Elastin-like recombinamer-based devices releasing Kv1.3 blockers for the prevention of intimal hyperplasia: An in vitro and in vivo study.

Elastin-like recombinamers Hydrogels Intimal hyperplasia Kv1.3 channels Local drug delivery Vascular smooth muscle cells

Journal

Acta biomaterialia
ISSN: 1878-7568
Titre abrégé: Acta Biomater
Pays: England
ID NLM: 101233144

Informations de publication

Date de publication:
01 10 2020
Historique:
received: 04 06 2020
revised: 25 07 2020
accepted: 30 07 2020
pubmed: 11 8 2020
medline: 15 5 2021
entrez: 11 8 2020
Statut: ppublish

Résumé

Coronary artery disease (CAD) is the most common cardiovascular disorder. Vascular surgery strategies for coronary revascularization (either percutaneous or open) show a high rate of failure because of restenosis of the vessel, due to phenotypic switch of vascular smooth muscle cells (VSMCs) leading to proliferation and migration. We have previously reported that the inhibition of Kv1.3 channel function with selective blockers represents an effective strategy for the prevention of restenosis in human vessels used for coronary angioplasty procedures. However, delivery systems for controlled release of these drugs have not been investigated. Here we tested the efficacy of several formulations of elastin like recombinamers (ELRs) hydrogels to deliver the Kv1.3 blocker PAP-1 in various restenosis models. The dose and time course of PAP-1 release from ELRs click hydrogels was able to inhibit human VSMC proliferation in vitro as well as remodeling of human vessels in organ culture and restenosis in in vivo models. We conclude that this combination of active compound and advanced delivery method could improve the outcomes of vascular surgery in patients. STATEMENT OF SIGNIFICANCE: Vascular surgery strategies for coronary revascularization show a high rate of failure, because of occlusion (restenosis) of the vessel, due to vascular smooth muscle cells proliferation and migration. We have previously reported that blockers of Kv1.3 channels represent an effective anti-restenosis therapy, but delivery systems for their controlled release have not being explored. Here we tested the efficacy of several formulations of elastin like recombinamers (ELRs) hydrogels to deliver the Kv1.3 blocker PAP-1 in various restenosis models, both in vivo and in vitro, and also in human vessels. We demonstrated that combination of active compound and advanced delivery method could improve the outcomes of vascular surgery in patients.

Identifiants

pubmed: 32771595
pii: S1742-7061(20)30450-5
doi: 10.1016/j.actbio.2020.07.053
pii:
doi:

Substances chimiques

Elastin 9007-58-3

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

264-274

Informations de copyright

Copyright © 2020. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Sara Moreno-Estar (S)

Departamento de Bioquímica y Biología Molecular y Fisiología and Instituto de Biología y Genética Molecular (IBGM), Universidad de Valladolid, and CSIC, c/ Sanz y Forés, 3, 47003 Valladolid, Spain.

Sofía Serrano (S)

BIOFORGE (Group for Advanced Materials and Nanobiotechnology), CIBER-BBN, Universidad de Valladolid, Spain.

Marycarmen Arévalo-Martínez (M)

Departamento de Bioquímica y Biología Molecular y Fisiología and Instituto de Biología y Genética Molecular (IBGM), Universidad de Valladolid, and CSIC, c/ Sanz y Forés, 3, 47003 Valladolid, Spain.

Pilar Cidad (P)

Departamento de Bioquímica y Biología Molecular y Fisiología and Instituto de Biología y Genética Molecular (IBGM), Universidad de Valladolid, and CSIC, c/ Sanz y Forés, 3, 47003 Valladolid, Spain.

José Ramón López-López (JR)

Departamento de Bioquímica y Biología Molecular y Fisiología and Instituto de Biología y Genética Molecular (IBGM), Universidad de Valladolid, and CSIC, c/ Sanz y Forés, 3, 47003 Valladolid, Spain.

Mercedes Santos (M)

BIOFORGE (Group for Advanced Materials and Nanobiotechnology), CIBER-BBN, Universidad de Valladolid, Spain.

M Teresa Pérez-Garcia (MT)

Departamento de Bioquímica y Biología Molecular y Fisiología and Instituto de Biología y Genética Molecular (IBGM), Universidad de Valladolid, and CSIC, c/ Sanz y Forés, 3, 47003 Valladolid, Spain. Electronic address: tperez@ibgm.uva.es.

F Javier Arias (FJ)

BIOFORGE (Group for Advanced Materials and Nanobiotechnology), CIBER-BBN, Universidad de Valladolid, Spain.

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Classifications MeSH