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普瑞纳洛尔:是部分β1肾上腺素能受体激动剂还是具有内在活性的β受体阻滞剂?

Prenalterol: a partial beta 1-adrenoceptor agonist or a beta-blocker with intrinsic activity?

作者信息

Wirtzfeld A, Klein G, Bibra H V, Sauer E

出版信息

Int J Clin Pharmacol Ther Toxicol. 1985 Jan;23(1):20-7.

PMID:2859252
Abstract

Hemodynamic studies have demonstrated a significantly reduced beta 1-adrenoceptor stimulating effect of prenalterol compared to dobutamine suggesting a partial agonism on the receptor. In order to prove this hypothesis we administered 80 micrograms/kg of prenalterol within 5 minutes in 8 healthy volunteers during a continuous infusion of dobutamine (15 micrograms/kg/min). In addition to heart rate, blood pressure and the double product, the systolic time intervals QS2I, PEP and LVET and the echocardiographically determined parameters FS and Vcf were measured for evaluation of ventrical function. The injection of prenalterol caused a distinct attenuation of the cardiostimulating effects of dobutamine: there was a prompt fall in heart rate and systolic blood pressure and a typical negative inotropic effect on the parameters of left ventricular function. In the experimental conditions selected, the effects of prenalterol were those of a beta-sympatholoytic agent. Prenalterol should therefore be classified as a partial beta 1-adrenoceptor agonist or as a beta-blocking agent with pronounced intrinsic sympathomimetic activity. The beta 1-stimulating potency of prenalterol amounts to about 60% of a full agonist.

摘要

血流动力学研究表明,与多巴酚丁胺相比,普瑞特罗对β1-肾上腺素能受体的刺激作用显著降低,提示其对该受体具有部分激动作用。为了验证这一假设,我们在8名健康志愿者持续输注多巴酚丁胺(15微克/千克/分钟)的过程中,于5分钟内给予他们80微克/千克的普瑞特罗。除了心率、血压和双乘积外,还测量了收缩期时间间期QS2I、PEP和LVET以及超声心动图测定的参数FS和Vcf,以评估心室功能。注射普瑞特罗导致多巴酚丁胺的心脏刺激作用明显减弱:心率和收缩压迅速下降,对左心室功能参数产生典型的负性肌力作用。在所选的实验条件下,普瑞特罗的作用与β-交感神经阻滞剂的作用相同。因此,普瑞特罗应归类为部分β1-肾上腺素能受体激动剂或具有明显内在拟交感活性的β-阻滞剂。普瑞特罗的β1刺激效力约为完全激动剂的60%。

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