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醋丁洛尔及其代谢产物双醋洛尔与美托洛尔和普萘洛尔在正常人体内的β-肾上腺素受体选择性比较。

Comparison of beta-adrenoceptor selectivity of acebutolol and its metabolite diacetolol with metoprolol and propranolol in normal man.

作者信息

Thomas M S, Tattersfield A E

出版信息

Eur J Clin Pharmacol. 1986;29(6):679-83. doi: 10.1007/BF00615958.

Abstract

The beta-adrenergic selectivity of diacetolol, the major metabolite of acebutolol, has been compared with that of acebutolol, metoprolol and propranolol in 11 normal subjects. Bronchial and cardiac beta-adrenoceptor blockade were assessed on separate occasions after diacetolol 600 mg, acebutolol 400 mg, metoprolol 200 mg, propranolol 80 mg and placebo. Bronchial beta-adrenoceptor blockade was assessed as the displacement of the bronchodilator dose response curve to inhaled isoprenaline after each beta blocking drug compared to placebo and expressed as the dose ratio. Bronchodilatation was measured as change in specific airway conductance (sGaw) in the body plethysmograph. Cardiac beta-adrenoceptor blockade was assessed as the percentage reduction in exercise heart rate during the 5th minute of exercise at 70% of the subject's maximum work rate. There was a significant reduction in exercise heart rate with all 4 beta-blocking drugs when compared with placebo, 22% for diacetolol, 24% for acebutolol, 25% for propranolol and 28% for metoprolol. The reduction with metoprolol was significantly greater than the reduction with the other three beta-adrenoceptor antagonists. Mean dose ratios for the airway isoprenaline dose response curves after each of the 4 beta-blocking drugs were 2.4 for diacetolol, 2.7 for metoprolol, 8 for acebutolol and 72 for propranolol. The difference between diacetolol and metoprolol was not significant. Thus diacetolol appears to be more cardioselective than acebutolol and both are more cardioselective than propranolol in man. Metoprolol is probably more cardioselective than diacetolol though interpretation of the differences in exercise heart rate is complicated by the fact that diacetolol has some intrinsic sympathomimetic activity.

摘要

已在11名正常受试者中比较了醋丁洛尔的主要代谢产物双醋洛尔与醋丁洛尔、美托洛尔和普萘洛尔的β-肾上腺素能选择性。在服用600mg双醋洛尔、400mg醋丁洛尔、200mg美托洛尔、80mg普萘洛尔和安慰剂后,分别在不同时间评估支气管和心脏β-肾上腺素能受体阻滞情况。支气管β-肾上腺素能受体阻滞通过比较每种β受体阻滞剂给药后吸入异丙肾上腺素的支气管扩张剂剂量反应曲线与安慰剂的位移来评估,并表示为剂量比。支气管扩张以体容积描记仪中特定气道传导率(sGaw)的变化来测量。心脏β-肾上腺素能受体阻滞通过在受试者最大工作率的70%运动的第5分钟内运动心率的降低百分比来评估。与安慰剂相比,所有4种β受体阻滞剂的运动心率均显著降低,双醋洛尔降低22%,醋丁洛尔降低24%,普萘洛尔降低25%,美托洛尔降低28%。美托洛尔的降低幅度显著大于其他三种β-肾上腺素能拮抗剂。4种β受体阻滞剂给药后气道异丙肾上腺素剂量反应曲线的平均剂量比,双醋洛尔为2.4,美托洛尔为2.7,醋丁洛尔为8,普萘洛尔为72。双醋洛尔和美托洛尔之间的差异不显著。因此,在人体中,双醋洛尔似乎比醋丁洛尔更具心脏选择性,且两者都比普萘洛尔更具心脏选择性。美托洛尔可能比双醋洛尔更具心脏选择性,不过由于双醋洛尔具有一些内在拟交感活性,运动心率差异的解释较为复杂。

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