Donor heart preservation with a novel long-term and slow-releasing hydrogen sulfide system

Donor heart preservation with a novel long-term and slow-releasing hydrogen sulfide system
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使用新型长期缓慢释放硫化氢系统保存供体心脏

DOI:
10.1016/j.niox.2018.09.001
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发表时间:
2018-12-01
影响因子:
3.9
通讯作者:
Wang, Yiqing
Wang, Yiqing
中科院分区:
生物学2区
文献类型:
--
作者:
Sun, Xiaotian;Wang, Wenshuo;Wang, Yiqing

文献摘要

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Cardiac transplantation has been limited by the inability to long preserve donor hearts safely. Hydrogen sulfide (H2S) has been recognized as an important gasotransmitter exerting potent cardioprotection from ischemia/reperfusion injury (I/R). Herein we investigated the cardioprotective effects of a novel long-term and slow releasing H2S system, namely DATS-MSN, in heart preservation solution using a heart transplantation models. The release of H2S from DATS-MSN was slow and continuous in the University of Wisconsin solution (UW), correspondingly, DATS-MSN application demonstrated superior cardioprotective effects over the control and traditional H2S donors after 6 h heart preservation and 1 h reperfusion, associated with greater allograft performance including left ventricular developed pressure (LVDP) and dP/dt (max), reduced plasmic CK-MB and troponin I levels, inhibited myocardial inflammation, increased antioxidant enzyme activities, preserved mitochondria structure and function, and decreased cardiomyocyte apoptosis index. Also, DATS-MSN application presented significant superiority in long-term allografts survival and function after 8 weeks of transplantation. In the in vitro experiments, cardiomyocytes injury from hypoxia was found to be relived with the treatment of DATS-MSN by anti-inflammatory effects via TLR4/NLRP3 pathway. The present work provides a long-term releasing H2S donor compatibly applied in the donor heart preservation, and preliminary explores its underlying mechanisms.