Correia Christopher J, Walsh Sharon L, Bigelow George E, Strain Eric C
Behavioral Pharmacology Research Unit, Johns Hopkins University School of Medicine, 5510 Nathan Shock Drive, Baltimore, MD 21224, USA.
Psychopharmacology (Berl). 2006 Dec;189(3):297-306. doi: 10.1007/s00213-006-0571-4. Epub 2006 Sep 30.
Buprenorphine has a long duration of action that allows less than daily dosing for opioid dependence, but pharmacologic characterization of buprenorphine's duration of effects over multiple days is incomplete.
This study assessed opioid blockade and spontaneous withdrawal effects of buprenorphine/naloxone (B/N) over a 98-h period.
Residential opioid-dependent volunteers (n = 8) were maintained, in randomized sequence, on each of three different daily sublingual B/N doses (8/2, 16/4, 32/8 mg). After 2 weeks on each maintenance dose, participants underwent challenge sessions on each weekday for 1 week. Challenges consisted of within-session, ascending dose administration of IM hydromorphone (H: 0, 6, and 12 mg). During that week, active B/N dose was given only on Monday; double-blind placebo was administered on the remaining weekdays. Thus, these sessions assessed the extent of both opioid blockade and spontaneous withdrawal at 2, 26, 50, 74, and 98 h after the last active B/N dose.
All three maintenance doses provided substantial but incomplete blockade against opioid agonist effects for 98 h. The extent of blockade diminished steadily but modestly over this time and did not differ as a function of B/N maintenance dose. In general, participants did not report marked spontaneous opioid withdrawal, although mild withdrawal effects were observed as time since the last active B/N dose increased. However, withdrawal did not differ as a function of B/N maintenance dose.
These findings suggest that B/N doses greater than 8/2 mg provide minimal incremental value in terms of opioid blockade and withdrawal suppression.
丁丙诺啡作用持续时间长,用于阿片类药物依赖时可减少每日给药次数,但丁丙诺啡多日效应的药理学特征尚不完全明确。
本研究评估了丁丙诺啡/纳洛酮(B/N)在98小时内的阿片类药物阻断和自发戒断效应。
居住的阿片类药物依赖志愿者(n = 8)按随机顺序接受三种不同的每日舌下B/N剂量(8/2、16/4、32/8毫克)维持治疗。每种维持剂量治疗2周后,参与者在每个工作日进行为期1周的激发试验。激发试验包括在试验期间递增剂量注射肌内注射氢吗啡酮(H:0、6和12毫克)。在那一周,仅在周一给予活性B/N剂量;其余工作日给予双盲安慰剂。因此,这些试验评估了最后一次活性B/N剂量后2、26、50、74和98小时的阿片类药物阻断和自发戒断程度。
所有三种维持剂量在98小时内均提供了显著但不完全的阿片类激动剂效应阻断。在此期间,阻断程度稳步但适度下降,且与B/N维持剂量无关。总体而言,参与者未报告明显的自发阿片类戒断症状,尽管随着距最后一次活性B/N剂量时间的增加,观察到了轻微的戒断效应。然而,戒断效应与B/N维持剂量无关。
这些发现表明,大于8/2毫克的B/N剂量在阿片类药物阻断和戒断抑制方面提供的增量价值最小。