Lynch J J, Wilson A W, Hernandez L E, Nelson R A, Marsh K C, Cox B F, Mittelstadt S W
Department of Integrative Pharmacology, Global Pharmaceutical Research and Development, Abbott Laboratories, Abbott Park, IL 60064-6119, USA.
Br J Pharmacol. 2008 Aug;154(7):1439-45. doi: 10.1038/bjp.2008.206. Epub 2008 Jun 2.
The non-selective beta-adrenoceptor antagonist, D,L-sotalol (sotalol) is commonly employed as a positive control during preclinical cardiovascular safety pharmacology testing, mainly because of its ability to prolong QT interval duration. However, no information appears in the literature, except in abstract form, regarding the dose-response effects of sotalol in unanesthetized monkeys. The current study was conducted to determine the dose- and plasma-response effects of orally administered sotalol on cardiovascular function in conscious non-human primates.
Male cynomolgus monkeys were implanted with telemetry devices and the effects of sotalol hydrochloride (5, 10 and 30 mg kg(-1) of body weight, p.o.) on arterial blood pressure, heart rate, body temperature and electrocardiogram waveform were continuously monitored for 6 h after dosing. Blood was sampled for the measurement of plasma concentrations of sotalol.
Sotalol dose dependently decreased heart rate and prolonged RR, PR, QT and corrected QT intervals, while having little or no effects on the QRS complex, arterial pressure or body temperature, over the dose range tested. When the data were related to plasma concentrations of sotalol, it was clear that the cardiovascular effects occurred in a similar pattern and to a comparable degree as those reported in human studies.
The current study helps demonstrate the validity of utilizing telemetry-instrumented non-human primates for the cardiovascular safety pharmacology assessment of drugs prior to first-in-human testing, and its findings may serve as a reference source for the dose- and plasma-response effects of orally administered sotalol in conscious monkeys.
非选择性β肾上腺素能受体拮抗剂D,L-索他洛尔(索他洛尔)在临床前心血管安全药理学测试中通常用作阳性对照,主要是因为它能够延长QT间期。然而,除了摘要形式外,文献中没有关于索他洛尔在未麻醉猴子中的剂量反应效应的信息。本研究旨在确定口服索他洛尔对清醒非人类灵长类动物心血管功能的剂量和血浆反应效应。
雄性食蟹猴植入遥测装置,给药后连续6小时监测盐酸索他洛尔(5、10和30mg/kg体重,口服)对动脉血压、心率、体温和心电图波形的影响。采集血液用于测定索他洛尔的血浆浓度。
在所测试的剂量范围内,索他洛尔剂量依赖性地降低心率,延长RR、PR、QT和校正QT间期,而对QRS波群、动脉压或体温几乎没有影响。当数据与索他洛尔的血浆浓度相关时,很明显心血管效应的发生模式和程度与人类研究报告的相似。
本研究有助于证明在首次人体试验前利用遥测仪器化的非人类灵长类动物进行药物心血管安全药理学评估的有效性,其结果可作为清醒猴子口服索他洛尔的剂量和血浆反应效应的参考来源。