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
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
CE - Biochemistry
OECD FORD branch
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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
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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
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