Comparison of Endothelial Barrier Functional Recovery After Implantation of a Novel Biodegradable-Polymer Sirolimus-Eluting Stent in Comparison to Durable- and Biodegradable-Polymer Everolimus-Eluting Stents

被引:11
作者
Sakamoto, Atsushi [1 ]
Torii, Sho [1 ]
Jinnouchi, Hiroyuki [1 ]
Guo, Liang [1 ]
Cornelissen, Anne [1 ]
Kuntz, Salome [1 ]
Cheng, Qi [1 ]
Fernandez, Raquel [1 ]
Paek, Ka Hyun [1 ]
Harris, Kathryn [2 ]
Srivastava, Mukta C. [2 ]
Kolodgie, Frank D. [1 ]
Virmani, Renu [1 ]
Finn, Aloke, V [1 ,2 ]
机构
[1] CVPath Inst Inc, 19 Firstfield Rd, Gaithersburg, MD 20878 USA
[2] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
关键词
Drug eluting stent; Biodegradable polymer; Durable polymer; Endothelial function; Vascular permeability;
D O I
10.1016/j.carrev.2020.08.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: The advantage of biodegradable-polymer drug-eluting stents (BP-DES) versus durable-polymer (DP) DES remains uncertain. We compared neointimal formation and endothelial barrier function of new BP sirolimus-eluting stents (BP-SES, BuMA Supreme (R)) to other contemporary BP-DES, DP-DES, and bare metal stents (BMS). Methods and results: Light microscopic assessment in swine coronary arteries showed comparable neointimal formation between BP-SES and DP everolimus-eluting stent (DP-EES). The performance of BP-SES was compared with DP-EES (Xience Xpedition (R)), BP-EES (Synergy (R)), and BMS (Multi-Link Vision (R)) at 45- and 90-days in rabbit ilio-femoral arteries using Evans blue dye (EBD) followed by immunostaining for endothelial barrier proteins (p120/vascular endothelial-cadherin [VE-cad]) to evaluate endothelial barrier function and scanning electron microscopy (SEM) to determine strut tissue coverage. BMS followed by BP-SES and BP-EES exhibited smaller EBD positive areas versus that of DP-EES at 45- and 90-days. p120/VE-cad immunostaining and SEM-determined strut coverage was greater at 45- and 90-days for BMS followed by all DESs. Regardless of stent type, the lack of p120/VE-cad co-localization showed greater leukocyte and platelet aggregation. Conclusion: Three types of DES showed different endothelial healing pattern regardless their equivalent suppression of neointimal formation. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
相关论文
共 26 条
[1]   Functional comparison between the BuMA Supreme biodegradable polymer sirolimus-eluting stent and a durable polymer zotarolimus-eluting coronary stent using quantitative flow ratio: PIONEER QFR substudy [J].
Asano, Taku ;
Katagiri, Yuki ;
Collet, Carlos ;
Tenekecioglu, Erhan ;
Miyazaki, Yosuke ;
Sotomi, Yohei ;
Amoroso, Giovanni ;
Aminian, Adel ;
Brugaletta, Salvatore ;
Vrolix, Mathias ;
Hernandez-Antolin, Rosana ;
van de Harst, Pim ;
Iniguez, Andres ;
Janssens, Luc ;
Smits, Pieter C. ;
Wykrzkowska, Joanna ;
Ribeiro, Vasco Gama ;
Pereira, Helder ;
da Silva, Pedro Canas ;
Piek, Jan J. ;
Reiber, Johan H. C. ;
von Birgelen, Clemens ;
Sabate, Manel ;
Onuma, Yoshinobu ;
Serruys, Patrick W. .
EUROINTERVENTION, 2018, 14 (05) :570-579
[2]   Local VE-cadherin mechanotransduction triggers long-ranged remodeling of endothelial monolayers [J].
Barry, Adrienne K. ;
Wang, Ning ;
Leckband, Deborah E. .
JOURNAL OF CELL SCIENCE, 2015, 128 (07) :1341-1351
[3]   Drug-Eluting or Bare-Metal Stents for Coronary Artery Disease [J].
Bonaa, K. H. ;
Mannsverk, J. ;
Wiseth, R. ;
Aaberge, L. ;
Myreng, Y. ;
Nygard, O. ;
Nilsen, D. W. ;
Klow, N. -E. ;
Uchto, M. ;
Trovik, T. ;
Bendz, B. ;
Stavnes, S. ;
Bjornerheim, R. ;
Larsen, A. -I. ;
Slette, M. ;
Steigen, T. ;
Jakobsen, O. J. ;
Bleie, O. ;
Fossum, E. ;
Hanssen, T. A. ;
Dahl-Eriksen, O. ;
Njolstad, I. ;
Rasmussen, K. ;
Wilsgaard, T. ;
Nordrehaug, J. E. .
NEW ENGLAND JOURNAL OF MEDICINE, 2016, 375 (13) :1242-1252
[4]   Mechanisms of disease:: Platelet activation and atherothrombosis [J].
Davi, Giovanni ;
Patrono, Carlo .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 357 (24) :2482-2494
[5]   The role of adherens junctions and VE-cadherin in the control of vascular permeability [J].
Dejana, Elisabetta ;
Orsenigo, Fabrizio ;
Lampugnani, Maria Grazia .
JOURNAL OF CELL SCIENCE, 2008, 121 (13) :2115-2122
[6]   The Role VE-Cadherin in Vascular Morphogenesis and Permeability Control [J].
Dejana, Elisabetta ;
Vestweber, Dietmar .
MOLECULAR BIOLOGY OF CADHERINS, 2013, 116 :119-144
[7]   Head-to-Head Comparison of a Drug-Free Early Programmed Dismantling Polylactic Acid Bioresorbable Scaffold and a Metallic Stent in the Porcine Coronary Artery Six-Month Angiography and Optical Coherence Tomographic Follow-Up Study [J].
Durand, Eric ;
Sharkawi, Tahmer ;
Leclerc, Guy ;
Raveleau, Marine ;
van der Leest, Machiel ;
Vert, Michel ;
Lafont, Antoine .
CIRCULATION-CARDIOVASCULAR INTERVENTIONS, 2014, 7 (01) :70-79
[8]   Sirolimus-FKBP12.6 Impairs Endothelial Barrier Function Through Protein Kinase C-α Activation and Disruption of the p120-Vascular Endothelial Cadherin Interaction [J].
Habib, Anwer ;
Karmali, Vinit ;
Polavarapu, Rohini ;
Akahori, Hirokuni ;
Cheng, Qi ;
Pachura, Kim ;
Kolodgie, Frank D. ;
Finn, Aloke V. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2013, 33 (10) :2425-2431
[9]   Direct Targeting of the mTOR (Mammalian Target of Rapamycin) Kinase Improves Endothelial Permeability in Drug-Eluting Stents-Brief Report [J].
Harari, Emanuel ;
Guo, Liang ;
Smith, Samantha L. ;
Paek, Ka Hyun ;
Fernandez, Raquel ;
Sakamoto, Atsushi ;
Mori, Hiroyoshi ;
Kutyna, Matthew D. ;
Habib, Anwer ;
Torii, Sho ;
Cornelissen, Anne ;
Jinnouchi, Hiroyuki ;
Gupta, Anuj ;
Kolodgie, Frank D. ;
Virmani, Renu ;
Finn, Aloke V. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2018, 38 (09) :2217-2224
[10]   Comparison of zotarolimus-eluting and sirolimus-eluting stents in patients with native coronary artery disease - A randomized controlled trial [J].
Kandzari, David E. ;
Leon, Martin B. ;
Popma, Jeffrey J. ;
Fitzgerald, Peter J. ;
O'Shaughnessy, Charles ;
Ball, Michael W. ;
Turco, Mark ;
Applegate, Robert J. ;
Gurbel, Paul A. ;
Midei, Mark G. ;
Badre, Sejal S. ;
Mauri, Laura ;
Thompson, Kweli P. ;
LeNarz, LeRoy A. ;
Kuntz, Richard E. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2006, 48 (12) :2440-2447