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Palmitoylated PrRP analog decreases body weight in DIO rats but not in ZDF rats

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985823%3A_____%2F16%3A00462516" target="_blank" >RIV/67985823:_____/16:00462516 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388963:_____/16:00462479 RIV/00216208:11110/16:10327339 RIV/00023761:_____/16:N0000007

  • Result on the web

    <a href="http://dx.doi.org/10.1530/JOE-15-0519" target="_blank" >http://dx.doi.org/10.1530/JOE-15-0519</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1530/JOE-15-0519" target="_blank" >10.1530/JOE-15-0519</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Palmitoylated PrRP analog decreases body weight in DIO rats but not in ZDF rats

  • Original language description

    Anorexigenic neuropeptides produced and acting in the brain have the potential to decrease food intake and ameliorate obesity, but are ineffective after peripheral application, owing to a limited ability to cross the blood–brain barrier. We have designed lipidized analogs of prolactin-releasing peptide (PrRP), which is involved in energy balance regulation as demonstrated by obesity phenotypes of both Prrp-knockout and Prrp receptor-knockout mice. The aim of this study was to characterize the subchronic effect of a palmitoylated PrRP analog in two rat models of obesity and diabetes: diet-induced obese Sprague–Dawley rats and leptin receptor-deficient Zucker diabetic (ZDF) rats. In the rats with diet-induced obesity (DIO), a two-week intraperitoneal treatment with palmitoylated PrRP lowered food intake by 24% and body weight by 8%. This treatment also improved glucose tolerance and tended to decrease leptin levels and adipose tissue masses in a dose-dependent manner. In contrast, in ZDF rats, the same treatment with palmitoylated PrRP lowered food intake but did not significantly affect body weight or glucose tolerance, probably in consequence of severe leptin resistance due to a nonfunctional leptin receptor. Our data indicate a good efficacy of lipidized PrRP in DIO rats. Thus, the strong anorexigenic, body weight-reducing, and glucose tolerance-improving effects make palmitoylated PrRP an attractive candidate for anti-obesity treatment.

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    ED - Physiology

  • OECD FORD branch

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2016

  • 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 Endocrinology

  • ISSN

    0022-0795

  • e-ISSN

  • Volume of the periodical

    229

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    12

  • Pages from-to

    85-96

  • UT code for WoS article

    000378643100006

  • EID of the result in the Scopus database

    2-s2.0-84977624840