Pharmacokinetics and Safety Assessment of l-Tetrahydropalmatine in Cocaine Users: A Randomized, Double-Blind, Placebo-Controlled Study.

IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Journal of clinical pharmacology Pub Date : 2017-02-01 Epub Date: 2016-08-04 DOI:10.1002/jcph.789
Hazem E Hassan, Deanna Kelly, Moshe Honick, Sagar Shukla, Ahmed Ibrahim, David A Gorelick, Matthew Glassman, Robert P McMahon, Heidi J Wehring, Ann Marie Kearns, Stephanie Feldman, Mingming Yu, Ken Bauer, Jia Bei Wang
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引用次数: 21

Abstract

Cocaine use disorder (CUD) remains a significant public health challenge. l-Tetrahydropalmatine (l-THP), a well-tolerated and nonaddictive compound, shows promise for the management of CUD. Its pharmacologic profile includes blockade at dopamine and other monoamine receptors and attenuation of cocaine self-administration, reinstatement, and rewarding properties in rats. This study evaluated the safety of l-THP in human cocaine users and its influence on the safety and pharmacokinetics (PK) of cocaine. Twenty-four cocaine-using adult men were randomized to receive l-THP (30 mg twice a day orally) or placebo double-blind for 4 days, with an intranasal cocaine (40 mg) challenge on the fourth day. Safety and tolerability were evaluated using vital signs, ECG, clinical laboratory tests, and standardized self-report instruments. Peripheral venous blood was collected periodically and later assayed for l-THP and cocaine using highly sensitive and specific ultraperformance liquid chromatography-fluorescence detection (UPLC-FLD) methods. Twenty subjects completed the study, of whom 19 provided complete PK data. The short 3.5-day course of l-THP was safe and well tolerated and did not affect cocaine's PK or its acute cardiovascular effects. The cocaine AUC0→∞ was 211.5 and 261.4 h·ng/mL, and the Cmax was 83.3 and 104.5 ng/mL for the l-THP and placebo groups, respectively. In addition there were no significant differences in the number of side effects reported in each group (l-THP group 22 [48%], placebo group 24 [52%]) or vital signs including, heart rate, blood pressure, complete blood count, or ECG. These findings suggest that oral THP has promise for further development as a treatment for CUD.

Abstract Image

l-四氢巴马汀在可卡因使用者体内的药代动力学和安全性评估:一项随机、双盲、安慰剂对照研究。
可卡因使用障碍(CUD)仍然是一个重大的公共卫生挑战。l-四氢巴马汀(l-THP)是一种耐受性良好且不会上瘾的化合物,有望用于治疗CUD。其药理学特征包括阻断多巴胺和其他单胺受体,减弱可卡因在大鼠体内的自我给药、恢复和奖励特性。本研究评估了l-THP在人类可卡因使用者中的安全性及其对可卡因安全性和药代动力学(PK)的影响。24名使用可卡因的成年男性随机接受l-THP(30毫克,每天两次口服)或安慰剂双盲治疗4天,第4天鼻内注射可卡因(40毫克)。使用生命体征、心电图、临床实验室检查和标准化自我报告仪器评估安全性和耐受性。定期采集外周静脉血,采用高灵敏、特异的超高效液相色谱-荧光检测(UPLC-FLD)方法检测l-THP和可卡因。20名受试者完成了研究,其中19人提供了完整的PK数据。3.5天的l-THP疗程是安全且耐受性良好的,不影响可卡因的PK或其急性心血管效应。l-THP组和安慰剂组的可卡因AUC0→∞分别为211.5和261.4 h·ng/mL, Cmax分别为83.3和104.5 ng/mL。此外,两组报告的副作用数量(l-THP组22例[48%],安慰剂组24例[52%])或包括心率、血压、全血细胞计数或心电图在内的生命体征无显著差异。这些发现表明口服THP作为CUD的治疗有进一步发展的希望。
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来源期刊
CiteScore
5.10
自引率
3.40%
发文量
176
审稿时长
2 months
期刊介绍: The Journal of Clinical Pharmacology (JCP) is a Human Pharmacology journal designed to provide physicians, pharmacists, research scientists, regulatory scientists, drug developers and academic colleagues a forum to present research in all aspects of Clinical Pharmacology. This includes original research in pharmacokinetics, pharmacogenetics/pharmacogenomics, pharmacometrics, physiologic based pharmacokinetic modeling, drug interactions, therapeutic drug monitoring, regulatory sciences (including unique methods of data analysis), special population studies, drug development, pharmacovigilance, womens’ health, pediatric pharmacology, and pharmacodynamics. Additionally, JCP publishes review articles, commentaries and educational manuscripts. The Journal also serves as an instrument to disseminate Public Policy statements from the American College of Clinical Pharmacology.
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