| Literature DB >> 28283218 |
Nuno Alexandre1, Irina Amorim2, Ana Rita Caseiro3, Tiago Pereira4, Rui Alvites4, Alexandra Rêma5, Ana Gonçalves5, Guilherme Valadares6, Elísio Costa7, Alice Santos-Silva7, Miguel Rodrigues8, Maria Ascensão Lopes8, André Almeida9, José Domingos Santos8, Ana Colette Maurício4, Ana Lúcia Luís10.
Abstract
The functional and structural performance of a 5cm synthetic small diameter vascular graft (SDVG) produced by the copolymerization of polyvinyl alcohol hydrogel with low molecular weight dextran (PVA/Dx graft) associated to mesenchymal stem cells (MSCs)-based therapies and anticoagulant treatment with heparin, clopidogrel and warfarin was tested using the ovine model during the healing period of 24 weeks. The results were compared to the ones obtained with standard expanded polyetetrafluoroethylene grafts (ePTFE graft). Blood flow, vessel and graft diameter measurements, graft appearance and patency rate (PR), thrombus, stenosis and collateral vessel formation were evaluated by B-mode ultrasound, audio and color flow Doppler. Graft and regenerated vessels morphologic evaluation was performed by scanning electronic microscopy (SEM), histopathological and immunohistochemical analysis. All PVA/Dx grafts could maintain a similar or higher PR and systolic/diastolic laminar blood flow velocities were similar to ePTFE grafts. CD14 (macrophages) and α-actin (smooth muscle) staining presented similar results in PVA/Dx/MSCs and ePTFE graft groups. Fibrosis layer was lower and endothelial cells were only detected at graft-artery transitions where it was added the MSCs. In conclusion, PVA/Dx graft can be an excellent scaffold candidate for vascular reconstruction, including clinic mechanically challenging applications, such as SDVGs, especially when associated to MSCs-based therapies to promote higher endothelialization and lower fibrosis of the vascular prosthesis, but also higher PR values.Entities:
Keywords: Dextran; Mesenchymal stem cells; Ovine model; PVA; Synthetic small diameter vascular graft
Mesh:
Substances:
Year: 2017 PMID: 28283218 DOI: 10.1016/j.ijpharm.2017.02.043
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875