A new glucagon and GLP-1 co-agonist eliminates obesity in rodents View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2009-10

AUTHORS

Jonathan W Day, Nickki Ottaway, James T Patterson, Vasily Gelfanov, David Smiley, Jas Gidda, Hannes Findeisen, Dennis Bruemmer, Daniel J Drucker, Nilika Chaudhary, Jenna Holland, Jazzminn Hembree, William Abplanalp, Erin Grant, Jennifer Ruehl, Hilary Wilson, Henriette Kirchner, Sarah Haas Lockie, Susanna Hofmann, Stephen C Woods, Ruben Nogueiras, Paul T Pfluger, Diego Perez-Tilve, Richard DiMarchi, Matthias H Tschöp

ABSTRACT

We report the efficacy of a new peptide with agonism at the glucagon and GLP-1 receptors that has potent, sustained satiation-inducing and lipolytic effects. Selective chemical modification to glucagon resulted in a loss of specificity, with minimal change to inherent activity. The structural basis for the co-agonism appears to be a combination of local positional interactions and a change in secondary structure. Two co-agonist peptides differing from each other only in their level of glucagon receptor agonism were studied in rodent obesity models. Administration of PEGylated peptides once per week normalized adiposity and glucose tolerance in diet-induced obese mice. Reduction of body weight was achieved by a loss of body fat resulting from decreased food intake and increased energy expenditure. These preclinical studies indicate that when full GLP-1 agonism is augmented with an appropriate degree of glucagon receptor activation, body fat reduction can be substantially enhanced without any overt adverse effects. More... »

PAGES

749

Journal

TITLE

Nature Chemical Biology

ISSUE

10

VOLUME

5

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  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1038/nchembio.209

    DOI

    http://dx.doi.org/10.1038/nchembio.209

    DIMENSIONS

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    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/19597507


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