubmed-meshheading:12769729-Glucagon-Like Peptide 2,
pubmed-meshheading:12769729-Glucagon-Like Peptides,
pubmed-meshheading:12769729-Humans,
pubmed-meshheading:12769729-Obesity,
pubmed-meshheading:12769729-Oxyntomodulin,
pubmed-meshheading:12769729-Peptide Fragments,
pubmed-meshheading:12769729-Peptides,
pubmed-meshheading:12769729-Proglucagon,
pubmed-meshheading:12769729-Protein Precursors,
pubmed-meshheading:12769729-Receptors, Glucagon
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pubmed:year |
2003
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pubmed:articleTitle |
Central pre-proglucagon derived peptides: opportunities for treatment of obesity.
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pubmed:affiliation |
Rheoscience, Glerupvej 2, 2610 Rødovre, Denmark. pjl@rheoscience.com
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pubmed:publicationType |
Journal Article,
Review
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