Tissue damage in the heart after cardiac arrest induced by asphyxia and hemorrhage in newborn pigs

被引:12
作者
Weber, Birte [1 ]
Mendler, Marc Robin [2 ]
Lackner, Ina [1 ]
Pressmar, Jochen [1 ]
Haffner-Luntzer, Melanie [3 ]
Hoefler, Severin [1 ]
Braun, Christian Karl [4 ]
Hummler, Helmut [2 ,5 ]
Schwarz, Stephan [2 ]
Kalbitz, Miriam [1 ]
机构
[1] Univ Ulm, Ctr Surg, Dept Traumatol Hand Plast & Reconstruct Surg, Ulm, Germany
[2] Ulm Univ, Dept Pediat & Adolescent Med, Div Neonatol & Pediat Crit Care, Ulm, Germany
[3] Univ Med Ctr Ulm, Inst Orthoped Res & Biomech, Ulm, Germany
[4] Univ Hosp Ulm, Inst Clin & Expt Trauma Immunol, Ulm, Germany
[5] Sidra Med, Div Neonatol, Dept Pediat, Doha, Qatar
关键词
EXTRACELLULAR HISTONES; TROPONIN; CARDIOMYOPATHY;
D O I
10.1038/s41390-019-0505-6
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
BACKGROUND: Asphyxia of newborns is a severe and frequent challenge of the peri- and postnatal period. METHODS: Forty-four neonatal piglets underwent asphyxia and hemorrhage (AH), followed by resuscitation with blood or crystalloid transfusion. In this study, 15 piglets (blood n = 9, NaCl n = 6, mean age 31 h) were randomly chosen. Four hours after return of spontaneous circulation, heart tissue and blood were collected. Analyses of heart fatty acid binding protein (HFABP), cardiac troponin I (TnI) levels, and activation of the complement system were performed. Histological staining for connexin 43 (Cx43) and complement C5a receptor 1 (C5aR1) was performed. RESULTS: Following AH, systemic elevation of cardiac TnI and HFABP revealed cardiac damage in both groups. Systemic activation of the complement system and the appearance of extracellular histones in plasma of the blood transfusion group were observed. The Cx43 was translocated from the intercalated discs to the cytosol after AH. Cardiac glycogen concentration was reduced in both groups. A significant reduction of C5aR1 in the left ventricle and a significant elevation of the heart injury score were investigated after blood transfusion. CONCLUSION: AH leads to alteration of the heart, particularly in Cx43 and glycogen reserves, as well as local inflammation.
引用
收藏
页码:709 / 718
页数:10
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