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dc.contributor.author
González, Germán Esteban
dc.contributor.author
Rabald, Steffen
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Briest, Wilfried
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Gelpi, Ricardo Jorge
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Seropian, Ignacio Miguel
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Zimmer, Heinz Gerd
dc.contributor.author
Deten, Alexander
dc.date.available
2020-04-14T17:09:58Z
dc.date.issued
2009-08
dc.identifier.citation
González, Germán Esteban; Rabald, Steffen; Briest, Wilfried; Gelpi, Ricardo Jorge; Seropian, Ignacio Miguel; et al.; Ribose Treatment Reduced the Infarct Size and Improved Heart Function after Myocardial Infarction in Rats; Karger; Cellular Physiology and Biochemistry; 24; 3-4; 8-2009; 211-218
dc.identifier.issn
1015-8987
dc.identifier.uri
http://hdl.handle.net/11336/102484
dc.description.abstract
Objective: In this study the effect of ribose on heart function and infarct-size was analyzed 6 h after myocardial infarction (MI) in rats. Methods: Continuous i.v.-infusion of NaCl or ribose (200 mg/ kg/h) was started one day prior to induction of MI in female Sprague-Dawley rats which was done by ligation of the left coronary artery. Six hours after MI heart function was measured with 3F tip catheter, cardiac output by thermodilution method. Thereafter the ischemic area was delineated by Evans Blue infusion, and the infarct area was visualized by triphenyltetrazolium chloride staining. The mRNA expression of interleukin (IL)-1β, IL-6, matrixmetalloproteinase (MMP)-8, and -9 was measured by ribonuclease protection assay. Results: Heart function was severely depressed 6 hours after coronary artery occlusion, but recovered significantly under the influence of ribose. Left ventricular (LV) systolic pressure (LVSP) and contractility (LVdP/dtmax) were restored to the normal levels of sham-operated animals, while parameters of LV relaxation (LVdP/dtmin and time constant of relaxation τ) were impaired compared to sham-operated animals, but significantly improved by ribose treatment compared to shamtreated MI-rats. Moreover, the infarct size was significantly smaller in the ribose treated animals despite a comparable ischemic area at risk in all MI-rats. The cytokine mRNA expression after MI was significantly reduced after ribose treatment, while there were no differences regarding MMP expression. Conclusion: MI size was significantly reduced and LV function significantly improved by ribose treatment at 6 h after MI. This seemed to be based on slowing the velocity of the necrotic wave front across the LV wall after MI resulting in smaller infarcts.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Karger
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
myocardial infarction
dc.subject
ribose
dc.subject.classification
Farmacología y Farmacia
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Medicina Básica
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CIENCIAS MÉDICAS Y DE LA SALUD
dc.title
Ribose Treatment Reduced the Infarct Size and Improved Heart Function after Myocardial Infarction in Rats
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2020-04-14T13:37:02Z
dc.journal.volume
24
dc.journal.number
3-4
dc.journal.pagination
211-218
dc.journal.pais
Suiza
dc.journal.ciudad
Basel
dc.description.fil
Fil: González, Germán Esteban. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Fisiopatología Cardiovascular; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
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Fil: Rabald, Steffen. University of Leipzig; Alemania
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Fil: Briest, Wilfried. University of Leipzig; Alemania
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Fil: Gelpi, Ricardo Jorge. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Fisiopatología Cardiovascular; Argentina
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Fil: Seropian, Ignacio Miguel. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Fisiopatología Cardiovascular; Argentina
dc.description.fil
Fil: Zimmer, Heinz Gerd. University of Leipzig; Alemania
dc.description.fil
Fil: Deten, Alexander. University of Leipzig; Alemania
dc.journal.title
Cellular Physiology and Biochemistry
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1159/000233247
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.karger.com/Article/Abstract/233247
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