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首页> 外文期刊>Journal of pharmacological sciences. >QT PRODACT: In Vivo QT Assay With a Conscious Monkey for Assessment of the Potential for Drug-Induced QT Interval Prolongation
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QT PRODACT: In Vivo QT Assay With a Conscious Monkey for Assessment of the Potential for Drug-Induced QT Interval Prolongation

机译:QT PRODACT:体内QT分析,用一只有意识的猴子评估药物诱导的QT间隔延长的可能性

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References(51) Cited-By(46) Supplementary materials(3) In safety pharmacology studies, the effects on the QT interval of electrocardiograms are routinely assessed using a telemetry system in cynomolgus monkeys. However, there is a lack of integrated databases concerning in vivo QT assays in conscious monkeys. As part of QT Interval Prolongation: Project for Database Construction (QT PRODACT), the present study examined 10 positive compounds with the potential to prolong the QT interval and 6 negative compounds considered to have no such effect on humans. The experiments were conducted at 7 facilities in accordance with a standard protocol established by QT PRODACT. The vehicle or 3 doses of each test compound were administered orally to male cynomolgus monkeys (n = 3 – 4), and telemetry signals were recorded for 24 h. None of the negative compounds prolonged the corrected QT using Bazett’s formula (QTcB) interval. On the other hand, almost all of the positive compounds prolonged the QTcB interval, but haloperidol, terfenadine, and thioridazine did not. The failure to detect the QTcB interval prolongation appeared to be attributable for the differences in metabolism between species and/or disagreement with Bazett’s formula for tachycardia. In the cynomolgus monkeys, astemizole induced Torsade de Pointes and cisapride caused tachyarrhythmia at lower plasma concentrations than those observed in humans and dogs. These results suggest that in vivo QT assays in conscious monkeys represent a useful model for assessing the risks of drug-induced QT interval prolongation. Supplementary material (Appendix): available only at http://dx.doi.org/10.1254/jphs.QT-A4
机译:参考文献(51)被引用的文献(46)补充材料(3)在安全药理研究中,常规使用遥测系统评估食蟹猴对心电图QT间隔的影响。然而,缺乏关于清醒猴子体内QT测定的综合数据库。作为“ QT间隔延长:数据库建设项目”(QT PRODACT)的一部分,本研究研究了10种可能延长QT间隔的阳性化合物和6种对人类无此影响的阴性化合物。根据QT PRODACT建立的标准协议,在7个设施中进行了实验。对雄性食蟹猴(n = 3-4)口服施用媒介物或每种试验化合物3剂,并记录遥测信号24小时。没有一种阴性化合物使用巴泽特公式(QTcB)间隔延长校正的QT。另一方面,几乎所有阳性化合物都延长了QTcB间隔,但是氟哌啶醇,特非那定和硫代哒嗪却没有。无法检测到QTcB间隔延长似乎是由于物种之间的代谢差异和/或与Bazett的心动过速公式不同所致。在食蟹猴中,阿司咪唑引起的尖锐湿疣和西沙必利引起的心律失常的血浆浓度低于人和狗所观察到的浓度。这些结果表明,在有意识的猴子中进行体内QT检测代表了评估药物诱导的QT间隔延长风险的有用模型。补充材料(附录):仅在http://dx.doi.org/10.1254/jphs.QT-A4提供

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