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Characterization of New Stable Ghrelin Analogs with Prolonged Orexigenic Potency

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F12%3A00376293" target="_blank" >RIV/61388963:_____/12:00376293 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1124/jpet.111.185371" target="_blank" >http://dx.doi.org/10.1124/jpet.111.185371</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1124/jpet.111.185371" target="_blank" >10.1124/jpet.111.185371</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Characterization of New Stable Ghrelin Analogs with Prolonged Orexigenic Potency

  • Original language description

    Ghrelin, the only known peripherally produced and centrally acting peptide that stimulates food intake, is synthesized primarily in the stomach and acts through the growth hormone secretagogue receptor (GHS-R1a). In addition to its orexigenic effect, ghrelin stimulates the release of growth hormone (GH). In this study, we investigated the biological properties of full-length and shortened ghrelin analogs in which octanoylated Ser(3) is replaced with an octanoic acid moiety coupled to diaminopropionic acid (Dpr). Ghrelin analogs stabilized with Dpr(N-octanoyl) in position 3 and noncoded amino acids in position 1 (sarcosine) and/or position 4 (naphthylalanine or cyclohexylalanine) were found to possess affinities similar to those of ghrelin for cell membranes with transfected GHS-R1a. In vivo, the prolonged orexigenic effects of analogs containing Dpr(N-octanoyl) 3 compared with that of ghrelin in adult mice and a similar impact on GH secretion in young mice were found. Full-length [Dpr(

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CE - Biochemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GA303%2F09%2F0744" target="_blank" >GA303/09/0744: Impact of ghrelin and estrogen on metabolic syndrom of female obese mice</a><br>

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2012

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Pharmacology and Experimental Therapeutics

  • ISSN

    0022-3565

  • e-ISSN

  • Volume of the periodical

    340

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    6

  • Pages from-to

    781-786

  • UT code for WoS article

    000300619000031

  • EID of the result in the Scopus database