首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Mechanisms underlying the antiarrhythmic properties of beta-adrenoceptor blockade against ischaemia-induced arrhythmias in acutely prepared rats.
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Mechanisms underlying the antiarrhythmic properties of beta-adrenoceptor blockade against ischaemia-induced arrhythmias in acutely prepared rats.

机译:β-肾上腺素受体阻滞剂抗缺血性心律失常的机制在急性准备的大鼠中。

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摘要

1. The mechanism underlying the limited antiarrhythmic effects of beta-adrenoceptor blocking agents against occlusion-induced arrhythmias in acutely prepared, pentobarbitone-anaesthetized rats has been investigated. 2. Atenolol, ICI 111,581 and propranolol were given at low, medium and high doses calculated to shift dose-response curves to exogenous agonists by factors of 10-30, 100-300 and 1000-3000, respectively. 3. Arrhythmias, blood pressure, heart rate, ECG changes and serum K+ were measured. 4. Antiarrhythmic activity was seen with beta-blocker treatment. This was minimal with atenolol (0.1, 1 and 10 mg kg-1) and only statistically significant with the highest dose of ICI 111,581 (5 mg kg-1), and propranolol (10 mg kg-1). 5. Treatment with beta-adrenoceptor blockers elevated serum potassium concentrations, as compared with saline controls, especially when measured at 30 min post-occlusion. 6. Only ICI 111,581 (5 mg kg-1) and propranolol (1 and 10 mg kg-1) prolonged P-R interval. 7. In order to evaluate possible mechanisms of antiarrhythmic action, attempts were made to correlate antiarrhythmic activity with beta-blockade, serum potassium concentrations, and/or with changes in the P-R interval of the ECG. 8. Reductions in arrhythmias did not correlate well with presumed beta-blockade. Better correlation was obtained with elevations of serum potassium concentration, and with prolongation of P-R interval (a presumed Class I antiarrhythmic action). 9. These results suggested that antiarrhythmic effects of adrenoceptor blocking agents in acutely-prepared anaesthetized rats, subjected to occlusion of a coronary artery, are unrelated to cardiac beta-blockade. The limited antiarrhythmic effects which were observed could be attributed to elevations in serum potassium concentration (due to peripheral beta-blockade) and/or possible Class I antiarrhythmic actions.
机译:1.研究了β-肾上腺素受体阻断剂在急性准备,戊巴比妥麻醉的大鼠中对阻塞性心律失常产生有限抗心律失常作用的机制。 2.分别以低,中和高剂量给予阿替洛尔,ICI 111,581和普萘洛尔,以将剂量-反应曲线分别转移到外源激动剂上分别为10-30、100-300和1000-3000倍。 3.测量心律不齐,血压,心率,ECG变化和血清K +。 4.用β-受体阻滞剂治疗可观察到抗心律失常活性。使用阿替洛尔(0.1、1和10 mg kg-1)的情况极少,只有最高剂量的ICI 111,581(5 mg kg-1)和普萘洛尔(10 mg kg-1)具有统计学意义。 5.与盐水对照组相比,用β-肾上腺素受体阻滞剂治疗可提高血清钾浓度,尤其是在闭塞后30分钟进行测量时。 6.只有ICI 111,581(5 mg kg-1)和普萘洛尔(1和10 mg kg-1)延长了P-R间隔。 7.为了评估抗心律不齐作用的可能机制,已尝试将抗心律不齐活性与β-受体阻滞剂,血清钾浓度和/或ECG的P-R间隔变化相关联。 8.心律失常的减少与推测的β-受体阻滞没有很好的相关性。与血清钾浓度升高和P-R间隔延长(推测的I类抗心律失常作用)相关性更好。 9.这些结果表明,肾上腺素受体阻滞剂在急性制备的麻醉大鼠中的冠状动脉闭塞的抗心律失常作用与心脏β阻滞无关。观察到的有限的抗心律失常作用可能归因于血清钾浓度升高(由于外周β阻滞)和/或可能的I类抗心律失常作用。

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