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酮色林对人体室性异位活动的影响。

The effects of ketanserin on ventricular ectopic activity in humans.

作者信息

Marks C, Dews I, Gould S E, Stephens J, VandenBurg M

机构信息

Department of Cardiology, Oldchurch Hospital, Romford, Essex, UK.

出版信息

Cardiovasc Drugs Ther. 1990 Jan;4 Suppl 1:93-5. doi: 10.1007/BF00053436.

DOI:10.1007/BF00053436
PMID:2285656
Abstract

Ketanserin is a serotonin S2-receptor antagonist that lowers blood pressure and inhibits platelet aggregation. Ketanserin treatment is also associated with prolongation of the corrected QT interval. The recently reported Prevention of Atherosclerotic Complications with Ketanserin (PACK) trial confirmed this prolongation of QT and also revealed a significant excess of deaths in patients receiving ketanserin together with potassium-losing diuretics. The investigators suggested that this excess of deaths may have been attributable to exacerbation of hypokalemia-induced ventricular arrhythmias by the repolarization-prolonging effect of ketanserin. However, drugs that prolong the QT interval may affect ventricular ectopic activity beneficially, and our study was designed to evaluate the effects of ketanserin on ventricular ectopic activity. Twenty patients (18 male, 2 female) aged 42-73 years were studied, each having at least 15 ventricular ectopic beats/hour. The study design was a double-blind, crossover comparison of ketanserin, 40 mg twice daily, and placebo, both given for 1 week. Ventricular ectopic activity was assessed by 48-hour Holter electrocardiogram (ECG) tapes at the end of each treatment period. Ketanserin treatment was associated with prolongation of repolarization, as reflected by the significant mean increases in both QT interval (+30 ms; p less than 0.001) and corrected QT interval (+20 ms; p less than 0.05). The mean overall degree of ventricular ectopic activity, as represented by a score based on the Lown classification, was significantly reduced (p less than 0.05). This was associated with a concordant improvement in the individual indices of ectopic activity. Our results show that ketanserin significantly suppressed ventricular ectopic activity in our normokalemic patients.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

酮色林是一种血清素S2受体拮抗剂,可降低血压并抑制血小板聚集。酮色林治疗还与校正QT间期延长有关。最近报道的酮色林预防动脉粥样硬化并发症(PACK)试验证实了QT间期的这种延长,并且还显示接受酮色林与排钾利尿剂联合治疗的患者死亡显著增多。研究人员认为,这种死亡过多可能归因于酮色林的复极延长作用加剧了低钾血症诱发的室性心律失常。然而,延长QT间期的药物可能对室性异位活动产生有益影响,我们的研究旨在评估酮色林对室性异位活动的影响。研究了20名年龄在42至73岁之间的患者(18名男性,2名女性),每人每小时至少有15次室性早搏。研究设计为双盲、交叉比较,每日两次给予40毫克酮色林和安慰剂,均给药1周。在每个治疗期结束时,通过48小时动态心电图(ECG)磁带评估室性异位活动。酮色林治疗与复极延长有关,QT间期(+30毫秒;p小于0.001)和校正QT间期(+20毫秒;p小于0.05)均显著平均增加即反映了这一点。以基于洛恩分类的评分表示的室性异位活动的平均总体程度显著降低(p小于0.05)。这与异位活动的各个指标的一致改善相关。我们的结果表明,酮色林在我们的正常血钾患者中显著抑制了室性异位活动。(摘要截短为250字)

相似文献

1
The effects of ketanserin on ventricular ectopic activity in humans.酮色林对人体室性异位活动的影响。
Cardiovasc Drugs Ther. 1990 Jan;4 Suppl 1:93-5. doi: 10.1007/BF00053436.
2
Incidence and clinical relevance of QT prolongation caused by the new selective serotonin antagonist ketanserin.新型选择性5-羟色胺拮抗剂酮色林所致QT间期延长的发生率及临床相关性。
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3
Incidence and clinical relevance of QT prolongation caused by the new selective serotonin antagonist ketanserin. Multicenter Ketanserin Research Group.新型选择性5-羟色胺拮抗剂酮色林所致QT间期延长的发生率及临床相关性。多中心酮色林研究组
Clin Physiol Biochem. 1990;8 Suppl 3:90-100.
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Prevention of atherosclerotic complications: controlled trial of ketanserin. Prevention of Atherosclerotic Complications with Ketanserin Trial Group.动脉粥样硬化并发症的预防:酮色林对照试验。酮色林预防动脉粥样硬化并发症试验组。
BMJ. 1989 Feb 18;298(6671):424-30. doi: 10.1136/bmj.298.6671.424.
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Effects of short-term ketanserin treatment on the QT interval and vagal function in healthy subjects.短期服用酮色林对健康受试者QT间期和迷走神经功能的影响。
J Auton Pharmacol. 1989 Feb;9(1):45-51. doi: 10.1111/j.1474-8673.1989.tb00195.x.
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QT prolongation and torsade de pointes ventricular tachycardia produced by Ketanserin.酮色林引起的QT间期延长和尖端扭转型室性心动过速。
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Retrospective analyses for hypothesis generation. A commentary on the PACK trial (prevention of atherosclerotic complications with ketanserin).用于假设生成的回顾性分析。关于PACK试验(酮色林预防动脉粥样硬化并发症)的述评。
Clin Exp Hypertens A. 1989;11(5-6):1117-36. doi: 10.3109/10641968909035395.
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[Cardiac interactions between ketanserin and the calcium antagonist nifedipine].[酮色林与钙拮抗剂硝苯地平之间的心脏相互作用]
Schweiz Med Wochenschr. 1992 Nov 7;122(45):1723-7.
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Ventricular arrhythmias and QT-prolongation during therapy with ketanserin: report of a case.酮色林治疗期间的室性心律失常和QT间期延长:一例报告。
Acta Cardiol. 1989;44(5):431-7.
10
Prolongation of the QT interval by ketanserin.酮色林导致QT间期延长。
Postgrad Med J. 1988 Feb;64(748):112-7. doi: 10.1136/pgmj.64.748.112.

引用本文的文献

1
A placebo-controlled crossover study of ketanserin in elderly hypertensive patients.酮色林在老年高血压患者中的安慰剂对照交叉研究。
Cardiovasc Drugs Ther. 1990 Jan;4 Suppl 1:115-7. doi: 10.1007/BF00053441.
2
Ketanserin. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential in hypertension and peripheral vascular disease.酮色林。对其药效学和药代动力学特性以及在高血压和外周血管疾病中的治疗潜力的综述。
Drugs. 1990 Dec;40(6):903-49. doi: 10.2165/00003495-199040060-00010.

本文引用的文献

1
Receptor binding profile of R 41 468, a novel antagonist at 5-HT2 receptors.新型5-羟色胺2受体拮抗剂R 41 468的受体结合情况
Life Sci. 1981 Mar 2;28(9):1015-22. doi: 10.1016/0024-3205(81)90747-5.
2
Inhibition of 5-hydroxytryptamine-induced and -amplified human platelet aggregation by ketanserin (R 41 468), a selective 5-HT2-receptor antagonist.酮色林(R 41 468),一种选择性5-HT2受体拮抗剂,对5-羟色胺诱导和增强的人血小板聚集的抑制作用。
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冠心病猝死的研究方法。
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Serotoninergic mechanisms in hypertension. Focus on the effects of ketanserin.高血压中的5-羟色胺能机制。聚焦于酮色林的作用。
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Prevention of atherosclerotic complications: controlled trial of ketanserin. Prevention of Atherosclerotic Complications with Ketanserin Trial Group.动脉粥样硬化并发症的预防:酮色林对照试验。酮色林预防动脉粥样硬化并发症试验组。
BMJ. 1989 Feb 18;298(6671):424-30. doi: 10.1136/bmj.298.6671.424.
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Cardiac electrophysiologic effects of intravenous ketanserin in humans.静脉注射酮色林对人体心脏电生理的影响。
J Cardiovasc Pharmacol. 1987;10 Suppl 3:S81-5.
7
The two-period cross-over clinical trial.两阶段交叉临床试验。
Br J Clin Pharmacol. 1979 Jul;8(1):7-20. doi: 10.1111/j.1365-2125.1979.tb05903.x.