Killingsworth Cheryl R, Wei Chih-Chang, Dell'Italia Louis J, Ardell Jeffrey L, Kingsley Melody A, Smith William M, Ideker Raymond E, Walcott Gregory P
Cardiac Rhythm Management Laboratory, Division of Cardiovascular Diseases, Department of Medicine, University of Alabama at Birmingham, AL 35294-0019, USA.
Circulation. 2004 May 25;109(20):2469-74. doi: 10.1161/01.CIR.0000128040.43933.D3. Epub 2004 May 3.
High catecholamine concentrations are cytotoxic to cardiac myocytes. We hypothesized that myocardial interstitial catecholamine levels are greatly elevated immediately after long-duration ventricular fibrillation (VF), defibrillation, and reperfusion and that the short-acting beta-antagonist esmolol administered at reperfusion would protect against this catecholamine surge and improve survival.
In part 1 of this study, catecholamines from myocardial interstitial fluid (ISF) and aortic and coronary sinus plasma were quantified by use of 3H-labeled radioenzymatic assay in 8 open-chest, anesthetized pigs. Eight minutes of electrically induced VF was followed by internal defibrillation and reperfusion. By 4 minutes of VF, ISF norepinephrine increased significantly, from 1.3+/-0.3 to 7.4+/-2.4 ng/mL. Epinephrine increased significantly, from 0.4+/-0.2 to 1.5+/-0.7 ng/mL. ISF norepinephrine and epinephrine peaked at 219.2+/-92.1 and 63.7+/-25.1 ng/mL after defibrillation and reperfusion and decreased significantly to 12.2+/-3.5 and 6.7+/-3.1 ng/mL 23 minutes after defibrillation. Transcardiac catecholamine changes were similar. In part 2, 8 minutes of VF was followed by external defibrillation in anesthetized, closed-chest pigs. Animals received 1.0 mg/kg esmolol (n=8) or saline (n=8) intravenously at the start of cardiopulmonary resuscitation (CPR). Advanced cardiac life support, including CPR and epinephrine, was delivered to both groups. Esmolol before reperfusion improved return of spontaneous circulation and 4-hour survival (7/8 versus 3/8 survivors, chi2 P<0.05).
Transcardiac and ISF norepinephrine and epinephrine levels are briefly massively elevated after 8 minutes of VF, defibrillation, and reperfusion. A short-acting beta-antagonist administered immediately after defibrillation improves return of spontaneous circulation and 4-hour survival after this prolonged VF.
高浓度儿茶酚胺对心肌细胞具有细胞毒性。我们推测,在长时间室颤(VF)、除颤及再灌注后即刻,心肌间质儿茶酚胺水平会大幅升高,且在再灌注时给予短效β受体阻滞剂艾司洛尔可预防这种儿茶酚胺激增并提高生存率。
在本研究的第1部分,通过使用³H标记的放射酶分析法,对8只开胸麻醉猪的心肌间质液(ISF)、主动脉和冠状窦血浆中的儿茶酚胺进行定量分析。进行8分钟的电诱导VF,随后进行体内除颤和再灌注。VF持续4分钟时,ISF去甲肾上腺素显著增加,从1.3±0.3 ng/mL增至7.4±2.4 ng/mL。肾上腺素也显著增加,从0.4±0.2 ng/mL增至1.5±0.7 ng/mL。除颤和再灌注后,ISF去甲肾上腺素和肾上腺素分别达到峰值219.2±92.1 ng/mL和63.7±25.1 ng/mL,并在除颤后23分钟显著降至12.2±3.5 ng/mL和6.7±3.1 ng/mL。经心脏的儿茶酚胺变化相似。在第2部分,对麻醉的闭胸猪进行8分钟VF后进行体外除颤。在心肺复苏(CPR)开始时,动物静脉注射1.0 mg/kg艾司洛尔(n = 8)或生理盐水(n = 8)。两组均给予包括CPR和肾上腺素在内的高级心脏生命支持。再灌注前给予艾司洛尔可提高自主循环恢复率和4小时生存率(存活者7/8 vs 3/8,χ² P<0.05)。
在8分钟VF、除颤及再灌注后,经心脏和ISF的去甲肾上腺素和肾上腺素水平会短暂大幅升高。除颤后立即给予短效β受体阻滞剂可改善这种长时间VF后的自主循环恢复率和4小时生存率。