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Tytuł oryginału: Preconditioning with millimolar concentrations of vitamin C or N-acetylcysteine protects L6 muscle cells insulin-stimulated viability and DNA synthesis under oxidative stress.
Autorzy: Orzechowski Arkadiusz, Łokociejewska Małgorzata, Muras Patrycja, Hocquette Jean-Francois
Źródło: Life Sci. 2002: 71 (15) s.1793-1808, il., tab., bibliogr. 54 poz.
Sygnatura GBL: 304,948

Hasła klasyfikacyjne GBL:
  • farmacja

    Typ dokumentu:
  • praca doświadczalna
  • praca opublikowana za granicą
  • tytuł obcojęzyczny

    Wskaźnik treści:
  • zwierzęta

    Streszczenie angielskie: The effect of reactive oxygen/nitrogen species (ROS/RNS)(hydrogen peroxide - H2O2, superoxide anion radical O2ú- and hydroxyl radical úOH - the reaction products of hypoxanthine/xanthine oxidase system), nitric oxide (NOú from sodium nitroprusside - SNP), and peroxynitrite (ONOO- from 3-morpholinosydonimine - SIN-1) on insulin mitogenic effect was studied in L6 muscle cells after one day pretreatment with/or without antioxidants.ROS/RNS inhibited insulin-induced mitogenicity (DNA synthesis). Insulin (0.1 ćM), however, markedly improved mitogenecity in the muscle cells treated with treated with increased concentrations (0.1, 0.5, 1 mM) of donors of H2O2, Oú2-, úOH, ONOO- and NOú. Cell viability assessed by morphological criteria was also monitored. Massive apoptosis was induced by 1 mM of donors of H2O2 and ONOO-, while NOú additionaly induced necrotic cell death. Taken together, these results have shown that ROS/RNS provide a good explanation for the developing resistance to the growth promoting activity of insulin in myoblasts under conditions of oxidative or nitrosative stress. Cell viability showed that neither donor induced cell death when given below 0.5 mM.In order to confirm the deleterious effects of ROS/RNS prior to the subsequent treatment with ROS/RNS plus insulin one day pretreatment with selected antioxidants (sodium ascorbate - ASC (0.01, 01, 1 mM), or N-acetylcysteine - NAC (0.1, 1, 10 mM) was carried out. Surprisingly, at a low dose (micromolar) antioxidants did not abrogate and even worsened the concentration-dependent effects of ROS/RNS...

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