Carbon Monoxide improves Hemodynamics during Extracorporeal Resuscitation in Pigs.
Carbon Monoxide improves Hemodynamics during Extracorporeal Resuscitation in Pigs.
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一氧化碳改善猪体外复苏期间的血流动力学
DOI:
10.1093/cvr/cvz075
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发表时间:
2020
影响因子:
10.8
通讯作者:
Goebel U
中科院分区:
文献类型:
--
作者:
Wollborn J;Steiger C;Ruetten E;Benk C;Kari FA;Wunder C;Meinel L;Buerkle H;Schick MA;Goebel U
AimsHeart disease of different aetiology remains the leading cause of cardiac arrest (CA). Despite efforts to improve the quality of cardiopulmonary resuscitation (CPR), subsequent myocardial and systemic damage after CA still present a major long-term burden. Low-dose carbon monoxide (CO) is known to exert protective effects in cardiovascular pathophysiology but clinical applications are challenged by unfavourable delivery modes. We tested the hypothesis that extracorporeal resuscitation (E-CPR) in combination with controlled fast onset CO delivery results in improved cardiac physiology and haemodynamics. Damage-associated molecular pattern (DAMP) signalling may be part of the molecular mechanism.Methods and resultsIn an established porcine model, E-CPR was performed. While E-CPR leads to similar results as compared to a conventional CPR strategy, CO delivery in combination with E-CPR demonstrated significant cardioprotection. Cardiac performance analysis using echocardiography and thermodilution techniques showed a CO-dependent improved cardiac function compared to severe myocardial dysfunction in CPR and E-CPR (left ventricular ejection fraction: Sham 49 ± 5; CPR 26 ± 2; E-CPR 25 ± 2; CO-E-CPR 31 ± 4;P< 0.05). While sublingual microcirculation was significantly compromised in CPR and E-CPR, CO delivery demonstrated a significant improvement in microvascular function (microvascular flow index: Sham 2.9 ± 0.1; CPR 2.2 ± 0.1; E-CPR 1.8 ± 0.1; CO-E-CPR 2.7 ± 0.1;P< 0.01). Histological and serological myocardial damage markers were significantly reduced (hsTroponin-T Sham 0.01 ± 0.001; CPR 1.9 ± 0.2; E-CPR 3.5 ± 1.2; CO-E-CPR 0.5 ± 0.2 ng/mL;P< 0.05). DAMP signalling was decreasedipse factoleading to influence of cardioprotective heat shock and cyclooxygenase response.ConclusionsCO treatment restores myocardial function and improves systemic macro- and microhaemodynamics in E-CPR through a reduction in DAMPs.
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影响因子:
13.6
作者:
Wegiel B;Hanto DW;Otterbein LE
通讯作者:
Otterbein LE
DOI:
10.1016/b978-0-12-394309-5.00006-7
发表时间:
2012
影响因子:
--
作者:
Kalogeris, Theodore;Baines, Christopher P.;Krenz, Maike;Korthuis, Ronald J.
通讯作者:
Korthuis, Ronald J.
影响因子:
37.8
作者:
Oyama, J;Blais, C;Bourcier, T
通讯作者:
Bourcier, T
影响因子:
4.6
作者:
Ahn C;Kim W;Cho Y;Choi KS;Jang BH;Lim TH
通讯作者:
Lim TH
影响因子:
20.1
作者:
Otterbein LE;Foresti R;Motterlini R
通讯作者:
Motterlini R