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本文引用的文献

1
THE EFFECT OF DESLANOSIDE ON THE DURATION OF THE PHASES OF VENTRICULAR SYSTOLE IN MAN.去乙酰毛花苷对人体心室收缩各期时长的影响。
Am J Cardiol. 1965 Feb;15:153-61. doi: 10.1016/0002-9149(65)90449-2.
2
Comparative pharmacokinetics and pharmacodynamics of cardiac glycosides.强心苷的比较药代动力学和药效学
Br J Clin Pharmacol. 1980 Aug;10(2):135-43. doi: 10.1111/j.1365-2125.1980.tb01730.x.
3
Systolic time interval v heart rate regression equations using atropine: reproducibility studies.使用阿托品的收缩期时间间期与心率回归方程:可重复性研究
Br J Clin Pharmacol. 1981 Jul;12(1):15-20. doi: 10.1111/j.1365-2125.1981.tb01849.x.
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Haemodynamic effects of prenalterol in patients with coronary heart disease.普瑞特罗对冠心病患者的血流动力学影响。
Br Heart J. 1980 Feb;43(2):134-7. doi: 10.1136/hrt.43.2.134.
5
Effect of beta adrenergic blockade on the hemodynamic responses to epinephrine in man.β-肾上腺素能阻滞对人体肾上腺素血流动力学反应的影响。
Am J Cardiol. 1966 Apr;17(4):484-92. doi: 10.1016/0002-9149(66)90238-4.
6
Shortening of electromechanical systole as a manifestation of excessive adrenergic stimulation in acute myocardial infarction.机电收缩期缩短作为急性心肌梗死中肾上腺素能过度刺激的一种表现。
Circulation. 1972 Nov;46(5):856-62. doi: 10.1161/01.cir.46.5.856.
7
Problems in echocardiographic volume determinations: echocardiographic-angiographic correlations in the presence of absence of asynergy.超声心动图容积测定中的问题:存在或不存在心肌运动不协调时超声心动图与血管造影的相关性
Am J Cardiol. 1976 Jan;37(1):7-11. doi: 10.1016/0002-9149(76)90491-4.
8
Cardiovascular effects of a new inotropic agent, U. K. 14275, in patients with coronary heart disease.新型正性肌力药物UK 14275对冠心病患者的心血管效应
Br J Clin Pharmacol. 1977 Oct;4(5):513-7. doi: 10.1111/j.1365-2125.1977.tb00778.x.
9
Comparative pharmacodynamics of betamethyl digoxin and digoxin in man.β-甲基地高辛与人用地高辛的比较药效学
Clin Pharmacol Ther. 1977 Sep;22(3):280-5. doi: 10.1002/cpt1977223280.
10
Measurement of systolic time intervals.收缩期时间间期的测量。
Br J Clin Pharmacol. 1978 Dec;6(6):549-50. doi: 10.1111/j.1365-2125.1978.tb00886.x.

新型口服活性正性肌力药物BM 10.188对健康志愿者的血流动力学影响。

Haemodynamic effects of BM 10.188, a new orally active inotropic agent, in healthy volunteers.

作者信息

Whiting B, Kelman A W, Sumner D J, Hillis W S, Ledermann H

出版信息

Br J Clin Pharmacol. 1982 Apr;13(4):529-32. doi: 10.1111/j.1365-2125.1982.tb01416.x.

DOI:10.1111/j.1365-2125.1982.tb01416.x
PMID:7066168
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1402041/
Abstract

1 BM 10.188 (Doxaminol, Boehringer Mannheim, GmbH) is a recently developed beta-sympathomimetic agent which has shown promising positive inotropic activity in experimental animal models. It is a dibenzoxepine derivative. 2 The effects of 20 mg oral BM 10.188 on systolic time intervals and standard echocardiographic parameters have been studied in six normal healthy male volunteers. 3 When assessed by repeated measured analysis of variance, QS2 and LVET shortened significantly (P less than 0.005) in the 8 h period following BM 10.188. Mean maximum shortening values were: QS2, 25.7 +/- 25.6 (s.d.) ms at 155 min and LVET, 10.7 +/- 9.5 (s.d.) ms at 155 min. There was a corresponding small but significant increase of 4.2 +/- 3.9 (s.d.) ml in stroke volume at 6 h (P less than 0.025). 4 These results indicate that in normal volunteers, BM 10.188 exhibits effects on noninvasive cardiological indices similar to those observed after cardiac glycosides.

摘要
  1. BM 10.188(多沙米诺,德国宝灵曼有限公司)是一种最近研发的β-拟交感神经药,在实验动物模型中已显示出有前景的正性肌力活性。它是一种二苯并氧杂卓衍生物。2. 已在6名正常健康男性志愿者中研究了口服20毫克BM 10.188对收缩期时间间期和标准超声心动图参数的影响。3. 通过重复测量方差分析评估时,在给予BM 10.188后的8小时内,QS2和LVET显著缩短(P小于0.005)。平均最大缩短值为:QS2在155分钟时为25.7±25.6(标准差)毫秒,LVET在155分钟时为10.7±9.5(标准差)毫秒。在6小时时,每搏输出量相应地有小但显著的增加,增加了4.2±3.9(标准差)毫升(P小于0.025)。4. 这些结果表明,在正常志愿者中,BM 10.188对无创心脏指标的影响与强心苷后观察到的影响相似。