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西拉普利抑制ACE对人体内脏和全身血流动力学的影响。

Effects of ACE inhibition with cilazapril on splanchnic and systemic haemodynamics in man.

作者信息

Gasic S, Heinz G, Kleinbloesem C, Korn A

机构信息

Medizinische Universitätsklinik, Division of Clinical Pharmacology, Wien, Austria.

出版信息

Br J Clin Pharmacol. 1989;27 Suppl 2(Suppl 2):225S-234S. doi: 10.1111/j.1365-2125.1989.tb03486.x.

Abstract
  1. There is recent experimental evidence that the renin-angiotensin-system may play an essential role in producing splanchnic vasoconstriction. However, controversy exists as to the influence of ACE inhibition on splanchnic haemodynamics in man. We therefore investigated whether cilazapril, a structurally new and long-acting ACE inhibitor, interacts with angiotensin I-dependent changes in splanchnic haemodynamics in man, using an experimental model. 2. The effects of cilazapril on angiotensin I-induced splanchnic and systemic haemodynamics were studied in seven normotensive men using the hepatic venous catheter technique (indocyanine-green dye), right-heart catheterisation (thermodilution method), intra-arterial blood pressure monitoring and systolic time-intervals. Dose-responses to angiotensin I were determined under control conditions and 60 min after ACE inhibition with 5 mg oral cilazapril. Angiotensin I was infused intravenously at constant rates in an increasing dose-sequence until systolic blood pressure was greater than 30 mm Hg. 3. ACE inhibition with cilazapril did not change basal splanchnic or systemic haemodynamics to any relevant extent. The angiotensin I dependent increase in systemic and pulmonary resistance and pulmonary capillary wedge pressure was attenuated by cilazapril, as indicated by the shift of the dose-response curves to the right. In the splanchnic vascular bed angiotensin I dose-dependently increased splanchnic vascular resistance and also wedge hepatic venous pressure and decreased splanchnic blood flow. These angiotensin I induced haemodynamic changes were clearly suppressed by cilazapril. The angiotensin I dose needed to produce a 30% increase in splanchnic vascular resistance, given as mean and s.e. mean, was 1.7 +/- 0.3 micrograms min-1 during control-trials vs 7.3 +/- 1.3 micrograms min-1 after ACE inhibition with cilazapril (P less than 0.001). 4. We conclude that, in man, the influence of cilazapril on acute angiotensin I-mediated haemodynamic responses is present in the splanchnic vascular bed, and that the overall effects of cilazapril are consistent with both arterial and venous effects of the ACE inhibitor. Cilazapril effectively counteracts angiotensin I-induced splanchnic vasoconstriction.
摘要
  1. 最近有实验证据表明,肾素-血管紧张素系统可能在产生内脏血管收缩中起重要作用。然而,关于ACE抑制对人体内脏血流动力学的影响仍存在争议。因此,我们使用实验模型研究了结构新颖的长效ACE抑制剂西拉普利是否会与人体内脏血流动力学中依赖血管紧张素I的变化相互作用。2. 采用肝静脉导管技术(吲哚菁绿染料)、右心导管插入术(热稀释法)、动脉内血压监测和收缩期时间间期,在7名血压正常的男性中研究了西拉普利对血管紧张素I诱导的内脏和全身血流动力学的影响。在对照条件下以及口服5mg西拉普利抑制ACE 60分钟后,测定对血管紧张素I的剂量反应。以递增的剂量序列静脉恒速输注血管紧张素I,直至收缩压大于30mmHg。3. 西拉普利抑制ACE并没有在任何相关程度上改变基础内脏或全身血流动力学。如剂量反应曲线右移所示,西拉普利减弱了血管紧张素I依赖性的全身和肺血管阻力以及肺毛细血管楔压的增加。在内脏血管床,血管紧张素I剂量依赖性地增加内脏血管阻力以及肝静脉楔压,并减少内脏血流量。这些血管紧张素I诱导的血流动力学变化被西拉普利明显抑制。在对照试验期间,使内脏血管阻力增加30%所需的血管紧张素I剂量,以平均值和标准误表示,为1.7±0.3μg·min⁻¹,而在用西拉普利抑制ACE后为7.3±1.3μg·min⁻¹(P<0.001)。4. 我们得出结论,在人体中,西拉普利对急性血管紧张素I介导的血流动力学反应的影响存在于内脏血管床,并且西拉普利的总体作用与ACE抑制剂的动脉和静脉作用均一致。西拉普利有效地抵消了血管紧张素I诱导的内脏血管收缩。

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本文引用的文献

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THE ESTIMATION OF HEPATIC BLOOD FLOW IN MAN.人体肝血流量的估计
J Clin Invest. 1945 Nov;24(6):890-7. doi: 10.1172/JCI101676.

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