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多巴胺1受体激动剂静脉注射非诺多泮在高血压患者中的药代动力学和药效学特性。

Pharmacokinetic and pharmacodynamic properties of intravenous fenoldopam, a dopamine1-receptor agonist, in hypertensive patients.

作者信息

Weber R R, McCoy C E, Ziemniak J A, Frederickson E D, Goldberg L I, Murphy M B

机构信息

Department of Pharmacological and Physiological Science, University of Chicago, Illinois 60637.

出版信息

Br J Clin Pharmacol. 1988 Jan;25(1):17-21. doi: 10.1111/j.1365-2125.1988.tb03276.x.

Abstract

1 The pharmacokinetic properties of intravenous fenoldopam, a selective dopamine1-receptor agonist, were studied in 10 patients with essential hypertension. 2 Reduction in blood pressure was linearly related to the log fenoldopam plasma concentration (r = 0.69) and the log fenoldopam infusion rate (r = 0.71). 3 The mean elimination half-life (+/- s. e. mean) was 9.8 +/- 1.0 min. The total body clearance was 30.3 +/- 2.3 ml kg-1 min-1 and the volume of distribution was 582 +/- 62 ml kg-1. 4 The rapid onset of action, short elimination half-life, linear dose-response relationship, and ease of administration suggest that fenoldopam may have a role where parenteral treatment of hypertension is required.

摘要
  1. 在10例原发性高血压患者中研究了静脉注射选择性多巴胺1受体激动剂非诺多泮的药代动力学特性。2. 血压降低与非诺多泮血浆浓度的对数呈线性相关(r = 0.69),与非诺多泮输注速率的对数也呈线性相关(r = 0.71)。3. 平均消除半衰期(±标准误)为9.8±1.0分钟。全身清除率为30.3±2.3 ml·kg⁻¹·min⁻¹,分布容积为582±62 ml·kg⁻¹。4. 起效迅速、消除半衰期短、剂量反应关系呈线性以及易于给药表明,在需要胃肠外治疗高血压的情况下,非诺多泮可能有一定作用。

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