• Title of article

    Direct intracellular nitric oxide detection in isolated adult cardiomyocytes: flow cytometric analysis using the fluorescent probe, diaminofluorescein

  • Author/Authors

    Hans Strijdom، نويسنده , , Christo Muller، نويسنده , , Amanda Lochner، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2004
  • Pages
    6
  • From page
    897
  • To page
    902
  • Abstract
    We assessed the possibility to detect intracellular nitric oxide (NO) with the NO-specific probe 4,5-diaminofluorescein-2/diacetate (DAF-2/DA), by flow cytometry, in fresh adult rat cardiomyocytes, and compared the findings with results obtained from quantitation of cellular nitrate/nitrite (NOx) levels. Methods. – Cardiomyocytes were isolated by collagenase perfusion, followed by incubation in a Krebs–Henseleit/2% bovine serum albumin buffer in the presence of 10 μM DAF-2/DA (~0.5 × 106 cells/ml). Experimental conditions were: (i) baseline control, (ii) NO donor (2-(N,N-diethylamino)-diazenolate 2-oxide, DEA/NO) administration, and (iii) 120 min simulated ischemia (hypoxia). In addition, control and hypoxic groups were incubated with the NO synthase (NOS) inhibitor, NW-nitro-l-arginine methyl ester (l-NAME). Following incubation and washing, intracellular fluorescence of DAF-triazol (DAF-2T, oxidized form of DAF-2/DA) was analyzed by flow cytometry. NOx levels were determined with an NOx assay. Fluorescence-activated cell sorter (FACS) data were expressed as mean fluorescence intensity (percentage of control) and NOx levels as pmol/106 cells. Results. – Optimal baseline fluorescence was obtained when myocytes were incubated with DAF-2/DA for 3 h at 37 °C. The NO donor DEA/NO (500 μM) and hypoxia significantly increased DAF fluorescence and NOx levels. l-NAME addition significantly reversed these trends in the hypoxia groups. Conclusions. – We have demonstrated that intracellular NO can be detected in fresh isolated adult cardiomyocytes by flow cytometry with 10 μM DAF-2/DA. Furthermore, we demonstrated that hypoxia is an activator of adult cardiomyocyte NOS, as demonstrated by both end-points. Reproducibility observed between results obtained by FACS analysis and NOx assays suggests that DAF-2/DA fluorescence can be regarded as an independent marker for intracellular NO in cardiomyocytes.
  • Keywords
    Nitric oxide detection , DAF-2/DA , Adult cardiomyocytes , flow cytometry , Nitrate/nitrite assay , hypoxia
  • Journal title
    Journal of Molecular and Cellular Cardiology
  • Serial Year
    2004
  • Journal title
    Journal of Molecular and Cellular Cardiology
  • Record number

    529044