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  • ISSN 1674-8301
  • CN 32-1810/R
Volume 33 Issue 4
Jun.  2019
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Article Contents
Abstract
References
Venakatesh Archana G., Mathew Johann J., Coleman Scott, Yang Longqiu, Liu Geoffrey L., Li Marilyn M., Liu Henry. Effects of milrinone on inflammatory response-related gene expressions in cultured rat cardiomyocytes[J]. The Journal of Biomedical Research, 2019, 33(4): 258-263. DOI: 10.7555/JBR.32.20170085
Citation: Venakatesh Archana G., Mathew Johann J., Coleman Scott, Yang Longqiu, Liu Geoffrey L., Li Marilyn M., Liu Henry. Effects of milrinone on inflammatory response-related gene expressions in cultured rat cardiomyocytes[J]. The Journal of Biomedical Research, 2019, 33(4): 258-263. DOI: 10.7555/JBR.32.20170085
shu

Effects of milrinone on inflammatory response-related gene expressions in cultured rat cardiomyocytes

  • 1.

    Department of Anesthesiology & Perioperative Medicine, Drexel University College of Medicine, Hahnemann University Hospital, Philadelphia, PA 19102, USA

  • 2.

    Department of Anesthesiology, Huangshi Central Hospital, Huangshi, Hubei 435002, China

  • 3.

    Division of Genomic Diagnostics, Department of Pathology & Laboratory Medicine, Children's Hospital of Philadelphia, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA 19104, USA

More Information
  • Corresponding author:

    Henry Liu, Department of Anesthesiology, Drexel University College of Medicine, Hahnemann University Hospital, 245 N. 15th Street, MS 310, Philadelphia, PA 19102, USA. Tel: (215)762-7877, E-mail: henryliupa@gmail.com

  • Received Date: July 31, 2017
  • Revised Date: September 20, 2017
  • Accepted Date: September 21, 2017
  • Available Online: October 28, 2017
    Graphical Abstract
    • Abstract
  • Congestive heart failure (CHF) is defined as a cardiac dysfunction leading to low cardiac output and inadequate tissue perfusion. Intravenous positive inotropes are used to increase myocardial contractility in hospitalized patients with advanced heart failure. Milrinone is a phosphodiesterase Ⅲ inhibitor and used most commonly for inotropic effect. The well-known PROMISE study investigated the effects of milrinone on mortality in patients with severe CHF, and concluded that long-term therapy with milrinone increased morbidity and mortality among patients with advanced CHF. Previous studies have suggested that phosphodiesterase inhibitors can have potential effects on inflammatory pathways. Hence, we hypothesized that milrinone may alter inflammatory gene expressions in cardiomyocytes, thus leading to adverse clinical outcomes. We used rat cardiomyocyte cell line H9C2 and studied the impact of exposing cardiomyocytes to milrinone (10 μmol/L) for 24 hours on inflammatory gene expressions. RNA extracted from cultured cardiomyocytes was used for whole rat genome gene expression assay (41 000 genes). The following changes in inflammatory response-related gene expressions were discovered. Genes with increased expressions included: THBS2 (+ 9.98), MMP2 (+3.47), DDIT3 (+2.39), and ADORA3 (+3.5). Genes with decreased expressions were: SPP1 (−5.28) and CD14 (−2.05). We found that the above mentioned gene expression changes seem to indicate that milrinone may hinder the inflammatory process which may potentially lead to adverse clinical outcomes. However, further in vivo and clinical investigations will be needed to illustrate the clinical relevance of these gene expression changes induced by milrinone.
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    • References (37)
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