Ciraulo Domenic A, Knapp Clifford, Rotrosen John, Sarid-Segal Ofra, Ciraulo Ann Marie, LoCastro Joseph, Greenblatt David J, Leiderman Deborah
Division of Psychiatry, Boston University School of Medicine, VA Boston Healthcare System Medication Development Research Unit (MDRU), Boston, MA, USA.
Addiction. 2005 Mar;100 Suppl 1:23-31. doi: 10.1111/j.1360-0443.2005.00984.x.
In the current study, nefazodone, an antidepressant with dual action on serotonin and norepinephrine reuptake as well as 5-HT(2A) receptor antagonist effects, was studied in subjects with cocaine dependence and depressive symptoms, to determine its efficacy in reducing cocaine use.
An 8-week, double blind, placebo-controlled design was used.
The study was conducted at the Medication Development Research Unit (MDRU) at the VA Boston Healthcare System and the Manhattan Department of Veterans Affairs (DVA) Medical Center.
Subjects (n = 69) met Diagnostic and Statistical Manual version IV (DSM-IV) criteria for cocaine dependence and had Hamilton Depression Scores of 12 or higher.
Subjects were assigned randomly to receive nefazodone 200 mg twice daily (n = 34) or matching placebo (n = 35). All subjects received individual counseling.
Urinary measurements of benzoylecgonine (BE, three times per week) and self-reports of cocaine use were the primary outcome measures. Secondary outcome measures included assessments of psychiatric functioning, cocaine craving and social functioning.
Median weekly BE declined more rapidly in the nefazodone than in the placebo group. Median urine BE at baseline was, however, significantly greater in nefazodone than in the placebo group. Scores for strength of cocaine craving also decreased more rapidly in the nefazodone group compared to the placebo group. Both groups had equivalent improvement in mood, psychosocial functioning and self-reported cocaine use.
These results suggest that nefazodone administration can reduce cocaine craving after it has been administered for several weeks. Although the nefazodone group had a greater rate of decrease in BE levels than the placebo group, the interpretation of this finding is obscured by significant group differences in baseline BE levels.
在本研究中,对具有5-羟色胺和去甲肾上腺素再摄取双重作用以及5-羟色胺2A(5-HT(2A))受体拮抗效应的抗抑郁药奈法唑酮进行了研究,以确定其在减少可卡因依赖和抑郁症状患者使用可卡因方面的疗效。
采用为期8周的双盲、安慰剂对照设计。
该研究在波士顿退伍军人事务部医疗系统的药物开发研究室(MDRU)和曼哈顿退伍军人事务部(DVA)医疗中心进行。
69名受试者符合《精神疾病诊断与统计手册》第四版(DSM-IV)可卡因依赖标准,汉密尔顿抑郁评分在12分及以上。
受试者被随机分配接受每日两次200毫克奈法唑酮治疗(n = 34)或匹配的安慰剂治疗(n = 35)。所有受试者均接受个体咨询。
主要测量指标为尿中苯甲酰爱康宁(BE,每周三次)的测定以及可卡因使用的自我报告。次要测量指标包括精神功能、对可卡因的渴望和社会功能的评估。
与安慰剂组相比,奈法唑酮组尿BE中位数下降更快。然而,奈法唑酮组基线时的尿BE中位数显著高于安慰剂组。与安慰剂组相比,奈法唑酮组对可卡因渴望强度的评分下降也更快。两组在情绪、心理社会功能和自我报告的可卡因使用方面均有同等程度的改善。
这些结果表明奈法唑酮给药数周后可减少对可卡因的渴望。尽管奈法唑酮组BE水平下降率高于安慰剂组,但由于两组基线BE水平存在显著差异,这一结果的解释受到影响。