The Effects of Alcohol on the Pharmacokinetics and Pharmacodynamics of the Selective Mu-Opioid Receptor Antagonist GSK1521498 in Healthy Subjects

被引:9
作者
Ziauddeen, Hisham [1 ,2 ,10 ,11 ]
Nathan, Pradeep J. [1 ,2 ,3 ]
Dodds, Chris [1 ]
Maltby, Kay [1 ]
Miller, Sam R. [1 ,6 ]
Waterworth, Dawn [4 ]
Song, Kijoung [4 ]
Warren, Liling [5 ]
Hosking, Louise [6 ]
Zucchetto, Mauro [7 ]
Bush, Mark [8 ]
Johnson, Lakshmi Vasist [8 ]
Sarai, Bhopinder [1 ]
Mogg, Karin [9 ]
Bradley, Brendan P. [9 ]
Richards, Duncan B. [12 ]
Fletcher, Paul C. [2 ,10 ,11 ]
Bullmore, Edward T. [1 ,2 ,11 ,12 ]
机构
[1] GlaxoSmithKline, Med Discovery & Dev, Clin Unit Cambridge, Addenbrookes Ctr Clin Invest, Cambridge, England
[2] Univ Cambridge, Dept Psychiat, Behav & Clin Neurosci Inst, Cambridge, England
[3] Monash Univ, Sch Psychol & Psychiat, Clayton, Vic, Australia
[4] GlaxoSmithKline, Projects Clin Platforms & Sci, King Of Prussia, PA USA
[5] GlaxoSmithKline, Projects Clin Platforms & Sci, Res Triangle Pk, NC USA
[6] GlaxoSmithKline, Projects Clin Platforms & Sci, Stevenage, Herts, England
[7] GlaxoSmithKline Res & Dev Ltd, Med Res Ctr, Stevenage, Herts, England
[8] Kinetigen, Res Triangle Pk, NC USA
[9] Univ Southampton, Dept Psychol, Southampton SO9 5NH, Hants, England
[10] Univ Cambridge, Inst Metab Sci, Metab Res Labs, Cambridge, England
[11] Cambridgeshire & Peterborough NHS Fdn Trust CPFT, Cambridge, England
[12] GlaxoSmithKline, Acad Discovery Performance Unit, Addenbrookes Ctr Clin Invest, Cambridge, England
基金
英国惠康基金;
关键词
mu-opioid receptor; pharmacokinetics; pharmacodynamics; safety; OPRM1; pharmacogenetics; alcohol; addiction; DOSE SAFETY; NALTREXONE; ASSOCIATION; VALIDATION; DEPENDENCE; ADDICTION; ETHANOL; ANXIETY; SEEKING; SYSTEM;
D O I
10.1002/jcph.110
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The mu-opioid system has a key role in hedonic and motivational processes critical to substance addiction. However, existing mu-opioid antagonists have had limited success as anti-addiction treatments. GSK1521498 is a selective and potent mu-opioid antagonist being developed for the treatment of overeating and substance addictions. In this study, 28 healthy participants were administered single doses of GSK1521498 20mg, ethanol 0.5g/kg body weight, or both in combination, in a double blind placebo controlled four-way crossover design. The primary objective was to determine the risk of significant adverse pharmacodynamic and pharmacokinetic (PK) interactions. The effects of GSK1521498 on hedonic and consummatory responses to alcohol and the attentional processing of alcohol-related stimuli, and their modulation by the OPRM1 A118G polymorphism were also explored. GSK1521498 20mg was well tolerated alone and in combination with ethanol. There were mild transient effects of GSK1521498 on alertness and mood that were greater when it was combined with ethanol. These effects were not of clinical significance. There were no effects of GSK1521498 on reaction time, hedonic or consummatory responses. These findings provide encouraging safety and PK data to support continued development of GSK1521498 for the treatment of alcohol addiction.
引用
收藏
页码:1078 / 1090
页数:13
相关论文
共 40 条
[1]  
[Anonymous], 2005, PROFILE MOOD STATES
[2]   Naltrexone Modification of Drinking Effects in a Subacute Treatment and Bar-Lab Paradigm: Influence of OPRM1 and Dopamine Transporter (SLC6A3) Genes [J].
Anton, Raymond F. ;
Voronin, Konstantin K. ;
Randall, Patrick K. ;
Myrick, Hugh ;
Tiffany, Abraham .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2012, 36 (11) :2000-2007
[3]   Combined pharmacotherapies and behavioral interventions for alcohol dependence - The COMBINE study: A randomized controlled trial [J].
Anton, RF ;
O'Malley, SS ;
Ciraulo, DA ;
Cisler, RA ;
Couper, D ;
Donovan, DM ;
Gastfriend, DR ;
Hosking, JD ;
Johnson, BA ;
LoCastro, JS ;
Longabaugh, R ;
Mason, BJ ;
Mattson, ME ;
Miller, WR ;
Pettinati, HM ;
Randall, CL ;
Swift, R ;
Weiss, RD ;
Williams, LD ;
Zweben, A .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2006, 295 (17) :2003-2017
[4]   Naltrexone effects on alcohol consumption in a clinical laboratory paradigm: temporal effects of drinking [J].
Anton, RF ;
Drobes, DJ ;
Voronin, K ;
Durazo-Avizu, R ;
Moak, D .
PSYCHOPHARMACOLOGY, 2004, 173 (1-2) :32-40
[5]  
Beck A.T., 1996, Manual for the BDI-II, DOI DOI 10.1037/T00742-000
[6]   DEVELOPMENT AND INITIAL VALIDATION OF A MEASURE OF DRINKING URGES IN ABSTINENT ALCOHOLICS [J].
BOHN, MJ ;
KRAHN, DD ;
STAEHLER, BA .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1995, 19 (03) :600-606
[7]   USE OF ANALOG SCALES IN RATING SUBJECTIVE FEELINGS [J].
BOND, A ;
LADER, M .
BRITISH JOURNAL OF MEDICAL PSYCHOLOGY, 1974, 47 (SEP) :211-218
[8]   Neural and Behavioral Effects of a Novel Mu Opioid Receptor Antagonist in Binge-Eating Obese People [J].
Cambridge, Victoria C. ;
Ziauddeen, Hisham ;
Nathan, Pradeep J. ;
Subramaniam, Naresh ;
Dodds, Chris ;
Chamberlain, Samuel R. ;
Koch, Annelize ;
Maltby, Kay ;
Skeggs, Andrew L. ;
Napolitano, Antonella ;
Farooqi, I. Sadaf ;
Bullmore, Edward T. ;
Fletcher, Paul C. .
BIOLOGICAL PSYCHIATRY, 2013, 73 (09) :887-894
[9]   Effects of mu opioid receptor antagonism on cognition in obese binge-eating individuals [J].
Chamberlain, Samuel R. ;
Mogg, Karin ;
Bradley, Brendan P. ;
Koch, Annelize ;
Dodds, Chris M. ;
Tao, Wenli X. ;
Maltby, Kay ;
Sarai, Bhopinder ;
Napolitano, Antonella ;
Richards, Duncan B. ;
Bullmore, Edward T. ;
Nathan, Pradeep J. .
PSYCHOPHARMACOLOGY, 2012, 224 (04) :501-509
[10]   Association of μ-opioid receptor (OPRM1) gene polymorphism with response to naltrexone in alcohol dependence: a systematic review and meta-analysis [J].
Chamorro, Antonio-Javier ;
Marcos, Miguel ;
Miron-Canelo, Jose-Antonio ;
Pastor, Isabel ;
Gonzalez-Sarmiento, Rogelio ;
Laso, Francisco-Javier .
ADDICTION BIOLOGY, 2012, 17 (03) :505-512