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    Online-Ressource
    Online-Ressource
    S. Karger AG ; 2005
    In:  Nephron Experimental Nephrology Vol. 100, No. 1 ( 2005-3-23), p. e54-e62
    In: Nephron Experimental Nephrology, S. Karger AG, Vol. 100, No. 1 ( 2005-3-23), p. e54-e62
    Kurzfassung: All-trans-retinoic acid (ATRA), a vitamin A derivative, was reported to suppress the interleukin-6 (IL-6) production and to downregulate the IL-6 receptor (IL-6R) and/or its signal transducer glycoprotein 130. We investigated the in vivo antinephritic effect of ATRA on IL-6 transgenic mice which had developed mesangial proliferative glomerulonephritis (PGN) as well as its in vitro inhibitory effect on the proliferation of rat mesangial cells. In vivo experiments on IL-6 transgenic mice showed that ATRA administration suppressed proteinuria and hematuria and reduced the IL-6 concentrations; furthermore, histological examination demonstrated that it improved PGN. In vitro experiments using rat mesangial cells demonstrated that ATRA inhibited cell growth in a dose-dependent manner within a range from 10 〈 sup 〉 –4 〈 /sup 〉 to 10 〈 sup 〉 –6 〈 /sup 〉 〈 i 〉 M 〈 /i 〉 . This inhibition by ATRA was partially counteracted by the addition of IL-6. RT-PCR assay results showed that ATRA also reduced IL-6R, but not the glycoprotein 130 expression in mesangial cells. These findings indicate that, by blocking of the IL-6 function, ATRA may be therapeutically effective in PGN.
    Materialart: Online-Ressource
    ISSN: 1660-2129
    Sprache: Englisch
    Verlag: S. Karger AG
    Publikationsdatum: 2005
    ZDB Id: 2098337-2
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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