Spontaneous and electrically evoked Ca2+ transients in cardiomyocytes of the rat pulmonary vein

Sunil Jit R J Logantha, Stuart F. Cruickshank, Edward G. Rowan, Robert M. Drummond

    Research output: Contribution to journalArticlepeer-review

    Abstract

    The pulmonary vein is surrounded by an external sleeve of cardiomyocytes that are widely recognised to play an important role in atrial fibrillation. While intracellular Ca2+ is thought to influence the electrical activity of cardiomyocytes, there have been relatively few studies examining Ca2+ signalling in these cells. Therefore, using fluo-4 and fluorescence imaging microscopy, we have investigated Ca2+ signalling in an intact section of the rat pulmonary vein. Under resting conditions cardiomyocytes displayed spontaneous Ca2+ transients, which were variable in amplitude and had a frequency of 1.6±0.03Hz. The Ca2+ transients were asynchronous amongst neighbouring cardiomyocytes and tended to propagate throughout the cell as a wave. Removing extracellular Ca2+ produced a slight reduction in the amplitude and frequency of the spontaneous Ca2+ transients; however, ryanodine (20μM) had a much greater effect on the amplitude and reduced the frequency by 94±2%. Blocking IP3 receptors with 2-aminoethoxydiphenyl borate (20μM) also reduced the amplitude and frequency (by 73±11%) of these events, indicating the importance of Ca2+ release from the SR. Electrical field stimulation of the pulmonary vein produced Ca2+ transients in cardiomyocytes that were significantly reduced by either voltage-gated Ca2+ channel blockers or ryanodine. © 2010 Elsevier Ltd.
    Original languageEnglish
    Pages (from-to)150-160
    Number of pages10
    JournalCell calcium
    Volume48
    Issue number2-3
    DOIs
    Publication statusPublished - Aug 2010

    Keywords

    • Fluorescence Ca2+ imaging
    • IP3 receptor
    • Pulmonary vein cardiomyocytes
    • Rat
    • Ryanodine receptor
    • Sarcoplasmic reticulum (SR)
    • Spontaneous Ca2+ transients
    • Voltage-gated Ca2+ channel

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