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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.

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。

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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.
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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.

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