Kranzler H R, Modesto-Lowe V, Nuwayser E S
Alcohol Research Center, Department of Psychiatry, University of Connecticut Health Center, Farmington 06030-2103, USA.
Alcohol Clin Exp Res. 1998 Aug;22(5):1074-9.
This 12-week study examined the bioavailability, tolerability, and potential efficacy of an injectable sustained-release preparation (SRP) of naltrexone (NTX). Twenty alcohol-dependent subjects took NTX 50 mg po daily for 2 weeks, followed by a 2-week, no-medication Washout Period, a 4-week Injection Period, and a 4-week Follow-up Period. Fifteen subjects (75%) received a single subcutaneous injection of 206 mg of sustained-release NTX, and five subjects (25%) received a placebo injection. All subjects also received eight weekly coping skills sessions during the Oral NTX, and the Washout and Injection Periods.
After injection, NTX plasma concentrations exceeded a mean of 1 ng/ml for 21 days. Adverse effects produced by the SRP of NTX were comparable with those resulting from oral NTX therapy. Compared with placebo, the SRP of NTX significantly reduced the frequency of heavy drinking days during the Injection and Follow-up Periods.
The results of this preliminary study support the potential clinical utility of the SRP of NTX for treatment of alcohol dependence.
这项为期12周的研究考察了纳曲酮(NTX)注射用缓释制剂(SRP)的生物利用度、耐受性和潜在疗效。20名酒精依赖受试者每日口服50毫克NTX,持续2周,随后是为期2周的无药物洗脱期、4周的注射期和4周的随访期。15名受试者(75%)接受了一次206毫克缓释NTX的皮下注射,5名受试者(25%)接受了安慰剂注射。在口服NTX、洗脱期和注射期,所有受试者还接受了为期八周的应对技能培训。
注射后,NTX血浆浓度在21天内超过平均1纳克/毫升。NTX缓释制剂产生的不良反应与口服NTX治疗产生的不良反应相当。与安慰剂相比,NTX缓释制剂在注射期和随访期显著降低了重度饮酒天数的频率。
这项初步研究的结果支持NTX缓释制剂治疗酒精依赖的潜在临床效用。