The susceptibility of bioprosthetic heart valve leaflets to oxidation

被引:37
作者
Christian, Abigail J. [1 ,2 ]
Lin, Hongqiao [3 ]
Alferiev, Ivan S. [2 ]
Connolly, Jeanne M. [2 ]
Ferrari, Giovanni [4 ]
Hazen, Stanley L. [3 ]
Ischiropoulos, Harry [1 ,5 ]
Levy, Robert J. [1 ,2 ]
机构
[1] Univ Penn, Dept Pharmacol, Perelman Sch Med, Philadelphia, PA 19104 USA
[2] Childrens Hosp Philadelphia, Dept Pediat, Div Cardiol, Philadelphia, PA 19104 USA
[3] Cleveland Clin, Lerner Res Inst, Dept Cellular & Mol Med, Cleveland, OH 44195 USA
[4] Univ Penn, Dept Surg, Perelman Sch Med, Philadelphia, PA 19104 USA
[5] Childrens Hosp Philadelphia, Dept Pediat, Div Neonatol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
Bioprosthesis; Heart valve; Oxidation; Antioxidant; Collagen; Calcification; SUBSTITUTE CARDIAC VALVES; STRUCTURAL-CHANGES; CROSS-LINKING; CALCIFICATION; COLLAGEN; PREVENTION; DEGENERATION; DEGRADATION; PATHWAYS; FAILURE;
D O I
10.1016/j.biomaterials.2013.11.045
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The clinical use of bioprosthetic heart valves (BHV) is limited due to device failure caused by structural degeneration of BHV leaflets. In this study we investigated the hypothesis that oxidative stress contributes to this process. Fifteen clinical BHV that had been removed for device failure were analyzed for oxidized amino acids using mass spectrometry. Significantly increased levels of ortho-tyrosine, meta-tyrosine and dityrosine were present in clinical BHV explants as compared to the non-implanted BHV material glutaraldehyde treated bovine pericardium (BP). BP was exposed in vitro to oxidizing conditions (FeSO4/H2O2) to assess the effects of oxidation on structural degeneration. Exposure to oxidizing conditions resulted in significant collagen deterioration, loss of glutaraldehyde cross-links, and increased susceptibility to collagenase degradation. BP modified through covalent attachment of the oxidant scavenger 3-(4-hydroxy-3,5-di-tert-butylphenyl) propyl amine (DBP) was resistant to all of the monitored parameters of structural damage induced by oxidation. These results indicate that oxidative stress, particularly via hydroxyl radical and tyrosyl radical mediated pathways, may be involved in the structural degeneration of BHV, and that this mechanism may be attenuated through local delivery of antioxidants such as DBP. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2097 / 2102
页数:6
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