The Myocardial Protection of Polarizing Cardioplegia Combined With Delta-Opioid Receptor Agonist in Swine

被引:9
|
作者
Wu, Ting
Dong, Peiqing [1 ]
Chen, Changcheng
Yang, Jing
Hou, Xiaotong
机构
[1] Capital Med Univ, Beijing Anzhen Hosp, Dept Cardiopulm Bypass, Beijing 100029, Peoples R China
来源
ANNALS OF THORACIC SURGERY | 2011年 / 91卷 / 06期
关键词
ADENOSINE-LIDOCAINE CARDIOPLEGIA; HIBERNATION INDUCTION TRIGGERS; SUPRANORMAL POTASSIUM; ARREST; WARM; MECHANISMS; ISCHEMIA; COLD;
D O I
10.1016/j.athoracsur.2011.02.069
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. The purpose of this study was to determine whether polarized arrest using adenosine/lidocaine cold crystalloid cardioplegia in combination with the hibernation inductor delta-opioid receptor agonist pentazocine would give satisfactory myocardial protection rather than using depolarized supranormal potassium cardioplegia, supranormal potassium cardioplegia with pentazocine, or adenosine/lidocaine cardioplegia. Methods. Twenty pigs were randomly divided into four groups (n = 5 each) to receive the four types of cold crystalloid cardioplegia with an aortic cross-clamp time of 1 hour. Hemodynamic data were continuously measured, as was the left ventricular end-diastolic pressure (LVEDP), left ventricular end-systolic pressure (LVESP), plus or minus derivative of change in diastolic pressure over time (+/- dp/dt), cardiac output, pulmonary artery pressure, pulmonary capillary wedge pressure, cardiac troponin I, and left ventricular ultrastructure. Results. Both the adenosine/lidocaine/pentazocine group and the adenosine/lidocaine group got significantly better results than the hyperkalemic and hyperkalemic pentazocine groups in improving hemodynamic values, pulmonary capillary wedge pressure, LVEDP, LVESP, +/- dp/dt, cardiac output, cardiac troponin I values, and left ventricular ultrastructure. There were no statistical differences between the adenosine/lidocaine/pentazocine group and the adenosine/lidocaine group at 1 hour after cross-clamp removal; but at 2 hours after crossclamp removal, the adenosine/lidocaine/pentazocine group stands out (LVEDP 3.3 +/- 0.5, LVESP 122.5 +/- 18.9, +dp/dt 2.9 +/- 0.1, -dp/dt 2.0 +/- 0.6, cardiac output 2.6 +/- 0.4, and troponin I 4.9 +/- 0.5), with significant differences from the adenosine/lidocaine group (LVEDP 5.8 +/- 1.0, LVESP 98.5 +/- 10.1, +dp/dt 2.5 +/- 0.2, -dp/dt 1.0 +/- 0.2, cardiac output 2.2 +/- 0.2, troponin I 8.2 +/- 0.8; p < 0.05). The defibrillation rate was largely decreased after the cross-clamp was released in the group containing pentazocine in cardioplegia. Conclusions. Adenosine/lidocaine/pentazocine cold crystalloid cardioplegia gave satisfactory cardiac arrest and better myocardial protection than the other three groups, especially with regard to improving prolonged postoperative cardiac function.
引用
收藏
页码:1914 / 1920
页数:7
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