4.5 Article

Rapid Lipid Modification of Endothelial Cell Membranes in Cardiac Ischemia/Reperfusion Injury: a Novel Therapeutic Strategy to Reduce Infarct Size

期刊

CARDIOVASCULAR DRUGS AND THERAPY
卷 35, 期 1, 页码 113-123

出版社

SPRINGER
DOI: 10.1007/s10557-020-07101-x

关键词

Ischemia; reperfusion; Myocardial infarction; Percutaneous coronary intervention; Endothelium; Lipid rafts; Liposomes; Membrane lipid therapy

资金

  1. National Institutes of Health [R43HL132649]
  2. Kentucky Science and Technology Corporation [KSTC184-512-16-235]

向作者/读者索取更多资源

The study aimed to test the efficacy of newly developed fusogenic nanoliposomes (FNL) in treating myocardial infarction reperfusion injury, with results showing that IC FNL-MLT significantly reduced infarct size and improved regional myocardial blood flow in the ischemic zone. This treatment approach may be a promising adjunct to PCI in the treatment of acute MI.
Purpose Plasma membranes constitute a gathering point for lipids and signaling proteins. Lipids are known to regulate the location and activity of signaling proteins under physiological and pathophysiological conditions. Membrane lipid therapies (MLTs) that gradually modify lipid content of plasma membranes have been developed to treat chronic disease; however, no MLTs have been developed to treat acute conditions such as reperfusion injury following myocardial infarction (MI) and percutaneous coronary intervention (PCI). A fusogenic nanoliposome (FNL) that rapidly incorporates exogenous unsaturated lipids into endothelial cell (EC) membranes was developed to attenuate reperfusion-induced protein signaling. We hypothesized that administration of intracoronary (IC) FNL-MLT interferes with EC membrane protein signaling, leading to reduced microvascular dysfunction and infarct size (IS). Methods Using a myocardial ischemia/reperfusion swine model, the efficacy of FNL-MLT in reducing IS following a 60-min coronary artery occlusion was tested. Animals were randomized to receive IC Ringer's lactate solution with or without 10 mg/mL/min of FNLs for 10 min prior to reperfusion (n = 6 per group). Results The IC FNL-MLT reduced IS (25.45 +/- 16.4% vs. 49.7 +/- 14.1%,P < 0.02) and enhanced regional myocardial blood flow (RMBF) in the ischemic zone at 15 min of reperfusion (2.13 +/- 1.48 mL/min/g vs. 0.70 +/- 0.43 mL/min/g,P < 0.001). The total cumulative plasma levels of the cardiac injury biomarker cardiac troponin I (cTnI) were trending downward but were not significant (999.3 +/- 38.7 ng/mL vs. 1456.5 +/- 64.8 ng/mL,P = 0.1867). However, plasma levels of heart-specific fatty acid binding protein (hFABP), another injury biomarker, were reduced at 2 h of reperfusion (70.3 +/- 38.0 ng/mL vs. 137.3 +/- 58.2 ng/mL,P= 0.0115). Conclusion The IC FNL-MLT reduced IS compared to vehicle in this swine model. The FNL-MLT maybe a promising adjuvant to PCI in the treatment of acute MI.

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