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Epicardial shock-wave therapy improves ventricular function in a porcine model of ischaemic heart disease
Journal of tissue engineering and regenerative medicine, 2016-12, Vol.10 (12), p.1057-1064
Holfeld, Johannes
Zimpfer, Daniel
Albrecht-Schgoer, Karin
Stojadinovic, Alexander
Paulus, Patrick
Dumfarth, Julia
Thomas, Anita
Lobenwein, Daniela
Tepeköylü, Can
Rosenhek, Raphael
Schaden, Wolfgang
Kirchmair, Rudolf
Aharinejad, Seyedhossein
Grimm, Michael
2016
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Holfeld, Johannes
Zimpfer, Daniel
Albrecht-Schgoer, Karin
Stojadinovic, Alexander
Paulus, Patrick
Dumfarth, Julia
Thomas, Anita
Lobenwein, Daniela
Tepeköylü, Can
Rosenhek, Raphael
Schaden, Wolfgang
Kirchmair, Rudolf
Aharinejad, Seyedhossein
Grimm, Michael
Titel
Epicardial shock-wave therapy improves ventricular function in a porcine model of ischaemic heart disease
Ist Teil von
Journal of tissue engineering and regenerative medicine, 2016-12, Vol.10 (12), p.1057-1064
Ort / Verlag
England: Blackwell Publishing Ltd
Erscheinungsjahr
2016
Quelle
MEDLINE
Beschreibungen/Notizen
Previously we have shown that epicardial shock‐wave therapy improves left ventricular ejection fraction (LVEF) in a rat model of myocardial infarction. In the present experiments we aimed to address the safety and efficacy of epicardial shock‐wave therapy in a preclinical large animal model and to further evaluate mechanisms of action of this novel therapy. Four weeks after left anterior descending (LAD) artery ligation in pigs, the animals underwent re‐thoracotomy with (shock‐wave group, n = 6) or without (control group, n = 5) epicardial shock waves (300 impulses at 0.38 mJ/mm2) applied to the infarcted anterior wall. Efficacy endpoints were improvement of LVEF and induction of angiogenesis 6 weeks after shock‐wave therapy. Safety endpoints were haemodynamic stability during treatment and myocardial damage. Four weeks after LAD ligation, LVEF decreased in both the shock‐wave (43 ± 3%, p < 0.001) and control (41 ± 4%, p = 0.012) groups. LVEF markedly improved in shock‐wave animals 6 weeks after treatment (62 ± 9%, p = 0.006); no improvement was observed in controls (41 ± 4%, p = 0.36), yielding a significant difference. Quantitative histology revealed significant angiogenesis 6 weeks after treatment (controls 2 ± 0.4 arterioles/high‐power field vs treatment group 9 ± 3; p = 0.004). No acute or chronic adverse effects were observed. As a potential mechanism of action in vitro experiments showed stimulation of VEGF receptors after shock‐wave treatment in human coronary artery endothelial cells. Epicardial shock‐wave treatment in a large animal model of ischaemic heart failure exerted a positive effect on LVEF improvement and did not show any adverse effects. Angiogenesis was induced by stimulation of VEGF receptors. Copyright © 2014 John Wiley & Sons, Ltd.
Sprache
Englisch
Identifikatoren
ISSN: 1932-6254
eISSN: 1932-7005
DOI: 10.1002/term.1890
Titel-ID: cdi_proquest_miscellaneous_1855073979
Format
–
Schlagworte
angiogenesis
,
Animals
,
Disease Models, Animal
,
endothelial cells
,
Female
,
High-Energy Shock Waves
,
Humans
,
left ventricular ejection fraction
,
myocardial infarction
,
Myocardial Ischemia - physiopathology
,
Myocardial Ischemia - therapy
,
Neovascularization, Physiologic
,
Pericardium
,
Regenerative medicine
,
shockwave therapy
,
Swine
,
Tissue engineering
,
Ultrasonic Therapy - methods
,
vascular endothelial growth factor
,
Ventricular Function, Left
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