Clonidine blocks stress-induced craving in cocaine users.
Clonidine blocks stress-induced craving in cocaine users.
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DOI:
10.1007/s00213-011-2230-7
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发表时间:
2011-11
影响因子:
3.4
通讯作者:
Preston, Kenzie L.
中科院分区:
文献类型:
--
作者:
Jobes, Michelle L.;Ghitza, Udi E.;Epstein, David H.;Phillips, Karran A.;Heishman, Stephen J.;Preston, Kenzie L.
Reactivity to stressors and environmental cues, a putative cause of relapse in addiction, may be a useful target for relapse-prevention medication. In rodents, alpha-2 adrenergic agonists such as clonidine block stress-induced reinstatement of drug seeking, but not drug cue-induced reinstatement. The objective of this study is to test the effect of clonidine on stress- and cue-induced craving in human cocaine users. Healthy, non-treatment-seeking cocaine users (n = 59) were randomly assigned to three groups receiving clonidine 0, 0.1, or 0.2 mg orally under double-blind conditions. In a single test session, each participant received clonidine or placebo followed 3 h later by exposure to two pairs of standardized auditory-imagery scripts (neutral/stress and neutral/drug). Subjective measures of craving were collected. Subjective responsivity (“crave cocaine” Visual Analog Scale) to stress scripts was significantly attenuated in the 0.1- and 0.2-mg clonidine groups; for drug-cue scripts, this attenuation occurred only in the 0.2-mg group. Other subjective measures of craving showed similar patterns of effects but Dose × Script interactions were not significant. Clonidine was effective in reducing stress-induced (and, at a higher dose, cue-induced) craving in a pattern consistent with preclinical findings, although this was significant on only one of several measures. Our results, though modest and preliminary, converge with other evidence to suggest that alpha-2 adrenergic agonists may help prevent relapse in drug abusers experiencing stress or situations that remind them of drug use.
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影响因子:
120.7
作者:
MCLELLAN, AT;ARNDT, IO;OBRIEN, CP
通讯作者:
OBRIEN, CP
影响因子:
3.4
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Erb, S;Shaham, Y;Stewart, J
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Stewart, J
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6
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Carter, BL;Tiffany, ST
通讯作者:
Tiffany, ST
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3.4
作者:
EHRMAN, RN;ROBBINS, SJ;OBRIEN, CP
通讯作者:
OBRIEN, CP
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作者:
Kilts, CD;Schweitzer, JB;Drexler, KPG
通讯作者:
Drexler, KPG