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04.07.2015 | Original Article

Intramyocardial delivery of VEGF₁₆₅ via a novel biodegradable hydrogel induces angiogenesis and improves cardiac function after rat myocardial infarction

Erschienen in: Heart and Vessels | Ausgabe 6/2016

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Abstract

Vascular endothelial growth factor (VEGF), an independent mitogen, has been reported to induce angiogenesis and thus attenuates the damage induced by myocardial infarction (MI). VEGF₁₆₅ is the most abundant and predominant isoform of VEGF. This study investigates whether this effect could be strengthened by local intramyocardial injection of VEGF₁₆₅ along with a novel biodegradable Dex-PCL-HEMA/PNIPAAm hydrogel and ascertains its possible mechanism of action. Rat models of myocardial infarction were induced by coronary artery ligation. Phosphate-buffered saline (PBS group), Dex-PCL-HEMA/PNIPAAm hydrogel (Gel group), phosphate-buffered saline containing VEGF₁₆₅ (VP group), and hydrogel containing VEGF₁₆₅ (VPG group) were injected into a peri-infarcted area of cardiac tissue immediately after myocardial infarction, respectively. The sham group was thoracic but without myocardial infarction. The injection of VEGF₁₆₅ along with a hydrogel induced angiogenesis, reduced collagen content and MI area, inhibited cell apoptosis, increased the level of VEGF₁₆₅ protein and the expression of flk-1 and flt-1, and improved cardiac function compared with the injection of either alone after MI in rats. The results suggest that injection of VEGF₁₆₅ along with a hydrogel acquires more cardioprotective effects than either alone in rat with MI by sustained release of VEGF₁₆₅, then may enhance the feedback between VEGF and its receptors flk-1 and flt-1.

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Titel: Intramyocardial delivery of VEGF165 via a novel biodegradable hydrogel induces angiogenesis and improves cardiac function after rat myocardial infarction
Publikationsdatum: 04.07.2015
Erschienen in: Heart and Vessels / Ausgabe 6/2016
Print ISSN: 0910-8327
Elektronische ISSN: 1615-2573
DOI: https://doi.org/10.1007/s00380-015-0710-0

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