<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-06-14T03:46:57Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/5119" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/5119</identifier><datestamp>2024-09-27T08:33:59Z</datestamp><setSpec>com_20.500.12105_19604</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19605</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Bobi, Joaquim</subfield>
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      <subfield code="a">Solanes, Nuria</subfield>
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      <subfield code="a">Fernandez-Jimenez, Rodrigo</subfield>
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      <subfield code="a">Galan-Arriola, Carlos</subfield>
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      <subfield code="a">Dantas, Ana Paula</subfield>
      <subfield code="e">author</subfield>
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      <subfield code="a">Fernandez-Friera, Leticia</subfield>
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      <subfield code="a">Galvez-Monton, Carolina</subfield>
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      <subfield code="a">Rigol-Monzo, Elisabet</subfield>
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      <subfield code="a">Aguero, Jaume</subfield>
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      <subfield code="a">Ramirez, Jose</subfield>
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      <subfield code="a">Roque, Merce</subfield>
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      <subfield code="a">Bayes-Genis, Antoni</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Sanchez-Gonzalez, Javier</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Garcia-Alvarez, Ana</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Sabaté, Manel</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Roura, Santiago</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Ibáñez, Borja</subfield>
      <subfield code="e">author</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Rigol, Montserrat</subfield>
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   <datafield ind2=" " ind1=" " tag="260">
      <subfield code="c">2017</subfield>
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      <subfield code="a">Background-Autologous adipose tissue-derived mesenchymal stem cells (ATMSCs) therapy is a promising strategy to improve post-myocardial infarction outcomes. In a porcine model of acute myocardial infarction, we studied the long-term effects and the mechanisms involved in allogeneic ATMSCs administration on myocardial performance. Methods and Results-Thirty-eight pigs underwent 50 minutes of coronary occlusion; the study was completed in 33 pigs. After reperfusion, allogeneic ATMSCs or culture medium (vehicle) were intracoronarily administered. Follow-ups were performed at short (2 days after acute myocardial infarction vehicle-treated, n=10; ATMSCs-treated, n=9) or long term (60 days after acute myocardial infarction vehicle-treated, n=7; ATMSCs-treated, n=7). At short term, infarcted myocardium analysis showed reduced apoptosis in the ATMSCs-treated animals (48.6 +/- 6\% versus 55.9 +/- 5.7\% in vehicle; P=0.017); enhancement of the reparative process with up-regulated vascular endothelial growth factor, granulocyte macrophage colony-stimulating factor, and stromal-derived factor-1 alpha gene expression; and increased M2 macrophages (67.2 +/- 10\% versus 54.7 +/- 10.2\% in vehicle; P=0.016). In long-term groups, increase in myocardial perfusion at the anterior infarct border was observed both on day-7 and day-60 cardiac magnetic resonance studies in ATMSCs-treated animals, compared to vehicle (87.9 +/- 28.7 versus 57.4 +/- 17.7 mL/min per gram at 7 days; P=0.034 and 99 +/- 22.6 versus 43.3 +/- 14.7 22.6 mL/min per gram at 60 days; P=0.0001, respectively). At day 60, higher vascular density was detected at the border zone in the ATMSCs-treated animals (118 +/- 18 versus 92.4 +/- 24.3 vessels/mm(2) in vehicle; P=0.045). Cardiac magnetic resonance-measured left ventricular ejection fraction of left ventricular volumes was not different between groups at any time point. Conclusions-In this porcine acute myocardial infarction model, allogeneic ATMSCs-based therapy was associated with increased cardioprotective and reparative mechanisms and with better cardiac magnetic resonance-measured perfusion. No effect on left ventricular volumes or ejection fraction was observed.</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">J Am Heart Assoc. 2017; 6(5):e005771</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">10.1161/JAHA.117.005771</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">2047-9980</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">Journal of the American Heart Association</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">28468789</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">http://hdl.handle.net/20.500.12105/5119</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">adipose tissue-derived mesenchymal stem cells</subfield>
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      <subfield code="a">allogeneic origin</subfield>
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      <subfield code="a">myocardial infarction</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">myocardial perfusion</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">vascular density</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">RANDOMIZED PHASE-1 TRIAL</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">CARDIAC-FUNCTION</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">ISCHEMIC CARDIOMYOPATHY</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">PROMOTE ANGIOGENESIS</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">PROGENITOR CELLS</subfield>
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      <subfield code="a">HEART-FAILURE</subfield>
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      <subfield code="a">PORCINE MODEL</subfield>
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      <subfield code="a">DISEASE</subfield>
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      <subfield code="a">THERAPY</subfield>
   </datafield>
   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">ISCHEMIA/REPERFUSION</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Intracoronary Administration of Allogeneic Adipose Tissue-Derived Mesenchymal Stem Cells Improves Myocardial Perfusion But Not Left Ventricle Function, in a Translational Model of Acute Myocardial Infarction</subfield>
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