Kakko Johan, von Wachenfeldt Joachim, Svanborg Kerstin Dybrandt, Lidström Jessica, Barr Christina S, Heilig Markus
Department of Clinical Neuroscience, Karolinska Institute, Stockholm, Sweden.
Biol Psychiatry. 2008 Jan 15;63(2):172-7. doi: 10.1016/j.biopsych.2007.05.001. Epub 2007 Sep 11.
Heroin dependence is associated with a hyperactive hypothalamic-pituitary-adrenal (HPA) axis, proposed as a biological correlate of craving. Maintenance treatment with methadone normalizes HPA axis activity. Here, we examined HPA axis activity under maintenance treatment with the increasingly utilized partial opiate agonist buprenorphine.
Responses to a metyrapone challenge were compared in 20 buprenorphine-maintained heroin addicts and 20 healthy volunteers (10 received a single 50 mg naltrexone dose [NTX+] and 10 received no naltrexone [NTX-]). Patients were 16 male subjects and 4 female subjects, aged 30 to 38 years, heroin-dependent and relapse-free under buprenorphine maintenance (BUP) for a minimum of 6 months. Healthy volunteers were 9 male subjects and 11 female subjects, aged 36 to 49 years, with no history of dependence. Serial measures were obtained of plasma adrenocorticotropic hormone (ACTH) and cortisol and Profile of Mood States (POMS) ratings over time. Subjects were genotyped for the OPRM1 118A/G polymorphism.
Buprenorphine maintenance showed a dampened HPA axis response to metyrapone, with OPRM1 118G carriers showing a significantly attenuated response compared with 118A carriers. The response of the NTX+ group was markedly increased. In contrast, negative affect was elevated in the BUP group but did not differ between NTX- and NTX+. Buprenorphine maintenance and NTX- groups did not differ in positive affect, whereas the NTX+ group was lower.
In contrast to exaggerated HPA axis responsiveness reported in untreated heroin dependence, response to metyrapone was subnormal in heroin addicts maintained on buprenorphine. Despite this, increased measures of negative affect were seen in this group. This implies a dissociation of HPA axis responsiveness and affect in heroin dependence.
海洛因依赖与下丘脑 - 垂体 - 肾上腺(HPA)轴功能亢进有关,这被认为是渴望的生物学关联。美沙酮维持治疗可使HPA轴活动正常化。在此,我们研究了在越来越多地使用的部分阿片类激动剂丁丙诺啡维持治疗下的HPA轴活动。
比较了20名接受丁丙诺啡维持治疗的海洛因成瘾者和20名健康志愿者(10名接受单次50mg纳曲酮剂量[NTX +],10名未接受纳曲酮[NTX -])对甲吡酮激发试验的反应。患者为16名男性和4名女性,年龄在30至38岁之间,依赖海洛因且在丁丙诺啡维持治疗(BUP)下至少6个月未复发。健康志愿者为9名男性和11名女性,年龄在36至49岁之间,无依赖史。随着时间的推移,连续测量血浆促肾上腺皮质激素(ACTH)、皮质醇以及情绪状态量表(POMS)评分。对受试者进行OPRM1 118A/G多态性基因分型。
丁丙诺啡维持治疗显示对甲吡酮的HPA轴反应减弱,与118A携带者相比,OPRM1 118G携带者的反应明显减弱。NTX +组的反应明显增强。相比之下,BUP组的消极情绪升高,但NTX -组和NTX +组之间没有差异。BUP维持治疗组和NTX -组在积极情绪方面没有差异,而NTX +组较低。
与未经治疗的海洛因依赖中报道的HPA轴反应过度不同,接受丁丙诺啡维持治疗的海洛因成瘾者对甲吡酮的反应低于正常水平。尽管如此,该组中消极情绪的测量值有所增加。这意味着在海洛因依赖中HPA轴反应性与情绪之间存在分离。