Abstract
High-affinity binding sites for glucagon-like peptide-1 7-36 amide (GLP-1 7-36 NH2) were identified in rat brain and lung membranes. Binding of [125I]GLP-1 7-36 NH2 was rapid, reversible, specific, saturable and pH dependent. Specific binding in the central nervous system was particularly high in the hypothalamus and the brain stem. Oxyntomodulin, glucagon-like peptide-1, glucagon-like peptide-2 and glucagon were 100-1000-fold less potent than GLP-1 7-36 NH2 in competition for this binding site.
MeSH terms
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Animals
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Binding, Competitive
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Brain / metabolism*
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Glucagon / metabolism*
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Glucagon-Like Peptide 1
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Glucagon-Like Peptides
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Kinetics
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Lung / metabolism*
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Organ Specificity
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Peptide Fragments*
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Peptides / metabolism*
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Rats
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Rats, Inbred Strains
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Receptors, Gastrointestinal Hormone / metabolism*
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Receptors, Glucagon
Substances
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Peptide Fragments
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Peptides
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Receptors, Gastrointestinal Hormone
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Receptors, Glucagon
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glucagon-like peptide 1 (7-36)amide
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Glucagon-Like Peptides
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Glucagon-Like Peptide 1
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Glucagon