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对硝酸异山梨酯耐受的缺血性心肌病患者对吗多明的血流动力学反应。

Hemodynamic response to molsidomine in patients with ischemic cardiomyopathy tolerant to isosorbide dinitrate.

作者信息

Unger P, Leone A, Staroukine M, Degré S, Berkenboom G

机构信息

Department of Cardiology, Erasme Hospital, Brussels, Belgium.

出版信息

J Cardiovasc Pharmacol. 1991 Dec;18(6):888-94. doi: 10.1097/00005344-199112000-00016.

DOI:10.1097/00005344-199112000-00016
PMID:1725903
Abstract

Unlike nitrates, molsidomine is able to relax vascular smooth muscle without depending on the availability of sulfhydryl groups. To assess the clinical relevance of this property, the hemodynamic effects of a 24-h i.v. infusion of molsidomine were studied in 14 patients with ischemic cardiomyopathy rendered tolerant to i.v. isosorbide dinitrate. In order to determine the role of neurohormonal activation, six of these patients were studied in the presence of an angiotensin-converting enzyme (ACE) inhibitor (enalapril, 5 mg, b.i.d.) (group 2). Six patients out of eight in group 1 (without ACE inhibition) and all patients in group 2 responded to molsidomine with a marked reduction of pulmonary artery wedge pressure (PAWP) (49% +/- 5 and 50% +/- 4 versus baseline value, respectively). However, the reduction of PAWP in group 1 was no longer significant at 12 h, and at 24 h the loss of the peak effect reached 67% +/- 7. On the contrary, PAWP remained persistently reduced in group 2 (loss of peak effect, 20% +/- 3 at 24 h, p less than 0.005). In addition, a significant decrease in hematocrit and increase in epinephrine occurred in group 1 but not in group 2. These results suggest that both the absence of dependence on sulfhydryl groups and the blockade of neurohormonal reactions are needed to avoid nitrate tolerance.

摘要

与硝酸盐不同,吗多明能够松弛血管平滑肌,而不依赖于巯基的可用性。为了评估这一特性的临床相关性,对14例对静脉注射硝酸异山梨酯产生耐受性的缺血性心肌病患者进行了为期24小时的静脉输注吗多明的血流动力学效应研究。为了确定神经激素激活的作用,其中6例患者在血管紧张素转换酶(ACE)抑制剂(依那普利,5毫克,每日两次)存在的情况下进行了研究(第2组)。第1组(无ACE抑制)的8例患者中有6例和第2组的所有患者对吗多明的反应是肺动脉楔压(PAWP)显著降低(分别为49%±5和50%±4,与基线值相比)。然而,第1组PAWP的降低在12小时时不再显著,在24小时时峰值效应的丧失达到67%±7。相反,第2组的PAWP持续降低(24小时时峰值效应的丧失为20%±3,p<0.005)。此外,第1组出现了血细胞比容显著降低和肾上腺素升高,而第2组没有。这些结果表明,既不依赖巯基又阻断神经激素反应对于避免硝酸盐耐受性都是必要的。

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1
Hemodynamic response to molsidomine in patients with ischemic cardiomyopathy tolerant to isosorbide dinitrate.对硝酸异山梨酯耐受的缺血性心肌病患者对吗多明的血流动力学反应。
J Cardiovasc Pharmacol. 1991 Dec;18(6):888-94. doi: 10.1097/00005344-199112000-00016.
2
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The influence of isosorbide dinitrate and molsidomine on migration of polymorphonuclear neutrophils in vivo.
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Pharm Res. 1999 May;16(5):633-6. doi: 10.1023/a:1018804003745.
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Clinical pharmacokinetics of vasodilators. Part II.血管扩张剂的临床药代动力学。第二部分。
Clin Pharmacokinet. 1998 Jul;35(1):9-36. doi: 10.2165/00003088-199835010-00002.
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Clinical pharmacokinetics of molsidomine.莫西多明的临床药代动力学
Clin Pharmacokinet. 1996 May;30(5):372-84. doi: 10.2165/00003088-199630050-00004.
4
Nitrates in congestive heart failure.充血性心力衰竭中的硝酸盐
Cardiovasc Drugs Ther. 1994 Jun;8(3):501-7. doi: 10.1007/BF00877928.
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Eur J Clin Pharmacol. 1992;43(3):273-6. doi: 10.1007/BF02333022.