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塞利洛尔:清醒犬体内一种具有正性肌力作用的β肾上腺素能受体阻滞剂。

Celiprolol: a positive inotropic beta-adrenoceptor blocking agent in conscious dogs.

作者信息

Nganele D M, DeLeonardis V M, Hintze T H

机构信息

Department of Physiology, New York Medical College, Valhalla 10595.

出版信息

Br J Pharmacol. 1988 Mar;93(3):501-8. doi: 10.1111/j.1476-5381.1988.tb10304.x.

Abstract
  1. beta-Adrenoceptor blocking agents are used to manage various cardiovascular disorders. A limiting factor in their use is the suppression of the cardiac contractile state. In our study, we examined the cardiac effects of celiprolol, a new beta-adrenoceptor blocking agent with reported positive inotropic effects. 2. Dogs were instrumented by use of sterile surgical techniques for the study of myocardial inotropic state, heart rate and internal left ventricular dimensions. Following complete recovery from surgery, experiments were conducted in the conscious state. 3. Intravenous injection of celiprolol (3 mg kg-1) in nine dogs, increased LV dP/dt by 13 +/- 2.6%, velocity of shortening (LV dD/dt) by 9.2 +/- 3.4%, and heart rate by 19 +/- 4.6% and decreased LV end-diastolic diameter by 1.8 +/- 0.8%, all significantly (P less than 0.05). Celiprolol blocked the inotropic actions of isoprenaline (0.5 micrograms kg-1) but only partially reduced its hypotensive effects. Propranolol, in contrast, reduced LV dP/dt by 17 +/- 3.3% and heart rate by 8.1 +/- 2.7% (P less than 0.05) while totally abolishing the hypotension, tachycardia and increase in LV dP/dt caused by isoprenaline. Following beta-adrenoceptor blockade with propranolol and with heart rate held constant by electrical pacing, celiprolol increased LV dP/dt by 16 +/- 4.0%, LV dD/dt by 12 +/- 3.0% and reduced LV end-diastolic diameter by 3.5 +/- 0.5% (P less than 0.05). 4. Thus, in conscious dogs, celiprolol increases inotropic state and reduces preload independently of beta 1-adrenoceptor mechanisms and the Bowditch phenomenon, while effectively blocking beta 1-receptors in the heart. These properties would make celiprolol useful in patients where a conventional beta-adrenoceptor blocking agent might lead to pump failure.
摘要
  1. β-肾上腺素受体阻滞剂用于治疗各种心血管疾病。其使用的一个限制因素是抑制心脏收缩状态。在我们的研究中,我们检测了塞利洛尔(一种新的据报道具有正性肌力作用的β-肾上腺素受体阻滞剂)对心脏的影响。2. 采用无菌手术技术对犬进行仪器植入,以研究心肌收缩状态、心率和左心室内径。手术完全恢复后,在清醒状态下进行实验。3. 对9只犬静脉注射塞利洛尔(3mg/kg),左室dp/dt增加13±2.6%,缩短速度(左室dD/dt)增加9.2±3.4%,心率增加19±4.6%,左室舒张末期直径减小1.8±0.8%,所有这些均具有显著性差异(P<0.05)。塞利洛尔阻断了异丙肾上腺素(0.5μg/kg)的正性肌力作用,但仅部分降低了其降压作用。相比之下,普萘洛尔使左室dp/dt降低17±3.3%,心率降低8.1±2.7%(P<0.05),同时完全消除了异丙肾上腺素引起的低血压、心动过速和左室dp/dt增加。在用普萘洛尔进行β-肾上腺素受体阻断且通过电起搏使心率保持恒定后,塞利洛尔使左室dp/dt增加16±4.0%,左室dD/dt增加12±3.0%,左室舒张末期直径减小3.5±0.5%(P<0.05)。4. 因此,在清醒犬中,塞利洛尔可增加心肌收缩状态并独立于β1-肾上腺素受体机制和鲍迪奇现象降低前负荷,同时有效阻断心脏中的β1-受体。这些特性将使塞利洛尔对传统β-肾上腺素受体阻滞剂可能导致泵衰竭的患者有用。

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CARDIAC METABOLISM.心脏代谢
Physiol Rev. 1965 Apr;45:171-213. doi: 10.1152/physrev.1965.45.2.171.

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