Bone-Marrow Stem Cells and Acellular Human Amniotic Membrane in a Rat Model of Heart Failure.
Gustavo Gavazzoni BlumePaulo André Bispo Machado-JuniorRossana Baggio SimeoniGiovana Paludo BertinatoMurilo Sgarbossa TonialSeigo NagashimaRicardo Aurino PinhoAnna Flávia Ribeiro Dos Santos MiggiolaroMarcia OlandoskiKatherine Athayde Teixeira de CarvalhoJulio César FranciscoLuiz César Guarita-SouzaPublished in: Life (Basel, Switzerland) (2021)
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.
Keyphrases
- left ventricular
- heart failure
- stem cells
- aortic stenosis
- ejection fraction
- bone marrow
- cardiac resynchronization therapy
- endothelial cells
- hypertrophic cardiomyopathy
- left atrial
- acute myocardial infarction
- high glucose
- mitral valve
- mesenchymal stem cells
- cell therapy
- poor prognosis
- induced apoptosis
- atrial fibrillation
- acute heart failure
- open label
- coronary artery
- pulmonary hypertension
- induced pluripotent stem cells
- pluripotent stem cells
- coronary artery disease
- vascular endothelial growth factor
- angiotensin ii
- long non coding rna
- binding protein
- drug induced
- clinical trial
- diabetic rats
- cell death
- data analysis
- transcatheter aortic valve replacement
- blood pressure