Aupetit J F, Frassati D, Bui-Xuan B, Freysz M, Faucon G, Timour Q
Department of Cardiology, St. Joseph-St. Luc Hospital, Lyon, France.
Cardiovasc Res. 1998 Mar;37(3):646-55. doi: 10.1016/s0008-6363(97)00304-0.
To investigate the prevention of ventricular fibrillation with a beta-adrenergic receptor (beta-AR) antagonist in anaesthetized, open-chest pigs in a model of ischaemia, intended to reproduce what happens either in anginal attack or in the first hour of infarction.
Ventricular fibrillation threshold (VFT) was determined with trains of diastolic stimuli of 100 ms duration delivered by a subepicardial electrode inserted in the area subjected to ischaemia. Ischaemia was obtained by the complete occlusion of the left anterior descending coronary artery, either near its origin during brief but increasing periods (30, 60, 90, 120, 150, 180, 240, 300 s), or half-way from its origin for a much longer time (more than 60 min).
During transient proximal occlusion and isoprenaline infusion (0.25 microgram/kg/min), propranolol (50 micrograms/kg plus 2 micrograms/kg/min) attenuated both tachycardia and the fall in VFT to 0 mA. The shortening of MAP duration accompanying depolarization of the fibres was concurrently slowed down, and time to fibrillation prolonged (122 +/- 15 to 262 +/- 14 s, p < 0.001). In the absence of isoprenaline infusion, propranolol exerted similar effects, but to a lesser degree, in proportion to heart rate dependent on sympathetic activity. In contrast, it became unable to raise VFT before and during ischaemia, when heart rate was kept constant by pacing. After persistent midportion occlusion, significant differences in VFT were found only at the 5th min, depending on whether heart rate was accelerated by isoprenaline (0.8 +/- 0.2 mA), left normal (1.8 +/- 0.3 mA) or slowed down by propranolol (1.6 +/- 0.3 mA). Later on, especially after 15 and 25 min of ischaemia, VFT, which was below 1.0 mA, did not appear to be influenced by the activation or blockade of beta-ARs: spontaneous fibrillations were observed in the same number in this period with or without the administration of propranolol. Beyond 30 min after occlusion, the rise in VFT, subsequent to the first irreversible cell damage, also occurred in the same way.
The prevention of ischaemic ventricular fibrillation by a beta-AR antagonist, judged from VFT, is easily checked experimentally when ischaemia is only transitory, especially if sympathetic activity is high. The maintenance of VFT at a relatively high level is essentially related to the depressant effect on the sinus rate. The same animal model does not give support to an effective protection in the first hour of infarction. However, the control of heart rate may also be beneficial in these circumstances by attenuating systemic haemodynamic disorders.
在麻醉开胸猪的缺血模型中研究β-肾上腺素能受体(β-AR)拮抗剂对心室颤动的预防作用,该模型旨在重现心绞痛发作或梗死最初1小时内发生的情况。
通过插入缺血区域的心外膜下电极给予持续100毫秒的舒张期刺激 trains 来测定心室颤动阈值(VFT)。通过完全阻断左前降支冠状动脉来诱导缺血,在其起始处附近进行短暂但逐渐延长的时段(30、60、90、120、150、180、240、300秒),或在距其起始处一半距离处进行更长时间(超过60分钟)的阻断。
在短暂近端阻断和输注异丙肾上腺素(0.25微克/千克/分钟)期间,普萘洛尔(50微克/千克加2微克/千克/分钟)减轻了心动过速以及VFT降至0毫安的情况。伴随纤维去极化的平均动脉压持续时间缩短同时减缓,颤动时间延长(从122±15秒至262±14秒,p<0.001)。在未输注异丙肾上腺素时,普萘洛尔发挥了类似作用,但程度较小,与依赖交感神经活动的心率成比例。相比之下,当通过起搏使心率保持恒定时,在缺血前和缺血期间它无法提高VFT。在持续中段阻断后,仅在第5分钟发现VFT存在显著差异,这取决于心率是被异丙肾上腺素加速(0.8±0.2毫安)、保持正常(1.8±0.3毫安)还是被普萘洛尔减慢(1.6±0.3毫安)。之后,特别是在缺血15和25分钟后,低于1.0毫安的VFT似乎不受β-ARs激活或阻断的影响:在此期间,无论是否给予普萘洛尔,观察到的自发性颤动数量相同。阻断后30分钟以上,在首次不可逆细胞损伤后VFT的升高也以相同方式发生。
从VFT判断,当缺血只是短暂性时,尤其是交感神经活动较高时,通过实验很容易检测到β-AR拮抗剂对缺血性心室颤动的预防作用。将VFT维持在相对较高水平主要与对窦性心率的抑制作用有关。同一动物模型不支持在梗死最初1小时内有有效保护作用。然而,在这些情况下控制心率也可能通过减轻全身血流动力学紊乱而有益。