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    ESC heart failure. 2017 Jun 30. doi: 10.1002/ehf2.12169
    Bioelectrical signals improve cardiac function and modify gene expression of extracellular matrix components.
    Macfelda K1,  Kapeller B2,  Holly A3,  Podesser BK4,  Losert U5,  Brandes K6,  Goettel P7,  Mueller J8
    Author information
    1Department of Biomedical Research (Cell Biology), Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
    2Department of Biomedical Research (Cell Biology), Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
    3Department of Biomedical Research (Cell Biology), Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
    4Department of Biomedical Research (Cell Biology), Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
    5Department of Biomedical Research (Cell Biology), Medical University of Vienna, Waehringer Guertel 18-20, 1090, Vienna, Austria.
    6Berlin Heals, Knesebeckstrasse 59-61, 10719, Berlin, Germany.
    7Berlin Heals, Knesebeckstrasse 59-61, 10719, Berlin, Germany.
    8Berlin Heals, Knesebeckstrasse 59-61, 10719, Berlin, Germany.
    Abstract

    AIMS: Beyond the influence of stimulating devices on cardiac excitation, their use in treating patients with heart failure has positive effects on the myocardium at the molecular level. Electrical signals can induce a wide spectrum of effects in living tissue. Therefore, we sought to determine whether applying electrical microcurrent directly to failing hearts leads to functional improvement.

    METHODS AND RESULTS: Sixteen male spontaneously hypertensive rats (SHRs) with heart failure underwent application of a patch electrode to the left ventricular epicardium and placement of a subcutaneous counter electrode. The electrode delivered a 0.35 μA microcurrent to nine of the SHRs for 45 ± 3 days; the other seven SHRs were used as controls. At baseline and before the SHRs were humanely put to death, we measured the left ventricular ejection fraction (LVEF) and the thickness of the LV posterior wall during systole and diastole (LVPWs/d). We used quantitative PCR to determine extracellular matrix parameters [collagen I-III, matrix metalloproteinase (MMP)-2, MMP-9, tissue inhibitor of metalloproteinases 3 (TIMP3), TIMP4, connexins (Cxs) 40/43/45, transforming growth factor (TGF)-β, and interleukin (IL)-6]. Among SHRs undergoing microcurrent application, LVEF normalized (mean decrease, 22.8%; P = 0.009), and LVPWs decreased (mean, 35.3%; P = 0.001). Compared with the control group, the SHRs receiving microcurrent exhibited a mean decrease in the gene expression of collagen I (10.6%, P = 0.003), TIMP3 (18.5%, P = 0.005), Cx43 (14.3%, P = 0.003), Cx45 (12.7%, P = 0.020), TGF-β (13.0%, P = 0.005), and IL-6 (53.7%, P = 0.000). Microcurrent application induced no changes in the expression of collagen III, MMP-2, MMP-9, TIMP4, or Cx40.

    CONCLUSIONS: Applying microcurrent to the LV epicardium of SHRs leads to statistically significant functional improvement and alterations in the levels of inflammatory and extracellular matrix components.


    © 2017 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology.

    KEYWORDS: Bioelectric, Collagen, Electrical stimulation, Extracellular matrix, Heart failure, Reverse remodelling

    Publikations ID: 28772035
    Quelle: öffnen
     
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