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Characterization of prolactin-releasing peptide: Binding, signaling and hormone secretion in rodent pituitary cell lines endogenously expressing its receptor

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388963%3A_____%2F11%3A00359843" target="_blank" >RIV/61388963:_____/11:00359843 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11150/11:10105705

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.peptides.2010.12.011" target="_blank" >http://dx.doi.org/10.1016/j.peptides.2010.12.011</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.peptides.2010.12.011" target="_blank" >10.1016/j.peptides.2010.12.011</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Characterization of prolactin-releasing peptide: Binding, signaling and hormone secretion in rodent pituitary cell lines endogenously expressing its receptor

  • Original language description

    The recently discovered prolactin-releasing peptide (PrRP) binds to the PrRP receptor and is involved in endocrine regulation and energy metabolism. However, its main physiological role is currently unknown. Two biologically active isoforms of PrRP exist: the 31 (PrRP31) and the 20 (PrRP20) amino acid forms, which both contain a C-terminal Phe amide sequence. In the present study, the PrRP receptor was immunodetected in three rodent tumor pituitary cell lines: GH3, AtT20 and RC-4B/C cells. Food intake after intracerebroventricular administration of PrRP analogs in fasted mice was followed. Both PrRP31 and PrRP20 decreased food intake, but PrRP13 did not show significant effect.

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GAP303%2F10%2F1368" target="_blank" >GAP303/10/1368: New pharmacological interventions influencing energy homeostasis and development of insulin resistance/ type 2 diabetes mellitus</a><br>

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2011

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Peptides

  • ISSN

    0196-9781

  • e-ISSN

  • Volume of the periodical

    32

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    7

  • Pages from-to

    811-817

  • UT code for WoS article

    000289707300026

  • EID of the result in the Scopus database