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卡托普利和纳洛酮对健康志愿者瓦尔萨尔瓦动作及收缩期时间间期的影响。

The influence of captopril and naloxone on the Valsalva manoeuvre and systolic time intervals in healthy volunteers.

作者信息

Richter J P, Sommers D K, Snyman J R

机构信息

Department of Pharmacology, University of Pretoria, Republic of South Africa.

出版信息

Clin Exp Pharmacol Physiol. 1994 Apr;21(4):301-5. doi: 10.1111/j.1440-1681.1994.tb02516.x.

Abstract
  1. The aim of the study was to ascertain whether the inhibition of the sympathetic nervous system by angiotensin-converting enzyme (ACE) inhibitors is mediated by endogenous opioids. Naloxone was used to evaluate the effects of the latter on systolic time intervals (STI) and Valsalva manoeuvre-induced blood pressure and heart rate changes. 2. Baseline recordings were done in 12 healthy male volunteers and repeated 2 h after oral administration of 75 mg of captopril and again after naloxone 0.4 mg/kg was administered intravenously over 10 min. 3. After captopril there was a significant reduction in systolic (P < 0.02) and mean blood pressure (P < 0.04) without any changes in heart rate. Furthermore, captopril increased the Valsalva ratio (P < 0.06) but did not influence inotropism as indicated by STI. Naloxone did not influence any of these findings. 4. The changes in the Valsalva ratio after captopril were mediated by an increase in the maximum bradycardia in nine of the 12 subjects. 5. The results indicate that endogenous opioids do not play a role in the putative sympatholytic effect of ACE inhibition.
摘要
  1. 本研究的目的是确定血管紧张素转换酶(ACE)抑制剂对交感神经系统的抑制作用是否由内源性阿片类物质介导。使用纳洛酮来评估后者对收缩期时间间期(STI)以及瓦尔萨尔瓦动作引起的血压和心率变化的影响。2. 对12名健康男性志愿者进行基线记录,并在口服75毫克卡托普利2小时后重复记录,在静脉注射0.4毫克/千克纳洛酮10分钟后再次记录。3. 服用卡托普利后,收缩压(P < 0.02)和平均血压(P < 0.04)显著降低,心率无任何变化。此外,卡托普利增加了瓦尔萨尔瓦比值(P < 0.06),但如STI所示,对心肌收缩力没有影响。纳洛酮对这些结果均无影响。4. 卡托普利后瓦尔萨尔瓦比值的变化是由12名受试者中9人的最大心动过缓增加介导的。5. 结果表明,内源性阿片类物质在ACE抑制假定的交感神经抑制作用中不起作用。

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