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Bone-Marrow Stem Cells and Acellular Human Amniotic Membrane in a Rat Model of Heart Failure. | LitMetric

AI Article Synopsis

  • Myocardial infarction (MI) is a leading cause of cardiovascular death and heart failure globally, and recent studies explore the use of bone marrow stem cells (BMSC) and human amniotic membrane (hAM) as therapies to improve heart function post-MI.
  • In a rat model, MI was induced, and rats with reduced heart function were treated with either BMSC, hAM, or left as a control group after coronary occlusion.
  • After 30 days, both BMSC and hAM groups showed significant improvements in heart function and structure compared to the control group, indicating potential benefits of these therapies in enhancing cardiac recovery through mechanisms like angiogenesis and heart cell regeneration.

Article Abstract

Myocardial infarction (MI) remains the leading cause of cardiovascular death worldwide and a major cause of heart failure. Recent studies have suggested that cell-based therapies with bone marrow stem cells (BMSC) and human amniotic membrane (hAM) would recover the ventricular function after MI; however, the mechanisms underlying these effects are still controversial. Herein, we aimed to compare the effects of BMSC and hAM in a rat model of heart failure. MI was induced through coronary occlusion, and animals with an ejection fraction (EF) < 50% were included and randomized into three groups: control, BMSC, and hAM. The BMSC and hAM groups were implanted on the anterior ventricular wall seven days after MI, and a new echocardiographic analysis was performed on the 30th day, followed by euthanasia. The echocardiographic results after 30 days showed significant improvements on EF and left-ventricular end-sistolic and end-diastolic volumes in both BMSC and hAM groups, without significant benefits in the control group. New blood vessels, desmine-positive cells and connexin-43 expression were also elevated in both BMSC and hAM groups. These results suggest a recovery of global cardiac function with the therapeutic use of both BMSC and hAM, associated with angiogenesis and cardiomyocyte regeneration after 30 days.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8471644PMC
http://dx.doi.org/10.3390/life11090958DOI Listing

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