Effects of escitalopram on attentional bias to cocaine-related stimuli and inhibitory control in cocaine-dependent subjects. (September 2013)

• Record Type: Journal Article
• Authors: Liu, Shijing; Lane, Scott D; Schmitz, Joy M; Cunningham, Kathryn A; John, Vineeth P; Moeller, F Gerard
• Is Part Of: Journal of psychopharmacology. Volume 27:Number 9(2013)
• Page Start: 801
• Page End: 807
• Publication Date: 2013-09
• Subjects: Escitalopram -- attentional bias -- cocaine Stroop task -- inhibitory control -- cocaine dependence; Psychopharmacology -- Periodicals; 615.78
• DOI: 10.1177/0269881113492898
• Languages: English
• ISSNs: 0269-8811

Abstract

Key characteristics of cocaine dependence include attentional bias to cocaine cues and impaired inhibitory control. Studies suggest that serotonin modulates both cocaine cue reactivity and inhibitory control. We investigated effects of the selective serotonin reuptake inhibitor escitalopram on cocaine cue reactivity and inhibitory processes in cocaine-dependent subjects. In a double-blind placebo-controlled design, cocaine-dependent subjects received placebo ( n =12) or escitalopram ( n =11; 10 mg on days 1–3, 20 mg on days 4–24 and 10 mg on days 25–28) orally, once daily for 4 weeks. The cocaine Stroop and immediate memory task (IMT) were administered at baseline, days 1, 4, 11, 18 and 25 after placebo or escitalopram initiation. There were no significant between-group differences in baseline performance on the cocaine Stroop task or the IMT. On day 1 (acute phase), escitalopram produced a significantly greater decrease from baseline than placebo in attentional bias measured by cocaine Stroop task 5 hours post-dose. No significant changes from baseline in attentional bias were observed on subsequent test days (chronic phase). Inhibitory control as measured by IMT commission error rate was not significantly different between two groups in either the acute or chronic phase. Consistent with preclinical data, serotonin-modulating drugs like escitalopram may have acute effects on cocaine cue reactivity in human cocaine users.